Evidence map›Paper›PMID 39906083›Full record

ReviewJGH open : an open access journal of gastroenterology and hepatology2025

Causal Exposures in Pancreatic Cancer Incidence: Insights From Mendelian Randomization Studies.

Ashraf Mohamadkhani, Reza Ghanbari, Ramin Shakeri, Mohammad Ali Mohammadkhani, Akram Pourshams

Abstract readReview
In one paragraph

Review in JGH open : an open access journal of gastroenterology and hepatology, 2025. 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

5 authors.

Ashraf MohamadkhaniLiver and Pancreatobiliary Diseases Research Center; Digestive Diseases Research Institute, Shariati Hospital, Tehran University of Medical Sciences Tehran Iran.
Reza GhanbariGene Therapy Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences Tehran Iran.ORCID https://orcid.org/0000-0003-3876-7584
Ramin ShakeriDigestive Oncology Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences Tehran Iran.
Mohammad Ali MohammadkhaniTechnical and Vocational University Tehran Iran.
Akram PourshamsLiver and Pancreatobiliary Diseases Research Center; Digestive Diseases Research Institute, Shariati Hospital, Tehran University of Medical Sciences Tehran Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Pancreatic cancer, marked by its high lethality and poor 5-year survival rate, requires a thorough understanding of its risk factors and etiological mechanisms. In this review, we collected the latest findings from Mendelian randomization (MR) studies to identify potential causal factors for pancreatic cancer. Method and Results: The present analysis encompasses MR studies on the gut and oral microbiomes, non-malignant phenotypes, blood metabolites, immune cells, and chronic inflammation. Specific gut and oral microbiome species have been identified as potential causal factors for pancreatic cancer, some with protective effects, and others increasing the risk. The review also highlights causal associations between obesity, type 2 diabetes, and pancreatic cancer, as well as the impact of blood metabolites and immune cell phenotypes on disease risk. Additionally, it investigates the causal effects of inflammatory bowel disease, showing a significant risk increase associated with Crohn's disease. Conclusion: These insights emphasize the need for interdisciplinary research and personalized medicine to enhance prevention and treatment strategies for pancreatic cancer.

Indexed as

causal factorsMendelian randomizationpancreatic cancer

Identifiers

PMID39906083
PMCPMC11790352

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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 OpenQuestion graph.