Key result
Endothelin-related genetic risks were associated with a 2.4 times greater decadal increase in arterial stiffness compared with no genetic risk (19.5% vs 8.1%), which was attenuated by regular aerobic exercise.
Why the study?
Do endothelin-related gene polymorphisms and regular aerobic exercise influence age-related arterial stiffening over 10 years?
Cohort (n=92)
Do endothelin-related gene polymorphisms and regular aerobic exercise influence age-related arterial stiffening over 10 years?
Absolute Event Rate: 19.5% vs 8.1%
Regular aerobic exercise attenuates age-related arterial stiffening independently of genetic risk factors related to the endothelin system.
Supports exercise to offset genetic arterial stiffening risk; hypothesis-generating and requires RCTs before practice change.
Increased arterial stiffness has emerged as a strong predictor of future cardiovascular events and all-cause mortality. The aim of this study was to elucidate influences of endothelin (ET)-related genetic polymorphisms and regular physical activity on age-related arterial stiffening through a 10-yr longitudinal study. A decadal change in brachial-ankle pulse wave velocity (baPWV), an index of arterial stiffness, was evaluated retrospectively among 92 volunteers (63 ± 14 yr, 51 men). The targeted single-nucleotide polymorphisms were ET-A receptor SNP rs5333 (ET-A) and ET-B receptor SNP rs5351 (ET-B). Subjects with either ET-A TC or CC genotypes exhibited significantly greater increases in baPWV (+15.3 ± 11.7 and +16.6 ± 15.7%/dec, respectively) than ET-A TT genotype holders (+9.2 ± 9.0%/dec), whereas subjects with the ET-B GG genotype showed a significantly greater increase in baPWV (+17.7 ± 14.1%/dec) than other ET-B genotype holders (AA: +9.5 ± 10.0%/dec; AG: +11.2 ± 9.6%/dec). The combination of these ET-related genetic risks was associated with a 2.4 times greater decadal increase in baPWV compared with no genetic risk (+8.1 ± 8.4 vs. 19.5 ± 16.0%/dec). In contrast, individuals engaging in >15 METs·h/wk of aerobic exercise showed substantially smaller increases in baPWV (+5.0 ± 9.7%/dec) compared with their physically inactive peers (approximately +13%/dec). These differences remained significant after adjusting for confounding factors, including baseline baPWV and ET-related genotype risk. Our current longitudinal study found that ET-related gene polymorphisms contribute to diverse age-related changes in arterial stiffness, and that regular sufficient aerobic exercise attenuates the age-related arterial stiffening independently of ET-related gene polymorphisms. NEW & NOTEWORTHY This 10-yr longitudinal study suggests that endothelin-related gene polymorphisms contribute to divergent increases in arterial stiffness with advancing age, whereas regular sufficient aerobic exercise attenuates age-related arterial stiffening independently of ET-related gene polymorphisms. This notion partly supports prevailing evidence that regular aerobic exercise contributes to a lower incidence of cardiovascular disease.
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Sugawara et al. (2017) conducted a cohort in Age-related arterial stiffening (n=92). Endothelin-related gene polymorphisms and aerobic exercise vs. No genetic risk and physical inactivity was evaluated on Decadal change in brachial-ankle pulse wave velocity (baPWV). Endothelin-related genetic risks were associated with a 2.4 times greater decadal increase in arterial stiffness compared with no genetic risk (19.5% vs 8.1%), which was attenuated by regular aerobic exercise.
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