Cited by 298Lipoproteins and Cardiovascular HealthCholesterol and Lipid MetabolismParaoxonase enzyme and polymorphisms

The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.

High-density lipoprotein subpopulation profile and coronary heart disease prevalence in male participants of the Framingham Offspring Study.

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Abstract

OBJECTIVE: High-density lipoprotein (HDL) is a heterogeneous lipoprotein class and there is no consensus on the value of HDL subspecies in coronary heart disease (CHD) risk assessment. We tested the hypothesis whether specific HDL subpopulations are significantly associated with CHD-prevalence. METHODS AND RESULTS: ApoA-I concentrations (mg/dL) in HDL subpopulations were quantitatively determined by native 2d gel electrophoresis, immunoblotting, and image analysis in male participants in the Framingham Offspring Study (FOS). CHD cases (n=169) had higher prebeta-1 and alpha-3 particle and lower alpha-1, prealpha-3, and prealpha-1 particle levels than either all (n=1277) or HDL cholesterol-matched (n=358) controls. alpha-1 and prealpha-3 levels had an inverse association, whereas alpha-3 and prealpha-1 particle levels had a positive association with CHD prevalence after adjusting the data for established CHD risk factors. Standardized logit coefficients indicated that alpha-1 HDL was most significantly associated with CHD prevalence. Moreover, each mg/dL increase in alpha-1 particle level decreased odds of CHD by 26% (P<0.0001), whereas each mg/dL increase in HDL cholesterol decreased odds of CHD by 2% in a model including all established CHD risk factors. CONCLUSIONS: Specific HDL subpopulations were positively correlated, whereas others were inversely correlated with CHD prevalence in male subject in the FOS, indicating that the various HDL particles might have different roles in the cause of CHD.

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Crossref · 10.1161/01.atv.0000146325.93749.a8

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Research works printed but not linked: 7

  1. 10.1161/circ.90.2.8044946 · DOI
  2. 10.1161/circ.85.1.1728453 · DOI
  3. 10.1161/atvb.20.12.2670 · DOI
  4. 10.1161/atvb.17.10.1885 · DOI
  5. 1996, Clin Chem, 42, 12;1992
  6. 10.1161/circ.100.6.594 · DOI
  7. 10.1161/atvb.21.8.1320 · DOI

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Metadata

Authors
Asztalos, B. F., Cupples, L. A., Demissie, S., Horvath, K. V., Cox, C. E., Batista, M. C., & Schaefer, E. J.
Affiliations
Boston University (US)
Venue
Arteriosclerosis, Thrombosis, and Vascular Biology
Published
2004-11
Volume
24
Issue
11
Pages
2181-2187
ISSN
  • 1079-5642 (ISSN-L)
  • 1524-4636
OpenAlex
W2103507414
Cited by
298
References
30
Citations by year
2025: 9 · 2024: 5 · 2023: 8 · 2022: 7 · 2021: 4 · 2020: 5 · 2019: 4 · 2018: 16 · 2017: 10 · 2016: 17 · 2015: 14 · 2014: 17 · 2013: 23 · 2012: 27
FWCI
15.79
Type
journal article
Language
en
Open access
Locations
  • Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (n01hc038038-022)
  • National Heart, Lung, and Blood Institute (HC 38038, HL54776, HL 64738, N01-HC, N01-HC-38038, R01HL054776, R01HL064738)
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Paraoxonase enzyme and polymorphisms
Keywords
high-density lipoprotein, HDL subpopulations, coronary artery disease, HDL cholesterol, apolipoprotein A-I, HDL heterogeneity, cardiovascular risk, Framingham Offspring Study, men
MeSH terms
Coronary Disease, Humans, Male, Prospective Studies, Risk Factors, Time, Prevalence, Apolipoprotein A-I, Observation

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