Tiev Kiet Phong, Diot Elisabeth, Clerson Pierre, Dupuis-Siméon Frédérique, Hachulla Eric, Hatron Pierre-Yves, Constans Joël, Cirstéa Daniéla, Farge-Bancel Dominique, Carpentier Patrick H
Service de Médecine Interne, Hôpital Saint Antoine, Paris, France.
J Rheumatol. 2009 Jul;36(7):1470-6. doi: 10.3899/jrheum.081044. Epub 2009 Jun 1.
Digital ulcers are the most frequent vascular manifestations of systemic sclerosis (SSc). Clinical features of patients with prior or current digital ulcers have not been extensively described. This cross-sectional analysis of a large multicenter cohort compared the characteristics of SSc patients with prior or current digital ulcers with those never affected.
Patients with prior/current digital ulcers or never affected were identified in the cohort of SSc patients enrolled in the French ItinérAIR-Sclérodermie registry. Rodnan skin scores, pulmonary function test results, and clinical and immunological data were analyzed to identify digital ulcerassociated clinical features.
Of 599 SSc patients, 317 had prior or current digital ulcers. These patients were more frequently male, with impaired diffusing capacity for carbon monoxide (DLCO), and higher Rodnan skin scores than patients never affected by digital ulcers. In a multivariate analysis, male gender, early onset of SSc, increased duration of SSc, high Rodnan skin score, and presence of anti-topoisomerase I antibodies (anti-topo I) were associated with prior or current digital ulcers. Comparison of patients with current digital ulcers versus patients never affected indicated that affected patients had increased duration of SSc, impaired DLCO, increased Rodnan score, and younger age at onset of SSc.
Male patients with early onset SSc, more severe skin fibrosis, impaired DLCO, and anti-topo I were most likely to exhibit prior or current digital ulcers. Confirmation of these results in a prospective longitudinal study may enable identification of patients at greatest risk of developing digital ulcers, facilitating management of this disabling complication.
指端溃疡是系统性硬化症(SSc)最常见的血管表现。既往或当前患有指端溃疡患者的临床特征尚未得到广泛描述。这项对大型多中心队列的横断面分析比较了既往或当前患有指端溃疡的SSc患者与从未患过指端溃疡患者的特征。
在法国ItinérAIR - 硬皮病登记处登记的SSc患者队列中识别出既往/当前患有指端溃疡或从未患过指端溃疡的患者。分析Rodnan皮肤评分、肺功能测试结果以及临床和免疫学数据,以确定与指端溃疡相关的临床特征。
在599例SSc患者中,317例有既往或当前指端溃疡。这些患者男性更为常见,一氧化碳弥散功能(DLCO)受损,且Rodnan皮肤评分高于从未患指端溃疡的患者。多变量分析显示,男性、SSc发病早、SSc病程延长、Rodnan皮肤评分高以及存在抗拓扑异构酶I抗体(抗拓扑异构酶I)与既往或当前指端溃疡相关。当前患有指端溃疡的患者与从未患过指端溃疡的患者比较表明,患病患者的SSc病程延长、DLCO受损、Rodnan评分增加且SSc发病年龄更小。
发病早、皮肤纤维化更严重、DLCO受损且有抗拓扑异构酶I的男性SSc患者最有可能出现既往或当前指端溃疡。在前瞻性纵向研究中证实这些结果可能有助于识别发生指端溃疡风险最高的患者,便于对这种致残性并发症进行管理。