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结合珠蛋白基因型与 2 型糖尿病患者的难治性高血压。

Haptoglobin genotypes and refractory hypertension in type 2 diabetes mellitus patients.

机构信息

Departamento de Patologia Clínica, Faculdade de Ciências Médicas, Unicamp, Campinas, SP, Brasil.

出版信息

Arq Bras Cardiol. 2011 Oct;97(4):338-45. doi: 10.1590/s0066-782x2011005000107. Epub 2011 Oct 21.

Abstract

BACKGROUND

It has been suggested that haptoglobin polymorphism may influence the pathogenesis of microvascular and macrovascular complications in diabetic patients.

OBJECTIVE

This cross sectional study was carried out to investigate the existence or not of an association between haptoglobin genotypes and prevalence of ischemic cardiovascular events (stable angina, unstable angina and acute myocardial infarction), systemic arterial hypertension, refractory hypertension, obesity and dyslipidemia in 120 type-2 diabetes mellitus patients followed up at Hospital de Clínicas da UNICAMP in Campinas, São Paulo state, southeastern Brazil.

METHODS

Haptoglobin genotyping was performed by allele-specific polymerase chain reactions. The frequencies of the haptoglobin genotypes were compared with the presence/absence of cardiovascular disease, systemic arterial hypertension, refractory hypertension, obesity and dyslipidemia; systolic and diastolic blood pressure measurements; plasma levels of glucose, cholesterol (total, high density lipoprotein-HDL and low density lipoprotein-LDL) and triglycerides; and serum creatinine levels.

RESULTS

Although no association between haptoglobin genotype and the presence of cardiovascular disease could be identified, we found a significant excess of patients with Hp2-1 genotype among those with refractory hypertension, who also had higher systolic and diastolic blood pressure, and total and LDL cholesterol levels.

CONCLUSION

Our results suggest that type-2 diabetes mellitus patients with the Hp2-1 genotype may have higher chances of developing refractory hypertension. Further studies in other diabetic populations are required to confirm these findings.

摘要

背景

有人提出血红蛋白多态性可能影响糖尿病患者微血管和大血管并发症的发病机制。

目的

本横断面研究旨在调查血红蛋白基因型与缺血性心血管事件(稳定性心绞痛、不稳定型心绞痛和急性心肌梗死)、系统性动脉高血压、难治性高血压、肥胖和血脂异常在巴西东南部圣保罗州坎皮纳斯 UNICAMP 临床医院随访的 120 例 2 型糖尿病患者中的存在与否之间是否存在关联。

方法

通过等位基因特异性聚合酶链反应进行血红蛋白基因分型。将血红蛋白基因型的频率与心血管疾病、系统性动脉高血压、难治性高血压、肥胖和血脂异常、收缩压和舒张压测量值、血糖、胆固醇(总胆固醇、高密度脂蛋白胆固醇和低密度脂蛋白胆固醇)和甘油三酯的血浆水平以及血清肌酐水平进行比较。

结果

尽管未能确定血红蛋白基因型与心血管疾病之间的关联,但我们发现难治性高血压患者 Hp2-1 基因型的患者明显过多,这些患者的收缩压和舒张压以及总胆固醇和 LDL 胆固醇水平也更高。

结论

我们的结果表明,2 型糖尿病患者的 Hp2-1 基因型可能更容易发生难治性高血压。需要在其他糖尿病人群中进行进一步的研究来证实这些发现。

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