Evidence map›Paper›PMID 38288469›Full record

ArticleFrontiers in endocrinology2023

Late age at first birth is a protective factor for oesophageal cancer and gastro-oesophageal reflux: the evidence from the genetic study.

Yani Su, Yiwei Xu, Yunfeng Hu, Yu Chang, Fangcai Wu, Mingyi Yang, Yuhui Peng

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. 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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1 · What the graph read from it

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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

7 authors.

Yani SuDepartment of Clinical Laboratory Medicine, Cancer Hospital of Shantou University Medical College, Shantou, China.
Yiwei XuDepartment of Clinical Laboratory Medicine, Cancer Hospital of Shantou University Medical College, Shantou, China.
Yunfeng HuDepartment of Radiotherapy, Yan'an University Affiliated Hospital, Yan'an, China.
Yu ChangDepartment of Radiotherapy, Yan'an University Affiliated Hospital, Yan'an, China.
Fangcai WuDepartment of Radiation Oncology, Cancer Hospital of Shantou University Medical College, Shantou, China.
Mingyi YangDepartment of Joint Surgery, HongHui Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Yuhui PengDepartment of Clinical Laboratory Medicine, Cancer Hospital of Shantou University Medical College, Shantou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The primary objective of this research endeavor was to examine the underlying genetic causality between the age at first birth (AFB) and four prevalent esophageal diseases, namely oesophageal obstruction (OO), oesophageal varices (OV), gastro-oesophageal reflux (GOR), and oesophageal cancer (OC). Methods: We conducted a two-sample Mendelian randomization (MR) analysis to examine the causal association between AFB and four prevalent esophageal disorders. We employed eight distinct MR analysis techniques to evaluate causal relationships, encompassing random-effects inverse variance weighted (IVW), MR Egger, weighted median, simple mode, weighted mode, maximum likelihood, penalized weighted median, and fixed-effects IVW. The random-effects IVW method served as the primary approach for our analysis. Furthermore, we executed several sensitivity analyses to assess the robustness of the genetic causal inferences. Results: The random-effects IVW analysis revealed a significant negative genetic causal association between AFB and both GOR (P < 0.001, Odds Ratio [OR] 95% Confidence Interval [CI] = 0.882 [0.828-0.940]) and OC (P < 0.001, OR 95% CI = 0.998 [0.998-0.999]). Conversely, there was insufficient evidence support to substantiate a genetic causal link between AFB and OO (P = 0.399, OR 95% CI = 0.873 [0.637-1.197]) or OV (P = 0.881, OR 95% CI = 0.978 [0.727-1.314]). The results of sensitivity analyses underscore the robustness and reliability of our MR analysis. Conclusion: The findings of this investigation substantiate the notion that elevated AFB confers a protective effect against GOR and OC. In addition, no causative association was discerned between AFB and OO or OV at the genetic level.

Indexed as

Esophageal NeoplasmsGastroesophageal RefluxBirth OrderHumansMendelian Randomization AnalysisProtective FactorsReproducibility of Resultsage at first birthcausalgastro-oesophageal refluxgeneticoesophageal cancer

Identifiers

PMID38288469
PMCPMC10823002

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