Basic Concepts of Muscular Conditioning Frank J. Cerny, PhD Increases in muscular strength or endurance • Neural MOTOR UNIT Basic Components • • • • – Central output – feedback • Muscle Nerve Cell Body Axon Neuromuscular Junction Muscle Fiber – Size – Characteristics Motor unit 1 Motor unit 1 + or - Motor neurons Motor neurons Motor unit 2 Motor unit 2 + or - Spinal cord Muscle fibers Descending cortical inputs (+ or -) Spinal cord Sensory input (feedback) Muscle fibers Motor unit recruitment Motor unit 1 • Dependent on speed and force of contraction + or - Motor neurons – Think specificity Motor unit 2 + or - Spinal cord Sensory input (feedback) Muscle fibers 1 Basic Concepts of Muscular Conditioning Frank J. Cerny, PhD Gating by interneurons Neural adaptations Descending cortical inputs (+ or -) • MU activation – Maximal = greater – Submaximal = fewer • MU Synchronization – Fine motor performance – Decreased variability Descending control signal Motor neuron -ve Motor unit 1 + or - +ve Motor neurons Sensory input Motor unit 2 Interneuron + or - • Muscular coordination • Within a muscle • Among muscles Muscle fibers Sensory input (feedback) Spinal cord “disinhibition” helps explain how a person can get “stronger” with resistance training without any change in size of the muscle Muscle adaptations Descending cortical inputs (+ or -) • Muscle fiber characteristics – “twitch” characteristics – Metabolic characteristics Motor unit 1 + or - Motor neurons Motor unit 2 + or - Spinal cord Muscle fibers Sensory input (feedback) Motor Unit Heterogeneity • Basic classification - Type I, IIa, IIb • Oversimplification • Human muscles have a variety of MU’s all with different characteristics • slow fast, oxidative glycolytic • provides a functional continuum Myosin ATPase stain in acid to show Type I fibers Myosin ATPase stained alkaline to show opposite 2 Basic Concepts of Muscular Conditioning Frank J. Cerny, PhD Factors to Consider when Developing a Training Program • Training quality • The specific effect of training on the muscles is dependent on the specific stimulus. – specificity • endurance • strength • Training quantity –Determine the metabolic and muscular demands and devise strategies that target those specific demands. – intensity – duration – frequency Training Overload % CHANGE TRAINING SPECIFICITY • To obtain an change in structure (strength) or function (endurance) the muscle must be taxed beyond some critical level • Progressive Increases in strength after 8 wks squat training 75 Specificity 50 25 SQUAT LEG PRESS KNEE EXTENSION Maximal Over training zone Training Rebuilding time Upper Threshold • Need recovery time Lower Threshold – The adaptive changes occur during periods of rest. • >24 hours for particularly strenuous The Overload Principle 3 Basic Concepts of Muscular Conditioning Frank J. Cerny, PhD Strength Training Conclusion Near maximum resistance • Change, or improvement, of a particular movement task • 6 - 10 repeats for best results • 2 - 4 sets for each muscle group or specific motion – Neural alterations – Muscle alterations • Specificity • overload 4 What do we Know about Exercise Based Treatments? Use it or Lose it Muscle Training Principles Influence Voice, Speech & Cough Failure to drive specific brain functions through training can lead to the degradation of that function Failure to drive muscle activity results in peripheral loss of function Christine Sapienza, Ph.D. University of Florida Brain Rehabilitation Research Center Malcom Randall VA z Kleim’ Kleim’s group and others (e.g. Vaynman & confirms that exercise training impacts molecular systems important for maintaining neural function and plasticity. z i.e. BDNF, survival and neurogenesis GomezGomez-Pinilla., 2005) But what about the science.. The concepts of strength training The challenges of developing the appropriate model to study training z The design and delivery of our methods and what we are measuring peripherally z Future design for testing changes to brain z And if we could… z z • • BUT EXERCISE IS NOT EXERCISE, IS NOT EXERCISE Results from limb and hand studies suggest that resistance/strength training, in particular,, changes the functional properties of spinal cord circuitry in humans, but does not substantially affect the organization of the motor cortex. z “Revenge of the "sit": how lifestyle impacts neuronal and cognitive health through molecular systems that interface energy metabolism with neuronal plasticity” Gomez-Pinella, 2006) plasticity” (Vaynman & Gomez“License to run: exercise impacts functional plasticity in the intact and injured central nervous system by using neurotrophins” Gomezneurotrophins” (Vaynman & Gomez- “Loud and Big, Keep on Talking and Moving… Moving… z “License for loaded breathing.. z Strength training for swallowing survival… survival…. z Pinella, 2005) z “Motor training induces experience specific patterns of plasticity across motor cortex and spinal cord” cord” (Adkins, Boychuk, Remple & Kleim, 2006 (eprint) What’s potentially changing? If this is true – should we not strength train because it may not change the brain z z z z z z z Carroll, T.J., Riek, S., & Carson, R.G. (2002). J. Physiology, 544(pt2), 641641-652. and Adkins, Boychuk, Remple & Kleim Don’t think so because even changes to corticospinal drive, changes to muscle are positive environmental changes and there is still not enough evidence….. Increased synchronization Descending drive Muscle activation Motor unit firing rates Strength Glycolytic enzymes Contractile properties of muscle including fiber type, CSA, and inorganic phosphate content (Leiber., 2002) 1 Multiple Levels of Plasticity z z z z Multiple Populations of Interest to Help and Study In those with PD That which changes brain (neural electromyographic evidence) That which changes muscle (myogenic(myogenicstructural evidence That which changes performance (behavioral) The clinical picture does not typically implicate muscle weakness z Yet, study outcomes show strength is reduced even when ample time is provided to generate force z Results point to insufficient neural activation as muscles during nerve stimulation have normal strength z Identify which level you intend to study and which mechanistic change you are defining e.g. Parkinson’ Parkinson’s disease, multiple sclerosis, spinal cord injury, laryngeal airway limitation, ataxia, TBI z Singers z Instrumentalists z z Glendinning (1994;1997) Forced Breathing Quiet expiration: begins when gravity and elastic forces act upon the ribcage, decrease lung volume, increase intrathoracic pressure (more (more than the atmospheric pressure) z Air flows out of the lungs when a balance is reached between the tendency of the chestwall to expand and the lungs to collapse. z How do we Breathe for Speech and other Tasks? Forced inspiration: accessory inspiratory muscles are recruited to help the diaphragm and the external intercostals increase the lung volume z Lung volume is increased, intrathoracic air pressure is more decreased (Much (Much less than the atmospheric pressure) pressure) z Respiratory System Forced expiration: All expiratory /abdominal muscles contract pushing against the diaphragm, which is raised z Decrease lung volume, increase intrathoracic pressure (Much more than the atmospheric pressure) z z z When we relax, diaphragm returns to its natural position (domed) The cycle is repeated-- increase in lung volume----air flows into the lungs------ Subglottal Pressure Demand Active Expiratory Mechanism 2 What happens when you have PD? Motor unit discharge is irregular z Larger number of motor units are recruited at lower thresholds z Antagonistic muscles are abnormally cocoactivated z The act of breathing is compromised by the disease state affecting anatomical sites ranging from the cerebral cortex, basal ganglia, brainstem to the alveolar sac. z Weakness of the respiratory muscles can dominate the clinical manifestations in the later stages z Structural abnormalities of the thoracic cage interfere with the action of the respiratory musclesmuscles-again in a unique manner z The hyperinflation