Department of Vascular Surgery, Red Cross Hospital of Athens, Greece.
Atherosclerosis. 2011 May;216(1):131-8. doi: 10.1016/j.atherosclerosis.2011.01.028. Epub 2011 Jan 26.
The aim of this study was to evaluate the iron burden of carotid atherosclerotic plaques removed from patients treated for carotid disease and find any relation with haptoglobin genotype and other common cardiovascular risk factors.
Consecutive patients undergoing carotid endarterectomy were included in the study. All patients had high-grade carotid stenosis (>70%). The clinical characteristics and serum parameters of the study population were recorded and the haptoglobin genotype was determined. The presence of hemosiderin deposits in the plaques was identified using Perl's stain on adjacent serial sections.
70 specimens were processed for histologic examination: 27 plaques from diabetic patients (16 with the Hp 1-1 or 2-1 genotype and 11 with the Hp 2-2 genotype) and 43 plaques from non diabetic patients (20 with the Hp 1-1 or 2-1 genotype and 23 with the Hp 2-2 genotype). In plaques from diabetic patients the density of Perl's iron stain was significantly higher in the Hp 2-2 group compared with that in the Hp 1-1 or 2-1 group (p = 0.008). The correlation and regression analysis of all possible clinical and laboratory predictors of intraplaque iron deposition showed that four factors were independently associated with intraplaque iron deposition: male gender, serum homocysteine, Hp 2-2 genotype and diabetes mellitus treatment.
Male diabetic patients with increased plasma levels of homocysteine and the Hp 2-2 genotype had higher carotid plaque iron deposition. Current evidence and pathophysiological considerations suggest that the increased intraplaque iron deposition may be associated with increased oxidative stress, affecting the stability of the carotid plaque.
本研究旨在评估接受颈动脉疾病治疗的患者颈动脉粥样硬化斑块中铁的负荷,并发现其与结合珠蛋白基因型和其他常见心血管危险因素之间的关系。
连续纳入接受颈动脉内膜切除术的患者。所有患者均存在重度颈动脉狭窄(>70%)。记录研究人群的临床特征和血清参数,并确定结合珠蛋白基因型。使用相邻连续切片上的 Perl 染色来确定斑块中是否存在含铁血黄素沉积。
共对 70 个标本进行了组织学检查:27 个斑块来自糖尿病患者(16 个为 Hp 1-1 或 2-1 基因型,11 个为 Hp 2-2 基因型),43 个斑块来自非糖尿病患者(20 个为 Hp 1-1 或 2-1 基因型,23 个为 Hp 2-2 基因型)。在糖尿病患者的斑块中,Hp 2-2 组的 Perl 铁染色密度明显高于 Hp 1-1 或 2-1 组(p = 0.008)。对所有可能与斑块内铁沉积相关的临床和实验室预测因素进行相关性和回归分析,结果表明有四个因素与斑块内铁沉积独立相关:男性、血清同型半胱氨酸、Hp 2-2 基因型和糖尿病治疗。
男性糖尿病患者血浆同型半胱氨酸水平升高和 Hp 2-2 基因型与颈动脉斑块铁沉积增加有关。现有证据和病理生理学考虑表明,斑块内铁沉积增加可能与氧化应激增加有关,从而影响颈动脉斑块的稳定性。