Int J Sports Med 2022; 43(02): 177-182
DOI: 10.1055/a-1529-6480
Training & Testing

Acute Cardiovascular Responses to Self-selected Intensity Exercise in Parkinson's Disease

1   Hospital Israelita Albert Einstein, São Paulo, Brazil
,
Gabriel Grizzo Cucato
1   Hospital Israelita Albert Einstein, São Paulo, Brazil
2   Northumbria University, Newcastle upon Tyne, United Kingdom of Great Britain and Northern Ireland
,
Paulo Longano
3   Universidade Nove de Julho – Campus Vergueiro, São Paulo, Brazil
,
Erika Okamoto
4   Brazil Parkinson Association, São Paolo, Brazil
,
Maria Elisa Pimentel Piemonte
5   University of São Paulo, São Paulo, Brazil
,
Marilia Almeida Correia
3   Universidade Nove de Julho – Campus Vergueiro, São Paulo, Brazil
,
Raphael Mendes Ritti-Dias
3   Universidade Nove de Julho – Campus Vergueiro, São Paulo, Brazil
› Author Affiliations
Funding We gratefully acknowledge the volunteers and the Brazil Parkinson Association. RR receive a research productivity fellowship granted by Brazilian National Council for Scientific and Technological Development and HK received fellowship granted by Fundação de Amparo à Pesquisa do Estado de São Paulo – FAPESP’ (2018/11564-6).

Abstract

Parkinson’s disease patients frequently present cardiovascular dysfunction. Exercise with a self-selected intensity has emerged as a new strategy for exercise prescription aiming to increase exercise adherence. Thus, the current study evaluated the acute cardiovascular responses after a session of aerobic exercise at a traditional intensity and at a self-selected intensity in Parkinson’s disease patients. Twenty patients (≥ 50 years old, Hoehn & Yahr 1–3 stages) performed 3 experimental sessions in random order: Traditional session (cycle ergometer, 25 min, 50 rpm, 60–80% maximum heart rate); Self-selected intensity: (cycle ergometer, 25 min, 50 rpm with self-selected intensity); and Control session (resting for 25 min). Before and after 30 min of intervention, brachial and central blood pressure (auscultatory method and pulse wave analysis, respectively), cardiac autonomic modulation (heart rate variability), and arterial stiffness (pulse wave analysis) were evaluated. Brachial and central systolic and diastolic blood pressure, heart rate, and the augmentation index increased after the control session, whereas no changes were observed after the exercise sessions (P<0.01). Pulse wave velocity and cardiac autonomic modulation parameters did not change after the three interventions. In conclusion, a single session of traditional intensity or self-selected intensity exercises similarly blunted the increase in brachial and central blood pressure and the augmentation index compared to a non-exercise control session in Parkinson’s disease patients.