that accompanies diseases of the airways interferes with the ability of the respiratory muscles to generate subatmospheric pressure and it increases the load on the respiratory muscles z (Glendinning & Enoka, 1994) Laghi & Tobin (2003) Reductions in Respiratory Muscle Strength z Lower airway obstruction, lower airway restriction, upper airway obstruction, and muscle weakness z Respiratory system involvement is REAL is more than what is perceived - and pneumonia is one of the common causes of death in this disorder. z z Flow Volume Loops show: Maximum Inspiratory and Expiratory Pressures Alterations in Flow and Volume 250 cmH2O 200 150 100 50 0 Actual MEP Predicted MEP (Black & Hyatt, 1969) Implementation of a Device Driven Program z From Pump to Larynx Supraglottal Laryngeal Healthy Design Intensity Matters PD Load versus No (Low) Load z Induction of plasticity (spinal or cortical) requires sufficient Is strength training with no load truly strength training or just a practice effect? z Respiratory Exercises z Vocal Exercises Silverman Voice Treatment z Expiratory Muscle Strength Training z Lee training intensity z Is it sensory or motor manipulation? Respiratory 3 Provides specific, constant,pressure load (spring loaded valve 00-150 cm/H20) Loaded Spring Hypothesized Target Muscles z Rectus abdominis, external abdominal oblique, internal abdominal oblique and transversus abdominis. Adjustable Valve Mouthpiece EMG activation during MEP Inductotrace (RC + AB) signal Result: Adaptations Defining changes? z Strength – defined by ability of muscle to move weight Progress Strength • Neural adaptations (6-8 weeks) Hypertrophy Rectus Abdominus Neural adaptations External Oblique (with likely contribution from Internal Obliques & Transverse Abdominis) • Myogenic adaptations (5+ weeks) Time Design and Delivery Current Study Maximum Expiratory Pressure Strength Defined by Changes in MEP 160 MEP Pre Post 140 200 180 160 140 120 100 80 60 40 MEP cmH20 120 Pre1 Pre2 1 2 3 4 Post (5) 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 Last cm H2O 90 Patients with PD Stage II and III Randomized Two Group Experimental (Device Driven) Sham (Modified from Sale, 1988) Baselines 100 84% increase 80 60 40 20 0 1 2 3 4 5 6 7 Subject 4 Dyspnea Scale Rating 5 4.5 4 3.5 3 2.5 2 1.5 1 0.5 0 Dyspnea Physiologic Effort Significantly Decreased Task Became Easier Improved Ability to Maintain High Levels of Ventilation During High Expiratory Loads Pre Post 1 2 3 4 5 6 7 Subglottal Pressure 1 = None; 2 = Mild; 3 = Moderate; 4 = Mod-Sever; 5 = Severe-Profound ¾ PostPost-hoc analysis indicated that the ratio of Ps to MEP decreased anywhere from 32 – 52% ¾ Proportion of subglottal pressure used relative to the MEP generated by the subjects decreased ¾ Decreased Ps/MEP ratio indicates less physiological stress because there is more reserve ¾ Relates to the decrease in sensation of breathlessness 25 Subglottal Pressure Maximizing the Container MIP (cm H20) Spinal Cord Injury 20 10 5 Tidal Volume (L) 0 ACOUSTIC CHANGE (Pre to Post IMST) % Change Sustained Vowel Production using Passy Muir Spontaneously Breathing 10 0 -10 -20 -30 -40 -50 -60 -70 -80 FF SDFF Jit Shim NHR Voice Handicap Index 48.5% Increase In MIP 15 1 2 3 1 2 3 4 Weeks 4 5 6 800 600 400 200 0 5 6 Age Matters Too Pre Post Functional 20 25 Physical 18 25 Emotional 19 24 Total 57 74 Training induced plasticity occurs more readily in the young brains and muscles z But don’ don’t ignore the old? Consider irreversible vs. reversible changes z dB SPL 5 Maximizing Performance: Reversible Muscle Changes Muscle Mass loss due to individual muscle fiber atrophy (Brooks, 2003) z Reversible and preventable through exercise MEP AND MIP Sedentary Elderly Taking advantage of reversible muscle changes z 140 •10 week balance training only vs. resistance training + balance training – • Combined group- 52% increase in strength F 1, 17 = 40.978, p < 0.001, 44% Mean ± 2SE (cm H2O) Mean +- 2 SE (cmH2O) 120 • Balance training only- 9% increase only • Improved sensory orientation • Improved balance with lesser falls (Hirsch et al., 2003) 100 110.70 ± 26.12 80 60 F 1, 17 = 18.513, p < 0.001, 49% 77.32 ± 20.12 58.42 ± 18.71 •Possible neuromuscular adaptations to reduce the abnormal agonist and antagonist muscle activation patterns 40 39.08 ± 13.18 20 MEP Post (Glendinning, 1997) MEP Pre MEP Post MIP Pre MIP Post MEP Pre MEP Pre 14 12 Cough Flow (L/s) 10 MANOVA - Wilks’ Λ = 0.351, F 5, 13 = 4.803, p = 0.010 CPD F 1, 17 = 13.590, p = 0.002, 53% PEFR F 1, 17 = 29.620, p < 0.001, 61% 6 Pre Strength Training Pre Strength Training z 2 0 -2 L/s .3 10 -6 9 14 8 12 0.35 ± 0.19 5 .1 0.16 ± 0.17 0.0 Pre Pre Post Training Post 4 Post Strength Training 8 8.00 ± 3.06 6 .2 Peak flow Lose it z Functional repercussions z Progressive loss of muscle mass z 30% loss of muscle mass from 50-80 years (Berger et al., 1988) 10 7 Pre Flow (L/s) .4 What if Nothing is Done at All? 4 -4 .5 milliseconds Peak flow 8 Post 4.89 ± 2.18 3 loss of Strength (due to force and power losses) 6 4 2 0 Pre z Progressive 1 61 121 181 241 301 361 421 481 541 601 661 721 781 841 901 961102110811141120112611321 -2 Post -4 -6 Time (msec) Current Projects Support for Cortical Plasticity z Neurogenic adaptations: TMS (Chhabra, Chhabra, Kleim, Kleim, Atkins & Pringle, Sapienza) z Examining the effects of motor experience (EMST) on the topography of movement representations in the abdominal muscles of healthy volunteers z Hypothesis: Increase in corticospinal excitability will be found with strength training increase 6 Parkinson Induced Rats Unilateral induced rats with 66-OHDA. z Multiple Aims but one Aim is: z More… z Expose to a respiratory obstructive load, via a tracheal occluder, occluder, allowing training of the respiratory muscles prior to lesion induction. This paradigm examines the presence of neuroprotective mechanisms. z Brain function will be defined by neuroanatomical analysis z IF IT WERE THIS EASY.. Future directions Translational Research Animal to Human Bench Research Exciting avenuesavenues- possibilitiespossibilities-different animal models z LimitationsLimitations- differences in fiber types of humans versus animals z How far can we stretch the animal model to answer questions in humans… humans…where do we draw the line? z z Thinking Loud Challenges (Animal) Thinking Loud z Say “ahhhh” for as long as you can Model Development z Picking the right animal data from spinal to cranial muscles z Transferring z Most work done in upper and lower extremities z Complexity of measuring cortical plasticity versus peripheral adaptations (special training for us) Say “ahhhh” for as long as you can Challenges (Human) z Model Development z Understanding the complexity of the disease measuring cortical plasticity versus peripheral adaptations z Variability in performance z Motivation z Interference (Fine line between Training and inducing Muscle Fatigue) z Complexity of 7 Translation… …. Team z z z z z z SLP Colleagues (J. Rosenbek & N. Musson) Study Coordinator (Michelle Troche, PhD student too) Neurology (M. Okun & H. Fernandez) Physiology & Physical Therapy (P. Davenport & D. Bolser) PostPost-Doc: Toni Chiara, Ph.D. Doctoral Students z Chris Carmichael z Teresa Pitts z Anuja Chhabra 8 Tongue Strengthening Exercises: Oral Motor Exercise Which Improves Swallowing JoAnne Robbins, PhD Professor, University of Wisconsin School of Medicine and Public Health Associate Director for Research Geriatric Research Education and Clinical Center (GRECC) William S. Middleton Memorial Veterans Hospital American Speech Language Hearing Association November 15, 2007 Swallowing Neural Control Swallowing: Moving food, liquid, secretions or medications from the mouth to the stomach, usually by a series of muscle contractions causing pressure changes in the aero-digestive tract Dysphagia A swallowing disorder characterized by difficulty… Lungs Esophagus Diagnostic Tools Interventions Until 1980’s: Brainstem Reflex • invariant • output at a “local” level Large scale distributed swallowing neural network Treatments Emerged: For the Patient through the