TY - JOUR
T1 - Clinical associations of vascular stiffness, microvascular dysfunction, and prevalent cardiovascular disease in a black cohort
T2 - The jackson heart study
AU - Cooper, Leroy L.
AU - Musani, Solomon K.
AU - Moore, Josiah A.
AU - Clarke, Victoria A.
AU - Yano, Yuichiro
AU - Cobbs, Keith
AU - Tsao, Connie W.
AU - Butler, Javed
AU - Hall, Michael E.
AU - Hamburg, Naomi M.
AU - Benjamin, Emelia J.
AU - Vasan, Ramachandran S.
AU - Mitchell, Gary F.
AU - Fox, Ervin R.
N1 - Funding Information:
The Jackson Heart Study (JHS) is supported and conducted in collaboration with Jackson State University (HHSN268201800013I), Tougaloo College (HHSN268201800014I), the Mississippi State Department of Health (HHSN268201800015I), and the University of Mississippi Medical Center (HHSN268201800010I, HHSN268201800011I, and HHSN268201800012I) contracts from the National Heart, Lung, and Blood Institute (NHLBI) and the National Institute for Minority Health and Health Disparities (NIMHD). Dr Mitchell is funded by research grants HL094898, DK082447, HL107385, HL104184, and HL126136 from the National Institutes of Health. Dr Benjamin was funded by research grants R01HL128914; 2R01 HL092577; American Heart Association18SFRN34110082; 1R01HL141434; 2U54HL120163, and HHSN26820130047C. Dr Tsao was funded partially by grant K23HL118529. Dr Cooper was partially funded by grant 2R25HL105400. The views expressed in this manuscript are those of the authors and do not necessarily represent the views of the National Heart, Lung, and Blood Institute; the National Institutes of Health; or the US Department of Health and Human Services.
Funding Information:
The Jackson Heart Study (JHS) is supported and conducted in collaboration with Jackson State University (HHSN268201800013I), Tougaloo College (HHSN268201800014I), the Mississippi State Department of Health (HHSN268201800015I), and the University of Mississippi Medical Center (HHSN268201800010I, HHSN268201800011I, and HHSN268201800012I) contracts from the National Heart, Lung, and Blood Institute (NHLBI) and the National Institute for Minority Health and Health Disparities (NIMHD). Dr Mitchell is funded by research grants HL094898, DK082447, HL107385, HL104184, and HL126136 from the National Institutes of Health. Dr Benjamin was funded by research grants R01HL128914; 2R01 HL092577; American Heart Association 18SFRN34110082; 1R01HL141434; 2U54HL120163, and HHSN26820130047C. Dr Tsao was funded partially by grant K23HL118529. Dr Cooper was partially funded by grant 2R25HL105400. The views expressed in this manuscript are those of the authors and do not necessarily represent the views of the National Heart, Lung, and Blood Institute; the National Institutes of Health; or the US Department of Health and Human Services.
Publisher Copyright:
© 2020 The Authors.
PY - 2020
Y1 - 2020
N2 - BACKGROUND: Measures of vascular dysfunction are related to adverse cardiovascular disease (CVD) outcomes in non-His-panic, White populations; however, data from Black individuals are limited. We aimed to investigate the associations between novel hemodynamic measures and prevalent CVD in a sample of Black individuals. METHODS AND RESULTS: Among older Black participants of the Jackson Heart Study, we assessed noninvasive vascular hemodynamic measures using arterial tonometry and Doppler ultrasound. We assessed 5 measures of aortic stiffness and wave reflection (carotid-femoral pulse wave velocity, pulse wave velocity ratio, forward pressure wave amplitude, central pulse pressure, and augmentation index), and 2 measures of microvascular function (baseline and hyperemic brachial flow veloc-ity). Using multivariable logistic regression models, we examined the relations between vascular hemodynamic measures and prevalent CVD. In models adjusted for traditional CVD risk factors, higher carotid-femoral pulse wave velocity (odds ratio [OR],1.25; 95% CI, 1.01–1.55; P=0.04), lower augmentation index (OR, 0.84; 95% CI, 0.70–0.99; P=0.05), and lower hyperemic brachial flow velocity (OR, 0.77; 95% CI, 0.65–0.90; P=0.001) were associated with higher odds of CVD. After further adjustment for hypertension treatment, lower augmentation index (OR, 0.84; 95% CI, 0.70–0.99; P=0.04) and hyperemic brachial flow velocity (OR, 0.79; 95% CI, 0.67–0.94; P=0.006), but not carotid-femoral pulse wave velocity (OR, 1.23; 95% CI, 0.99–1.051; P=0.06), were associated with higher odds of CVD. CONCLUSIONS: In a sample of older Black individuals, more severe microvascular damage and aortic stiffness were associated with prevalent CVD. Further research on hemodynamic mechanisms that contribute to cardiovascular risk among older Black individuals is merited.
AB - BACKGROUND: Measures of vascular dysfunction are related to adverse cardiovascular disease (CVD) outcomes in non-His-panic, White populations; however, data from Black individuals are limited. We aimed to investigate the associations between novel hemodynamic measures and prevalent CVD in a sample of Black individuals. METHODS AND RESULTS: Among older Black participants of the Jackson Heart Study, we assessed noninvasive vascular hemodynamic measures using arterial tonometry and Doppler ultrasound. We assessed 5 measures of aortic stiffness and wave reflection (carotid-femoral pulse wave velocity, pulse wave velocity ratio, forward pressure wave amplitude, central pulse pressure, and augmentation index), and 2 measures of microvascular function (baseline and hyperemic brachial flow veloc-ity). Using multivariable logistic regression models, we examined the relations between vascular hemodynamic measures and prevalent CVD. In models adjusted for traditional CVD risk factors, higher carotid-femoral pulse wave velocity (odds ratio [OR],1.25; 95% CI, 1.01–1.55; P=0.04), lower augmentation index (OR, 0.84; 95% CI, 0.70–0.99; P=0.05), and lower hyperemic brachial flow velocity (OR, 0.77; 95% CI, 0.65–0.90; P=0.001) were associated with higher odds of CVD. After further adjustment for hypertension treatment, lower augmentation index (OR, 0.84; 95% CI, 0.70–0.99; P=0.04) and hyperemic brachial flow velocity (OR, 0.79; 95% CI, 0.67–0.94; P=0.006), but not carotid-femoral pulse wave velocity (OR, 1.23; 95% CI, 0.99–1.051; P=0.06), were associated with higher odds of CVD. CONCLUSIONS: In a sample of older Black individuals, more severe microvascular damage and aortic stiffness were associated with prevalent CVD. Further research on hemodynamic mechanisms that contribute to cardiovascular risk among older Black individuals is merited.
KW - Aortic stiffness
KW - Cardiovascular disease
KW - Microvascular function
KW - Ultrasound
KW - Vascular function
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U2 - 10.1161/JAHA.120.017018
DO - 10.1161/JAHA.120.017018
M3 - Article
C2 - 32873113
AN - SCOPUS:85091125210
VL - 9
JO - Journal of the American Heart Association
JF - Journal of the American Heart Association
SN - 2047-9980
IS - 18
M1 - e017018
ER -