Evidence map›Paper›PMID 40591000›Full record

ArticleClinical and experimental medicine2025

Dynamics of serum tumor markers may indicate the progression of interstitial lung disease in Sjögren's syndrome patients: new roles for old friends.

Jiamin Song, Ronglin Gao, Fang Han, Jincheng Pu, Yuanyuan Liang, Yanqing Wang, Zhenzhen Wu, Shengnan Pan, Huihong Wu, Yuhang Sun and 3 more

Abstract read
In one paragraph

Article in Clinical and experimental medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Jiamin Song *Department of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0001-9815-8508
Ronglin Gao *Department of Pulmonary and Critical Care Medicine, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0002-4507-480X
Fang HanDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0003-2271-7646
Jincheng PuDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0001-9242-3067
Yuanyuan LiangDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0003-0360-286X
Yanqing WangDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0002-9946-159X
Zhenzhen WuDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0003-4384-3473
Shengnan PanDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0002-4520-0239
Huihong WuDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0000-0002-2842-4812
Yuhang SunDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0009-0003-6248-7424
Kailong LinDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China.ORCID http://orcid.org/0009-0006-8296-5229
Jianping TangDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China. tangjp6512@126.com.ORCID http://orcid.org/0000-0003-4629-7631
Xuan WangDepartment of Rheumatology and Immunology, Tongji Hospital, School of Medicine, Tongji University, No. 389 Xincun Road, Shanghai, 200065, China. xuan2018@tongji.edu.cn.ORCID http://orcid.org/0000-0002-6588-2951

Funding

Clinical research program of Tongji Hospital Tongji University ITJZD2408, ITJZD1909, ITJQN2001Fundamental Research Funds for the Central Universities 22120240361National Natural Science Foundation of China 81671598National Natural Science Foundation of China 81801601Natural Science Foundation of Shanghai 20ZR1451400Science and technology commission of Shanghai 20Y11911600Shanghai Pujiang Rheumatic Youth Cultivation Program SPROG2007, SPROG2210, SPROG2310Shanghai Wu Mengchao Medical Foundation JJHXM-2019011Sixth cycle of key cultivation disciplines of Tongji Hospital Tongji University ZDPY24-YD-2the Shanghai Sailing Program 17YF1417200
6 · The paper itself

Abstract

A retrospective case-control study was designed to identify the characteristics and predictors of primary Sjögren's syndrome (pSS)-associated progressive fibrosing interstitial lung disease (ILD). Patients who diagnosed pSS-ILD were enrolled from Shanghai Tongji Hospital between January 1, 2015, and September 30, 2023. Relevant clinical data, including medical history, laboratory test results, and imaging findings, were collected at baseline. Progressive pulmonary fibrosis (PPF) was defined as established standard during one year of follow-up. Multiple linear regression was used to assess the relationship between tumor markers and ILD activity status. Characteristics associated with progression were determined by COX regression analysis. Kaplan-Meier survival analysis was employed to evaluate the predictive accuracy of the model. A total of 58 patients with pSS-ILD were included. The incidence of pleuritis and baseline levels of carbohydrate antigen 50 (CA50) were significantly higher in the pSS-PPF group. No significant differences were observed in arterial blood gas analysis, tumor marker levels, or CT scores at baseline. A negative correlation was found between cancer antigen 199 (CA199) levels and forced vital capacity, while carcinoembryonic antigen (CEA) and carbohydrate antigen 125 (CA125) levels were positively correlated with the severity of CT lesions. Cox regression analysis identified CEA and CA50 as significant predictors of pulmonary prognosis, and survival analysis indicated that elevated levels of CEA and CA50 were associated with disease progression. Serum tumor markers, such as CEA and CA50, may serve as potential indicators of radiographic progression and declines in lung function in pSS-ILD patients, possibly identifying individuals at higher risk of poor prognosis.

Indexed as

Biomarkers, TumorLung Diseases, InterstitialSjogren's SyndromeAdultAgedAntigens, Tumor-Associated, CarbohydrateCase-Control StudiesDisease ProgressionFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisRetrospective StudiesAntigens, Tumor-Associated, CarbohydrateBiomarkers, TumorInterstitial lung diseasePrimary Sjogren syndromePrognosisTumor markers

Identifiers

PMID40591000
PMCPMC12214032

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.