Franck Marcus, Staub Henrique L, Petracco João B, Norman Gary L, Lassen Andrew J, Schiavo Nádia, Borges Rodrigo B K, von Mühlen Carlos A
Department of Rheumatology, Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
Angiology. 2007 Jun-Jul;58(3):295-302. doi: 10.1177/0003319707302493.
Peripheral artery disease (PAD) is mostly related to atherosclerosis. Autoimmunity and, in particular, antibodies to cardiolipin (aCL) and phospholipid cofactors such as beta2-glycoprotein I (beta2-gpI) might influence the development of atheroma. Beta2-glycoprotein I (beta2-gpI) has been found in atheroma. It has previously been shown that immunoglobulin A (IgA) anti-beta2-gpI antibodies are associated with a risk of cerebral ischemia and myocardial infarction. This case control study aimed to determine whether elevated levels of aCL/anti-beta2-gpI antibodies are associated with a risk of symptomatic PAD (sPAD). Cases comprised a nonselected population of patients with sPAD (intermittent claudication or critical ischemia). Patient recruitment was based on arteriography changes. Controls were selected from patients admitted to orthopedic wards as a result of fractures or muscle-ligamentous disorders. Age, sex, race, hypertension, smoking, diabetes mellitus, and hypercholesterolemia were evaluated as risk factors in both groups. IgG/IgM/IgA aCL and anti-beta2-gpI were detected by enzyme-linked immunoabsorbant assays (ELISA). To estimate the grade of association of antibodies with sPAD, odds ratios (OR) were calculated. Logistic regression was utilized for adjustment of confounding factors. Seventy-seven cases and 93 controls were studied. The mean age was 61.5 years for cases and 47.5 years for controls (p <0.001). Among the risk factors evaluated, the presence of hypertension showed the strongest association with sPAD (OR 12.1; 95%CI 5.8-30). The presence of IgA anti-beta2-gpI was independently associated with sPAD (OR 5.4; 95%CI 1.8-15.8; p = 0.01). IgA aCL was strongly associated with the outcome (nonadjusted OR 11.5 after Agresti correction). IgA aCL and IgA anti-beta2-gpI antibodies were not associated with any known risk factors for sPAD or with arteriography changes. The occurrence of these autoantibodies might represent one of the links between autoimmunity and atherosclerosis in patients with sPAD.
外周动脉疾病(PAD)大多与动脉粥样硬化有关。自身免疫,尤其是抗心磷脂(aCL)抗体和磷脂辅助因子如β2-糖蛋白I(β2-gpI)可能会影响动脉粥样硬化的发展。在动脉粥样硬化斑块中已发现β2-糖蛋白I(β2-gpI)。此前已有研究表明,免疫球蛋白A(IgA)抗β2-gpI抗体与脑缺血和心肌梗死风险相关。本病例对照研究旨在确定aCL/抗β2-gpI抗体水平升高是否与有症状外周动脉疾病(sPAD)风险相关。病例组为未经过筛选的有症状外周动脉疾病患者(间歇性跛行或严重缺血)。患者招募基于血管造影结果。对照组选自因骨折或肌肉韧带疾病入住骨科病房的患者。对两组患者的年龄、性别、种族、高血压、吸烟、糖尿病和高胆固醇血症等危险因素进行评估。采用酶联免疫吸附测定(ELISA)检测IgG/IgM/IgA aCL和抗β2-gpI。为评估抗体与sPAD的关联程度,计算比值比(OR)。采用逻辑回归调整混杂因素。共研究了77例病例和93例对照。病例组平均年龄为61.5岁,对照组为47.5岁(p<0.001)。在评估的危险因素中,高血压与sPAD的关联最为密切(OR 12.1;95%CI 5.8 - 30)。IgA抗β2-gpI的存在与sPAD独立相关(OR 5.4;95%CI 1.8 - 15.8;p = 0.01)。IgA aCL与结果密切相关(经阿格雷斯蒂校正后未调整的OR为11.5)。IgA aCL和IgA抗β2-gpI抗体与sPAD的任何已知危险因素或血管造影改变均无关联。这些自身抗体的出现可能代表了sPAD患者自身免疫与动脉粥样硬化之间的联系之一。