Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease: a nested case-control study in men

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Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease : a nested case-control study in men. / Cahill, Leah E; Sacks, Frank M; Rimm, Eric B; Jensen, Majken K.

I: Journal of Lipid Research, Bind 60, Nr. 8, 2019, s. 1457-1464.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Cahill, LE, Sacks, FM, Rimm, EB & Jensen, MK 2019, 'Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease: a nested case-control study in men', Journal of Lipid Research, bind 60, nr. 8, s. 1457-1464. https://doi.org/10.1194/jlr.P093823

APA

Cahill, L. E., Sacks, F. M., Rimm, E. B., & Jensen, M. K. (2019). Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease: a nested case-control study in men. Journal of Lipid Research, 60(8), 1457-1464. https://doi.org/10.1194/jlr.P093823

Vancouver

Cahill LE, Sacks FM, Rimm EB, Jensen MK. Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease: a nested case-control study in men. Journal of Lipid Research. 2019;60(8):1457-1464. https://doi.org/10.1194/jlr.P093823

Author

Cahill, Leah E ; Sacks, Frank M ; Rimm, Eric B ; Jensen, Majken K. / Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease : a nested case-control study in men. I: Journal of Lipid Research. 2019 ; Bind 60, Nr. 8. s. 1457-1464.

Bibtex

@article{7104927a59964dd69bff4bd35e79bd3c,
title = "Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease: a nested case-control study in men",
abstract = "The capacity of HDLs to accept cholesterol effluxing from macrophages has been proposed as a new biomarker of HDLs' anti-atherogenic function. Whether cholesterol efflux capacity (CEC) is independent of HDL cholesterol (HDL-C) as a biomarker for coronary heart disease (CHD) risk in a generally healthy primary-prevention population remains unanswered. Therefore, in this nested case-control study, we simultaneously assessed CEC (using J774 cells) and plasma HDL-C levels as predictors of CHD in healthy middle-aged and older men not receiving treatment affecting blood lipid concentrations. We used risk-set sampling of participants free of disease at baseline from the Health Professionals Follow-Up Study, and matched cases (n = 701) to controls 1:1 for age, smoking, and blood sampling date. We applied conditional logistic regression models to calculate the multivariable relative risk and 95% CIs of CHD over 16 years of follow-up. CEC and HDL-C were correlated (r = 0.50, P < 0.0001). The risk (95% CI) of CHD per one SD higher CEC was 0.82 (0.71-0.96), but completely attenuated to 1.08 (0.85-1.37) with HDL-C in the model. The association per one SD between HDL-C and CHD (0.66; 0.58-0.76) was essentially unchanged (0.68; 0.53-0.88) after adjustment for CEC. These findings indicate that CEC's ability to predict CHD may not be independent of HDL-C in a cohort of generally healthy men.",
keywords = "Aged, Biomarkers/blood, Case-Control Studies, Cholesterol, HDL/blood, Coronary Disease/blood, Female, Humans, Male, Middle Aged, Models, Cardiovascular, Risk Assessment",
author = "Cahill, {Leah E} and Sacks, {Frank M} and Rimm, {Eric B} and Jensen, {Majken K}",
note = "Copyright {\textcopyright} 2019 Cahill et al.",
year = "2019",
doi = "10.1194/jlr.P093823",
language = "English",
volume = "60",
pages = "1457--1464",
journal = "Journal of Lipid Research",
issn = "0022-2275",
publisher = "American Society for Biochemistry and Molecular Biology, Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Cholesterol efflux capacity, HDL cholesterol, and risk of coronary heart disease

T2 - a nested case-control study in men

AU - Cahill, Leah E

AU - Sacks, Frank M

AU - Rimm, Eric B

AU - Jensen, Majken K

N1 - Copyright © 2019 Cahill et al.

PY - 2019

Y1 - 2019

N2 - The capacity of HDLs to accept cholesterol effluxing from macrophages has been proposed as a new biomarker of HDLs' anti-atherogenic function. Whether cholesterol efflux capacity (CEC) is independent of HDL cholesterol (HDL-C) as a biomarker for coronary heart disease (CHD) risk in a generally healthy primary-prevention population remains unanswered. Therefore, in this nested case-control study, we simultaneously assessed CEC (using J774 cells) and plasma HDL-C levels as predictors of CHD in healthy middle-aged and older men not receiving treatment affecting blood lipid concentrations. We used risk-set sampling of participants free of disease at baseline from the Health Professionals Follow-Up Study, and matched cases (n = 701) to controls 1:1 for age, smoking, and blood sampling date. We applied conditional logistic regression models to calculate the multivariable relative risk and 95% CIs of CHD over 16 years of follow-up. CEC and HDL-C were correlated (r = 0.50, P < 0.0001). The risk (95% CI) of CHD per one SD higher CEC was 0.82 (0.71-0.96), but completely attenuated to 1.08 (0.85-1.37) with HDL-C in the model. The association per one SD between HDL-C and CHD (0.66; 0.58-0.76) was essentially unchanged (0.68; 0.53-0.88) after adjustment for CEC. These findings indicate that CEC's ability to predict CHD may not be independent of HDL-C in a cohort of generally healthy men.

AB - The capacity of HDLs to accept cholesterol effluxing from macrophages has been proposed as a new biomarker of HDLs' anti-atherogenic function. Whether cholesterol efflux capacity (CEC) is independent of HDL cholesterol (HDL-C) as a biomarker for coronary heart disease (CHD) risk in a generally healthy primary-prevention population remains unanswered. Therefore, in this nested case-control study, we simultaneously assessed CEC (using J774 cells) and plasma HDL-C levels as predictors of CHD in healthy middle-aged and older men not receiving treatment affecting blood lipid concentrations. We used risk-set sampling of participants free of disease at baseline from the Health Professionals Follow-Up Study, and matched cases (n = 701) to controls 1:1 for age, smoking, and blood sampling date. We applied conditional logistic regression models to calculate the multivariable relative risk and 95% CIs of CHD over 16 years of follow-up. CEC and HDL-C were correlated (r = 0.50, P < 0.0001). The risk (95% CI) of CHD per one SD higher CEC was 0.82 (0.71-0.96), but completely attenuated to 1.08 (0.85-1.37) with HDL-C in the model. The association per one SD between HDL-C and CHD (0.66; 0.58-0.76) was essentially unchanged (0.68; 0.53-0.88) after adjustment for CEC. These findings indicate that CEC's ability to predict CHD may not be independent of HDL-C in a cohort of generally healthy men.

KW - Aged

KW - Biomarkers/blood

KW - Case-Control Studies

KW - Cholesterol, HDL/blood

KW - Coronary Disease/blood

KW - Female

KW - Humans

KW - Male

KW - Middle Aged

KW - Models, Cardiovascular

KW - Risk Assessment

U2 - 10.1194/jlr.P093823

DO - 10.1194/jlr.P093823

M3 - Journal article

C2 - 31142574

VL - 60

SP - 1457

EP - 1464

JO - Journal of Lipid Research

JF - Journal of Lipid Research

SN - 0022-2275

IS - 8

ER -

ID: 244969538