High-Density Lipoprotein Subspecies Defined by Presence of Apolipoprotein C-III and Incident Coronary Heart Disease in Four Cohorts

Majken K. Jensen, Sarah A. Aroner, Kenneth J. Mukamal, Jeremy D. Furtado, Wendy S. Post, Michael Y. Tsai, Anne Tjønneland, Joseph F. Polak, Eric B. Rimm, Kim Overvad, Robyn L. McClelland, Frank M. Sacks

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Background: The causal role of high-density lipoprotein (HDL) cholesterol in cardioprotection has been questioned by genetic and randomized studies. Novel measures that relate to HDL function may contribute new information to the prediction of cardiovascular risk. Apolipoprotein C-III (apoC-III) is a key regulator of lipoprotein metabolism. We investigated whether subspecies of HDL defined by apoC-III are associated with coronary heart disease (CHD). Methods: We used immunoaffinity chromatography to measure the apoA-I concentrations of HDL that contains and lacks apoC-III in 2 prospective studies of adults free of CHD. In MESA (Multi-Ethnic Study of Atherosclerosis), 5657 participants (52% women, 52-72 years of age) were followed for risk of CHD from 2000 to 2002 through 2013. In a case-cohort study nested within the DCH study (Danish Diet, Cancer, and Health), 3642 participants (47% women, 51-64 years of age) were followed from 1994 to 1997 through 2010. Subsequently, we conducted a meta-analysis that combined these results with the previously published findings from 2 cohort studies that used similar laboratory methodology to measure lipoproteins, totaling 2997 incident cases. Results: ApoC-III was found on 6% to 8% of apoA-I. The 2 HDL subspecies showed opposing associations, with risk of CHD in each of the individual cohorts and in the meta-analysis (P heterogeneity between the 2 subspecies <0.01). HDL that contains apoC-III was associated with a higher risk of CHD (pooled relative risk per standard deviation, 1.09; 95% confidence interval, 1.01-1.18), whereas HDL that lacks apoC-III was associated with lower risk (relative risk, 0.76; 95% confidence interval, 0.70-0.83). The relative risk for HDL lacking apoC-III was even more negative than the relative risk for total HDL (relative risk, 0.80; 95% confidence interval, 0.74-0.87). Conclusions: Our findings from 4 prospective studies support the hypothesis that apoC-III may mark a subfraction of HDL that is associated with higher risk of CHD. New measures reflecting HDL structure and function may provide novel insights for cardiovascular risk that extend beyond traditional plasma HDL cholesterol concentrations.

Original languageEnglish (US)
Pages (from-to)1364-1373
Number of pages10
JournalCirculation
Volume137
Issue number13
DOIs
StatePublished - Mar 27 2018

Bibliographical note

Funding Information:
and UL1-TR-001079 from the National Center for Research Resources, and contracts N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, and N01-HC-95169 from National Heart, Lung, and Blood Institute. HDL apoC-III measurements were supported by an independent research grant from Roche Pharmaceuticals and by the William F. Milton Fund, Harvard Medical School. The DCH study is supported by the Danish Independent Research Council and the Danish Cancer Society. HDL apoC-III measurements were funded by a Young Research Award from the Danish Independent Research Council. The funding sources had no role in the conduct of the study.

Funding Information:
MESA is a National Heart, Lung, and Blood Institute–funded study supported by grants R01 HL071739 and R21 HL091217 from the National Heart, Lung, and Blood Institute, grants T32 DK 007703 from the National Institute of Diabetes and Digestive and Kidney Diseases, grants UL1-TR-000040

Publisher Copyright:
© 2018 American Heart Association, Inc.

Keywords

  • CHD
  • HDL
  • biomarker
  • cohort study
  • plasma

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