environment Food Fluid Positioning By the Patient Chin tuck Head turn Jaw extension (“jaw jut”) Mendelsohn manuever Exercise Increasingly demanding (Zald & Pardo; Robbins, Annals of Neurology, 1999) 1 Exponential growth of the population of older adults: • As of July 1, 2005, there were an estimated 78.2 million American baby boomers (those born between 1946 & 1964) • In 2006, baby boomers began turning 60 at a rate of about 330 every hour • Increase in longevity = potential for increase in Years of Healthy Life (YHL) (DHHS, PHS, 1996) 1991 - 1998 Hospitalization of elderly Medicare beneficiaries for aspiration pneumonia increased by 93.5% WHY? (Baine et al. Amer J of Pub Health, 2001) Adults over age 65 swallow slower than younger counterparts Initiation of laryngeal & pharyngeal events, including: • laryngeal vestibule closure • maximal hyolaryngeal excursion • upper esophageal sphincter (UES) opening Are all delayed significantly longer relative to oral bolus transport than in younger adults. Thus, the bolus is next to an open airway longer. (Tracy et al, 1989; Robbins et al, 1992; Shaw et al,1990; Shaw et al, 1995) Neural Plasticity PRESBYPHAGIA: age-related changes in swallowing as demonstrated by healthy older individuals 56 year old female Changes in the functioning of a neural substrate and the possible alteration in behavior can be secondary to influences such as: • • • • • • • • Experience Learning Development Aging Change in use Injury Response to injury REHABILITATION (Tinazzi et al, Brain, 1998; Urasaki et al, J Clin Neurophysiol, 2005; Ziemann et al, J Neurosci, 1998) Grade = 0, Higher Cortical Grade = 1, Lower Cortical Single UBO with subcortical region (white small) (Levine, Robbins and Maser, Dysphagia, 1992) 2 Horizontal Pressure applied V e r t i c a l Hypothesize that pressure changes with age Strength as measured by pressure applied to air-filled bulb Isometric Lingual Resistance Isometric Lingual Resistance • Iowa Oral Performance Instrument (IOPI) • Press tongue to roof of mouth (isometric) • Anterior & posterior tongue • Iowa Oral Performance Instrument (IOPI) • Press tongue to roof of mouth (isometric) • Anterior & posterior tongue Isometric Pressures IOPI Protocol (3 Trials) “Press your tongue against the bulb as hard as possible” • Measured using the IOPI • One repetition maximum: highest value achieved one time only • 2 sets of 3 repetitions • Average of sets do not differ > 5% Isometric Pressure (kPa) Set 1 Set 2 32 29 28 27 • press bulb with tongue as hard as possible – maximum isometric pressure • swallow with tongue bulb in place – maximum swallow pressure 31 28 (Robbins et al, J of Gerontol, 1995) 3 Tongue Strength Findings: Older adults generate reduced isometric pressures relative to their younger counterparts… But swallow pressures remain the same as young Swallowing Functional Reserve Findings: max isometric pressure: swallowing pressures • ability to adapt to stress (Pendergast et al, 1993) • decreases with age • risk factor for dysphagia in elderly when combined with poor medical condition, chronic or acute illness, mechanical perturbation (Robbins et al, J of Gerontol, 1995; Nicosia et al, J of Gerontol, 2000) Why does lingual strength change with age? Anatomical MRI Data Eight weeks of progressive resistance training on skeletal muscle in the frail elderly population has been associated with increased: • • • • • Gait speed Activity level Stair climbing Endurance Function (Fiatarone et al., JAMA 1990; N Engl J Med, 1994) 38 Yr Old Female 81 Yr Old Female Evidence in oropharynx fat/connective tissue cross-sectional area fiber density 4 Lingual Resistance Exercise (Non-Swallowing Specific) ¾ Iowa Oral Performance Instrument (IOPI) ¾ Press tongue to roof of mouth (isometric/static) ¾ Anterior and posterior tongue sites Repetition Matters American College of Sports Med, 2002: Low repetition, high resistance builds strength 8-12 reps improves strength in older adults 8 weeks of exercise increases limb strength 10 repetitions per set Intensity Matters ¾ One repetition maximum (1RM) Highest amount that can be lifted one time ¾ 80% RM improves strength ¾ Duration of contraction is correlated with rate of strength increase 60% RM Week 1 3 sets per day 80% RM Week 2-8 3 days per week for 8 weeks 3-5 sec. contraction Healthy Normals (>65yo) Healthy Normals (>65yo) Change in Isometric Pressures Change in Swallowing Pressures Tongue Tongue Blade Blade 3mL Thin Liquid 50 50 35 Pressure (kPa) 40 40 Pressure (kPa) (kPa) Pressure 3mL Semi-Solid 40 30 30 20 20 10 10 30 25 20 15 10 5 00 0 Baseline Baseline Post-Exercise Post-Exercise (Robbins et al., JAGS, 2005) Baseline Post-Exercise (Robbins et al., JAGS, 2005) 5 Magnetic Resonance Imaging • Total Lingual Volume • Fat fraction 4 Subjects 74-84 years old Scanner FOV Thickness Plane Pulse Sequence ΔLingual Volume (Reeder, IDEAL) Demographics of Stroke Subjects 1.5 Tesla GE 8 channel head coil 20 cm 3 mm Coronal T2 2D-FSE • • • • • • N=10 Age (51-90yrs) Ischemic stroke Acute (6) Chronic (4) *acute:< 3 mos. post-stroke ↑ x 5.10 cm3 (Robbins et al, Arch Phys Med Rehabil, 2007) Baseline Max Isometric Pressures Time Matters Posterior Tongue Anterior Tongue 70 ¾ Effects dependent on time post-lesion Pressure (kPa) ¾ Plastic change depends upon time post-training Neural changes may precede hypertrophy Pressure (kPa) 70 50 30 10 Week 0 Data collected at 4 and 8 weeks post- exercise 10 Week 8 Week 0 Week 4 Week 8 (Robbins et al. JAGS, 2005) Significant Week 8 Max Isometric Pressures Penetration/Asperation Scale Scores 10mL liquid (p=0.005) ; 3mL liquid (p=0.003) Posterior Tongue Anterior Tongue 70 50 * 30 Week 0 Week 4 Week 8 50 8 30 6 10 4 Week 0 Week 4 Week 8 Significant Change (p=0.0001) in Anterior & Posterior Tongue Strength after 8 Weeks of Exercise 2 0 Aspiration Penetration Penetration-Aspiration Scale Score Pressure (kPa) 70 Pressure (kPa) 30 Healthy Lingual Pressures (65+yrs) 40 kPa anterior, 39 kPa posterior Chronic and acute stroke subjects 10 Week 4 50 Baseline Week 4 = Mean Pen/Asp Score (10mL Liquid) Week 8 (Rosenbek et al. 1996, Robbins et al., 1999) 6 Swallowing Pressures Kay Swallowing Workstation Isometric Exercise Increases Dynamic Swallowing Pressures (Kay Elemetrics Corp.) Significance Levels: 10mL liquid (p=0.03) 3mL liquid (p=0.004) 3mL semisolid (p=0.02) Anatomical Results Muscles of Interest Tongue • • • • • • • • • Longitudinal Vertical Transverse Genioglossus Hyoglossus Styloglossus Nasal conchae Septum Stroke Subject Sample Percent Change in Lingual Volume 63 yo male 2% 54 yo female 6.7 % Floor of mouth Myohyoid Geniohyoid Anterior Bellies of the Digastric Epiglottis Significant Increase in Lingual Volume in 2 subjects 51 yr old stroke patient- acute post stroke Weak image Does a stronger muscular framework make ALL the difference for skilled movement? (stronger/faster) 7 Stroke patient after 8 weeks lingual strengthening exercise/Strong movie 10mm 10mm Madison Oral Strengthening Therapeutic Device (MOST) 6mm 8mm Specificity: Nature of the Experience Specifies the Plasticity Isometric/Non-Specific Swallow-Specific Strength – Spinal synaptogenesis Skill – Cortical map reorganization and Cortical synaptogenesis 8mm Dynamic Cerebral Blood Flow and Functional Synchrony in Dysphagia Functional Outcome Measures Neural Plasticity… Another level of Influence/Evidence ? Fatigue ? Effort ? QOL Physiological: Oropharyngeal biomechanics Temporospatial (duration, range of motion) Strength (pressure) Bolus flow kinematics: Direction Duration Clearance Functional: Swallowing Related QOL Diet Health status (respiration, hydration, nutrition) The Future: Neural Plasticity and Dysphagia Rehabilitation 8 Acknowledgements National Institutes of Health Department of Veteran’s Affairs Geriatric Research Education and Clinical Center (GRECC) UW Graduate School UW Institute on Aging Jackie Hind, MS, CCC-SLP, BRS-S Stephanie Kays, MS, CCC-SLP Ianessa Humbert, PhD, CCC-SLP Scott Reeder, MD, PhD Sterling Johnson, PhD Steven Barczi, MD Andy Taylor, MD Ross Levine, MD Abby Duane, BS Mark Nicosia, PhD Angela Hewitt, MS Eva