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Could aerobic exercise applied before constraint-induced movement therapy change circulating molecular biomarkers in chronic post-stroke? |
Garcia-Salazar LF, Pereira ND, Silva ESM, Ribeiro JAM, Nagai Ocamoto G, Mendes Zambetta R, de Oliveira SG, Catai AM, Borstad A, Russo TL |
Physiotherapy Theory and Practice 2024;41(6):1191-1202 |
clinical trial |
This trial has not yet been rated. |
BACKGROUND: Integrating aerobic exercise (AE) into rehabilitation programs for post-stroke individuals could enhance motor recovery and cardiovascular health by increasing brain-derived neurotrophic factor (BDNF) and the myokine irisin. Chronic stroke survivors typically exhibit elevated matrix metalloproteinase-9 (MMP-9) activity, which is negatively correlated with steps and time in medium cadence, although the impact of AE on this biomarker remains unclear. OBJECTIVE: To evaluate the effect of high-intensity AE training prior to modified constraint-induced movement therapy (mCIMT) on BDNF and irisin concentration, and on MMP-2 and MMP-9 activity in chronic post-stroke individuals and to associate these results with functional improvements. METHODS: Nine participants received AE combined with mCIMT for two weeks, while the control group (n = 7) received mCIMT alone. Manual dexterity and functional capacity were assessed before and after the intervention. Serum samples were analyzed for BDNF, irisin, MMP-2 and MMP-9. RESULTS: There were no significant main effects of assessment, group or interaction on molecular biomarkers. However, the AE group had a significant increase in MMP-9 activity post-intervention (p = 0.033; d 0.67). For the Box and Block Test, there were significant main effects of assessment (F[1, 14] 33.27, p = 0.000, etap2 0.70) and group (F[1, 14] 5.43, p = 0.035, etap2 0.028). No correlations were found between biomarkers and clinical assessments. CONCLUSION: AE prior to mCIMT did not influence circulating BDNF and irisin levels but did induce an acute rise in MMP-9 activity, suggesting potential effects on cardiovascular remodeling in this population.
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