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2 型糖尿病患者血清热休克蛋白 70 和氧化型低密度脂蛋白:性别有影响吗?

Serum heat shock protein 70 and oxidized LDL in patients with type 2 diabetes: does sex matter?

机构信息

Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Cell Stress Chaperones. 2011 Mar;16(2):195-201. doi: 10.1007/s12192-010-0232-8. Epub 2010 Sep 26.

Abstract

Several studies suggest that the response to various stressors differs between the sexes. We aimed to study serum HSP70 and levels of oxidized-LDL (ox-LDL) as markers of oxidative stress in men and women with type 2 diabetes. We quantified serum HSP70 and levels of ox-LDL in three cohorts; patients with newly diagnosed diabetes, patients with long-standing diabetes and normal controls. The cohort of patients with newly diagnosed diabetes was followed up for 3 months under glucose-lowering therapy with metformin. Our findings showed that serum HSP70 level was increased in women with long-standing diabetes in comparison with men. HSP70 did not decrease after glucose lowering therapy in women with newly diagnosed diabetes, but it did decrease in men. There was no significant difference on ox-LDL between men and women in any of the studied cohorts. It decreased significantly in the cohort of patients with newly diagnosed diabetes after treatment, regardless of sex. There was no significant correlation between HSP70 and ox-LDL in any of the studied cohorts except among normal women. We suggest that diabetes induces an immune response and impairs cellular defense mechanisms against oxidative stress more commonly in women with type 2 diabetes than in men.

摘要

一些研究表明,对于不同的应激源,男女的反应不同。我们旨在研究 2 型糖尿病患者中血清 HSP70 和氧化型 LDL(ox-LDL)水平作为氧化应激的标志物。我们在三个队列中定量了血清 HSP70 和 ox-LDL 水平:新诊断的糖尿病患者、长期糖尿病患者和正常对照组。新诊断的糖尿病患者队列在接受二甲双胍降糖治疗的情况下进行了 3 个月的随访。我们的研究结果表明,与男性相比,长期糖尿病的女性血清 HSP70 水平升高。在新诊断的糖尿病女性中,HSP70 并未随着血糖降低而降低,但在男性中则降低了。在任何研究队列中,男性和女性之间的 ox-LDL 均无显著差异。在接受治疗后,新诊断的糖尿病患者队列中的 ox-LDL 显著降低,而与性别无关。除了在正常女性中,我们没有发现任何研究队列中 HSP70 和 ox-LDL 之间存在显著相关性。我们认为,糖尿病在 2 型糖尿病女性中比男性更常见地诱导免疫反应,并损害细胞对抗氧化应激的防御机制。

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