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本文引用的文献

1
Plasma levels of Hsp70 and anti-Hsp70 antibody predict risk of acute coronary syndrome.血浆 Hsp70 水平和抗 Hsp70 抗体可预测急性冠状动脉综合征的风险。
Cell Stress Chaperones. 2010 Sep;15(5):675-86. doi: 10.1007/s12192-010-0180-3. Epub 2010 Mar 19.
2
Circulating heat shock protein 70 (HSPA1A) in normal and pathological pregnancies.正常妊娠和病理妊娠循环中的热休克蛋白 70(HSPA1A)。
Cell Stress Chaperones. 2010 May;15(3):237-47. doi: 10.1007/s12192-009-0146-5. Epub 2009 Oct 12.
3
ANTI-HSP60 and ANTI-HSP70 antibody levels and micro/ macrovascular complications in type 1 diabetes: the EURODIAB Study.1 型糖尿病患者的抗 HSP60 和抗 HSP70 抗体水平与微血管/大血管并发症:EURODIAB 研究。
J Intern Med. 2009 Dec;266(6):527-36. doi: 10.1111/j.1365-2796.2009.02129.x. Epub 2009 May 8.
4
The atheroprotective properties of Hsp70: a role for Hsp70-endothelial interactions?Hsp70 的抗动脉粥样硬化特性:Hsp70-内皮相互作用的作用?
Cell Stress Chaperones. 2009 Nov;14(6):545-53. doi: 10.1007/s12192-009-0113-1. Epub 2009 Apr 9.
5
Elevated heat shock protein 60 levels are associated with higher risk of coronary heart disease in Chinese.在中国,热休克蛋白60水平升高与冠心病风险较高相关。
Circulation. 2008 Dec 16;118(25):2687-93. doi: 10.1161/CIRCULATIONAHA.108.781856.
6
Reduction of heat shock protein antibody levels by statin therapy.他汀类药物治疗降低热休克蛋白抗体水平。
Lipids. 2009 Apr;44(4):317-24. doi: 10.1007/s11745-008-3265-3. Epub 2008 Nov 26.
7
Gender differences in genetic risk profiles for cardiovascular disease.心血管疾病遗传风险概况中的性别差异。
PLoS One. 2008;3(10):e3615. doi: 10.1371/journal.pone.0003615. Epub 2008 Oct 31.
8
Inflammation, heat shock proteins, and type 2 diabetes.炎症、热休克蛋白与2型糖尿病
Cell Stress Chaperones. 2009 Mar;14(2):113-5. doi: 10.1007/s12192-008-0073-x. Epub 2008 Aug 22.
9
Guidelines for the nomenclature of the human heat shock proteins.人类热休克蛋白命名指南。
Cell Stress Chaperones. 2009 Jan;14(1):105-11. doi: 10.1007/s12192-008-0068-7. Epub 2008 Jul 29.
10
Heat shock protein 60 induces inflammatory mediators in mouse adipocytes.
FEBS Lett. 2008 Aug 6;582(18):2731-6. doi: 10.1016/j.febslet.2008.07.002. Epub 2008 Jul 11.

人群中外周热休克蛋白 70(HSPA1A)与经典血管危险因素。

Extracellular heat shock protein 70 (HSPA1A) and classical vascular risk factors in a general population.

机构信息

Biochemistry Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

出版信息

Cell Stress Chaperones. 2010 Nov;15(6):929-37. doi: 10.1007/s12192-010-0201-2. Epub 2010 May 20.

DOI:10.1007/s12192-010-0201-2
PMID:20490736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3024077/
Abstract

Atherosclerosis is a chronic inflammatory and autoimmune disease. Candidate molecules/autoantigens include heat shock proteins (HSPs); Hsp70 (HSPA1A) is one of the best studied HSPs. Various studies have shown a correlation between extracellular Hsp70 (eHsp70) and anti-Hsp70/anti-Hsp60 antibody concentration and development of atherosclerosis. A random sample of 456 people aged 40-60 (218 males, 234 females) was studied to investigate the prevalence of traditional vascular risk factors and eHsp70 and anti-Hsp70/anti-Hsp60 antibodies levels, according to the risk of vascular disease. Task Force Chart was applied for classification. Subjects were divided into three groups: G0 (with no vascular risk factor or a risk lower than 5%), n = 239; G1 (moderated 10-20% risk, who do not have established disease) n = 161; and G2 (established atherosclerosis disease) n = 52. eHsp70 and anti-Hsp70 were significantly lower in the atherosclerosis group (group 2) with respect to the other groups. Disease-free people showed the highest anti-Hsp60 concentration compared with the other two groups. A correlation has not been demonstrated between the concentrations of circulating Hsp70 (HSPA1A), anti-Hsp70, and anti-Hsp60 and classical vascular risk factors and C-reactive protein. Low levels of eHsp70 and anti-Hsp70 antibodies should be considered as candidate FRV. Simultaneous decrease of eHsp70 and anti-Hsp70 antibodies would be explained by circulating immune complex formation, and both could be proposed as biomarkers for the progression of atherosclerotic disease. Levels of circulating anti-Hsp60 antibodies may constitute a marker of inflammation in atherosclerosis.

摘要

动脉粥样硬化是一种慢性炎症性自身免疫性疾病。候选分子/自身抗原包括热休克蛋白(HSPs);热休克蛋白 70(HSPA1A)是研究最多的 HSP 之一。多项研究表明,细胞外热休克蛋白 70(eHsp70)与抗 HSP70/抗 HSP60 抗体浓度之间存在相关性,与动脉粥样硬化的发展有关。随机抽取 456 名年龄在 40-60 岁的人群(218 名男性,234 名女性),根据血管疾病风险,研究传统血管危险因素、eHsp70 和抗 HSP70/抗 HSP60 抗体水平的患病率。应用工作队图表进行分类。将受试者分为三组:G0(无血管危险因素或风险低于 5%),n=239;G1(中度 10-20%风险,无已确诊疾病),n=161;G2(已确诊动脉粥样硬化疾病),n=52。与其他两组相比,动脉粥样硬化组(G2 组)的 eHsp70 和抗 HSP70 显著降低。与其他两组相比,无疾病人群的抗 HSP60 浓度最高。循环 HSP70(HSPA1A)、抗 HSP70 和抗 HSP60 浓度与经典血管危险因素和 C 反应蛋白之间未显示相关性。eHsp70 和抗 HSP70 抗体的低水平应被视为 FRV 的候选物。循环免疫复合物形成会导致 eHsp70 和抗 HSP70 抗体同时减少,这两种物质都可以作为动脉粥样硬化疾病进展的生物标志物。循环抗 HSP60 抗体水平可能构成动脉粥样硬化炎症的标志物。