Evidence map›Paper›PMID 41329431›Full record

ArticleClinical rheumatology2026

The clinical features, pathological findings, and risk factors of intracardiac thrombus in Behçet's syndrome.

Xiaoou Wang, Hongqin Dai, Xun Wang, Weida Liu, Xin Yu, Menghao Zhang, Yeling Liu, Yiyuan Ao, Jinjing Liu, Qi Miao and 3 more

Abstract read
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Article in Clinical 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

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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Xiaoou WangDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China.
Hongqin DaiDepartment of Nephrology and Rheumatology, The Fourth Hospital of Changsha (Changsha Integrated Traditional Chinese and Western Medicine Hospital), Changsha, 410000, China.
Xun WangDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Weida LiuState Key Laboratory for Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Xin YuDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China.
Menghao ZhangDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China.
Yeling LiuDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China.
Yiyuan AoDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China.
Jinjing LiuDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China.
Qi MiaoDepartment of Cardiac Surgery, Peking Union Medical College Hospital, Dongcheng District, Beijing, 100730, China.
Wenze WangDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Jun ZhengDepartment of Cardiac Surgery, Peking Union Medical College Hospital, Dongcheng District, Beijing, 100730, China. zhengjun@pumch.cn.
Wenjie ZhengDepartment of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, Beijing, 100730, China. wenjzheng@gmail.com.ORCID http://orcid.org/0000-0002-3165-8185

Funding

CAMS Innovation Fund for Medical Sciences 2023-I2M-C&T-B-049Fundamental Research Funds for the Central Universities, Peking Union Medical College 3332025116National High Level Hospital Clinical Research Funding 2022-PUMCH-C-008National Natural Science Foundation of China 82371822National Natural Science Foundation of China 82402117
6 · The paper itself

Abstract

objectivesTo investigate the clinical features, pathological findings, and risk factors of intracardiac thrombus (ICT) in Behçet's syndrome (BS).

methodsWe conducted a case-control study using our BS registry database. BS patients with ICT were enrolled as the cases, and controls were selected using risk-set-sampling. Multivariable logistic regression identified risk factors, and outcomes were also analyzed. Pathology of six ICT specimens was reanalyzed by preoperative disease activity.

resultsSeventeen BS patients with ICT (14 males, 3 females, BS onset age: 26.4 ± 8.0 years) were enrolled. Compared to controls, ICT patients had higher venous involvement (70.6% vs. 13.7%, p < 0.001), pulmonary artery thrombosis (64.7% vs. 3.9%, p < 0.001), elevated ESR (26.0 vs. 9.8 mm/h, p = 0.013), CRP (34.7 vs. 10.1 mg/L, p < 0.001), and monocyte count (0.5 vs. 0.4*10^9/L, p = 0.024). Multivariable logistic regression identified CRP > 20 mg/L (OR 11.27, 95% CI 1.13-112.26, p = 0.039) and venous involvement (OR 11.71, 95% CI 2.79-49.20, p < 0.001) as ICT risk factors. Pathology revealed increased infiltration of neutrophils and CD68

conclusionICT in BS is a severe complication with a high relapse rate and pathological features of neutrophils and macrophages' infiltration. Elevated CRP (> 20 mg/L) and venous involvement are potential risk factors. These findings support the potential benefit of adequate immunosuppressive treatment before surgery for improving outcomes in BS patients with ICT. Key Points • ICT is a serious complication of BS, with a high relapse rate. • CRP > 20 mg/L and venous involvement are potential risk factors for ICT in BS. • Adequate immunosuppressive treatment before surgery is essential for improving outcomes in BS patients with ICT.

Indexed as

Behcet SyndromeHeart DiseasesThrombosisAdultCase-Control StudiesFemaleHumansLogistic ModelsMaleRisk FactorsYoung AdultBehçet’s syndromeIntracardiac thrombusRisk factors

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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.