Aortic stiffness, a precursor to adverse cardiovascular outcomes, is worsened in conditions of general and abdominal obesity, low cardiorespiratory fitness (CRF), and physical inactivity. Elevated carotid-femoral pulse wave velocity (cfPWV) is an indicator of aortic stiffness. Behavioral weight loss interventions promote decreased caloric intake and increased moderate-vigorous physical activity (MVPA), but whether increases in MVPA and CRF have independent or additive effects with weight loss on aortic stiffness remains unclear. PURPOSE: To determine the overall and independent effects of changes in general and abdominal obesity, CRF, and MVPA on cfPWV in overweight and obese adults. METHODS: Eighty three (N=83) sedentary, overweight and obese adults (age 44.5 ± 8.1 years; BMI 32.4 ± 4.0 kg/m2) completed 6 months of a standard behavioral weight loss intervention. Assessments included cfPWV (m/s) by applanation tonometry, abdominal obesity by dual X-ray absorptiometry (DXA), MVPA (min/wk, MET-min/wk) by objective activity monitoring and CRF by graded exercise testing. Changes in systolic and diastolic blood pressure (SBP, DBP) were also evaluated. Multiple linear regression was performed to determine the effect of changes in CRF and MVPA on cfPWV with changes in body weight and abdominal fat as covariates. RESULTS: After 6 months, body weight, BMI, waist circumference, and abdominal fat significantly decreased, while CRF and MVPA significantly increased (all p0.1). Reductions in body weight, BMI, waist circumference, and abdominal fat were not associated with the decrease in cfPWV (all p>0.1). The decrease in cfPWV was moderately correlated with decreases in SBP (r=0.379, p<0.001) and DBP (r=0.317, p=0.004). CONCLUSION: These data did not support that changes in fatness were associated with improved aortic stiffness, however, the significant improvements in CRF and cfPWV suggest that targeting fitness in lifestyle interventions for a sedentary, obese population maybe be important for better vascular health. Supported by NIH (HL103646)
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