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血压和高血压与日本人种中的 7 个位点相关。

Blood pressure and hypertension are associated with 7 loci in the Japanese population.

机构信息

Department of Gene Diagnostics and Therapeutics, Research Institute, International Medical Center of Japan, Tokyo, Japan.

出版信息

Circulation. 2010 Jun 1;121(21):2302-9. doi: 10.1161/CIRCULATIONAHA.109.904664. Epub 2010 May 17.

Abstract

BACKGROUND

Two consortium-based genome-wide association studies have recently identified robust and significant associations of common variants with systolic and diastolic blood pressures in populations of European descent, warranting further investigation in populations of non-European descent.

METHODS AND RESULTS

We examined the associations at 27 loci reported by the genome-wide association studies on Europeans in a screening panel of Japanese subjects (n=1526) and chose 11 loci showing association signals (1-tailed test in the screening, P<0.3) for an extensive replication study with a follow-up panel of 3 Japanese general-population cohorts (n < or =24 300). Significant associations were replicated for 7 loci-CASZ1, MTHFR, ITGA9, FGF5, CYP17A1-CNNM2, ATP2B1, and CSK-ULK3-with any or all of these 3 traits: systolic blood pressure (P=1.4x10(-14) to 0.05), diastolic blood pressure (P=1.9x10(-12) to 0.05), and hypertension (P=2.0x10(-14) to 0.006; odds ratio, 1.10 to 1.29). The strongest association was observed for FGF5. In the whole study panel, the variance (R(2)) for blood pressure explained by the 7 single-nucleotide polymorphism loci was calculated to be R(2)=0.003 for male and 0.006 for female participants. Stratified analysis implied the potential presence of a gene-age-sex interaction, although it did not reach a conclusive level of statistical significance after adjustment for multiple testing.

CONCLUSIONS

We have confirmed 7 loci associated with blood pressure and/or hypertension in the Japanese. These loci can guide fine-mapping efforts to pinpoint causal variants and causal genes with the integration of multiethnic results.

摘要

背景

两项基于联盟的全基因组关联研究最近在欧洲血统人群中发现了常见变异与收缩压和舒张压之间存在稳健且显著的关联,这使得有必要在非欧洲血统人群中进一步研究。

方法和结果

我们在日本受试者的筛查面板(n=1526)中检查了欧洲人全基因组关联研究报告的 27 个位点的关联,并选择了 11 个显示关联信号的位点(在筛查中进行单侧检验,P<0.3),以便在 3 个日本普通人群队列的随访面板中进行广泛的复制研究(n <或=24300)。在任何或所有这 3 个特征中都复制到了 7 个显著关联的位点-CASZ1、MTHFR、ITGA9、FGF5、CYP17A1-CNNM2、ATP2B1 和 CSK-ULK3-收缩压(P=1.4x10(-14)至 0.05)、舒张压(P=1.9x10(-12)至 0.05)和高血压(P=2.0x10(-14)至 0.006;优势比,1.10 至 1.29)。最强的关联发生在 FGF5 上。在整个研究面板中,通过 7 个单核苷酸多态性位点解释的血压方差(R(2))男性参与者为 0.003,女性参与者为 0.006。分层分析表明存在基因年龄性别相互作用的潜在可能性,尽管在进行多次测试调整后,这种相互作用并未达到统计学上的显著水平。

结论

我们在日本人中证实了与血压和/或高血压相关的 7 个位点。这些位点可以通过整合多民族研究结果,指导精细映射工作,以确定因果变异和因果基因。

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