Evidence map›Paper›PMID 42337778›Full record

ArticleBMC rheumatology2026

Tumor markers in rheumatoid arthritis -associated interstitial lung disease: a systematic review and meta-analysis.

Zeng Qiaoqian, Wu Qing, Li Bowen, Wei Qijiao, Wang Na

Abstract read
In one paragraph

Article in BMC rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zeng Qiaoqian *Department of Rheumatology, Children's Hospital of Fudan University, National Pediatric Medical Center of China, Shanghai, China.
Wu Qing *Department of Renal Rheumatology and Immunology, Affiliated Children's Hospital of Jiangnan University (Wuxi Children's Hospital), Wuxi, China.
Li Bowen *Department of General Practice, The First Affiliated Hospital of Naval Medical University, Shanghai, Shanghai, 200000, China.
Wei QijiaoDepartment of Rheumatology, Children's Hospital of Fudan University, National Pediatric Medical Center of China, Shanghai, China. weiqijiao@126.com.
Wang NaDepartment of Traditional Chinese Medicine, Children's Hospital of Fudan University, Shanghai, China. 18203638814@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInterstitial lung disease (ILD) is a serious extra-articular complication of rheumatoid arthritis (RA) and a leading cause of mortality. This meta-analysis aims to comprehensively evaluate the diagnostic utility and clinical relevance of tumor-associated biomarkers in patients with Rheumatoid Arthritis-Associated Interstitial Lung Disease (RA-ILD).

methodsA systematic literature search was conducted in PubMed, EMBASE, Web of Science, CBM, Wan-Fang, and CNKI databases from inception to April 1, 2025. We included case-control and cohort studies that compared tumor marker levels between RA-ILD and RA-non-ILD patients, following the PICOS framework. Study quality was assessed using the Newcastle-Ottawa Scale (NOS). Pooled effect sizes were calculated as standardized mean differences (SMD) with 95% confidence intervals (CI) using random-effects models. Diagnostic accuracy was evaluated using summary receiver operating characteristic (ROC) curves.

resultsThirty-six studies comprising 7300 RA patients were included. Compared to RA-non-ILD patients, those with RA-ILD showed significantly elevated levels of CA125 (SMD = 1.10, 95%CI 0.47-1.72), CA199 (SMD = 0.90, 95%CI 0.56-1.23), CA153 (SMD = 1.70, 95%CI 1.16-2.23), CEA (SMD = 0.58, 95%CI 0.24-0.92), KL-6 (SMD = 1.68, 95%CI 1.22-2.14), NSE (SMD = 0.32, 95%CI 0.16-0.48), and HE4 (SMD = 1.87, 95%CI 1.60-2.14). After adjustment for publication bias using trim-and-fill analysis, CYFRA21-1 was also significantly elevated (SMD = 0.48, 95%CI 0.06-0.89). For distinguishing RA-ILD, KL-6 demonstrated the highest diagnostic accuracy (AUC = 0.964), followed by CYFRA21-1 (AUC = 0.906).

conclusionOur findings, which are primarily based on evidence from Chinese cohorts, support the utility of CA125, CA199, CA153, CEA, KL-6, NSE, HE4, and CYFRA21-1 as biomarkers for RA-ILD. The superior diagnostic performance of KL-6 and CYFRA21-1 suggests their potential clinical utility as part of a multi-marker panel discriminating RA-ILD from RA-non-ILD and risk stratification, offering a complementary approach to imaging for identifying this high-risk RA complication. REGISTRATION NUMBER: PROSPERO CRD42022362487.

Indexed as

Meta-analysisRheumatoid arthritisRheumatoid arthritis-associated interstitial lung diseaseSystematic reviewTumor markers

Identifiers

PMID42337778
PMCPMC13551961

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.