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1.
Kaohsiung J Med Sci ; 33(1): 1-10, 2017 Jan.
Article in English | MEDLINE | ID: mdl-28088267

ABSTRACT

The aim of this meta-analysis was to detect whether three identified single nucleotide polymorphisms (SNPs) (rs646776, rs599839, and rs17465637) at 1p13.3 and 1q41 are associated with lipid levels and the risk of coronary artery disease (CAD). Databases of MEDLINE, EMBASE, the Cochrane Library, and BIOSIS were systematically searched. The pooled effects were expressed as odds ratio or standardized mean difference or mean difference with 95% confidence intervals. A total of 14 studies with 57,916 patients were included in the meta-analysis. Pooled effects showed that the AA group of 1p13.3 rs599839 had higher total cholesterol (TC) and low-density lipoprotein cholesterol (LDLC), and lower high-density lipoprotein cholesterol (HDLC) levels than the GA/GG group, and the CAD group had higher AA genotype frequency than the control group. The TT group of 1p13.3 rs646776 had higher TC and LDLC levels and lower HDLC levels than the CT/CC group. The CAD group also had higher CC genotype frequency of 1q41 rs17465637 than the control group. The SNPs of 1p13 rs599839 and rs646776 were associated with serum lipid levels. The genetic variants of 1p13 rs599839 and 1q41 rs17465637 SNPs were prominently related to CAD, and the genetic variants of chromosome 1p13 promote the risk of CAD by increased TC and LDLC levels and decreased HDLC levels.


Subject(s)
Chromosomes, Human, Pair 1/chemistry , Coronary Artery Disease/genetics , Genetic Loci , Genetic Predisposition to Disease , Polymorphism, Single Nucleotide , Aged , Alleles , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Coronary Artery Disease/blood , Coronary Artery Disease/diagnosis , Coronary Artery Disease/pathology , Female , Gene Frequency , Genotype , Humans , Male , Middle Aged , Odds Ratio , Risk
2.
Neurobiol Aging ; 35(6): 1513.e13-23, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24468472

ABSTRACT

The purpose of this meta-analysis was to detect the association between the cholesteryl ester transfer protein gene polymorphisms and the risk of Alzheimer's disease (AD), carotid atherosclerosis, longevity, and the efficacy of statin therapy. Databases of MEDLINE, EMBASE, BIOSIS, the Cochrane Library, and the Chinese National Knowledge Infrastructure were systematically searched. Thirty-two studies were included in this meta-analysis. There was no difference in the I405V, C629A, and Taq1B polymorphisms between AD and control groups. However, stratified analysis showed that AD group had higher B2B2 genotype frequency than control group in Asian populations with APOE4+ in Taq1B. I405V and Taq1B polymorphisms were not associated with the risk of carotid atherosclerosis and longevity. The efficacy of statin therapy was not associated with Taq1B polymorphism. In conclusion, there was no association between cholesteryl ester transfer protein gene polymorphisms and the risk of AD, carotid atherosclerosis, longevity, and the efficacy of statin therapy in the pooled effects of overall population. However, the B2B2 genotype of Taq1B was associated with increased risk of AD in the Asian populations with APOE4+.


Subject(s)
Alzheimer Disease/genetics , Carotid Artery Diseases/genetics , Cholesterol Ester Transfer Proteins/genetics , Databases, Bibliographic , Genetic Association Studies , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Longevity/genetics , Polymorphism, Genetic/genetics , Aged , Aged, 80 and over , Apolipoprotein E4 , Asian People , Female , Humans , Male , Middle Aged , Risk
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