Evidence map›Paper›PMID 40193675›Full record

ArticleMedicine2025

Gastroesophageal reflux disease and osteoporosis: A bidirectional Mendelian randomization study.

Qinghua Yang, Longao Huang, Hongyuan Xu, Junfei Feng, Dun Liu, Shengwang Wei, Hua Jiang

Abstract read
In one paragraph

Article in Medicine, 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

The trial behind it

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Qinghua YangDepartment of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Longao HuangDepartment of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Hongyuan XuDepartment of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Junfei FengDepartment of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Dun LiuDepartment of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Shengwang WeiDepartment of Orthopedics, The Fourth Affiliated Hospital of Guangxi Medical University/Liuzhou Worker's Hospital, Liuzhou, China.
Hua JiangDepartment of Spine Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID 0000-0001-9347-5782

Funding

Joint Project on Regional High-Incidence Diseases Research of Guangxi Natural Science Foundation 2024GXNSFDA010043Liuzhou Science and Technology Plan Project 2021CBB0110The National Natural Science Foundation of China 82360438
6 · The paper itself

Abstract

In observational studies, associations between osteoporosis (OP) and gastroesophageal reflux disease (GERD) have been found. We conducted a 2-way, 2-sample Mendelian randomization (MR) analysis to determine whether these associations have a causal relationship. Data on GERD at the summary-level were sourced from extensive genome-wide association studies encompassing 129,080 cases and 473,524 control subjects. Bone mineral density (BMD) served as the phenotypic indicator for OP. BMD metrics were compiled from a cohort of 537,750 individuals, encompassing total body BMD (TB-BMD) and stratified TB-BMD across age groups, along with BMD measurements at 4 anatomical locations: lumbar spine, femoral neck, heel, and ultra-distal forearm. Multiple MR approaches, such as the inverse-variance weighted (IVW) method, MR-Egger regression, and the MR-PRESSO test, were employed, among which findings obtained by IVW method were designated as the primary outcomes. For quality assurance, sensitivity analyses were conducted using the MR-Egger intercept, Cochran Q, and leave-one-out test. There were no significant causal links between genetic inclination towards GERD and reduced BMD levels. Nonetheless, the genetic evidence suggests a causal link between higher BMD levels and lower incidence of GERD [TB-BMD: OR = 0.941, 95% confidence intervals (CI) = 0.910-0.972, P < .001; TB-BMD-1: OR = 0.919, 95% CI = 0.885-0.954, P < .001; TB-BMD-3: OR = 0.945, 95% CI = 0.915-0.977, P = .001; TB-BMD-4: OR = 0.926, 95% CI = 0.896-0.957, P < .001]. Sensitivity analyses corroborate our findings. The MR analysis indicates no significant causal link between genetic inclination towards GERD and OP or reduced BMD within the European demographic. In addition, the study suggests that lower BMD or OP, as predicted by genetics, may contribute to the development of GERD.

Indexed as

Gastroesophageal RefluxOsteoporosisAdultBone DensityFemaleGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisMiddle Agedbone mineral densitygastroesophageal reflux diseaseGWAS dataMendelian randomizationosteoporosis

Identifiers

PMID40193675
PMCPMC11977714

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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.