Lira Sheezara T, Costa Maxsuel R, Gonçalves Barros Wérgila R, Gonçalves Junior Jucier
Internal Medicine, Universidade Federal do Cariri (UFCA), Barbalha, BRA.
Internal Medicine, Escola de Saúde Pública (ESP), Juazeiro do Norte, BRB.
Cureus. 2024 Aug 8;16(8):e66422. doi: 10.7759/cureus.66422. eCollection 2024 Aug.
Despite advances in the study of rheumatoid arthritis-associated interstitial lung disease (RA-ILD), the pulmonary manifestation remains an important cause of morbidity and mortality. However, there is a lack of biochemical markers for this manifestation in the literature. Therefore, the objective of this study was to carry out a qualitative systematic review on biochemical markers associated with RA-ILD in the PubMed, Web of Science, Embase, Cochrane Library, and Virtual Health Library (VHL) between January 2015 and July 2024, using the following descriptors: #1 "biomarkers" (MeSH) AND #2 "rheumatoid arthritis" (MeSH) AND #3 "Lung Diseases, Interstitial" (MeSH). Of the 1497 articles found, 27 presented eligibility criteria. The findings were divided into three sessions: "Main biomarkers for RA-ILD," "Other biomarkers for RA-ILD activity," and "Other biomarkers for RA-ILD prognosis." Among the evaluated markers, KL-6, RF, ACPA, ESR, and CRP appear to have prognostic value and association with damage in patients with RA-ILD. The association of some molecules such as sPD-1, sCD25, VCAM-1, MCP-1, and ADMA with tissue damage is intriguing. Longitudinal and randomized studies are imperative to comprehensively delineate the history of RA-ILD and evaluate potential serum biomarkers.
尽管类风湿关节炎相关间质性肺疾病(RA - ILD)的研究取得了进展,但肺部表现仍然是发病和死亡的重要原因。然而,文献中缺乏针对这种表现的生化标志物。因此,本研究的目的是在2015年1月至2024年7月期间,使用以下描述词:#1“生物标志物”(医学主题词)、#2“类风湿关节炎”(医学主题词)和#3“间质性肺疾病”(医学主题词),对PubMed、科学网、Embase、Cochrane图书馆和虚拟健康图书馆(VHL)中与RA - ILD相关的生化标志物进行定性系统评价。在找到的1497篇文章中,27篇符合纳入标准。研究结果分为三个部分:“RA - ILD的主要生物标志物”、“RA - ILD活动度的其他生物标志物”和“RA - ILD预后的其他生物标志物”。在评估的标志物中,KL - 6、类风湿因子(RF)、抗环瓜氨酸肽抗体(ACPA)、红细胞沉降率(ESR)和C反应蛋白(CRP)似乎对RA - ILD患者具有预后价值并与损伤相关。一些分子如可溶性程序性死亡受体1(sPD - 1)、可溶性白细胞介素 - 2受体α链(sCD25)、血管细胞黏附分子1(VCAM - 1)、单核细胞趋化蛋白 - 1(MCP - 1)和不对称二甲基精氨酸(ADMA)与组织损伤的关联很有趣。纵向和随机研究对于全面描绘RA - ILD的病程并评估潜在的血清生物标志物至关重要。