Capillaroscopic findings in individuals with Sjögren’s syndrome, systemic sclerosis, and primary Raynaud’s phenomenon at a capillaroscopy referral centre in Medellin, Colombia

Simón Hoyos-Patiño , Alejandro Arango-Martínez , Libia María Rodriguez-Padilla , Andrés Chavarriaga-Restrepo , Carlos Jaime Velasquez-Franco
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Abstract

Introduction

Nailfold capillaroscopy is a fundamental technique for studying systemic autoimmune diseases such as Sjögren’s syndrome, particularly in patients with Raynaud’s phenomenon and sclerodermiform features. However, in this condition, studies are scarce and often use instruments less precise than digital videocapillaroscopy, limiting the available evidence.

Objective

To compare capillaroscopic findings among individuals with Sjögren's syndrome (SS), primary Raynaud's phenomenon (PRP), and systemic sclerosis (SSc) at a national referral centre for nailfold videocapillaroscopy in Medellin, Colombia, between 2016 and 2022.

Materials and methods

An analytical cross-sectional observational study that included individuals over 18 years of age with SS, SSc, and PRP. Clinical and capillaroscopic characteristics information was obtained from capillaroscopy reports at an expert centre. Pearson's chi-square test was used to compare qualitative variables, and the Kruskal-Wallis test for quantitative variables. A P-value <.05 was considered statistically significant.

Results

A total of 195 patients were included. Subjects with SS had a lower prevalence of abnormal capillaroscopic variables than patients with SSc (P < .001). All abnormal capillaroscopic variables were more frequent in the SS group compared to PRP. There were statistically significant differences among the three patient groups in the capillaroscopic pattern (P < .001). The main capillaroscopic finding in SS was the presence of dilated capillaries (55.4%; 36/65). In the SS group, an early scleroderma pattern was present in 4.6%, and an active scleroderma pattern in 13.8%, both findings less frequent than in SSc but more common than in PRP.

Conclusions

In a population of SS patients with a high prevalence of secondary Raynaud's phenomenon and anticentromere antibodies, a high prevalence of capillaroscopic abnormalities was found. Although less frequent compared to the SSc group, these abnormalities were more common than in the PRP group.
在哥伦比亚麦德林的一个毛细血管镜检查转诊中心,对Sjögren综合征、系统性硬化症和原发性雷诺氏现象患者的毛细血管镜检查结果
甲襞毛细血管镜检查是研究系统性自身免疫性疾病(如Sjögren综合征)的一项基本技术,特别是在有雷诺现象和硬皮样特征的患者中。然而,在这种情况下,研究很少,而且通常使用的仪器不如数字视频毛细血管镜精确,限制了可用的证据。目的比较2016年至2022年在哥伦比亚麦德林的一个国家甲折视频毛细血管镜转诊中心,Sjögren综合征(SS)、原发性雷诺现象(PRP)和系统性硬化症(SSc)患者的毛细血管镜检查结果。材料和方法一项分析性横断面观察研究,包括18岁以上的SS、SSc和PRP患者。临床和毛细血管镜特征信息从专家中心的毛细血管镜检查报告中获得。定性变量比较采用Pearson卡方检验,定量变量比较采用Kruskal-Wallis检验。p值<; 0.05被认为具有统计学意义。结果共纳入195例患者。与SSc患者相比,SS患者的毛细血管镜变量异常发生率较低(P < .001)。与PRP组相比,SS组的所有毛细血管镜异常变量都更频繁。三组患者在毛细管镜模式上差异有统计学意义(P < 0.001)。SS的主要毛细血管镜检查结果是毛细血管扩张(55.4%;36/65)。在SS组中,4.6%的患者出现早期硬皮病,13.8%的患者出现活动性硬皮病,这两种情况都比SSc少,但比PRP更常见。结论继发性雷诺现象和抗着丝点抗体高发的SS患者中,毛细血管镜下异常高发。虽然与SSc组相比,这些异常发生率较低,但比PRP组更常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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