TY - JOUR
T1 - Cardiometabolic Traits and Systolic Mechanics in the Community
AU - Ho, Jennifer E.
AU - McCabe, Elizabeth L.
AU - Wang, Thomas J.
AU - Larson, Martin G.
AU - Levy, Daniel
AU - Tsao, Connie
AU - Aragam, Jayashri
AU - Mitchell, Gary F.
AU - Benjamin, Emelia J.
AU - Vasan, Ramachandran S.
AU - Cheng, Susan
N1 - Funding Information:
This work was partially supported by the National Heart, Lung and Blood Institute's Framingham Heart Study (contracts N01- HC-25195 and HHSN268201500001I). Dr Ho is supported by National Institutes of Health (NIH) grant K23-HL116780 and the MGH Hassenfeld Scholar Award. Dr Cheng is supported in part by R00-HL-107642, R01-HL131532, R01-HL134168, and a grant from the Ellison Foundation. Dr Tsao is supported by K23-HL118259. Dr Benjamin was supported by R01-HL128914, R01-HL076784, and R01-AG028321.
Publisher Copyright:
© 2017 The Authors.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Background - Obesity and cardiometabolic dysfunction are associated with increased risk of heart failure and other cardiovascular diseases. We sought to examine the association of cardiometabolic traits with left ventricular (LV) cardiac mechanics. We hypothesized that specific obesity-related phenotypes are associated with distinct aspects of LV strain. Methods and Results - We evaluated the associations of obesity-related phenotypes, including central adiposity, diabetes mellitus, insulin resistance, and circulating adipokine concentrations with echocardiographic measures of LV mechanical function among participants of the Framingham Heart Study Offspring and Third Generation cohorts. Among 6231 participants, the mean age was 51±16 years, and 54% were women. Greater body mass index was associated with worse LV longitudinal strain, radial strain (apical view), and longitudinal synchrony (multivariable-adjusted P<0.0001). After accounting for body mass index, we found that central adiposity, as measured by waist circumference, was associated with worse global longitudinal strain and synchrony (P≤0.006). Measures of insulin resistance, dyslipidemia, and diabetes mellitus also were associated with distinct aspects of LV mechanical function. Circulating leptin concentrations were associated with global longitudinal and radial strain (apical view, P<0.0001), whereas no such association was found with leptin receptor, adiponectin, or C-reactive protein. Conclusions - Our findings highlight the association of central obesity and related cardiometabolic phenotypes above and beyond body mass index with subclinical measures of LV mechanical function. Interestingly, obesity-related traits were associated with distinct aspects of LV mechanics, underscoring potential differential effects along specific LV planes of deformation. These findings may shed light onto obesity-related cardiac remodeling and heart failure.
AB - Background - Obesity and cardiometabolic dysfunction are associated with increased risk of heart failure and other cardiovascular diseases. We sought to examine the association of cardiometabolic traits with left ventricular (LV) cardiac mechanics. We hypothesized that specific obesity-related phenotypes are associated with distinct aspects of LV strain. Methods and Results - We evaluated the associations of obesity-related phenotypes, including central adiposity, diabetes mellitus, insulin resistance, and circulating adipokine concentrations with echocardiographic measures of LV mechanical function among participants of the Framingham Heart Study Offspring and Third Generation cohorts. Among 6231 participants, the mean age was 51±16 years, and 54% were women. Greater body mass index was associated with worse LV longitudinal strain, radial strain (apical view), and longitudinal synchrony (multivariable-adjusted P<0.0001). After accounting for body mass index, we found that central adiposity, as measured by waist circumference, was associated with worse global longitudinal strain and synchrony (P≤0.006). Measures of insulin resistance, dyslipidemia, and diabetes mellitus also were associated with distinct aspects of LV mechanical function. Circulating leptin concentrations were associated with global longitudinal and radial strain (apical view, P<0.0001), whereas no such association was found with leptin receptor, adiponectin, or C-reactive protein. Conclusions - Our findings highlight the association of central obesity and related cardiometabolic phenotypes above and beyond body mass index with subclinical measures of LV mechanical function. Interestingly, obesity-related traits were associated with distinct aspects of LV mechanics, underscoring potential differential effects along specific LV planes of deformation. These findings may shed light onto obesity-related cardiac remodeling and heart failure.
KW - adipokine
KW - echocardiography
KW - epidemiology
KW - left ventricular function
KW - obesity
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U2 - 10.1161/CIRCHEARTFAILURE.116.003536
DO - 10.1161/CIRCHEARTFAILURE.116.003536
M3 - Article
C2 - 28495953
AN - SCOPUS:85019636814
SN - 1941-3289
VL - 10
JO - Circulation: Heart Failure
JF - Circulation: Heart Failure
IS - 5
M1 - e003536
ER -