Evidence map›Paper›PMID 41818289›Full record

SynthesisPloS one2026

Diagnostic potential of total serum ghrelin in autoimmune gastritis: A systematic review and meta-analysis.

Iqbal Taufiqqurrachman, Andro Pramana Witarto, Ari Fahrial Syam, Murdani Abdullah, Sigit Ari Saputro, Irine Normalina, Muhammad Miftahussurur, Yoshio Yamaoka

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Iqbal TaufiqqurrachmanDepartment of Environmental and Preventive Medicine, Oita University Faculty of Medicine, Yufu, Japan.
Andro Pramana WitartoInternal Medicine Specialist Study Program, Department of Internal Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.ORCID https://orcid.org/0000-0003-4292-3738
Ari Fahrial SyamDivision of Gastroenterology, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia, Cipto Mangunkusumo General Hospital, Central Jakarta, Indonesia.
Murdani AbdullahDivision of Gastroenterology, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia, Cipto Mangunkusumo General Hospital, Central Jakarta, Indonesia.
Sigit Ari SaputroDepartment of Epidemiology, Biostatistics, Population and Health Promotion, Faculty of Public Health, Airlangga University, Surabaya, East Java, Indonesia.
Irine NormalinaHelicobacter pylori and Microbiota Study Group, Institute Tropical Disease, Universitas Airlangga.
Muhammad MiftahussururHelicobacter pylori and Microbiota Study Group, Institute Tropical Disease, Universitas Airlangga.ORCID https://orcid.org/0000-0003-1415-6033
Yoshio YamaokaDepartment of Environmental and Preventive Medicine, Oita University Faculty of Medicine, Yufu, Japan.ORCID https://orcid.org/0000-0002-1222-5819

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutoimmune gastritis (AIG) is a chronic inflammatory condition characterized by the destruction of gastric parietal cells. The invasive nature of diagnostic procedures and risk of confounding factors hinder the development of reliable diagnostic tools for AIG.

methodsWe conducted a systematic search of four databases. After assessing the study quality using the ROBINS-E tool, a meta-analysis was performed using a random-effects model. Meta-regression and sensitivity analyses were conducted to explore the sources of heterogeneity and impact of study bias.

resultsThe pooled mean difference in total serum ghrelin (pmol/L) between patients with AIG and healthy controls was -65.28 (95% CI: -178.54, 47.97). Subgroup analysis showed that the mean differences in serum ghrelin for mild, moderate, and severe atrophy were -78.85 (95% CI: -165.17, to 7.48), -91.97 (95% CI: -183.11, to -0.84), and -110.67 (95% CI: -204.77, to -16.56), respectively. The sensitivity analysis confirmed that the exclusion of studies with high-risk bias did not significantly alter the results. Meta-regression indicated that BMI contributed substantially to heterogeneity.

conclusionsAlthough total serum ghrelin levels were not significantly different between patients with AIG and healthy controls, significantly lower levels were observed in patients with moderate-to-severe gastric atrophy. Given the high heterogeneity and limitations of existing studies, the diagnostic utility of serum ghrelin in AIG warrants further investigation.

Indexed as

Autoimmune DiseasesGastritisGhrelinHumansGhrelin

Identifiers

PMID41818289
PMCPMC12981498

What Socratic holds

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Registered trials

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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 Socratic graph.