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血清可溶性血管细胞黏附分子-1 过表达是首次诊断抗核抗体患者的疾病标志物:一项前瞻性、观察性的初步研究。

Serum Soluble Vascular Cell Adhesion Molecule-1 Overexpression Is a Disease Marker in Patients with First-Time Diagnosed Antinuclear Antibodies: A Prospective, Observational Pilot Study.

机构信息

Praxis für Rheumatologie, Köln, Germany.

Medizinische Klinik III, Hematology, Oncology and Rheumatology, University Hospital of Bonn, Bonn, Germany.

出版信息

Biomed Res Int. 2018 Feb 1;2018:8286067. doi: 10.1155/2018/8286067. eCollection 2018.

Abstract

OBJECTIVE

Antinuclear antibodies (ANA) serve as screening tests for connective tissue diseases but have low specificity. In this pilot study, we aimed to identify patients with first-time positive ANA and musculoskeletal complaints and correlate serum soluble vascular adhesion molecules as biomarkers.

METHODS

Prospective, observational study with 100 ANA-positive patients, comparing them to age- and gender-matched healthy controls (HC, = 75), was conducted. Serum levels of soluble intercellular adhesion molecule-1 (sICAM-1), endothelial-leukocyte adhesion molecule-1 (sELAM-1), and vascular cell adhesion molecule-1 (sVCAM-1) were measured. A subgroup of patients with systemic sclerosis (SSc) treated with immunosuppressants was followed over 10 months.

RESULTS

Patients belonged to three main entities: rheumatoid arthritis (RA, = 32), collagen diseases (CD, = 56) also including systemic sclerosis (SSc, = 11), and other autoimmune diseases ( = 12). sICAM-1 was similar among groups. sELAM-1 was elevated by 1.9-fold in only in SSc. sVCAM-1 was elevated by 3.1-fold in RA and by 3.3-fold in CD and in other autoimmune diseases by 3.4-fold. Seven SSc patients with immunosuppression had a 2.7-fold increased sVCAM-1 at baseline and reached the levels of healthy controls after 5 months, while CRP, ESR, and clinical parameters remained unchanged.

CONCLUSION

Our study suggests that sVCAM-1 is a disease marker independent of standard serum parameters in several rheumatic diseases. This study is registered with EU PAS Register number: EUPAS22154.

摘要

目的

抗核抗体(ANA)可作为结缔组织疾病的筛查试验,但特异性低。在这项初步研究中,我们旨在确定首次出现 ANA 阳性和肌肉骨骼投诉的患者,并将血清可溶性血管黏附分子作为生物标志物进行相关分析。

方法

进行了一项前瞻性、观察性研究,纳入 100 例 ANA 阳性患者,并与年龄和性别匹配的健康对照者(HC,n=75)进行比较。检测血清可溶性细胞间黏附分子-1(sICAM-1)、内皮白细胞黏附分子-1(sELAM-1)和血管细胞黏附分子-1(sVCAM-1)水平。对接受免疫抑制剂治疗的系统性硬化症(SSc)患者亚组进行了 10 个月的随访。

结果

患者主要归为以下三种疾病实体:类风湿关节炎(RA,n=32)、胶原疾病(CD,n=56),也包括系统性硬化症(SSc,n=11)和其他自身免疫性疾病(n=12)。各组间 sICAM-1 水平相似。仅在 SSc 患者中 sELAM-1 升高 1.9 倍。RA 和 CD 患者以及其他自身免疫性疾病患者 sVCAM-1 分别升高 3.1 倍、3.3 倍和 3.4 倍。7 例接受免疫抑制治疗的 SSc 患者基线时 sVCAM-1 升高 2.7 倍,在 5 个月后达到健康对照者水平,而 CRP、ESR 和临床参数保持不变。

结论

我们的研究表明,sVCAM-1 是几种风湿性疾病中独立于标准血清参数的疾病标志物。本研究在 EU PAS 登记处注册,注册号:EUPAS22154。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de39/5816882/593e30ce19ef/BMRI2018-8286067.001.jpg

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