Porcaro, MS 9 References 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. Baine WB; Yu W; Summe JP. Trends in hospitalization of elderly medicare patients with pneumonia. Am J of Pub Health 91: 1121-1123 Buchner DM et al. Evidence for a non-linear relationship between leg strength and gait speed. Age and Aging 1996;25:386-391. Campbell MJ et al. Physiological changes in ageing muscles. J Neurol Neurosurg Psychiatry 1973;36:174-182. Evans WJ. What is sarcopenia? J Gerontol 1995;50A:5-8. Fiatarone MA, Marks EC, Ryan ND, Meredith CN, Lipsitz LA, Evans WJ. High intensity strength training in non-agenarians. Effects on skeletal muscle. JAMA 1990; 263:3029-3034. Fiatarone MA, O'Neill EF, Ryan ND et al. Exercise training and nutritional supplementation for physical fraility in very elderly people. N Engl J Med 1994; 330:1769-1775. Hamdy S, et al. Explaining oropharyngeal dysphagia after unilateral hemispheric stroke. Lancet 1997;350(9079):686-92 Hodges SH et al. Neuromuscular junction changes in aged rat genioglossus. Ann Otol Rhinol Laryngol 2004;113:175-179. Kays SA, Robbins JA. Framing oral motor exercise in principles of neural plasticity. ASHA SID 2: Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders (In Press) Kraemer W et al. Progression models in resistance training for healthy adults. Med Sci Sports Exerc 2002;34(2):364-380. Lazarus C et al. Effects of two types of tongue strengthening exercises in young normals. Folia Phoniatr Logop. 2003 Jul-Aug;55(4):199-205. Levine R, Robbins JA, Maser A. Periventricular white matter changes and oropharyngeal swallowing in normal individuals. Dysphagia 1992; 7:142-147 Luschei ES (1991). Development of objective standards of non-speech oral strength and performance: An advocate's views. In Moore CA, Yorkston KM, & Beukelman DR (Eds.), Dysarthria and Apraxia of Speech (Baltimore: Brookes Publishing). McDonagh MJN. Adaptive response of mammalian skeletal muscle to exercise with high loads. Eur J Appl Physiol 1984;52:139-155. Narici MV. Changes in force, cross-sectional area, and neural activation during strength training and detraining of the human quadriceps. Euro J Appl Physiol 1989;59:310-319. Newton JP et al. Changes in human masseter and medial pterygoid muscles with age: A study by computed tomography. Gerondontics 1987; 3:151-154. Nicosia M et al. Age effects on the temporal evolution of isometric and swallowing pressure. J of Gerontol 2000;55A(11):M634-M640. Robbins J, Kays S, Gangnon R, Hewitt A, Hind J. The Effects of Lingual Exercise in Stroke Patients with Dysphagia. Archives of Physical Medicine and Rehabilitation 88: 150-158, 2007 19. Robbins J et al. The effects of lingual exercise on swallowing in older adults. JAGS 2005;53(9): 1483-1489. 20. Robbins J. Invited Editorial: The evolution of swallowing neuroanatomy and physiology in humans: A practical perspective. Annals of Neurology 1999; 36:279-280 21. Robbins JA, Coyle J, Rosenbek J, et al. Differentiation of normal and abnormal airway protection during swallowing using Penetration Aspiration scale. Dysphagia 1999; 14:228-232. 22. Robbins JA, Levine RL, Wood J, et al. Age effects on lingual pressure generation as a risk factor for dysphagia. Journal of Gerontology, Medical Sciences, 50A(5):M257M262, 1995. 23. Robbins JA, Levine RL, Maser A, Rosenbek JC, Kempster GL. Swallowing after unilateral stroke of the cerebral cortex. Archives of Physical Medicine and Rehabilitation, 74:1295-1300, 1993. 24. Robbins JA, Hamilton JW, Lof GL, Kempster G. Oropharyngeal swallowing in normal adults of different ages. Gastroenterology 1992; 103:823-829. 25. Rosenbek JC, Robbins JA, Roecker EB, Coyle JL, Wood JL. A Penetration-Aspiration Scale. Dysphagia 1996; 11:93-98. 26. Saleem AF et al. Respiratory muscle strength training: treatment and response duration in a patient with early idiopathic Parkinson's disease. NeuroRehabilitation 2005;20(4):323-333. 27. Shaker R et al. Rehabilitation of swallowing by exercise in tube-fed patients with pharyngeal dysphagia secondary to abnormal UES opening. Gastroenterology. 2002 May;122(5):1314-21. 28. Shaw DW et al. Influence of normal aging on oropharyngeal and upper esophageal sphincter function during swallow. Am J Physiol 1995;L68:G389-390. 29. Shaw DW, Cook IJ, Dent J et al. Age influences oropharyngeal and upper esophageal sphincter function during swallowing. Gastroenterology 1990; 98:A390. 30. Tinazzi M, Zanette G, Volpato D et al. Neurophysiological evidence of neuroplasticity at multiple levels of the somatosensory system in patients with carpal tunnel syndrome. Brain 1998; 121:1785-1794. 31. Tracy F, Logemann JA, Kahrilas PJ, Jacob P, Kobara M, Krugla C. Preliminary observations on the effects of age on oropharyngeal deglutition. Dysphagia 1989; 4:9094. 32. Urasaki E, Genmoto T, Wada S, Yokota A, Akamatsu N. Dynamic changes in area 1 somatosensory cortex during transient sensory deprivation: A preliminary study. Journal of Clinical Neurophysiology 2002; 19:219-231. 33. Zald DH, Pardo JV. The functional neuroanatomy of voluntary swallowing. Annals of Neurology 1999; 46:281-286. 34. Zeynep E et al. Effects of aging on motor-unit control properties. J Neurophysiol 1999;82:2081-2091. 35. Ziemann U, Hallett M, Cohen LG. Mechanisms of deafferentation-induced plasticity in human motor cortex. Journal of Neuroscience 1998; 18:7000-7007. G. Lof ASHA 2007: Why not strength exercises Page 1 MUSCLE TRAINING PRINCIPLES AND RESULTING CHANGES TO SPEECH AND SWALLOWING (Invited Session) 2007 ASHA National Convention, Boston, MA Strength Exercises: Why not for Childhood Speech Sound Disorders Gregory L. Lof, Ph.D., CCC-SLP Graduate Program In Communication Sciences and Disorders MGH Institute of Health Professions Boston, MA [email protected] Is strength targeted by SLPS? Nationwide survey of 537 SLPs by Lof & Watson (2004; 2008) • Most frequently used exercises (in rank order): Blowing; Tongue Push-Ups; Pucker-Smile; Tongue Wags; Big Smile; Tongue-to-Nose-to-Chin; Cheek Puffing; Blowing Kisses; Tongue Curling. • Reported benefits (in rank order): Tongue Elevation; Awareness of Articulators; Tongue Strength; Lip Strength; Lateral Tongue Movements; Jaw Stabilization; Lip/Tongue Protrusion; Drooling Control; VP Competence; Sucking Ability. Websites and self published materials encourages the use of strength exercises. Question 1: How much strength is necessary for speaking? • • • • Articulator strength needs are VERY low for speech and the speaking strength needs do not come anywhere close to maximum strength abilities of the articulators. For example, lip muscle force for speaking is only about 10-20% of the maximal capabilities for lip force, and the jaw uses only about 1115% of the available amount of force that can be produced (Forrest, 2002). “…only a fraction of maximum tongue force is used in speech production, and such strength tasks are not representative of the tongue's role during typical speaking. As a result, caution should be taken when directly associating tongue strength to speech…” (Wenke, Goozee, Murdoch, & LaPointe, 2006). Children with speech sound disorders actually had stronger tongues than typically developing children (Sudberry, Wilson, Broaddus, & Potter, 2006). Agility and fine articulatory movements, rather than strong articulators, are required for the ballistic movements of speaking. Usually, non-speech exercises encourage gross and exaggerated ranges of motion, not small, coordinated movements that are required for talking. Question 2: Do typical non-speech oral motor exercises actually increase strength? • These non-speech exercises may not actually increase articulator strength. To strengthen muscle, the exercise must be done with multiple repetitions, against resistance, following a basic strengthtraining paradigm; there are probably no actual strength gains occurring due to these non-speech exercises. G. Lof • • • ASHA 2007: Why not strength exercises Page 2 Articulators can be strengthened (e.g., the tongue for oral phase of swallowing or the VP complex) but these strengthened articulators will probably not help with the production