Evidence map›Paper›PMID 35971954›Full record

ReviewJournal of medical virology2022

COVID-19 and inflammatory bowel disease crosstalk: From emerging association to clinical proposal.

Sha-Sha Tao, Xin-Yi Wang, Xiao-Ke Yang, Yu-Chen Liu, Zi-Yue Fu, Li-Zhi Zhang, Zhi-Xin Wang, Jing Ni, Zong-Wen Shuai, Hai-Feng Pan

Abstract readReview
In one paragraph

Review in Journal of medical virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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

  1. Pooled it
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  7. Review
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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

10 authors.

Sha-Sha TaoDepartment of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.ORCID 0000-0002-3054-4370
Xin-Yi WangDepartment of Radiation Oncology, The First Affiliated Hospital of Anhui Medical University, First Clinical Medical College, Anhui Medical University, Hefei, Anhui, China.
Xiao-Ke YangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yu-Chen LiuDepartment of Otolaryngology, Head, and Neck Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Zi-Yue FuDepartment of Clinical Medicine, The Second School of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
Li-Zhi ZhangDepartment of Clinical Medicine, The First School of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
Zhi-Xin WangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Jing NiDepartment of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.
Zong-Wen ShuaiDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Hai-Feng PanDepartment of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can cause coronavirus disease 2019 (COVID-19), an acute respiratory inflammation that has emerged worldwide since December 2019, and it quickly became a global epidemic. Inflammatory bowel disease (IBD) is a group of chronic nonspecific intestinal inflammatory diseases whose etiology has not been elucidated. The two have many overlapping symptoms in clinical presentation, such as abdominal pain, diarrhea, pneumonia, etc. Imbalance of the autoimmune system in IBD patients and long-term use of immunosuppressive drugs may increase the risk of infection; and systemic symptoms caused by COVID-19 may also induce or exacerbate intestinal inflammation. It has been found that the SARS-CoV-2 receptor angiotensin converting enzyme 2, which is highly expressed in the lung and intestine, is an inflammatory protective factor, and is downregulated and upregulated in COVID-19 and IBD, respectively, suggesting that there may be a coregulatory pathway. In addition, the immune activation pattern of COVID-19 and the cytokine storm in the inflammatory response have similar roles in IBD, indicating that the two diseases may influence each other. Therefore, this review aimed to address the following research questions: whether SARS-CoV-2 infection leads to the progression of IBD; whether IBD increases the risk of COVID-19 infection and poor prognosis; possible common mechanisms and genetic cross-linking between the two diseases; new treatment and care strategies for IBD patients, and the feasibility and risk of vaccination in the context of the COVID-19 epidemic.

Indexed as

COVID-19Inflammatory Bowel DiseasesAngiotensin-Converting Enzyme 2Cytokine Release SyndromeHumansPeptidyl-Dipeptidase ASARS-CoV-2Angiotensin-Converting Enzyme 2Peptidyl-Dipeptidase AACE2COVID-19IL-17inflammatory bowel diseaseSARS-CoV-2

Identifiers

PMID35971954
PMCPMC9538900

What Socratic holds

Textmetadata
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 Socratic graph.