Evidence map›Paper›PMID 40622608›Full record

ArticleClinical rheumatology2025

Relieving the discrimination dilemma of adult autoimmune enteropathy and common variable immunodeficiency disease: two rare causes of chronic diarrhea and small intestinal villous atrophy.

Muhan Li, Qipu Wang, Yang Chen, Xiaoxing Feng, Yanjun Lai, Chengzhu Ou, Xiaoqing Li, Gechong Ruan, Tianming Xu, Hao Tang and 5 more

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. 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

15 authors.

Muhan LiDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Qipu WangDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Yang ChenDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Xiaoxing FengDepartment of Pathology, Affiliated Hospital of Jiangnan University, Wuxi, 214122, China.
Yanjun LaiDepartment of Gastroenterology, Zhangzhou Municipal Hospital of Fujian Province, Zhangzhou, 363000, China.
Chengzhu OuDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Xiaoqing LiDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Gechong RuanDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Tianming XuDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Hao TangDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China.
Yujie ZhangDepartment of Pathology, Tianjin First Central Hospital, Nankai University, Tianjin, 300192, China.
Yan YouDepartment of Pathology, Peking Union Medical College and Chinese Academy of Medical Science, Peking Union Medical College Hospital, Beijing, 100730, China.
Ji LiDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China. liji0235@pumch.cn.ORCID http://orcid.org/0000-0002-0285-2966
Weixun ZhouDepartment of Pathology, Peking Union Medical College and Chinese Academy of Medical Science, Peking Union Medical College Hospital, Beijing, 100730, China. zweixun@163.com.
Jingnan LiDepartment Gastroenterology, Peking Union Medical College Hospitalof, Peking Union Medical College and Chinese Academy Medical Scienceof, Beijing, 100730, China. lijn2008@126.com.

Funding

CAMS Innovation Fund for Medical Sciences 2021-1-I2M-003National High Level Hospital Clinical Research Funding 2022-PUMCH-B-022National High Level Hospital Clinical Research Funding 2022-PUMCH-D-002National key clinical specialty construction project ZK108000Undergraduate Innovation Program 2023-zglc-06034Undergraduate Innovation Program 2024dcxm025
6 · The paper itself

Abstract

backgroundAutoimmune enteropathy (AIE) and common variable immunodeficiency (CVID) can both manifest as chronic diarrhea and small intestinal villous atrophy, making their differentiation challenging.

aimsTo explore the similarities and differences in the clinical manifestations, laboratory tests, pathological features, and long-term prognoses between these two diseases.

methodsThis retrospective study included 26 AIE patients and 29 CVID patients with gastrointestinal (GI) involvement who were admitted to our center from June 2012 to May 2024, with all their medical records reviewed. Differences between the two diseases were evaluated via statistical tests.

resultsCompared with CVID patients, AIE patients experienced a shorter duration of severe diarrhea, greater weight loss, and more severe hypoalbuminemia and electrolyte imbalances. Furthermore, CVID patients exhibited a notable history of recurrent respiratory infections; significantly lower serum levels of IgG, IgM, and IgA; a marked decrease in B-cell and CD4 + T-cell counts; and a significant inversion of the CD4 + /CD8 + ratio within peripheral blood lymphocyte subsets. Endoscopically, AIE patients are more likely to present with active inflammatory changes, such as erosions and hyperemia. On the basis of histopathological analysis of 23 AIE patients and 24 CVID patients, AIE patients presented with reduced goblet and Paneth cells, pronounced neutrophilic infiltration, and more frequent apoptotic bodies, while CVID patients demonstrated reduced plasma cells and deep crypt lymphocytosis. The diagnostic efficiency of the five pathological items in the duodenum (AUC 0.937), which includes goblet cell and Paneth cell reduction, was greater than that of the four-item combination (AUC 0.622). Long-term follow-up indicated that patients with both conditions were prone to diarrhea relapse, and CVID patients showed a slightly longer median relapse-free survival than did AIE patients.

conclusionsAlthough AIE patients and CVID patients share many similarities, they exhibit significant differences. A thorough medical history, laboratory tests, and endoscopic and histopathological results provide compelling evidence for their differential diagnosis. Key Points • Both AIE and CVID with gastrointestinal involvement are immune-mediated diseases characterized by chronic diarrhea and small intestinal villi atrophy, making clinical diagnosis difficult. • AIE and CVID have different characteristics that can be used to distinguish them, especially pathological findings.

Indexed as

Common Variable ImmunodeficiencyDiarrheaIntestinal MucosaIntestine, SmallPolyendocrinopathies, AutoimmuneAdultAgedAtrophyChronic DiseaseDiagnosis, DifferentialFemaleHumansMaleMiddle AgedRetrospective StudiesYoung AdultAutoimmune enteropathyCommon variable immunodeficiencyDifferential diagnosisPathologyPrognosis

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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.