Interaction of common sequence variants and selected risk factors in determination of HDL cholesterol levels.

doi:10.1016/j.clinbiochem.2010.04.001

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Article

Interaction of common sequence variants and selected risk factors in determination of HDL cholesterol levels.

Clinical biochemistry - 1 Jun 2010

Katerina Hirschfeldova, Michaela Sedova, Michal Vrablik, Helena Svobodova, Jana Zvarova, Jaroslav Hubacek, Richard Ceska

Abstract excerpt

OBJECTIVES: The aim of our study was to assess the association of common sequence variants, and selected interactions, with HDL-c plasma levels. DESIGN AND METHODS: We analysed 743 individuals (340 men and 403 women) with high mean triglyceride and LDL-c levels. The association of five polymorphic sites (ABCA1 g.1051G>A, APOA1 g.-75G>A, CETP g.-629C>A, HNF1A g.102A>C, and LIPG g.584C>T), apoE isoforms and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20394740
DOI: 10.1016/j.clinbiochem.2010.04.001

Genes

CETP
ABCA1
APOA1
APOE
LIPG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.