作者
Myocardial Infarction Genetics Consortium Investigators, Erin Austin, Ph.D., Zi Ye, M.D., Ph.D., Iftikhar J. Kullo M.D, (authors from Mayo Clinic)
发表日期
2014/11/27
期刊
N Engl J Med.
卷号
371
期号
22
页码范围
2072
简介
Background
Ezetimibe lowers plasma levels of low-density lipoprotein (LDL) cholesterol by inhibiting the activity of the Niemann–Pick C1-like 1 (NPC1L1) protein. However, whether such inhibition reduces the risk of coronary heart disease is not known. Human mutations that inactivate a gene encoding a drug target can mimic the action of an inhibitory drug and thus can be used to infer potential effects of that drug.
Methods
We sequenced the exons of NPC1L1 in 7364 patients with coronary heart disease and in 14,728 controls without such disease who were of European, African, or South Asian ancestry. We identified carriers of inactivating mutations (nonsense, splice-site, or frameshift mutations). In addition, we genotyped a specific inactivating mutation (p.Arg406X) in 22,590 patients with coronary heart disease and in 68,412 controls. We tested the association between the presence of an inactivating mutation …
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