High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures: MESA (The Multi-Ethnic Study of Atherosclerosis)

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High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures : MESA (The Multi-Ethnic Study of Atherosclerosis). / Aroner, Sarah A.; Koch, Manja; Mukamal, Kenneth J.; Furtado, Jeremy D.; Stein, James H.; Tattersall, Matthew C.; McClelland, Robyn L.; Jensen, Majken K.

In: Journal of the American Heart Association, Vol. 7, No. 6, e007824, 20.03.2018.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Aroner, SA, Koch, M, Mukamal, KJ, Furtado, JD, Stein, JH, Tattersall, MC, McClelland, RL & Jensen, MK 2018, 'High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures: MESA (The Multi-Ethnic Study of Atherosclerosis)', Journal of the American Heart Association, vol. 7, no. 6, e007824. https://doi.org/10.1161/JAHA.117.007824

APA

Aroner, S. A., Koch, M., Mukamal, K. J., Furtado, J. D., Stein, J. H., Tattersall, M. C., McClelland, R. L., & Jensen, M. K. (2018). High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures: MESA (The Multi-Ethnic Study of Atherosclerosis). Journal of the American Heart Association, 7(6), [e007824]. https://doi.org/10.1161/JAHA.117.007824

Vancouver

Aroner SA, Koch M, Mukamal KJ, Furtado JD, Stein JH, Tattersall MC et al. High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures: MESA (The Multi-Ethnic Study of Atherosclerosis). Journal of the American Heart Association. 2018 Mar 20;7(6). e007824. https://doi.org/10.1161/JAHA.117.007824

Author

Aroner, Sarah A. ; Koch, Manja ; Mukamal, Kenneth J. ; Furtado, Jeremy D. ; Stein, James H. ; Tattersall, Matthew C. ; McClelland, Robyn L. ; Jensen, Majken K. / High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures : MESA (The Multi-Ethnic Study of Atherosclerosis). In: Journal of the American Heart Association. 2018 ; Vol. 7, No. 6.

Bibtex

@article{39c7bbfc1f1242dc83794bfee1f15b33,
title = "High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures: MESA (The Multi-Ethnic Study of Atherosclerosis)",
abstract = "Background--Apolipoprotein C-III (apoC-III), a small proinflammatory protein present on 6% to 7% of high-density lipoprotein (HDL) particles, defines a subspecies of HDL adversely associated with coronary heart disease in primarily white cohorts. In a multi-ethnic population free of clinical cardiovascular disease, we evaluated the relationship between apoC-III-defined HDL subspecies and subclinical markers of atherosclerotic pathology. Methods and Results--We investigated cross-sectional associations between apolipoprotein A-I concentrations of apoC-III- defined HDL subspecies, measured via ELISA and imaging measures of subclinical atherosclerosis, among 4659 participants in the MESA (The Multi-Ethnic Study of Atherosclerosis) at baseline (2000-2002). HDL particles containing and lacking apoC-III were divergently associated with coronary artery calcification in women (P-heterogeneity=0.002) but not in men (P-heterogeneity=0.31) and with carotid plaque score (P-heterogeneity=0.02) and intima-media thickness (P-heterogeneity=0.06) in the overall study population. HDL lacking apoC-III was inversely associated with all outcome measures (coronary artery calcification, women: odds ratio per SD=0.81 [95% confidence interval [CI], 0.73-0.90]; carotid plaque, overall: odds ratio per SD=0.92 [95% CI, 0.84-1.00]; intima-media thickness, overall: mean difference per SD=-14.0 μm [95% CI, -21.1 to -6.7 lm]), whereas HDL containing apoCIII was positively associated (coronary artery calcification, women: odds ratio=1.10 [95% CI, 0.99-1.22]; plaque, overall: odds ratio=1.10 [95% CI, 1.01-1.19]) or unassociated. Neither total HDL nor HDL subspecies was associated with changes in subclinical atherosclerosis measures up to 10 years later. Conclusions--The presence of apoC-III defined a subspecies of HDL not inversely associated with baseline measures of subclinical atherosclerosis, supporting a role of apoC-III in the pathophysiology of cardiovascular disease.",
keywords = "Apolipoprotein, Atherosclerosis, Coronary artery calcium, High-density lipoprotein, Plaque",
author = "Aroner, {Sarah A.} and Manja Koch and Mukamal, {Kenneth J.} and Furtado, {Jeremy D.} and Stein, {James H.} and Tattersall, {Matthew C.} and McClelland, {Robyn L.} and Jensen, {Majken K.}",
year = "2018",
month = mar,
day = "20",
doi = "10.1161/JAHA.117.007824",
language = "English",
volume = "7",
journal = "Journal of the American Heart Association",
issn = "2047-9980",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - High-density lipoprotein subspecies defined by apolipoprotein C-III and subclinical atherosclerosis measures

T2 - MESA (The Multi-Ethnic Study of Atherosclerosis)

AU - Aroner, Sarah A.

