ApoC-III gene polymorphisms and risk of coronary artery disease
Open accessAbstract
Several polymorphisms in the apolipoprotein C-III (apoC-III) gene have been associated with hypertriglyceridemia, but the link with coronary artery disease risk is still controversial. In particular, apoC-III promoter sequence variants in the insulin responsive element (IRE), constitutively resistant to downregulation by insulin, have never been investigated in this connection. We studied a total of 800 patients, 549 of whom had angiographically documented coronary atherosclerosis, whereas 251 had normal coronary arteriograms. We measured plasma lipids, insulin, apoA-I, apoB, and apoC-III and assessed three polymorphisms in the apoC-III gene, namely, T-455C in the IRE promoter region, C1100T in exon 3, and Sst1 polymorphic site (S1/S2) in the 3' untranslated region. Each variant influenced triglyceride levels, but only the T-455C (in homozygosity) and S2 alleles influenced apoC-III levels. In coronary artery disease (CAD) patients, 18.6% were homozygous for the -455C variant compared with only 9.2% in CAD-free group (P < 0.001). In logistic regression models, homozygosity for -455C variant was associated with a significantly increased risk of CAD (OR = 2.5 and 2.18 for unadjusted and adjusted models, respectively) suggesting that it represents an independent genetic susceptibility factor for CAD.
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Previous studies have suggested that two single-nucleotide polymorphisms in the gene encoding apolipoprotein C3 (APOC3) may be associated with hypertriglyceridemia.
“Previous studies have suggested that two single-nucleotide polymorphisms (SNPs) in the gene encoding apolipoprotein C3 (APOC3) may be associated with hypertriglyceridemia.4–8”
From Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease (2010) · cites this paper as [6]
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Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease
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Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease
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- Authors
- Olivieri, O., Stranieri, C., Bassi, A., Zaia, B., Girelli, D., Pizzolo, F., Trabetti, E., Cheng, S., Grow, M. A., Pignatti, P. F., & Corrocher, R.
- Affiliations
- University of Verona (IT)
- Corresponding author
- Olivieri, Oliviero
- Venue
- Journal of Lipid Research
- Publisher
- Elsevier BV
- Published
- 2002-09
- Volume
- 43
- Issue
- 9
- Pages
- 1450-1457
- ISSN
- 0022-2275 (ISSN-L)
- OpenAlex
- W2144970509
- Cited by
- 70
- References
- 39
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 3 · 2022: 1 · 2021: 2 · 2020: 2 · 2019: 1 · 2018: 3 · 2017: 4 · 2016: 3 · 2015: 2 · 2014: 3 · 2013: 6 · 2012: 2
- FWCI
- 2.84
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Lipid Research (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- INFM-OAR (INFN Catania) (submittedVersion, cc-by)
- Funders
- Fondazione Cassa di Risparmio di Verona Vicenza Belluno e Ancona
- Regione del Veneto
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- apolipoprotein C-III, genetic polymorphism, coronary artery disease, genetic susceptibility, promoter, 3' untranslated region, hypertriglyceridemia, triglyceride levels
- MeSH terms
- Adult, Apolipoproteins B, Apolipoproteins C, Coronary Artery Disease, Female, Genotype, Humans, Insulin, Male, Middle Aged, Polymorphism, Genetic, Biomarkers, Odds Ratio, Apolipoprotein A-I, Genetic Predisposition to Disease, Apolipoprotein C-III
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