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系统性红斑狼疮中的骨缺血性坏死与抗磷脂抗体

Avascular necrosis of bone and antiphospholipid antibodies in systemic lupus erythematosus.

作者信息

Asherson R A, Lioté F, Page B, Meyer O, Buchanan N, Khamashta M A, Jungers P, Hughes G R

机构信息

Lupus/Arthritis Research Unit, Rayne Institute, St. Thomas' Hospital, London, England.

出版信息

J Rheumatol. 1993 Feb;20(2):284-8.

PMID:8474066
Abstract

Of a total of 800 patients with systemic lupus erythematosus, 37 were found to have developed avascular necrosis of bone (4.6%). Routine radiological screening of all joints was not performed and these 37 represented symptomatic patients only. Twenty-seven of these were positive for antiphospholipid antibodies (aPL) (73%). Both aPL positive and aPL negative patients had received large doses of oral steroids. The frequency of vasculitis and livedo reticularis, as well as arterial thrombosis was higher in the aPL positive group, but this did not reach statistical significance, perhaps because of the small numbers of patients involved. Although the difference in the frequency of thrombocytopenia was more marked in the aPL positive group (p < 0.08), once again, this was not statistically significant at the 5% level. Since the prevalence of aPL positivity in the general lupus population is about 30-40%, the presence of the aPL may be associated with an increased tendency to develop avascular necrosis. This is supported by recent reports of avascular necrosis occurring in patients with primary antiphospholipid syndrome in the absence of previous steroid administration.

摘要

在总共800例系统性红斑狼疮患者中,发现37例发生了骨缺血性坏死(4.6%)。未对所有关节进行常规放射学筛查,这37例仅代表有症状的患者。其中27例抗磷脂抗体(aPL)呈阳性(73%)。aPL阳性和aPL阴性患者均接受过大剂量口服类固醇治疗。aPL阳性组血管炎、网状青斑以及动脉血栓形成的发生率更高,但这未达到统计学显著性,可能是因为涉及的患者数量较少。尽管血小板减少症发生率在aPL阳性组的差异更为明显(p < 0.08),但同样,在5%水平上这也无统计学显著性。由于一般狼疮人群中aPL阳性的患病率约为30% - 40%,aPL的存在可能与发生骨缺血性坏死的倾向增加有关。原发性抗磷脂综合征患者在未预先使用类固醇的情况下发生骨缺血性坏死的近期报道支持了这一点。

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