of speech. Task specificity: The same structures used for speaking and other “mouth tasks” (e.g., feeding, swallowing, sucking, breathing, etc.) function in different ways depending on the task and each task is mediated by different parts of the brain. The organization of movements within the nervous system is not the same for speech and non-speech gestures. Although identical structures are used, these structures function differently for speech and for non-speech activities. Non-speech motor movements elicit activation of different parts of the brain than do speech motor movements (Bonilha, Moser, Rorden, Baylis, & Fridriksson, 2006; Stathopoulos & Duchane, 2006; Weismer, 2006). Question 3: How do speech-language pathologists objectively measure strength? • • Clinical measurements of strength are usually highly subjective (e.g., feeling the force of the tongue pushing against a tongue depressor or against the cheek or just “observing” weakness), so clinicians cannot initially verify that strength is actually diminished and then they cannot report increased strength following NS-OME. Only objective measures (e.g., tongue force transducers) can corroborate statements of strength needs and improvement. Without such objective measurements, testimonials of articulator strength gains must be considered suspect. Strength estimation is unreliable, with student clinicians actually better than practicing clinicians (Solomon & Monson, 2004). Why strength for certain speech sound disorders? Cleft Lip and Palate • The VP mechanism can be strengthened through exercise, but added strength will not improve speech • • • production. Blowing exercises for strength are not appropriate. “Do not invest time or advise a parent to invest time and money addressing a muscle strength problem that may not (and probably does not) exist. It is very frustrating to see clinicians working on “exercises” to strengthen the lips and tongue tip when bilabial and lingua-alveolar sounds are already evident in babble, or when bilabial and lingual/lingua-alveolar functions are completely intact for feeding and other non-speech motor behaviors.” (Peterson-Falzone, Trost-Cardamone, Karnell, Hardin-Jones, 2006). “Having a repaired cleft does not mean a child will lack the muscle strength needed to produce consonant sounds adequately. The presence of a cleft palate (repaired or unrepaired) has no bearing on tongue strength or function (why would it?). The majority of children who demonstrate VPI do so because their palate is too short to achieve VP closure. Muscle strength or lack thereof is not a primary causal factor associated with phonological delays in this population.” (Peterson-Falzone, Trost-Cardamone, Karnell, Hardin-Jones, 2006). “…blowing should never be used to ‘strengthen’ labial or soft palate musculature; it does not work. Children who appear to improve over time in therapy when using these tools are likely demonstrating improvement related to maturation and to learning correct motor speech patterns. Had therapy focused only on speech sound development, these children probably would have shown progress much sooner.” (Peterson-Falzone, Trost-Cardamone, Karnell, Hardin-Jones, 2006). G. Lof ASHA 2007: Why not strength exercises Page 3 Childhood Apraxia of Speech (CAS) • By definition, children with CAS have adequate oral structure movements for non-speech activities • but not for volitional speech, and have adequate amounts of strength (Caruso & Strand, 1999). The focus of intervention for the child diagnosed with CAS is on improving the planning, sequencing, and coordination of muscle movements for speech. Isolated exercises designed to "strengthen" the oral muscles will not help. CAS is a disorder of speech coordination, not strength. (http://www.asha.org/public/speech/disorders/ChildhoodApraxia.htm#tx). Language-Based Speech Sound Disorders • It makes no sense that strengthening exercises could help improve the speech of children who have non-motor problems, such as language-phonemic-phonological problems, for children in Early Interventions diagnosed as late talkers. Why would children with a language-based sound problem improve with strengthening exercises using a motor-based treatment approach? References ASHA: http://www.asha.org/public/speech/disorders/ChildhoodApraxia.htm#tx Bonilha, L., Moser, D., Rorden, C., Baylis, G., & Fridriksson, J. (2006). Speech apraxia without oral apraxia: Can normal brain function explain the physiopathology? Neuro Report, 17 (10), 1027-1031. Caruso, A., & Strand, E. (1999). Clinical management of motor speech disorders in children. New York: Thieme. Davis, B., & Velleman, S. (2000). Differential diagnosis and treatment of developmental apraxia of speech in infants and toddlers. Infant-Toddler Intervention, 10, 177-192. Forrest, K. (2002). Are oral-motor exercises useful in the treatment of phonological/articulatory disorders? Seminars in Speech and Language, 23, 15-25. Golding-Kushner, K. (2001). Therapy techniques for cleft palate speech and related disorders. Clifton Park, NY:Thompson/Delmar Lof, G.L., & Watson, M. (in press 2008). A nationwide survey of non-speech oral motor exercise use: Implications for evidence-based practice. Language, Speech, and Hearing Services in the Schools. Peter-Falzone, S., Trost-Cardamone, J., Karnell, M., & Hardin-Jones, M. (2006). The clinician’s guide to treating cleft palate speech. St. Louis, MO: Mosby. Robbins, J., Gangnon, R., Theis, S., Kays, S., Hewitt, A., & Hind, J. (2005). The effects of lingual exercise on swallowing in older adults. Journal of the American Geriatrics Society, 53, 1483-1489. Solomon, N., & Munson, B. (2004). The effect of jaw position on measures of tongue strength and endurance, Journal of Speech, Language, and Hearing Research, 47, 584-594. Stathopoulous, E., & Duchan, J. (2006). History and principles of exercise-based therapy: How they inform our current treatment. Seminars in Speech and Language, 24(4), 227-235. Sudbery, A., Wilson, E, Broaddus, T., & Potter, N. (2006, November). Tongue strength in preschool children: Measures, implications, and revelations. Poster presented at the annual meeting of the American SpeechLanguage-Hearing Association, Miami Beach, FL. Weismer, G. (2006). Philosophy of research in motor speech disorders. Clinical Linguistics & Phonetics, 20, 315-349. Wenke, R., Goozee, J., Murdoch, B., & LaPointe, L. (2006). Dynamic assessment of articulation during lingual fatigue in myasthenia gravis. Journal of Medical Speech-Language Pathology, 14, 13-32. Wide Smiles: Cleft Lip and Palate Resource. http://www.widesmiles.org/cleftlinks/WS-563.html. The following article will be published in the December issue (Vol. 17, No. 4) of /Perspectives on Neurophysiology and Neurogenic Speech and Language Disorders/, the peer-reviewed publication of ASHA Special Interest Division 2, Neurophysiology and Neurogenic Speech and Language Disorders. This article is being distributed at this ASHA Convention forum with permission of the publisher, ASHA. It may not be reprinted, copied, or distributed by any other individual or organization without express written permission from the publisher. Framing Oral Motor Exercise in Principles of Neural Plasticity Stephanie Kays and JoAnne Robbins University of Wisconsin-Madison, Department of Medicine and William S. Middleton Memorial Veterans Hospital, Geriatric, Research, Education and Clinic Center (GRECC) Introduction For decades the relationship between motor speech and swallowing production has been debated, with the use of oral motor exercise to remediate speech and swallowing disorders remaining a contentious issue. The field of speech pathology, which includes in its scope swallowing and dysphagia, has evolved with two primary viewpoints. The task-specific or taskdependent model, which postulates that distinct neuromotor systems are responsible for specific motor activities, suggests that speech or swallowing-specific tasks are the optimal stimuli for influencing motor speech or swallowing production, respectively. In contrast, a non-specific or task-independent