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[Prevalence of antiphospholipid antibodies in Horton's disease and in polymyalgia rheumatica].

作者信息

Hulin C, Hachulla E, Michon-Pasturel U, Hatron P Y, Masy E, Gillot J M, Caron C, Arvieux J, Flipo R M, Devulder B

机构信息

Service de médecine interne, hôpital Clauae-Huriez, CHRU, Lille.

出版信息

Rev Med Interne. 1999 Aug;20(8):659-63. doi: 10.1016/s0248-8663(99)80485-8.

Abstract

PURPOSE

Antiphospholipid antibodies (APL) are frequently observed in the course of giant cell arteritis and polymyalgia rheumatica. However, their role and relationships with potential ischemic events are still debated.

METHODS

To determine the prevalence of APL in relation with ischemic events, 62 patients with giant cell arteritis and/or polymyalgia rheumatica were retrospectively studied.

RESULTS

Before corticosteroid treatment 41% of the 51 patients with giant cell arteritis and 64% of the 11 patients with isolated polymyalgic rheumatica had high IgG ACL levels, with a frequency significantly higher than that (15.6%) of the control group which was composed of healthy elderly. IgM ACL were found in only two patients with giant cell arteritis. There was no correlation between the occurrence of an ischemic event (22 ischemic events in the 51 patients with giant cell arteritis) and the presence of ACL, even though the latter were more frequently observed in the giant cell arteritis group (52% versus 41% in non ischemic patients). The prevalence of ACL increased, reaching 59% if lupus anticoagulant was associated, but the difference was not significant. ACL disappeared soon after corticosteroid therapy had been initiated.

CONCLUSION

Though ACL are frequently seen in giant cell arteritis and/or polymyalgia rheumatica, they are not related to ischemic events and disappear rapidly after corticosteroid treatment.

摘要

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