Publication History

Received: 09 December 2020

Accepted: 04 June 2021

Article published online:
11 August 2021

© 2021. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Dickson DW. Neuropathology of Parkinson disease. Parkinsonism Relat Disord 2018; 46: S30-S33
  • 2 Kanegusuku H, Silva-Batista C, Peçanha T. et al. Blunted maximal and submaximal responses to cardiopulmonary exercise tests in patients with Parkinson disease. Arch Phys Med Rehabil 2016; 97: 720-725
  • 3 Low DA, Vichayanrat E, Iodice V. et al. Exercise hemodynamics in Parkinson’s disease and autonomic dysfunction. Parkinsonism Relat Disord 2014; 20: 549-553
  • 4 Miyasato RS, Silva-Batista C, Peçanha T. et al. Cardiovascular responses during resistance exercise in patients with Parkinson disease. PM R 2018; 10: 1145-1152
  • 5 Roberson KB, Signorile JF, Singer C. et al. Hemodynamic responses to an exercise stress test in Parkinson’s disease patients without orthostatic hypotension. Appl Physiol Nutr Metab 2019; 44: 751-758
  • 6 Sabino-Carvalho J, Vianna LC. Altered cardiorespiratory regulation during exercise in patients with Parkinson’s disease: a challenging non-motor feature. SAGE Open Med 2020; 8: 2050312120921603 doi:10.1177/2050312120921603
  • 7 Bocalini DS, Bergamin M, Evangelista AL. et al. Post-exercise hypotension and heart rate variability response after water- and land-ergometry exercise in hypertensive patients. PLoS One 2017; 12: e0180216
  • 8 GjØvaag T, Berge H, Olsrud M. et al. Acute post-exercise blood pressure responses in middle-aged persons with elevated blood pressure/stage 1 hypertension following moderate and high-intensity isoenergetic endurance exercise. Int J Exerc Sci 2020; 13: 1532-1548
  • 9 Jones MD, Munir M, Wilkonski A. et al. Post-exercise hypotension time-course is influenced by exercise intensity: a randomised trial comparing moderate-intensity, high-intensity, and sprint exercise. J Hum Hypertens 2020; DOI: 10.1038/s41371-020-00421-3.
  • 10 Ben-Shlomo Y, Marmot MG. Survival and cause of death in a cohort of patients with Parkinsonism: possible clues to aetiology?. J Neurol Neurosurg Psychiatry 1995; 58: 293-299
  • 11 Diem-Zangerl A, Seppi K, Wenning GK. et al. Mortality in Parkinson's disease: A 20-year follow-up study. Mov Disord 2009; 24: 819-825
  • 12 Fanciulli A, Campese N, Goebel G. et al. Association of transient orthostatic hypotension with falls and syncope in patients with Parkinson disease. Neurology 2020; 95: e2854-e2865
  • 13 Feito Y. Parkinson disease: etiology, clinical characteristics and the role of exercise. ACSM’s Certified News 2009; 19: 9-12
  • 14 Kim Y, Lai B, Mehta T, Thirumalai M. et al. Exercise training guidelines for multiple sclerosis, stroke, and Parkinson disease: Rapid review and synthesis. Am J Phys Med Rehabil 2019; 98: 613-621
  • 15 Ekkekakis P. Let them roam free? Physiological and psychological evidence for the potential of self-selected exercise intensity in public health. Sports Med 2009; 39: 857-888
  • 16 Mavrommati F, Collett J, Franssen M. et al. Exercise response in Parkinson’s disease: insights from a cross-sectional comparison with sedentary controls and a per-protocol analysis of a randomised controlled trial. BMJ Open 2017; 7: e017194
  • 17 Van der Kolk NM, King LA. Effects of exercise on mobility in people with Parkinson’s disease. Mov Disord 2013; 28: 1587-1596
  • 18 Costa IBB, Schwade D, Macedo GAD. et al. Acute antihypertensive effect of self-selected exercise intensity in older women with hypertension: a crossover trial. Clin Interv Aging 2019; 14: 1407-1418
  • 19 Harriss DJ, MacSween A, Atkinson G. Ethical standards in sport and exercise science research: 2020 update. Int J Sports Med 2019; 40: 813-817
  • 20 Goetz CG, Poewe W, Rascol O. et al. Movement Disorder Society Task Force report on the Hoehn and Yahr staging scale: status and recommendations. Mov Disord 2004; 9: 1020-1028
  • 21 Nasreddine ZS, Phillips NA, Bedirian V. et al. The Montreal Cognitive Assessment, MoCA: A brief screening tool for mild cognitive impairment. J Am Geriatr Soc 2005; 53: 695-699
  • 22 Kanegusuku H, de Almeida Correia M, Longano P. et al. Cardiovascular, perceived exertion and affective responses during aerobic exercise performed with imposed and a self-selected intensity in patients with Parkinson's disease. NeuroRehabilitation 2021; 48: 267-272
  • 23 Longano P, Kanegusuku H, Correia MA. et al. Are cardiovascular function and habitual physical activity levels similar with classic and atypical claudication symptoms? A cross-sectional study. Vascular 2020; 28: 360-367
  • 24 Siebenhofer A, Kemp C, Sutton A. et al. The reproducibility of central aortic blood pressure measurements in healthy subjects using applanation tonometry and sphygmocardiography. J Hum Hypertens 1999; 13: 625-629
  • 25 Van Bortel LM, Duprez D, Starmans-Kool MJ. et al. Clinical applications of arterial stiffness, Task Force III: Recommendations for user procedures. Am J Hypertens 2002; 15: 445-452
  • 26 Heart rate variability: standards of measurement, physiological interpretation and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology Circulation 1996; 96: 1043-1065
  • 27 Fanciulli A, Göbel G, Ndayisaba JP. et al. Supine hypertension in Parkinson’s disease and multiple system atrophy. Clin Auton Res 2016; 26: 97-105
  • 28 Goldstein DS, Pechnik S, Holmes C. et al. Association between supine hypertension and orthostatic hypotension in autonomic failure. Hypertension 2003; 42: 136-142
  • 29 Pathak A, Senard JM. Blood pressure disorders during Parkinson’s disease: Epidemiology, pathophysiology and management. Expert Rev Neurother 2006; 6: 1173-1180
  • 30 Sabino-Carvalho JL, Falquetto B, Takakura AC. et al. Baroreflex dysfunction in Parkinson's disease: Integration of central and peripheral mechanisms. J Neurophysiol 2021; 125: 1425-1439
  • 31 Senard JM, Valet P, Durrieu G. et al. Adrenergic supersensitivity in Parkinsonians with orthostatic hypotension. Eur J Clin Invest 1990; 20: 613-619
  • 32 Shannon JR, Jordan J, Diedrich A. et al. Sympathetically mediated hypertension in autonomic failure. Circulation 2000; 101: 2710-2715
  • 33 Szili-Torok T, Kalman J, Paprika D. et al. Depressed baroreflex sensitivity in patients with Alzheimer's and Parkinson's disease. Neurobiol Aging 2001; 22: 435-438
  • 34 Nichols WW, Singh BM. Augmentation index as a measure of peripheral vascular disease state. Curr Opin Cardiol 2002; 17: 543-551
  • 35 Halliwill JR, Minson CT, Joyner MJ. Effect of systemic nitric oxide synthase inhibition on postexercise hypotension in humans. J Appl Physiol (1985) 2000; 89: 1830-1836
  • 36 Halliwill JR, Taylor JA, Eckberg DL. Impaired sympathetic vascular regulation in humans after acute dynamic exercise. J Appl Physiol (1985) 1996; 495: 279-288
  • 37 McCord JL, Halliwill JR. H1 and H2 receptors mediate postexercise hyperemia in sedentary and endurance exercise-trained men and women. J Appl Physiol (1985) 2006; 101: 1693-1701
  • 38 Peçanha T, Silva-Júnior ND, Forjaz CL. Heart rate recovery: autonomic determinants, methods of assessment amd association with mortality and cardiovascular disease. Clin Physiol Funct Imaging 2014; 34: 327-339
  • 39 Perini R, Orizio C, Comande A. et al. Plasma norepinephrine and heart rate dynamics during recovery from submaximal exercise in man. Eur J Appl Physiol Occup Physiol 1989; 58: 879-883
  • 40 Chandrakumar D, Boutcher SH, Boutcher YN. Acute exercise effects on vascular and autonomic function in overweight men. J Sports Med Phys Fitness 2015; 55: 91-102
  • 41 Enweze L, Oke LM, Thompson T. et al. Acute exercise and postexercise blood pressure in African American women. Autumn 2007; 17: 664-668