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Progression of nailfold microvascular damage and antinuclear antibody pattern in systemic sclerosis

机译:系统性硬化中指甲皱纹微血管损伤和抗核抗体谱的研究进展

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Objective. This study evaluates possible correlations between the pattern of antinuclear antibodies (ANA) on indirect immunofluorescence (IIF) testing and nailfold microangiopathy stage (early, active, and late stage) in systemic sclerosis (SSc). Patients with SSc were followed prospectively to monitor progression of microvascular damage. Methods. The ANA pattern on IIF was searched in 42 patients with SSc showing an early pattern of nailfold microangiopathy at baseline, and was followed using nailfold videocapillaroscopy (NVC) for a median time of 91 months. Results. Among patients whose microangiopathy showed a rapid progression from early to late pattern on NVC, the IIF pattern was fine-speckled + nucleolar (Scl-70+) in 44%, centromeric in 33%, nucleolar in 11%, and homogeneous in 11% of patients with SSc. Antitopoisomerase I antibodies were significantly more frequent (57%) in patients with late pattern of microangiopathy on NVC. The median time of progression from early to active disease was significantly lower in patients with both fine-speckled + nucleolar and nucleolar ANA positivity. The severity of microangiopathy was higher in patients with the nucleolar pattern on IIF. Patients already showing a slight reduction of capillary number at baseline were likely to have either the nucleolar or the fine-speckled + nucleolar pattern on IIF. Of note, 37% of patients still showing the early microangiopathy pattern on NVC at the end of the followup were ANA-negative. Conclusion. ANA-negative patients with SSc display a slower progression of nailfold microangiopathy characterized by the early pattern on NVC. Progression to the late NVC pattern (more advanced stage of microvascular damage) seems to be associated with a different autoantibody pattern on IIF (fine-speckled + nucleolar pattern being the most prevalent). (First Release March 1 2013; J Rheumatol 2013;40:634-9;) The Journal of Rheumatology
机译:目的。这项研究评估间接免疫荧光(IIF)测试中的抗核抗体(ANA)模式与系统性硬化症(SSc)的指甲褶皱性微血管病变阶段(早期,活动和晚期)之间的可能相关性。前瞻性跟踪SSc患者以监测微血管损伤的进展。方法。在42名SSc患者中搜索了IIF上的ANA模式,该患者在基线时显示出指甲皱纹性微血管病的早期模式,随后使用指甲皱纹毛细血管镜(NVC)进行了中位时间为91个月。结果。在微血管病变在NVC上从早期到晚期迅速发展的患者中,IIF模式为44%的细斑点+核仁(Scl-70 +),33%的着丝粒+ 11%的核仁和11%的均质SSc患者。在NVC上出现微血管病晚期模式的患者中,抗拓扑异构酶I抗体的发生率明显更高(57%)。散斑+核仁和核仁ANA阳性患者的从早期疾病发展为活动性疾病的中位时间显着降低。 IIF上具有核仁模式的患者微血管病变的严重程度更高。在基线时已经显示毛细血管数目略有减少的患者可能在IIF上出现核仁或斑点状+核仁图案。值得注意的是,在随访结束时仍有37%的患者在NVC上仍表现出早期的微血管病变模式,而ANA阴性。结论。 ANA阴性的SSc患者表现出较慢的指甲皱纹性微血管病进展,其特征是NVC呈早期模式。晚期NVC模式(微血管损伤的更晚期)的进展似乎与IIF上不同的自身抗体模式(细斑+核仁模式最为普遍)有关。 (2013年3月1日首次发布; J Rheumatol 2013; 40:634-9;)风湿病学杂志

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