model assumes that overlapping neuromotor systems comprise an integrated sensorimotor network organized by general functions (e.g., force and timing), rather than specific motor behaviors (e.g., speech or swallowing) (Ballard, Robin, & Folkin, 2003; Ziegler, 2003). In this latter model, the use of volitional oral motor tasks is endorsed for promoting both speech and swallowing rehabilitation (Ballard et al., 2003; Kent, 2004). While the theoretical debate over task-specificity has received a great deal of attention in the field of communicative disorders, speech-language pathologists have only recently been considering systematic treatment protocols within a larger framework of principles shown to effect neural plasticity, the mechanism by which the brain encodes, learns or relearns behaviors (Grossman, Churchill, Bates, Kleim, & Greenough, 2002). As neuroscientists continue to elucidate the factors that guide brain recovery through investigative activities such as animal research and neuroimaging, clinicians are beginning to apply these principles in treatment designs and modes of delivery. Our profession is just beginning to provide evidence to validate and establish treatment procedures by understanding and systematically manipulating principles of exercise and neural plasticity. Exercise physiology principles and techniques that were based on clinical intuition in the past are now aligned with principles of neural plasticity and are leading to objective and quantifiable measures for evidence-based treatment designs. An understanding of fundamental processes that underlie motor learning is necessary in order to translate the phenomenon of neural plasticity into speech and swallowing clinical research and, ultimately, practice. Ten principles derived from animal research and neuroscience have been identified by Kleim and Jones (in press) as being relevant to speech and swallowing rehabilitation. Three of these principles that have received the most attention in efficacy-based studies of therapy are repetition, intensity, and specificity. Repetition Animal research suggests that one mechanism critical for inducing neural plastic changes in the central nervous system is repetitive performance of a skill even after the skill has been acquired. For instance, although a patient may demonstrate correct performance of a behavior such as a Mendelsohn maneuver (Kahrilas, Logemann, Krugler, & Flanagan, 1991) after one or two therapy sessions, changes in neuronal synapses or cortical organization require continued performance of the maneuver over time. It is hypothesized that plasticity influenced by repetition results in an acquired behavior that is resistant to decay, such that the patient is able to continue to use the function outside of therapy while maintaining and advancing gains (Kleim & Jones, in press), (Monfils, Plautz, & Kleim, 2005). Traditional treatment methods for motor speech disorders, such as childhood apraxia of speech, are based on principles of motor learning, with one of the most important aspects being the encouragement of a high number of responses within each therapy session. Yorkston and colleagues stated that, “Probably the most common error made by speech-language pathologists who treat motor speech disorders is failure to provide adequate practice in the form of hundreds of trials or responses per session” (Yorkston, Beukelman, Strand, & Bell, 1991, p. 550). A high frequency of practice was shown to facilitate phoneme acquisition in acquired apraxia of speech in a recent single-subject design. However, minimal generalization of the trained behavior to more complex behaviors was observed, despite the high number of repetitions within each treatment session (Kendall, Rodriguez, Rosenbek, Conway, & Gonzalez Rothi, 2006). An example of an exercise program that has incorporated the principle of repetition is provided by Kuehn and colleagues in their study of patients with speech disorders secondary to structural deviations (Kuehn et al., 2002). Results of this multi-center clinical trial with 43 children with congenital cleft palate demonstrated that eight weeks of speaking against transnasal continuous positive airway pressure (CPAP) resistance six days per week resulted in a significant reduction in nasality during speech, although the response was variable across patients and centers. The authors stated that the “response trend [was] minimal after four weeks of therapy with accelerated benefit during the second month” (p. 273). This suggests that a certain level of practice is necessary to induce robust skill acquisition. The principle of repetition also is a key component of active resistance exercises, which are more commonly being applied to the oropharyngeal musculature. Studies continue to emerge demonstrating positive changes in strength and function subsequent to regimens that traditionally have been reserved for the limb muscles. The concept of repetition has been incorporated as a key principle of exercise for years, with the recognition that the outcome of a training program can be manipulated by varying the number of repetitions with which an exercise is performed. For instance, training programs designed to build muscle strength (force-generating capacity) typically use a low number of repetitions against a near-maximal resistance. In contrast, regimens designed to increase muscle endurance (fatigue-resistance) rely on a higher number of repetitions with a sub-maximal load. Robbins and colleagues developed an eight-week progressive resistance exercise regimen that they applied to the lingual musculature. This regimen consists of 10 repetitions at two tongue locations performed three times a day on three days of the week (Robbins et al., 2005; Robbins et al., 2007). The American College of Sports Medicine confirms that eight to fifteen repetitions performed one to three times a day is optimal for building strength in the limb musculature (Kraemer et al., 2002). The most effective number of repetitions required to build strength in the orofacial muscles remains to be discovered and likely varies with factors such as age or underlying disease processes. However, healthy older adults and acute and chronic stroke 2 patients have demonstrated statistically significant improvements in lingual strength (pressure) during a series of non-swallowing isometric lingual presses with spontaneous generalization to natural swallowing tasks (Robbins et al., 2005). Moreover, stroke subjects demonstrated a reduction in liquid aspiration and pharyngeal residue, likely related to a longer pharyngeal response duration observed during liquid swallows (Robbins et al., 2007). After eight weeks of exercise, stroke subjects continued to demonstrate improvements in isometric tongue strength, suggesting that a longer program of exercise may yield even greater improvements in swallowing function. Future studies incorporating anatomic magnetic resonance imaging (MRI) to understand changes at the muscle level (e.g., lingual volume and tissue composition) and at the neural level via functional MRI (fMRI) are underway (Humbert et al., in press; Kays et al., in press) to confirm that these behavioral changes indeed represent neuromuscular changes in response to repetitive exercise. Such study designs will incorporate measures at multiple time points throughout an exercise program to determine patient response to various exercise doses. Shaker and colleagues (Shaker et al., 1997; Shaker et al., 2002) similarly have demonstrated an improvement in maximum anterior hyolaryngeal excursion and upper esophageal sphincter opening during swallowing following a program of repetitive head lifting. The Shaker protocol includes a dynamic component of 30 repetitive head lifts followed by three sustained contractions, performed three times daily for six weeks. More recent findings by Easterling, Grande, Kern, Sears, and Shaker (2005) demonstrate the importance of repetition over time for skill acquisition, as participants who committed to the entire 6-week program were more likely to attain the predetermined