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A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach
This study examines the instrument selection strategies currently employed throughout the type-2 diabetes and HbA(1c) MR literature. We then argue for a more integrated and thorough approach, providing a framework to do this in the context of HbA(1c) and diabetes. We conducted a literature search fo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614590/ https://www.ncbi.nlm.nih.gov/pubmed/36669000 http://dx.doi.org/10.2337/db22-0110 |
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author | Garfield, Victoria Salzmann, Antoine Burgess, Stephen Chaturvedi, Nish |
author_facet | Garfield, Victoria Salzmann, Antoine Burgess, Stephen Chaturvedi, Nish |
author_sort | Garfield, Victoria |
collection | PubMed |
description | This study examines the instrument selection strategies currently employed throughout the type-2 diabetes and HbA(1c) MR literature. We then argue for a more integrated and thorough approach, providing a framework to do this in the context of HbA(1c) and diabetes. We conducted a literature search for Mendelian randomisation studies that have instrumented diabetes and/or HbA(1c). We also used data from the UK Biobank (N=349,326) to calculate instrument strength metrics that are key in MR studies (the F-statistic for average strength and R(2) for total strength) with two different methods (‘Individual-level data regression’ and Cragg-Donald formula). We used a 157-SNP instrument for diabetes and a 51-SNP instrument (as well as partitioned into glycaemic and erythrocytic) for HbA(1c). Our literature search yielded 48 studies for diabetes and 22 for HbA1c. Our UKB empirical examples showed that irrespective of, the method used to calculate metrics of strength and whether the instrument was the main one or was partitioned by function, the HbA1c genetic instrument is strong in terms of both average and total strength. For diabetes, a 157-SNP instrument was shown to have good average and total strength, but these were both substantially smaller than those of the HbA(1c) instrument. We provide a careful set of five recommendations to researchers who wish to genetically instrument type-2 diabetes and/or HbA(1c). MR studies of glycaemia should take a more integrated approach when selecting genetic instruments and we give specific guidance on how to do this. |
format | Online Article Text |
id | pubmed-7614590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76145902023-05-30 A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach Garfield, Victoria Salzmann, Antoine Burgess, Stephen Chaturvedi, Nish Diabetes Article This study examines the instrument selection strategies currently employed throughout the type-2 diabetes and HbA(1c) MR literature. We then argue for a more integrated and thorough approach, providing a framework to do this in the context of HbA(1c) and diabetes. We conducted a literature search for Mendelian randomisation studies that have instrumented diabetes and/or HbA(1c). We also used data from the UK Biobank (N=349,326) to calculate instrument strength metrics that are key in MR studies (the F-statistic for average strength and R(2) for total strength) with two different methods (‘Individual-level data regression’ and Cragg-Donald formula). We used a 157-SNP instrument for diabetes and a 51-SNP instrument (as well as partitioned into glycaemic and erythrocytic) for HbA(1c). Our literature search yielded 48 studies for diabetes and 22 for HbA1c. Our UKB empirical examples showed that irrespective of, the method used to calculate metrics of strength and whether the instrument was the main one or was partitioned by function, the HbA1c genetic instrument is strong in terms of both average and total strength. For diabetes, a 157-SNP instrument was shown to have good average and total strength, but these were both substantially smaller than those of the HbA(1c) instrument. We provide a careful set of five recommendations to researchers who wish to genetically instrument type-2 diabetes and/or HbA(1c). MR studies of glycaemia should take a more integrated approach when selecting genetic instruments and we give specific guidance on how to do this. 2023-02-01 /pmc/articles/PMC7614590/ /pubmed/36669000 http://dx.doi.org/10.2337/db22-0110 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license. |
spellingShingle | Article Garfield, Victoria Salzmann, Antoine Burgess, Stephen Chaturvedi, Nish A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach |
title | A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach |
title_full | A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach |
title_fullStr | A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach |
title_full_unstemmed | A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach |
title_short | A Guide for Selection of Genetic Instruments in Mendelian randomisation (MR) studies of Type-2 diabetes and HbA(1c): towards an integrated approach |
title_sort | guide for selection of genetic instruments in mendelian randomisation (mr) studies of type-2 diabetes and hba(1c): towards an integrated approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614590/ https://www.ncbi.nlm.nih.gov/pubmed/36669000 http://dx.doi.org/10.2337/db22-0110 |
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