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GWAS Study

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection.

Pollin TI, Damcott CM, Shen H et al.

19074352 PubMed ID
GWAS Study Type
1507 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PT
Pollin TI
DC
Damcott CM
SH
Shen H
OS
Ott SH
SJ
Shelton J
HR
Horenstein RB
PW
Post W
MJ
McLenithan JC
BL
Bielak LF
PP
Peyser PA
MB
Mitchell BD
MM
Miller M
OJ
O'Connell JR
SA
Shuldiner AR
Chapter II

Abstract

Summary of the research findings

Apolipoprotein C-III (apoC-III) inhibits triglyceride hydrolysis and has been implicated in coronary artery disease. Through a genome-wide association study, we have found that about 5% of the Lancaster Amish are heterozygous carriers of a null mutation (R19X) in the gene encoding apoC-III (APOC3) and, as a result, express half the amount of apoC-III present in noncarriers. Mutation carriers compared with noncarriers had lower fasting and postprandial serum triglycerides, higher levels of HDL-cholesterol and lower levels of LDL-cholesterol. Subclinical atherosclerosis, as measured by coronary artery calcification, was less common in carriers than noncarriers, which suggests that lifelong deficiency of apoC-III has a cardioprotective effect.

809 Old Order Amish individuals

Chapter III

Study Statistics

Key metrics and study information

1507
Total Participants
GWAS
Study Type
Yes
Replicated
698 Old Order Amish individuals
Replication Participants
Other
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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