Evidence map›Paper›PMID 34930143›Full record

SynthesisBMC gastroenterology2021

Association of HSD17B13 rs72613567: TA allelic variant with liver disease: review and meta-analysis.

Shan Tang, Jing Zhang, Ting-Ting Mei, Wen-Yan Zhang, Su-Jun Zheng, Hai-Bin Yu

Open access · goldAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in BMC gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Heterogeneity, dynamics and organelle interactions of lipid droplets.Nature reviews. Molecular cell biology · 2026
    Review
  2. Review
  3. Gene-based therapies for steatotic liver disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Impact of a Loss-of-Function Variant inInternational journal of molecular sciences · 2022
    Article
  10. 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

6 authors at 2 institutions in 1 country.

Shan TangBeijing YouAn Hospital, Capital Medical University, 8 Xitoutiao, Youanmenwai Street, Beijing, 100069, China.
Jing ZhangBeijing YouAn Hospital, Capital Medical University, 8 Xitoutiao, Youanmenwai Street, Beijing, 100069, China.
Ting-Ting MeiBeijing YouAn Hospital, Capital Medical University, 8 Xitoutiao, Youanmenwai Street, Beijing, 100069, China.
Wen-Yan ZhangBeijing YouAn Hospital, Capital Medical University, 8 Xitoutiao, Youanmenwai Street, Beijing, 100069, China.
Su-Jun ZhengBeijing YouAn Hospital, Capital Medical University, 8 Xitoutiao, Youanmenwai Street, Beijing, 100069, China. zhengsujun@ccmu.edu.cn.
Hai-Bin YuBeijing YouAn Hospital, Capital Medical University, 8 Xitoutiao, Youanmenwai Street, Beijing, 100069, China. dryuhaibin@ccmu.edu.cn.
Beijing YouAn Hospital · CNCapital Medical University · CN

Funding

National Major Science and Technology Projects of China 2017ZX10202203-006National Major Science and Technology Projects of China 2017ZX10302201-004the Key Medical Professional Development Plan(Sailing plan) of Beijing Hospital Management Center ZYLX202125
6 · The paper itself

Abstract

backgroundTo assess the association of HSD17B13 rs72613567:TA allelic variant with liver disease, we performed the current review and meta-analysis.

methodsSeven studies were identified by a search of CNKI,CBM,MEDLINE, PubMed, EMBASE, and CENTRAL databases from inception to November 2021. Odds ratios (ORs) with 95% confidence interval (CI) were calculated using random effects model or fixed effects model based on the between-study heterogeneity. The Stata 14.0 software was employed for data analysis.

resultsStatistical analysis showed that the HSD17B13 rs72613567:TA allelic variant can decrease the risk of hepatocellular carcinoma(HCC) in nonalcoholic fatty liver disease (NAFLD) patients, alcoholic fatty liver disease (ALD) patients and viral hepatitis patients (TA vs T OR = 0.766, 95% CI = 0.682-0.860, P = 0.000; TATA + TAT vs TT OR = 0.755, 95% CI = 0.645-0.885, P = 0.001) or healthy controls(TA vs T OR = 0.649, 95% CI = 0.431-0.977, P = 0.038). Besides, the HSD17B13 rs72613567:TA allelic variant can also provide protection from nonalcoholic fatty liver disease (NAFLD) not only in entire population (TA vs T OR = 0.669, 95% CI = 0.524-0.856, P = 0.001) but also in healthy people (TA vs T OR = 0.600, 95% CI = 0.464-0.777, P = 0.000). No significant publication bias found in this airticle.

conclusionThe present findings suggest HSD17B13 rs72613567:TA allelic variant can reduce the risk of HCC and NAFLD in the entire population studied.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNon-alcoholic Fatty Liver Disease17-Hydroxysteroid DehydrogenasesAllelesHumansOdds Ratio17-Hydroxysteroid DehydrogenasesHSD17B13 protein, humanHSD17B13 rs72613567:TA allelic variantLiver diseaseMeta-analysis

Identifiers

PMID34930143
PMCPMC8686634
OpenAlexW4225337631

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.