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触珠蛋白基因型是人类动脉粥样硬化斑块中铁含量的主要决定因素。

Haptoglobin genotype is a major determinant of the amount of iron in the human atherosclerotic plaque.

作者信息

Moreno Pedro R, Purushothaman K Raman, Purushothaman Meera, Muntner Paul, Levy Nina S, Fuster Valentin, Fallon John T, Lento Patrick A, Winterstern Aaron, Levy Andrew P

机构信息

Department of Medicine (Cardiology), Mount Sinai Medical Center, New York, New York, USA.

出版信息

J Am Coll Cardiol. 2008 Sep 23;52(13):1049-51. doi: 10.1016/j.jacc.2008.06.029.

DOI:10.1016/j.jacc.2008.06.029
PMID:18848136
Abstract

OBJECTIVES

We sought to test the hypothesis that haptoglobin (Hp) genotype is a determinant of the amount of iron in the atherosclerotic plaque.

BACKGROUND

In atherosclerotic lesions, intraplaque hemorrhage releases free hemoglobin (Hb), whose incorporated iron can act as an oxidant and inflammatory stimulus. These effects are antagonized by Hp, which binds free Hb and facilitates its clearance from the plaque. The Hp gene has 2 alleles (1 and 2), giving rise to 3 genotypes: Hp 1-1, Hp 2-1, and Hp 2-2. We previously hypothesized that Hp 2-2 individuals with diabetes mellitus (DM) have impaired clearance of Hb and its iron cargo from the plaque.

METHODS

We identified the presence or absence of Perl's iron stain in 189 plaques obtained from 37 decedents at autopsy.

RESULTS

Among DM, the prevalence of Perl's iron stain was increased in Hp 2-2 compared with that seen in Hp 1-1 or 2-1 (46.2% vs. 11.8%). After accounting for the within-decedent correlation of plaques, the prevalence ratio of Perl's iron stain associated with Hp 2-2 was 3.97 (95% confidence interval: 1.38 to 11.5; p = 0.025). In non-DM plaques, there was a nonsignificant trend towards a higher prevalence of iron staining in Hp 2-2 compared with that in Hp 1-1 or 2-1 (26.8% vs. 11.1%; prevalence ratio =2.40 [95% confidence interval: 0.81 to 7.09]; p = 0.114).

CONCLUSIONS

These data support an impaired clearance of Hb from plaques in Hp 2-2 individuals, particularly in DM. The higher prevalence of plaque iron in Hp 2-2 DM individuals may contribute to the increased incidence of atherothrombotic events in these patients.

摘要

目的

我们试图验证如下假设,即触珠蛋白(Hp)基因型是动脉粥样硬化斑块中铁含量的一个决定因素。

背景

在动脉粥样硬化病变中,斑块内出血会释放游离血红蛋白(Hb),其所包含的铁可作为氧化剂和炎症刺激物。这些作用会被Hp拮抗,Hp能结合游离Hb并促进其从斑块中清除。Hp基因有两个等位基因(1和2),产生三种基因型:Hp 1-1、Hp 2-1和Hp 2-2。我们之前曾假设,患有糖尿病(DM)的Hp 2-2个体对Hb及其携带的铁从斑块中的清除存在障碍。

方法

我们在尸检时从37名死者身上获取了189个斑块,检测其中Perl铁染色的有无。

结果

在糖尿病患者中,与Hp 1-1或Hp 2-1相比,Hp 2-2个体中Perl铁染色的患病率更高(46.2%对11.8%)。在考虑了同一死者斑块之间的相关性后,与Hp 2-2相关的Perl铁染色患病率比值为3.97(95%置信区间:1.38至11.5;p = 0.025)。在非糖尿病斑块中,与Hp 1-1或Hp 2-1相比,Hp 2-2中铁染色患病率有升高的趋势,但无统计学意义(26.8%对11.1%;患病率比值 = 2.40 [95%置信区间:0.81至7.09];p = 0.114)。

结论

这些数据支持了Hp 2-2个体,尤其是糖尿病患者,从斑块中清除Hb的能力受损。Hp 2-2糖尿病个体中斑块铁的患病率较高,可能导致这些患者动脉粥样血栓形成事件的发生率增加。

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