Systemic Autoimmune Diseases Unit, Department of Internal Medicine, Parc Taulí, Hospital Universitari, Sabadell, Barcelona, and Universitat Autònoma de Barcelona, Spain.
Systemic Autoimmune Diseases Unit, Department of Internal Medicine, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
Clin Exp Rheumatol. 2023 Aug;41(8):1695-1703. doi: 10.55563/clinexprheumatol/8lrofr. Epub 2023 Aug 1.
To assess the associations and prognostic value of scleroderma patterns by nailfold videocapillaroscopy (NVC) in patients with systemic sclerosis (SSc) and cutaneous subsets.
At baseline, 1356 SSc patients from the RESCLE registry were compared according to the scleroderma pattern as Late pattern and non-Late pattern, which included Early and Active patterns. Patient characteristics, disease features, survival time and causes of death were analysed.
Late pattern was identified in 540 (39.8%), and non-Late pattern in 816 (60.2%) patients (88% women; 987 lcSSc/251 dcSSc). Late pattern was associated to dcSSc (OR=1.96; p<0.001), interstitial lung disease (ILD) (OR=1.29; p=0.031), and scleroderma renal crisis (OR=3.46; p<0.001). Once the cutaneous subset was disregarded in an alternative analysis, both digital ulcers (DU) (OR=1.29; p<0.037) and anti-topoisomerase I antibodies (OR=1.39; p< 0.036) emerged associated with the Late pattern. By cutaneous subsets, associations with Late pattern were: (1) in dcSSc, acro-osteolysis (OR=2.13; p=0.022), and systolic pulmonary artery pressure >40 mmHg by Doppler echocardiogram (OR=2.24; p<0.001); and (2) in lcSSc, ILD (OR=1.38; p=0.028). Survival was reduced in dcSSc with Late pattern compared to non-Late pattern (p=0.049). Risk factors for SSc mortality in multivariate regression Cox analysis were age at diagnosis (HR=1.03; p<0.001), dcSSc (HR=2.48; p<0.001), DU (HR=1.38; p=0.046), ILD (HR=2.81; p<0.001), and pulmonary arterial hypertension (HR=1.99; p<0.001).
SSc patients with Late pattern more frequently present dcSSc and develop more fibrotic and vascular manifestations. Advanced microangiopathy by NVC identifies dcSSc patients at risk of reduced survival due to SSc-related causes.
通过甲襞毛细血管显微镜(NVC)评估系统性硬化症(SSc)和皮肤亚型患者的硬皮病模式的相关性和预后价值。
根据硬皮病模式(晚期和非晚期),将 RESCLE 登记处的 1356 例 SSc 患者在基线时进行比较,其中晚期模式包括早期和活跃模式。分析患者特征、疾病特征、生存时间和死亡原因。
540 例(39.8%)为晚期模式,816 例(60.2%)为非晚期模式(88%为女性;987 例局限型 SSc/251 例弥漫型 SSc)。晚期模式与弥漫型 SSc(OR=1.96;p<0.001)、间质性肺病(ILD)(OR=1.29;p=0.031)和硬皮病肾危象(OR=3.46;p<0.001)相关。在替代分析中不考虑皮肤亚型时,晚期模式与手指溃疡(OR=1.29;p<0.037)和抗拓扑异构酶 I 抗体(OR=1.39;p<0.036)相关。根据皮肤亚型,与晚期模式相关的因素为:(1)弥漫型 SSc 中,肢端骨溶解(OR=2.13;p=0.022)和多普勒超声心动图显示收缩期肺动脉压>40mmHg(OR=2.24;p<0.001);(2)局限型 SSc 中,ILD(OR=1.38;p=0.028)。与非晚期模式相比,晚期模式的弥漫型 SSc 患者的生存时间缩短(p=0.049)。多变量回归 Cox 分析显示,SSc 死亡率的危险因素为诊断时年龄(HR=1.03;p<0.001)、弥漫型 SSc(HR=2.48;p<0.001)、手指溃疡(HR=1.38;p=0.046)、ILD(HR=2.81;p<0.001)和肺动脉高压(HR=1.99;p<0.001)。
晚期模式的 SSc 患者更常出现弥漫型 SSc,并出现更多的纤维化和血管表现。NVC 检测到的晚期微血管病变可识别因 SSc 相关原因导致生存时间缩短的弥漫型 SSc 患者。