Evidence map›Paper›PMID 39863728›Full record

ArticleScientific reports2025

Genetic association of lipid-lowering drug target genes with pancreatic cancer: a Mendelian randomization study.

Bohan Su, Zhiyao Fan, Jiexi Wu, Hanxiang Zhan

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Bohan Su *Division of Pancreatic Surgery, Department of General Surgery, Qilu Hospital, Shandong University, Jinan, 250012, China.
Zhiyao Fan *Division of Pancreatic Surgery, Department of General Surgery, Qilu Hospital, Shandong University, Jinan, 250012, China.
Jiexi WuDivision of Pancreatic Surgery, Department of General Surgery, Qilu Hospital, Shandong University, Jinan, 250012, China.
Hanxiang ZhanDivision of Pancreatic Surgery, Department of General Surgery, Qilu Hospital, Shandong University, Jinan, 250012, China. zhanhanxiang@hotmail.com.

Funding

Clinical Research Foundation of Shandong University 2020SDUCRCC016National Natural Science Foundation of China 81972274Natural Science Foundation of Shandong Province ZR2021LSW004Taishan Scholars Program for Young Experts of Shangdong Province tsqn202103172
6 · The paper itself

Abstract

Previous studies have found that dyslipidemia is a risk factor for pancreatic cancer (PC), and that lipid-lowering drugs may reduce the risk of PC. However, it is not clear whether dyslipidemia causes PC. The Mendelian randomization (MR) study aimed to investigate the causal role of lipid traits in pancreatic cancer and to assess the potential impact of lipid-lowering drug targets on pancreatic cancer. Genetic variants associated with lipid traits and variants of genes encoding lipid-lowering drug targets were extracted from the Global Lipids Genetics Consortium genome-wide association study (GWAS). Summary statistics for PC were obtained from an independent GWAS datasets. Colocalization analyses were performed to validate the robustness of the results. No significant effect of lipid-lowering drug targets on PC risk was found. Genetic mimicry of lipoprotein lipase (LPL) was potentially associated with PC risks. Significant MR associations were observed in the discovery dataset (OR 1.64 [95% CI 1.24-2.16], p = 4.48*10

Indexed as

DyslipidemiasHypolipidemic AgentsPancreatic NeoplasmsGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLipoprotein LipaseMendelian Randomization AnalysisPolymorphism, Single NucleotideHypolipidemic AgentsLipoprotein LipaseeQTLMendelian randomizationPancreatic cancerTG

Identifiers

PMID39863728
PMCPMC11762976

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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.