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Arterioscler Thromb Vasc Biol. 2010 Feb;30(2):353-9. doi: 10.1161/ATVBAHA.109.196402. Epub 2009 Dec 3.

Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.

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1
Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, Calif 90095-7088, USA.

Abstract

BACKGROUND AND PURPOSE:

Although the Mexican population has a high predisposition to dyslipidemias and premature coronary artery disease, this population is underinvestigated for the genetic factors conferring the high susceptibility. This study attempted to determine these genetic factors.

METHODS AND RESULTS:

First, we investigated apolipoprotein B (apoB) levels in Mexican extended families with familial combined hyperlipidemia using a two-step testing strategy. In the screening step, we screened 5721 single-nucleotide polymorphisms (SNPs) for linkage signals with apoB. In the test step, we analyzed the 130 SNPs residing in regions of suggestive linkage signals for association with apoB. We identified significant associations with two SNPs (ie, rs1424032 [P=6.07x10(-6)] and rs1349411 [P=2.72x10(-4)]) that surpassed the significance level for the number of tests performed in the test step (P<3.84x10(-4)). Second, these SNPs were tested for replication in Mexican hyperlipidemic case-control samples. The same risk alleles as in the families with familial combined hyperlipidemia were significantly associated (P<0.05) with apoB in the case-control samples. The rs1349411 resides near the apoB messenger RNA editing enzyme (APOBEC1) involved in the processing of APOB messenger RNA in the small intestine. The rs1424032 resides in a highly conserved noncoding region predicted to function as a regulatory element.

CONCLUSIONS:

We identified two novel variants, rs1349411 and rs1424032, for serum apoB levels in Mexicans.

PMID:
19965785
PMCID:
PMC2809779
DOI:
10.1161/ATVBAHA.109.196402
[Indexed for MEDLINE]
Free PMC Article

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