García Bolao J I, Iglesias I, Fidalgo M L, Alegría E, Mejía S, Huelmos A, Garrote C
Departamento de Cardiología y Cirugía Cardiovascular, Facultad de Medicina, Universidad de Navarra, Pamplona.
Rev Med Univ Navarra. 1990 Jul-Sep;34(3):151-5.
Recurrent thrombosis, abortion and thrombocytopenia are the most frequent manifestation of antiphospholipid syndrome, which usually presents antibodies against some anionic phospholipids. A few years ago, this syndrome was considered as a manifestation of systemic lupus erythematosus; nowadays it is classified as an isolated systemic lupus erythematosus; nowadays it is classified as an isolated autoimmune disease. Hypotheses have been proposed to explain the origin of antiphospholipid antibodies, including infectious and autoimmune diseases with high titles of anticardiolipin antibodies. Genetic factors have also been involved. Laboratory tests of choice for the detection of anticardiolipin antibodies are RIA and ELISA tests; there are some structural differences among them depending on the underlying disease. Hypercoagulability and recurrent thrombosis are the main features of this entity; ischemic heart disease is in this context of outmost importance. Despite the lack of any clinically demonstrated association between antiphospholipid syndrome and ischemic heart disease, there are many "in vitro" studies that support this possibility.
复发性血栓形成、流产和血小板减少是抗磷脂综合征最常见的表现,该综合征通常会出现针对某些阴离子磷脂的抗体。几年前,这种综合征被认为是系统性红斑狼疮的一种表现;如今它被归类为一种独立的自身免疫性疾病。已经提出了一些假说来解释抗磷脂抗体的起源,包括具有高滴度抗心磷脂抗体的感染性和自身免疫性疾病。遗传因素也与之相关。检测抗心磷脂抗体的首选实验室检测方法是放射免疫分析(RIA)和酶联免疫吸附测定(ELISA)检测;根据潜在疾病的不同,它们之间存在一些结构差异。高凝状态和复发性血栓形成是该疾病的主要特征;在这种情况下,缺血性心脏病至关重要。尽管抗磷脂综合征与缺血性心脏病之间缺乏任何临床证实的关联,但有许多“体外”研究支持这种可能性。