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Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study
AIMS/HYPOTHESIS: Observational studies have found an increased risk of latent autoimmune diabetes in adults (LADA) associated with low birthweight and adult overweight/obese status. We aimed to investigate whether these associations are causal, using a two-sample Mendelian randomisation (MR) design....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345833/ https://www.ncbi.nlm.nih.gov/pubmed/35606578 http://dx.doi.org/10.1007/s00125-022-05725-2 |
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author | Wei, Yuxia Zhan, Yiqiang Löfvenborg, Josefin E. Tuomi, Tiinamaija Carlsson, Sofia |
author_facet | Wei, Yuxia Zhan, Yiqiang Löfvenborg, Josefin E. Tuomi, Tiinamaija Carlsson, Sofia |
author_sort | Wei, Yuxia |
collection | PubMed |
description | AIMS/HYPOTHESIS: Observational studies have found an increased risk of latent autoimmune diabetes in adults (LADA) associated with low birthweight and adult overweight/obese status. We aimed to investigate whether these associations are causal, using a two-sample Mendelian randomisation (MR) design. In addition, we compared results for LADA and type 2 diabetes. METHODS: We identified 43 SNPs acting through the fetal genome as instrumental variables (IVs) for own birthweight from a genome-wide association study (GWAS) of the Early Growth Genetics Consortium (EGG) and the UK Biobank. We identified 820 SNPs as IVs for adult BMI from a GWAS of the UK Biobank and the Genetic Investigation of ANthropometric Traits consortium (GIANT). Summary statistics for the associations between IVs and LADA were extracted from the only GWAS involving 2634 cases and 5947 population controls. We used the inverse-variance weighted (IVW) estimator as our primary analysis, supplemented by a series of sensitivity analyses. RESULTS: Genetically determined own birthweight was inversely associated with LADA (OR per SD [~500 g] decrease in birthweight 1.68 [95% CI 1.01, 2.82]). In contrast, genetically predicted BMI in adulthood was positively associated with LADA (OR per SD [~4.8 kg/m(2)] increase in BMI 1.40 [95% CI 1.14, 1.71]). Robust results were obtained in a range of sensitivity analyses using other MR estimators or excluding some IVs. With respect to type 2 diabetes, the association with birthweight was not stronger than in LADA while the association with adult BMI was stronger than in LADA. CONCLUSIONS/ INTERPRETATION: This study provides genetic support for a causal link between low birthweight, adult overweight/obese status and LADA. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00125-022-05725-2) contains peer-reviewed but unedited supplementary material. |
format | Online Article Text |
id | pubmed-9345833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93458332022-08-04 Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study Wei, Yuxia Zhan, Yiqiang Löfvenborg, Josefin E. Tuomi, Tiinamaija Carlsson, Sofia Diabetologia Article AIMS/HYPOTHESIS: Observational studies have found an increased risk of latent autoimmune diabetes in adults (LADA) associated with low birthweight and adult overweight/obese status. We aimed to investigate whether these associations are causal, using a two-sample Mendelian randomisation (MR) design. In addition, we compared results for LADA and type 2 diabetes. METHODS: We identified 43 SNPs acting through the fetal genome as instrumental variables (IVs) for own birthweight from a genome-wide association study (GWAS) of the Early Growth Genetics Consortium (EGG) and the UK Biobank. We identified 820 SNPs as IVs for adult BMI from a GWAS of the UK Biobank and the Genetic Investigation of ANthropometric Traits consortium (GIANT). Summary statistics for the associations between IVs and LADA were extracted from the only GWAS involving 2634 cases and 5947 population controls. We used the inverse-variance weighted (IVW) estimator as our primary analysis, supplemented by a series of sensitivity analyses. RESULTS: Genetically determined own birthweight was inversely associated with LADA (OR per SD [~500 g] decrease in birthweight 1.68 [95% CI 1.01, 2.82]). In contrast, genetically predicted BMI in adulthood was positively associated with LADA (OR per SD [~4.8 kg/m(2)] increase in BMI 1.40 [95% CI 1.14, 1.71]). Robust results were obtained in a range of sensitivity analyses using other MR estimators or excluding some IVs. With respect to type 2 diabetes, the association with birthweight was not stronger than in LADA while the association with adult BMI was stronger than in LADA. CONCLUSIONS/ INTERPRETATION: This study provides genetic support for a causal link between low birthweight, adult overweight/obese status and LADA. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00125-022-05725-2) contains peer-reviewed but unedited supplementary material. Springer Berlin Heidelberg 2022-05-23 2022 /pmc/articles/PMC9345833/ /pubmed/35606578 http://dx.doi.org/10.1007/s00125-022-05725-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wei, Yuxia Zhan, Yiqiang Löfvenborg, Josefin E. Tuomi, Tiinamaija Carlsson, Sofia Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study |
title | Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study |
title_full | Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study |
title_fullStr | Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study |
title_full_unstemmed | Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study |
title_short | Birthweight, BMI in adulthood and latent autoimmune diabetes in adults: a Mendelian randomisation study |
title_sort | birthweight, bmi in adulthood and latent autoimmune diabetes in adults: a mendelian randomisation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345833/ https://www.ncbi.nlm.nih.gov/pubmed/35606578 http://dx.doi.org/10.1007/s00125-022-05725-2 |
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