goals than those who discontinued within the first two weeks. Continued work in this area is warranted to determine if the frequency of this regimen and others is sufficient for eliciting changes in swallowing biomechanics that are resistant to decay or if a maintenance program is necessary. Recent findings by Sapienza and colleagues also have demonstrated a significant increase in maximum expiratory pressure after four weeks of expiratory muscle strength training (EMST), following a slightly different protocol of five repetitions, five times a day on five days of the week (Sapienza & Wheeler, 2006). While short-term increases in electromyographic activity of the anterior suprahyoid musculature have been measured during performance of EMST (Wheeler, Chiara, & Sapienza, 2007), the optimal regimen for eliciting long-term changes remains unknown. For example, a case study of an older patient with Parkinson disease revealed continued improvements in maximum expiratory muscle strength over a period of 20 weeks of EMST as opposed to the traditional regimen of four weeks (Saleem, Sapienza, & Okun, 2005). The degree of repetition necessary to obtain a level of brain reorganization and skill acquisition sufficient for a patient to maintain functional gains clearly requires more evidence. One of the most well-known programs of therapy for improving speech and voice in individuals with Parkinson disease is the Lee Silverman Voice Treatment® (LSVT/LOUD). LSVT/LOUD utilizes highly-repetitive practice of a salient and simple treatment target (higheffort voice) to trigger system-wide effects across the speech and swallowing production systems. The program requires an unprecedented amount of repetition that was not seen in earlier models of speech and voice therapy, consisting of 16 individual 60-minute sessions performed over a period of four weeks. LSVT/LOUD also promotes long-term maintenance of the target speech behavior by including specific strategies for incorporating exercise into repetitive or routine aspects of daily living (Fox et al., 2006; Ramig, Countryman, Thompson, & Horii, 1995; Ramig, Countryman, O'Brien, Hoehn, & Thompson, 1996). The examples provided clearly demonstrate that repetition is being recognized as a key component of treatments that result in lasting changes hypothesized to represent neural plastic modifications. The optimal frequency of repetition remains to be discovered and likely differs depending on variables such as the desired behavior, treatment goals, and the patient population. 3 Intensity In many cases, it is hypothesized that repetition alone generally is not adequate for affecting sustainable neural modifications related to functional parameters, such as muscle strength, endurance, or power. The intensity with which an exercise is performed also requires consideration. Intensity is expressed by the overload principle, which states that the load placed on a motor system must be progressively increased over time in order to increase demands as a system adapts. Strength and endurance training protocols both incorporate the overload principle, but use different levels of intensity, depending on whether the goal is to improve muscle strength or endurance. Strength Training In order to build oropharyngeal muscle strength, clinical researchers have applied a traditional load of 60% to 80% of an individual’s one repetition maximum (abbreviated 60-80% RM), which refers to the highest amount of force that can be generated once. To build lingual strength, Robbins and colleagues recommend an initial week of isometric exercise using a load of 60% RM until proper technique and form are learned, followed by 7 weeks using an 80% RM load that is progressively increased every 2 weeks relative to individual strength gains (Robbins et al., 2005; Robbins et al., 2007). Sapienza and Wheeler (2006) follow a similar approach using a load of 75% RM, and, unlike traditional breathing exercises that allow airflow rate to vary, stress the importance of maintaining a consistent intensity throughout EMST. Intensity is also emphasized in the LSVT/LOUD treatment program discussed earlier. A hallmark of the LSVT/LOUD program is to encourage high-effort vocal loudness with increasing demands for consistency and accuracy of loud performance in speech tasks (Ramig, Countryman, Thompson, & Horii, 1995). Unlike the strengthening regimens discussed above, LSVT does not specify a target value to apply across subjects but simply demands the highest stimulable vocal effort while advancing the demands of the context. The positive effects, which have shown to extend to articulatory precision (Sapir, Spielman, Ramig, Story, & Fox, 2007), facial expression (Spielman, Borod, & Ramig, 2003) and swallowing (El Sharkawi et al., 2002), are attributed in large part to the intensive delivery of this treatment. The findings from LSVT also raise the appealing speculation that intensive stimulation of one sensorimotor system may result in positive neural plastic changes in the brain that relate to other systems, a phenomenon known as transference (Kleim and Jones, in press; Fox et al., 2006; Liotti et al., 2003). Endurance Training Depending on the goal of a program, a submaximal target load may be more effective than a highly intense program. The principles of exercise recommend an intensity of 40 to 60% RM performed with an increased number of repetitions to improve muscle endurance, as opposed to muscle strength. Progressive exercises to improve the endurance of the speech and swallowing systems have not been investigated over multiple time points, although a number of studies exist that have devised methods of measuring the fatigue-resistance of the head and neck musculature (Cahill et al., 2004; Goozee, Murdoch, & Theodoros, 2001; Lazarus, Logemann, Huang, & Rademaker, 2003; McAuliffe, Ward, Murdoch, & Farrell, 2005; Solomon, 2004). Solomon demonstrated a decrement in articulatory precision after exercising the tongue to the point of fatigue; however, a strenuous fatigue-producing protocol involving repetitive maximal force production was necessary to elicit changes in speech intelligibility, and no changes in speaking rate were observed. This suggests that speech is a relatively robust system (Solomon, 2000). Preliminary work by Kays et al. (2007) taking a more functional approach, is beginning to examine whether a similar relationship exists between ability of the tongue to withstand fatigue during the sequential swallowing performed when consuming an entire meal, which may be a challenging condition for frail elders and dysphagic individuals. Specificity 4 Animal research has shown that experience is necessary, but not always sufficient, for inducing long-lasting plasticity, and that the importance of a behavior to an individual is equally as important as its frequency or intensity for stimulating learning (Kilgard & Merzenich, 1999). For example, the proportion of motor cortex representing forelimb movement was shown to increase in rats trained to perform skilled reaching (i.e., for a food reward) compared to nonskilled reaching. Moreover, the addition of a progressive resistance to the task did not affect the cortical outcome despite improvements in forelimb strength. That is, both skilled reaching and skilled reaching against a resistance equally resulted in cortical reorganization (Remple, Bruneau, VandenBerg, Goertzen, & Kleim, 2001). While this evidence may lead some to conclude that speech and swallowing can only be improved through performance of the behavior itself, clinicians frequently are faced with the dilemma that individuals lack the strength to even approximate an accurate or complete production of the target behavior. In such cases, the value of practicing an incorrect target with any degree of repetition or intensity is questionable. In some treatment models, basic resistance exercises may be paired with more traditional treatments to build a foundation of strength reserve, such that more dynamic, task-specific techniques can be successfully performed over time. This is not unlike the