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携带血红蛋白 2-2 基因型的 64 岁女性,患有已确诊的糖尿病,其颈动脉粥样硬化的风险增加。

The haptoglobin 2-2 genotype is associated with carotid atherosclerosis in 64-year old women with established diabetes.

机构信息

Center for Cardiovascular and Metabolic Research, Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Sweden.

出版信息

Clin Chim Acta. 2010 Apr 2;411(7-8):500-4. doi: 10.1016/j.cca.2009.12.025. Epub 2010 Jan 12.

Abstract

BACKGROUND

Haptoglobin polymorphism generates three common human genotypes: Hp1-1, Hp2-1 and Hp2-2. Among subjects with diabetes, Hp2-2 is associated with an elevated risk to develop cardiovascular disease. The impact of haptoglobin genotype on subclinical carotid atherosclerosis is not known. We hypothesized that Hp2-2 was associated with increased occurrence of carotid atherosclerosis in subjects with diabetes.

METHODS

We studied a population-based sample of 64-year old women with diabetes (n=226), either established diabetes known before study entry (n=116) or new diabetes detected at study screening (n=110). Haptoglobin genotype was determined by PCR. Carotid atherosclerosis was assessed by ultrasound imaging.

RESULTS

In the entire diabetes cohort, no differences were observed in carotid intima-media thickness (IMT) or plaque prevalence between the genotype groups. However, among those with established diabetes, Hp2-2 was associated with higher plaque prevalence and larger carotid IMT compared with the Hp2-1 and Hp1-1 genotypes. Common cardiovascular risk factors did not differ between the genotype groups.

CONCLUSIONS

The Hp2-2 genotype was associated with increased occurrence of subclinical carotid atherosclerosis in 64-year old women with established diabetes. This association was not explained by traditional risk factors for cardiovascular disease. These results extend previous observations that Hp2-2 is associated with clinical cardiovascular disease in diabetes.

摘要

背景

触珠蛋白多态性产生三种常见的人类基因型:Hp1-1、Hp2-1 和 Hp2-2。在糖尿病患者中,Hp2-2 与发生心血管疾病的风险增加相关。触珠蛋白基因型对亚临床颈动脉粥样硬化的影响尚不清楚。我们假设 Hp2-2 与糖尿病患者颈动脉粥样硬化的发生增加有关。

方法

我们研究了一个基于人群的 64 岁女性糖尿病样本(n=226),包括研究前已知的已确诊糖尿病(n=116)或研究筛查时新诊断的糖尿病(n=110)。触珠蛋白基因型通过 PCR 确定。颈动脉粥样硬化通过超声成像评估。

结果

在整个糖尿病队列中,基因型组之间的颈动脉内膜中层厚度(IMT)或斑块患病率没有差异。然而,在已确诊的糖尿病患者中,与 Hp2-1 和 Hp1-1 基因型相比,Hp2-2 与更高的斑块患病率和更大的颈动脉 IMT 相关。常见心血管危险因素在基因型组之间没有差异。

结论

在 64 岁患有已确诊糖尿病的女性中,Hp2-2 基因型与亚临床颈动脉粥样硬化的发生增加有关。这种关联不能用心血管疾病的传统危险因素来解释。这些结果扩展了之前的观察结果,即 Hp2-2 与糖尿病患者的临床心血管疾病相关。

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