Evidence map›Paper›PMID 39230635›Full record

ArticleDigestive diseases and sciences2024

Does Gastroesophageal Reflux Disease Increase the Risk of Sepsis and Its 28-day Mortality? A Causal Study Using a Mendelian Randomization Approach.

Runquan Zhou, Wenjuan Li, Fan Wu, Yuanhui Sheng, Shan Xu, Yi Liu, Dan Zhang, Mingxing Wang

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Article in Digestive diseases and sciences, 2024. 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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8 authors.

Runquan ZhouDepartment of Emergency, First Affiliated Hospital of Chongqing Medical University, 12th Floor, Building 5A, 1 Youyi Rd, Yuzhong Qu, Chongqing, 400016, People's Republic of China.
Wenjuan LiIntensive Care Unit, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Fan WuDepartment of Emergency, First Affiliated Hospital of Chongqing Medical University, 12th Floor, Building 5A, 1 Youyi Rd, Yuzhong Qu, Chongqing, 400016, People's Republic of China.
Yuanhui ShengIntensive Care Unit, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Shan XuDepartment of Emergency, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yi LiuIntensive Care Unit, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Dan ZhangDepartment of Emergency, First Affiliated Hospital of Chongqing Medical University, 12th Floor, Building 5A, 1 Youyi Rd, Yuzhong Qu, Chongqing, 400016, People's Republic of China. 201966@hospital.cqmu.edu.cn.
Mingxing WangIntensive Care Unit, First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Funding

Science and Technology Commission of Chongqing cstc2020jcyj-msxmX0922Science and Technology Commission of Chongqing Yuzhong District 20210138
6 · The paper itself

Abstract

backgroundGastroesophageal reflux disease (GERD) is a prevalent gastrointestinal disorder. Recent studies indicate that GERD may exert systemic effects, potentially elevating the risk of severe infections, including sepsis. Nevertheless, the causal relationship between GERD and sepsis, as well as sepsis-related 28-day mortality, remains uncertain.

aimThe aim of this study is to investigate the causal relationship between GERD and the risk of sepsis, including 28-day mortality of sepsis.

methodsThis study utilized a two-sample Mendelian Randomization (MR) approach to analyze data from publicly available genome-wide association studies (GWAS) databases ( https://gwas.mrcieu.ac.uk/ ). The analysis comprised 129,080 cases and 473,524 controls for GERD; 11,643 patients and 474,841 controls for sepsis; and 1,896 patients and 484,588 controls for 28-day mortality from sepsis. The objective was to evaluate the causal impact of GERD on the risk of sepsis and 28-day sepsis mortality. Genetic variation data pertinent to GERD were obtained from the most recent genome-wide association studies (GWAS). The primary analysis employed the Inverse Variance Weighted (IVW) method. Sensitivity and pleiotropy analyses were performed to validate the robustness of the findings.

resultsMR analysis revealed a notable link between genetically predicted GERD and increased sepsis risk (odds ratio [OR] 1.37, 95% confidence interval [CI] 1.24-1.52; p = 2.79 × 10-9). Moreover, GERD correlated with elevated 28-day mortality of sepsis (OR 1.44, 95% CI 1.11-1.85; p = 5.34 × 10-3). These results remained consistent throughout various sensitivity analyses, indicating their resilience against potential pleiotropy and other biases.

conclusionThis study indicates that genetic predisposition to GERD may be linked to an elevated risk of sepsis and its associated 28-day mortality. However, the study does not establish a direct causal relationship for GERD itself, nor does it assess the impact of GERD treatment. Further research is needed to explore the underlying mechanisms and potential therapeutic interventions involved.

Indexed as

Gastroesophageal RefluxGenome-Wide Association StudyMendelian Randomization AnalysisSepsisCase-Control StudiesGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideRisk Factors28-day mortalityGastroesophageal reflux disease (GERD)Genetic epidemiologyMendelian randomizationSepsis

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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.