Faculty of Medicine, Benha University, Benha, Al-Qalyubia Governorate, Egypt.
Faculty of Medicine, Tanta University, Tanta, Egypt.
Clin Rheumatol. 2022 Nov;41(11):3401-3409. doi: 10.1007/s10067-022-06301-0. Epub 2022 Jul 25.
Systemic sclerosis (SSc) is an autoimmune disorder that causes vasculopathy and scarring, most commonly in the lungs and skin, but it can also affect other organs. Endothelial vinculin plays a critical role in angiogenesis regulation. Therefore, vinculin overexpression in SSc may give rise to anti-vinculin antibodies, which may contribute to the development of SSc vasculopathy. The current research aims to (1) determine whether anti-vinculin autoantibodies play a significant role in the diagnosis of SSc and (2) compare anti-vinculin serum levels between two scleroderma patient populations, namely, pulmonary artery hypertension (PAH)-predominant and interstitial pulmonary fibrosis (IPF)-predominant groups.
This research included 140 participants categorized into three groups: group I-patients with PAH-predominant; group II-patients with ILD-predominant; group III-the control group. Anti-vinculin antibodies were detected in serum samples collected from all participants using ELISA. All subjects underwent high-resolution computed tomography (CT), diffusing capacity for carbon monoxide, and pulmonary function tests.
Patients in group I (PAH-predominant group, N = 35) were 41.3 [± 11.4] years old, with 80% being women. Patients in group II (ILD-predominant group, N = 35) were 41.0 [± 11.5] years old. The SSc group showed significantly higher anti-vinculin antibody levels than the control group (P < 0.001). The PAH-predominant group demonstrated significantly higher anti-vinculin antibody levels and anti-vinculin positivity than the ILD-predominant group.
Anti-vinculin antibodies in the blood appear to be diagnostic biomarkers for scleroderma. Furthermore, they shed light on some novel perspectives on the pathophysiology of specific lung fibrotic changes. Key Points • This study included two groups of systemic sclerosis patients (PAH-predominant group, ILD-predominant group) as well as a control group to investigate the significance of anti-vinculin antibodies in such cases. • Our results have demonstrated that anti-vinculin antibodies can play a significant role in diagnosing and monitoring systemic sclerosis disease.
系统性硬化症(SSc)是一种自身免疫性疾病,可导致血管病变和瘢痕形成,最常见于肺部和皮肤,但也可能影响其他器官。内皮细胞粘着斑蛋白在血管生成调节中起着关键作用。因此,SSc 中的粘着斑蛋白过度表达可能会产生抗粘着斑蛋白抗体,这可能有助于 SSc 血管病变的发展。目前的研究旨在:(1)确定抗粘着斑蛋白自身抗体在 SSc 的诊断中是否具有重要作用;(2)比较两种硬皮病患者群体(即肺动脉高压(PAH)为主型和间质性肺纤维化(IPF)为主型)之间的抗粘着斑蛋白血清水平。
本研究纳入了 140 名参与者,分为三组:I 组-肺动脉高压(PAH)为主型患者;II 组-间质性肺纤维化(ILD)为主型患者;III 组-对照组。使用 ELISA 法检测所有参与者血清中的抗粘着斑蛋白抗体。所有受试者均接受高分辨率计算机断层扫描(CT)、一氧化碳弥散量和肺功能检查。
I 组(PAH 为主型组,N=35)患者年龄为 41.3[±11.4]岁,其中 80%为女性。II 组(ILD 为主型组,N=35)患者年龄为 41.0[±11.5]岁。SSc 组的抗粘着斑蛋白抗体水平明显高于对照组(P<0.001)。PAH 为主型组的抗粘着斑蛋白抗体水平和抗粘着斑蛋白阳性率明显高于 ILD 为主型组。
血液中的抗粘着斑蛋白抗体似乎是硬皮病的诊断生物标志物。此外,它们为特定肺纤维化变化的病理生理学提供了一些新的视角。关键点:• 本研究纳入了两组系统性硬化症患者(PAH 为主型组、ILD 为主型组)和一组对照组,旨在探讨抗粘着斑蛋白抗体在这些病例中的意义。• 我们的研究结果表明,抗粘着斑蛋白抗体在诊断和监测系统性硬化症疾病方面具有重要作用。