AU - Koch, Manja

AU - Mukamal, Kenneth J.

AU - Furtado, Jeremy D.

AU - Stein, James H.

AU - Tattersall, Matthew C.

AU - McClelland, Robyn L.

AU - Jensen, Majken K.

PY - 2018/3/20

Y1 - 2018/3/20

N2 - Background--Apolipoprotein C-III (apoC-III), a small proinflammatory protein present on 6% to 7% of high-density lipoprotein (HDL) particles, defines a subspecies of HDL adversely associated with coronary heart disease in primarily white cohorts. In a multi-ethnic population free of clinical cardiovascular disease, we evaluated the relationship between apoC-III-defined HDL subspecies and subclinical markers of atherosclerotic pathology. Methods and Results--We investigated cross-sectional associations between apolipoprotein A-I concentrations of apoC-III- defined HDL subspecies, measured via ELISA and imaging measures of subclinical atherosclerosis, among 4659 participants in the MESA (The Multi-Ethnic Study of Atherosclerosis) at baseline (2000-2002). HDL particles containing and lacking apoC-III were divergently associated with coronary artery calcification in women (P-heterogeneity=0.002) but not in men (P-heterogeneity=0.31) and with carotid plaque score (P-heterogeneity=0.02) and intima-media thickness (P-heterogeneity=0.06) in the overall study population. HDL lacking apoC-III was inversely associated with all outcome measures (coronary artery calcification, women: odds ratio per SD=0.81 [95% confidence interval [CI], 0.73-0.90]; carotid plaque, overall: odds ratio per SD=0.92 [95% CI, 0.84-1.00]; intima-media thickness, overall: mean difference per SD=-14.0 μm [95% CI, -21.1 to -6.7 lm]), whereas HDL containing apoCIII was positively associated (coronary artery calcification, women: odds ratio=1.10 [95% CI, 0.99-1.22]; plaque, overall: odds ratio=1.10 [95% CI, 1.01-1.19]) or unassociated. Neither total HDL nor HDL subspecies was associated with changes in subclinical atherosclerosis measures up to 10 years later. Conclusions--The presence of apoC-III defined a subspecies of HDL not inversely associated with baseline measures of subclinical atherosclerosis, supporting a role of apoC-III in the pathophysiology of cardiovascular disease.

AB - Background--Apolipoprotein C-III (apoC-III), a small proinflammatory protein present on 6% to 7% of high-density lipoprotein (HDL) particles, defines a subspecies of HDL adversely associated with coronary heart disease in primarily white cohorts. In a multi-ethnic population free of clinical cardiovascular disease, we evaluated the relationship between apoC-III-defined HDL subspecies and subclinical markers of atherosclerotic pathology. Methods and Results--We investigated cross-sectional associations between apolipoprotein A-I concentrations of apoC-III- defined HDL subspecies, measured via ELISA and imaging measures of subclinical atherosclerosis, among 4659 participants in the MESA (The Multi-Ethnic Study of Atherosclerosis) at baseline (2000-2002). HDL particles containing and lacking apoC-III were divergently associated with coronary artery calcification in women (P-heterogeneity=0.002) but not in men (P-heterogeneity=0.31) and with carotid plaque score (P-heterogeneity=0.02) and intima-media thickness (P-heterogeneity=0.06) in the overall study population. HDL lacking apoC-III was inversely associated with all outcome measures (coronary artery calcification, women: odds ratio per SD=0.81 [95% confidence interval [CI], 0.73-0.90]; carotid plaque, overall: odds ratio per SD=0.92 [95% CI, 0.84-1.00]; intima-media thickness, overall: mean difference per SD=-14.0 μm [95% CI, -21.1 to -6.7 lm]), whereas HDL containing apoCIII was positively associated (coronary artery calcification, women: odds ratio=1.10 [95% CI, 0.99-1.22]; plaque, overall: odds ratio=1.10 [95% CI, 1.01-1.19]) or unassociated. Neither total HDL nor HDL subspecies was associated with changes in subclinical atherosclerosis measures up to 10 years later. Conclusions--The presence of apoC-III defined a subspecies of HDL not inversely associated with baseline measures of subclinical atherosclerosis, supporting a role of apoC-III in the pathophysiology of cardiovascular disease.

KW - Apolipoprotein

KW - Atherosclerosis

KW - Coronary artery calcium

KW - High-density lipoprotein

KW - Plaque

U2 - 10.1161/JAHA.117.007824

DO - 10.1161/JAHA.117.007824

M3 - Journal article

C2 - 29540426

AN - SCOPUS:85043702305

VL - 7

JO - Journal of the American Heart Association

JF - Journal of the American Heart Association

SN - 2047-9980

IS - 6

M1 - e007824

ER -

ID: 244626002