SynthesisFrontiers in medicine2026
The impact of gut microbiome on intrahepatic cholestasis of pregnancy-systematic literature review.
Synthesis in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In recent years, there has been a growing interest in the gut microbiome and its potential role in the etiopathogenesis of both gastrointestinal and extraintestinal diseases. Dysbiosis, characterized by a pathological alteration in the composition of the gut microbiome, has been implicated in various gastrointestinal diseases. This paradigm extends to pregnancy-specific conditions, including intrahepatic cholestasis of pregnancy (ICP). ICP exhibits a multifactorial etiopathogenesis, involving hormonal, genetic and environmental factors, among others. Despite growing scientific evidence, there is currently a lack of comprehensive reviews that specifically examine the causal mechanisms through which gut microbiota dysbiosis might contribute to the pathogenesis of ICP, as well as the resulting implications for the development of new targeted therapeutic approaches. Notably, shifts in microbial taxa and the depletion of bacteria involved in certain metabolic pathways have been observed in ICP. These findings suggest that alterations in the gut microbiome composition may contribute to the pathophysiology of ICP. Such microbiome-associated alterations may have important implications for risk stratification and early identification of patients at increased risk of adverse maternal and fetal outcomes. Further investigation into these microbial changes and molecular pathways could offer novel insights and identify potential pharmacological targets for ICP development and management. In particular, modulation of the gut microbiome could represent a future adjunctive strategy to existing therapeutic approaches, potentially improving disease monitoring and individualized management. The precise role of gut microbiome composition in the management and treatment of ICP is still not fully understood, highlighting the need for a systematic review to synthesize existing evidence and identify critical gaps relevant to the future development of screening, prevention, and targeted therapeutic strategies.
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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.