theory underlying intensive speech therapies such as LSVT/LOUD, in which a single, simplified component of speech production (vocal loudness) is emphasized and enhanced in order to induce widespread system effects in progressively complex contexts (Ramig et al., 1995). Another example is a study of effortful swallowing, which indicated that middle-aged adults were able to increase swallowing pressures to a greater degree than older adults when cued to swallow hard (Hind, Nicosia, Roecker, Carnes, & Robbins, 2001), indicating that agerelated reductions in maximum isometric tongue strength may limit one’s ability to change dynamic swallowing behavior. These findings suggest that a foundation of muscle strength may increase the ability to utilize therapeutic strategies, thus improving prognostic outcomes. Strengthening therefore may be a reasonable goal, particularly when performed in conjunction with more skilled movements. Finally, resistance training provides an effective means of stimulating orofacial muscle and related neural pathways to maintain or build muscle strength without compromising patient safety. For example, some dysphagic patients may be unable to safely perform swallowingspecific training due to the risk of aspiration. Resistance training also may be an important early intervention for patients with muscle weakness secondary to disease-related weakness potentially overlaid on the natural age-related loss of muscle mass and strength (sarcopenia). Such treatments can maintain saliency by utilizing creative taste, temperature, and tactile inputs when possible. Although the interaction among systems of speech, swallowing and respiration remains the focus of many researchers, several differences in these functions cannot be ignored and may lead to divergent rehabilitation strategies. The muscles of speech are specialized to favor speed over force. As Kent and others recognized (Kent, 2004; Adams, Weismer, & Kent, 1993), studies show that normal speaking rates are more aligned in kinematic and force profiles with fast speaking rates than slow rates. These findings suggest that the speech system is habitually geared toward rapid production. Nonetheless, age-related changes in speech precision and durations have been reported in adults over 60, suggesting that even though older adults may produce speech that sounds normal, the manner of production may differ to account for physiological age-related changes. Shawker and Sonies (1984) found significant differences in the direction and extent of tongue movements in older versus younger speakers during production of /a/. More recently, Goozee, Stephenson, Murdoch, Darnell, and LaPointe (2005) demonstrated that older and younger adults used similar strategies to increase their speaking 5 rates, but that young adults were more likely to economize effort by reducing the distance traveled by the tongue under very fast rate demands, while older adults showed smaller decreases in distance and associated reductions in velocity. It was hypothesized that the smaller changes in distance observed in older adults represent reduced neuromotor control, proprioception, or stability of tongue movements. Swallowing, in contrast to speech, sacrifices a degree of speed yet utilizes higher lingual contractile forces to prepare and propel a bolus. Also unlike speech, swallowing durations have been shown to decrease with age relative to declines in lingual muscle strength or force-generating capacity (Nicosia et al., 2000; Robbins, Levine, Wood, Roecker, & Luschei, 1995). In addition, the sensory afferent pathways differ for speech and swallowing, most notably in the undeniable importance of the auditory perceptual pathway in speech development and rehabilitation and the consistency, temperature and taste inputs involved in swallowing. Luschei’s comments on the relationship between tongue strength and velocity of movement remain relevant as the exploration of oral strengthening exercises grows (Luschei, 1991). He compared the motion of the lingual hydrostat to opening a door with a dashpot, a device designed to keep the door from banging shut when released: “Although it does not take much force to open the door slowly or hold it open, it requires a very large force to move the door rapidly” (p. 8). Thus, there is reason to believe that the relationship between force, speed, and accuracy of oral motor movements across the lifespan is still not well-understood and may differ depending on the sensorimotor system in question. Evidence from higher levels of motor control, available with innovative imaging techniques, will begin to elucidate the longstanding question of whether oral neuromotor systems are topographically distinct or overlapping. Summary Recent imaging studies suggest that the speech, swallowing and respiratory systems may be controlled by widespread cortical and subcortical networks with more shared regions than traditionally predicted (Kern et al., 2001; Loucks, Poletto, Simonyan, Reynolds, & Ludlow, 2007; Riecker et al., 2005; Suzuki et al., 2003; Toogood et al., 2005; Zald & Pardo, 2000). Martin and colleagues have begun to explore relationships between brain activity during tongue elevation and saliva swallowing (Martin et al., 2004), demonstrating overlapping regions of cortical activity (post central gyrus, cuneus and precuneus, supramarginal gyrus) that argues against the existence of a “swallowing-specific” region. However, tongue elevation was represented by distinctly larger cortical regions, indicating that the two behaviors also have unique aspects of cortical control. Early PET imaging findings in individuals who have completed LSVT reflect increased activity in neural systems that are hypothesized to be involved in vocalization and loudness (basal ganglia, limbic system, prefrontal cortex, right hemispheric cortex), yet decreased activity in the motor/pre-motor cortices (Liotti et al., 2003). Whether decreased brain activity in this or other studies represents a “normalization” of brain effort remains to be understood. Studies investigating changes in brain activity in response to various intervention doses are on the horizon, and will depend on our ability to acquire and interpret imaging data reliably. Advances in technology and neuroscience paired with lasting scientific principles and therapy designs are leading the way to stimulate much-needed development in the field of speech and swallowing rehabilitation. Much remains to be understood, including interactions among age, disease, severity and cross-system impairments, such that only the systematic application of interventions according to selected principles of neural plasticity will yield outcomes that can be interpreted meaningfully and applied to patients efficaciously. Most importantly, new levels of evidence are being pursued enthusiastically by teams of clinicians and researchers, which will advance our understanding and discovery of critical patient-oriented approaches to drive recovery. 6 Acknowledgements: This is GRECC manuscript #2007-19. Stephanie Kays is a clinical and research speech-language pathologist at the University of Wisconsin, Department of Medicine, and the Geriatric Research, Education and Clinical Center (GRECC) of the William S. Middleton Memorial Veterans Hospital. She is a member of the UW/VA Speech, Swallowing and Dining Enhancement Program and a primary contributor to research on the effects of aging and lingual exercise on swallowing. JoAnne Robbins is a Professor of Medicine and Radiology at the University of Wisconsin School of Medicine and Public Health. She is also the Associate Director for Research at the Geriatric Research, Education and Clinical Center at the William S. Middleton VA Hospital. Her current research initiatives are examining the effects of oral motor exercise on swallowing skills in the geriatric population. References Adams, S. G., Weismer, G., & Kent, R. D. (1993). Speaking rate and speech movement velocity profiles. Journal of Speech and Hearing Research, 36(1), 41-54. 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