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转化生长因子-β1 多态性与颈动脉斑块及老年中国男性颈动脉内膜中层厚度增加相关:广州生物银行队列研究-心血管疾病亚队列。

A polymorphism in transforming growth factor-β1 is associated with carotid plaques and increased carotid intima-media thickness in older Chinese men: the Guangzhou Biobank Cohort Study-Cardiovascular Disease Subcohort.

机构信息

Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong.

出版信息

Atherosclerosis. 2011 Feb;214(2):391-6. doi: 10.1016/j.atherosclerosis.2010.11.025. Epub 2010 Nov 26.

DOI:10.1016/j.atherosclerosis.2010.11.025
PMID:21167485
Abstract

OBJECTIVE

Polymorphisms of the transforming growth factor-β1 (TGFB1) gene have not been associated with asymptomatic atherosclerosis previously. We investigated the relationship between a single nucleotide polymorphism (SNP) rs4803455 in TGFB1 and atherosclerosis identified by the presence of carotid plaque and increased intima-media thickness (IMT) in an older Chinese population.

METHODS

1996 subjects (992 (49.7%) men aged 50-85 years) from the Guangzhou Biobank Cohort Study-Cardiovascular Subcohort (GBCS-CVD) were genotyped. Carotid plaque and IMT were assessed by B-mode ultrasonography.

RESULTS

In male subjects, the C allele of TGFB1 rs4803455 was significantly associated with prevalence of carotid plaque (adjusted OR: 2.49, 95% CI: 1.16-5.36, P = 0.03). The C allele was related to increased number of common carotid artery (CCA) plaques (P=0.03) and larger carotid plaque area (P = 0.02) in men. The homozygous carriers of allele C in male subjects also had a higher risk of having carotid IMT ≥ 1 mm (adjusted OR: 1.75, 95% CI: 1.05-2.93, P = 0.03). These associations were independent of age, smoking, physical activity, body mass index, blood pressure, lipid profile, fasting glucose and high sensitivity C-reactive protein.

CONCLUSION

This is the first study to show that the C allele in TGFB1 was associated with increased risk of atherosclerosis in older Chinese men. Further investigations on the linkage between the TGFB1 gene and progression of atherosclerosis in asymptomatic populations are warranted.

摘要

目的

转化生长因子-β1(TGFB1)基因的多态性与无症状动脉粥样硬化之前尚未相关联。我们研究了 TGFB1 中的单核苷酸多态性(SNP)rs4803455 与颈动脉斑块和内膜-中层厚度(IMT)增加在老年中国人群中动脉粥样硬化之间的关系。

方法

1996 名受试者(1996 名受试者,992 名男性,年龄 50-85 岁)来自广州生物库队列研究-心血管亚队列(GBCS-CVD)进行基因分型。颈动脉斑块和 IMT 通过 B 型超声进行评估。

结果

在男性受试者中,TGFB1 rs4803455 的 C 等位基因与颈动脉斑块的患病率显着相关(调整后的 OR:2.49,95%CI:1.16-5.36,P = 0.03)。C 等位基因与男性颈总动脉(CCA)斑块数量增加(P = 0.03)和颈动脉斑块面积增大(P = 0.02)有关。男性受试者等位基因 C 的纯合子携带者也具有颈动脉 IMT≥1mm 的较高风险(调整后的 OR:1.75,95%CI:1.05-2.93,P = 0.03)。这些关联独立于年龄,吸烟,体力活动,体重指数,血压,血脂,空腹血糖和高敏 C 反应蛋白。

结论

这是第一项表明 TGFB1 中的 C 等位基因与老年中国男性动脉粥样硬化风险增加相关的研究。需要进一步研究 TGFB1 基因与无症状人群中动脉粥样硬化进展之间的联系。

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