TY - JOUR
T1 - Sex differences in the association of vital exhaustion with regional fat deposition and subclinical cardiovascular disease risk
AU - Pester, Mollie S.
AU - Gonzalez, Alex
AU - Schmaus, Jennifer A.
AU - Wohlgemuth, William
AU - McCabe, Philip M.
AU - Iacobellis, Gianluca
AU - Schneiderman, Neil
AU - Hurwitz, Barry E.
N1 - Funding Information:
This study was supported by a research grant ( HL081817 ) awarded to B.E.H. and a training grant ( HL007426 ) awarded to N.S. from the National Heart, Lung and Blood Institute of the National Institutes of Health .
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/6
Y1 - 2022/6
N2 - Objective: Vital exhaustion (VE) is more strongly associated with cardiovascular disease (CVD) risk for women than men. This study examined whether sex differences in associations of VE with CVD risk markers are accounted for by unique associations of VE with regional adiposity. Methods: The study enrolled 143 persons (18–55 years) without diagnosed conditions. VE was assessed by the Maastricht questionnaire. CVD indices were measured using the euglycemic-hyperinsulinemia clamp, resting blood pressure, and blood draws. Regional adiposity was measured using computed tomography and 2-D echocardiography. This cross-sectional study employed a path analysis approach, including relevant covariates. Results: Of the cohort, aged 38.7 ± 8.4 years, 65% were men, and 41% were obese. The final model had excellent fit (χ2(36) = 36.5, p =.45; RMSEA = 0.009, CFI = 0.999). For women, but not men, the model indicated paths from VE to: 1) lower insulin sensitivity (B = −0.10, p =.04), and higher total cholesterol to HDL ratio (B = 0.12, p =.09), triglycerides (B = 0.10, p =.08), and C-reactive protein (B = 0.08, p =.09) through visceral adiposity; 2) higher mean arterial pressure (B = 0.14, p =.04), lower insulin sensitivity (B = −0.09, p =.08), and higher C-reactive protein (B = 0.12, p =.07) through subcutaneous adiposity; 3) lower insulin sensitivity (B = −0.07, p =.08) and higher total cholesterol to HDL ratio (B = 0.16, p =.03) through liver adiposity; and 4) higher C-reactive protein (B = 0.08, p =.09) through epicardial adiposity. Conclusion: Results extend prior evidence by showing that the association of VE with CVD risk in women is linked with specific regional adiposity elevation. Further study of adiposity-related mechanisms in women who experience early decline in vitality may inform clinical targets for CVD prevention.
AB - Objective: Vital exhaustion (VE) is more strongly associated with cardiovascular disease (CVD) risk for women than men. This study examined whether sex differences in associations of VE with CVD risk markers are accounted for by unique associations of VE with regional adiposity. Methods: The study enrolled 143 persons (18–55 years) without diagnosed conditions. VE was assessed by the Maastricht questionnaire. CVD indices were measured using the euglycemic-hyperinsulinemia clamp, resting blood pressure, and blood draws. Regional adiposity was measured using computed tomography and 2-D echocardiography. This cross-sectional study employed a path analysis approach, including relevant covariates. Results: Of the cohort, aged 38.7 ± 8.4 years, 65% were men, and 41% were obese. The final model had excellent fit (χ2(36) = 36.5, p =.45; RMSEA = 0.009, CFI = 0.999). For women, but not men, the model indicated paths from VE to: 1) lower insulin sensitivity (B = −0.10, p =.04), and higher total cholesterol to HDL ratio (B = 0.12, p =.09), triglycerides (B = 0.10, p =.08), and C-reactive protein (B = 0.08, p =.09) through visceral adiposity; 2) higher mean arterial pressure (B = 0.14, p =.04), lower insulin sensitivity (B = −0.09, p =.08), and higher C-reactive protein (B = 0.12, p =.07) through subcutaneous adiposity; 3) lower insulin sensitivity (B = −0.07, p =.08) and higher total cholesterol to HDL ratio (B = 0.16, p =.03) through liver adiposity; and 4) higher C-reactive protein (B = 0.08, p =.09) through epicardial adiposity. Conclusion: Results extend prior evidence by showing that the association of VE with CVD risk in women is linked with specific regional adiposity elevation. Further study of adiposity-related mechanisms in women who experience early decline in vitality may inform clinical targets for CVD prevention.
KW - Cardiovascular disease
KW - Fatigue
KW - Regional adiposity
KW - Sex
KW - Vitality
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U2 - 10.1016/j.jpsychores.2022.110785
DO - 10.1016/j.jpsychores.2022.110785
M3 - Article
C2 - 35366516
AN - SCOPUS:85127149193
VL - 157
JO - Journal of Psychosomatic Research
JF - Journal of Psychosomatic Research
SN - 0022-3999
M1 - 110785
ER -