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对氧磷酶1(PON1)Q192R基因多态性与冠心病的关联:英国女性心脏与健康队列研究及一项荟萃分析的结果

The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis.

作者信息

Lawlor Debbie A, Day Ian N M, Gaunt Tom R, Hinks Lesley J, Briggs Patricia J, Kiessling Matthew, Timpson Nick, Smith George Davey, Ebrahim Shah

机构信息

Department of Social Medicine, University of Bristol, UK.

出版信息

BMC Genet. 2004 Jun 23;5:17. doi: 10.1186/1471-2156-5-17.

Abstract

BACKGROUND

There have been inconsistent results from case-control studies assessing the association of the PON1 Q192R polymorphism with coronary heart disease (CHD). Most studies have included predominantly men and the association in women is unclear. Since lipid levels vary between the sexes the antioxidant effect of PON1 and any genes associated with it may also vary by sex. We have examined the association of the PON1 Q192R polymorphism with CHD in a large cohort of British women and combined the results from our cohort study with those from all other published studies.

RESULTS

The distribution of genotypes was the same among women with CHD and those without disease. The odds ratio (95% confidence interval) of having CHD comparing those with either the QR or RR genotype to those with QQ genotype (dominant model of association) was 1.03 (0.89, 1.21) and the per allele odds ratio was 0.98 (0.95, 1.01). In a meta-analysis of this and 38 other published studies (10,738 cases and 17,068 controls) the pooled odds ratio for the dominant effect was 1.14 (1.08, 1.20) and for the per allele effect was 1.10 (1.06, 1.13). There was evidence of small study bias in the meta-analyses and the dominant effect among those studies with 500 or more cases was 1.05 (0.96, 1.15). Ethnicity and reporting of whether the genotyping was done blind to the participants clinical status also contributed to heterogeneity between studies, but there was no difference in effect between studies with 50% or more women compared to those with fewer women and no difference between studies of healthy populations compared to those at high risk (with diabetes, renal disease of familial hypercholesterolaemia).

CONCLUSION

There is no robust evidence that the PON1 Q192R polymorphism is associated with CHD risk in Caucasian women or men.

摘要

背景

在评估对氧磷酶1(PON1)Q192R基因多态性与冠心病(CHD)关联的病例对照研究中,结果并不一致。大多数研究主要纳入男性,女性中的关联尚不清楚。由于血脂水平存在性别差异,PON1的抗氧化作用及其相关基因的作用可能也因性别而异。我们在一大群英国女性中研究了PON1 Q192R基因多态性与冠心病的关联,并将我们队列研究的结果与所有其他已发表研究的结果相结合。

结果

冠心病女性患者和非冠心病女性患者的基因型分布相同。将具有QR或RR基因型者与具有QQ基因型者(关联的显性模型)相比,患冠心病的比值比(95%置信区间)为1.03(0.89,1.21),每个等位基因的比值比为0.98(0.95,1.01)。在对本研究和其他38项已发表研究(10738例病例和17068例对照)的荟萃分析中,显性效应的合并比值比为1.14(1.08,1.20),每个等位基因效应的合并比值比为1.10(1.06,1.13)。荟萃分析中有证据表明存在小规模研究偏倚,病例数在500例或以上的研究中的显性效应为1.05(0.96,1.15)。种族以及基因分型是否对参与者的临床状态设盲的报告也导致了研究之间的异质性,但女性比例在50%或以上的研究与女性比例较低的研究之间,以及健康人群研究与高危人群(患有糖尿病、肾病或家族性高胆固醇血症)研究之间,效应没有差异。

结论

没有确凿证据表明PON1 Q192R基因多态性与白种女性或男性的冠心病风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7a/449704/38675d9b31b2/1471-2156-5-17-1.jpg

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