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Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish
Background: Autozygosity, the proportion of the genome that is homozygous by descent, has been associated with variation in multiple health-related traits impacting evolutionary fitness. Autozygosity (FROH) is typically measured from runs of homozygosity (ROHs) that arise when identical-by-descent (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029202/ https://www.ncbi.nlm.nih.gov/pubmed/36941539 http://dx.doi.org/10.1186/s12864-023-09208-5 |
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author | Lynch, Megan T. Maloney, Kristin A. Xu, Huichun Perry, James A. Center, Regeneron Genetics Shuldiner, Alan R. Mitchell, Braxton D. |
author_facet | Lynch, Megan T. Maloney, Kristin A. Xu, Huichun Perry, James A. Center, Regeneron Genetics Shuldiner, Alan R. Mitchell, Braxton D. |
author_sort | Lynch, Megan T. |
collection | PubMed |
description | Background: Autozygosity, the proportion of the genome that is homozygous by descent, has been associated with variation in multiple health-related traits impacting evolutionary fitness. Autozygosity (FROH) is typically measured from runs of homozygosity (ROHs) that arise when identical-by-descent (IBD) haplotypes are inherited from each parent. Population isolates with a small set of common founders have elevated autozygosity relative to outbred populations. Methods: In this study, we examined whether degree of autozygosity was associated with variation in 96 cardiometabolic traits among 7221 Old Order Amish individuals residing in Lancaster County, PA. We estimated the average length of an ROH segment to be 6350 KB, with each individual having on average 17.2 segments 1.5 KB or larger. Measurements of genome-wide and regional FROH were used as the primary predictors of trait variation in association analysis. Results: In genome-wide FROH analysis, we did not identify any associations that withstood Bonferroni-correction (p = 0.0005). However, on regional FROH analysis, we identified associations exceeding genome-wide thresholds for two traits: serum bilirubin levels, which were significantly associated with a region on chromosome 2 localized to a region surrounding UGT1A10 (p = 1 × 10− 43), and HbA1c levels, which were significantly associated with a region on chromosome 8 localized near CHRNB3 (p = 8 × 10− 10). Conclusions: These analyses highlight the potential value of autozygosity mapping in founder populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09208-5. |
format | Online Article Text |
id | pubmed-10029202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100292022023-03-22 Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish Lynch, Megan T. Maloney, Kristin A. Xu, Huichun Perry, James A. Center, Regeneron Genetics Shuldiner, Alan R. Mitchell, Braxton D. BMC Genomics Research Background: Autozygosity, the proportion of the genome that is homozygous by descent, has been associated with variation in multiple health-related traits impacting evolutionary fitness. Autozygosity (FROH) is typically measured from runs of homozygosity (ROHs) that arise when identical-by-descent (IBD) haplotypes are inherited from each parent. Population isolates with a small set of common founders have elevated autozygosity relative to outbred populations. Methods: In this study, we examined whether degree of autozygosity was associated with variation in 96 cardiometabolic traits among 7221 Old Order Amish individuals residing in Lancaster County, PA. We estimated the average length of an ROH segment to be 6350 KB, with each individual having on average 17.2 segments 1.5 KB or larger. Measurements of genome-wide and regional FROH were used as the primary predictors of trait variation in association analysis. Results: In genome-wide FROH analysis, we did not identify any associations that withstood Bonferroni-correction (p = 0.0005). However, on regional FROH analysis, we identified associations exceeding genome-wide thresholds for two traits: serum bilirubin levels, which were significantly associated with a region on chromosome 2 localized to a region surrounding UGT1A10 (p = 1 × 10− 43), and HbA1c levels, which were significantly associated with a region on chromosome 8 localized near CHRNB3 (p = 8 × 10− 10). Conclusions: These analyses highlight the potential value of autozygosity mapping in founder populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09208-5. BioMed Central 2023-03-20 /pmc/articles/PMC10029202/ /pubmed/36941539 http://dx.doi.org/10.1186/s12864-023-09208-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lynch, Megan T. Maloney, Kristin A. Xu, Huichun Perry, James A. Center, Regeneron Genetics Shuldiner, Alan R. Mitchell, Braxton D. Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish |
title | Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish |
title_full | Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish |
title_fullStr | Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish |
title_full_unstemmed | Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish |
title_short | Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish |
title_sort | associations of genome-wide and regional autozygosity with 96 complex traits in old order amish |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029202/ https://www.ncbi.nlm.nih.gov/pubmed/36941539 http://dx.doi.org/10.1186/s12864-023-09208-5 |
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