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Pulse Wave Velocity and Sarcopenia in Older Persons-A Systematic Review and Meta-Analysis

Publisher

MDPI
DOI: 10.3390/ijerph19116477

Keywords

arterial stiffness; sarcopenia; meta-analysis; PWV

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This study conducted a systematic review and meta-analysis to explore the relationship between pulse wave velocity (PWV) and sarcopenia. The findings showed that sarcopenic individuals had higher PWV values and a greater probability of concurrent sarcopenia with higher PWV values. The study also suggested that increased stiffness of the aorta may be associated with sarcopenia and that sarcopenia could potentially accelerate age-related large arterial remodeling.
Sarcopenia and cardiovascular disease share some of the pathophysiologic mechanisms. Sarcopenia is likewise an important feature of frailty and the one potentially related to cardiovascular pathology. Previously, the relationship between arterial stiffness and frailty has been established. In this study, we conducted a systematic review and a meta-analysis of studies where the relationship between pulse wave velocity (PWV) and sarcopenia has been addressed. We included six cross-sectional studies that enrolled 5476 participants. Using the WebPlotDigitizer, RevMan5, and SAS 9.4, we extracted or calculated the summary statistics. We then calculated standardized mean differences (SMD) of PWV in the sarcopenic and non-sarcopenic participants. The pooled SMD was 0.73 (95% CI 0.39-1.08, p < 0.0001, I-2 = 90%) indicating higher value in the sarcopenic subjects. The three studies that presented odds ratios for sarcopenia as a function of PWV homogenously indicated a greater probability of concomitant sarcopenia with higher values of PWV. Greater stiffness of the aorta is associated with sarcopenia. It is impossible to establish the causation. However, the plausible explanation is that increased stiffness may translate into or be an intermediary phenotype of common vascular and muscle damage. On the other hand, sarcopenia, which shares some of the inflammatory mechanisms with cardiovascular disease, may wind up the age-related large arterial remodeling.

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