Evidence map›Paper›PMID 40937292›Full record

ArticleRheumatology advances in practice2025

Genetically proxied tumour necrosis factor inhibition and pregnancy-related maternal and foetal outcomes in the general population: a Mendelian randomization study.

Sizheng Steven Zhao, Benjamin Woolf, Tormod Rogne, Dipender Gill

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Article in Rheumatology advances in practice, 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sizheng Steven ZhaoCentre for Musculoskeletal Research, Division of Musculoskeletal and Dermatological Sciences, School of Biological Sciences, Faculty of Biology Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.ORCID https://orcid.org/0000-0002-3558-7353
Benjamin WoolfSchool of Psychological Science and MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-1505-2570
Tormod RogneDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, USA.
Dipender GillDepartment of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Evidence on the safety of TNF inhibitors (TNFi) for pregnancy-related maternal and foetal outcomes remains limited. While some studies report increased rates of preterm delivery, others have suggested a possible protective role for gestational diabetes. We used population-level data to examine the effect of genetically proxied TNFi on these outcomes. Methods: We proxied TNFi using rs1800693, a splicing variant within the Results: We found no strong association between genetically proxied TNFi and any adverse pregnancy-related outcome, including spontaneous abortion (odds ratio [OR] 1.07, 95% CI: 0.41, 2.81), preterm birth (OR 0.48, 95% CI 0.14, 1.60), hyperemesis gravidarum (OR 0.20, 95% CI 0.02, 2.57), pre-eclampsia or eclampsia (OR 0.59, 95% CI 0.13, 2.65). Genetically proxied TNFi was associated with lower risk of gestational diabetes (OR 0.16, 95% CI 0.05, 0.52). There was no statistical evidence to suggest genetic confounding through linkage disequilibrium. Conclusion: This genetic investigation found no evidence linking TNFi to adverse pregnancy-related outcomes. The suggestive association with a reduced risk of gestational diabetes warrants further research and may support its consideration for at-risk pregnant women.

Indexed as

birthweighteclampsiaectopic pregnancygestational diabeteshyperemesis gravidarumpreterm birthspontaneous abortionTNF inhibitor

Identifiers

PMID40937292
PMCPMC12422557

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