ReviewInternational journal of women's health2026
Gut and Gastric Dysbiosis in Hyperemesis Gravidarum: A Scoping Review of Microbiome-Targeted Evidence and Translational Pathways.
Review in International journal of women's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Hyperemesis gravidarum (HG) is defined by severe nausea and/or vomiting beginning in early pregnancy, impaired ability to eat or drink normally, and a marked restriction of daily activities. Although gastrointestinal dysbiosis has been proposed in HG, its role remains uncertain within the emerging growth differentiation factor 15 (GDF15)-centered model of susceptibility. Methods: Guided by PRISMA-ScR, this scoping review searched PubMed/MEDLINE, Scopus, Web of Science, publisher websites, and reference lists for contemporary evidence published between 1 January 2021 and 2 May 2026. Pre-2021 foundational publications were excluded from the charted evidence map and included-study count and were cited only as methodological or biological background. Results: Thirty-six sources of evidence were synthesized across five thematic domains. Direct human studies identified associations between HG and altered microbial diversity or composition, as well as gastric Conclusion: Current evidence supports dysbiosis as an associated modifier, consequence, or endotype marker rather than an established independent cause of HG. Priority studies should use Windsor-compatible definitions, early longitudinal sampling, harmonized sequencing and metabolomic methods, concurrent assessment of GDF15 and nutritional status, and biologically stratified trials of confirmed H. pylori infection or reproducible functional dysbiosis.
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Registered trials
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.