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A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S.
INTRODUCTION: Polygenic Risk Scores (PRSs) are summaries of genetic risk alleles for an outcome. METHODS: We used summary statistics from five GWASs of AD to construct PRSs in 4,189 diverse Hispanics/Latinos (mean age 63 years) from the Study of Latinos-Investigation of Neurocognitive Aging (SOL-INC...
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/PMC10469805/ https://www.ncbi.nlm.nih.gov/pubmed/37649099 http://dx.doi.org/10.1186/s13195-023-01298-3 |
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author | Sofer, Tamar Kurniansyah, Nuzulul Granot-Hershkovitz, Einat Goodman, Matthew O. Tarraf, Wassim Broce, Iris Lipton, Richard B. Daviglus, Martha Lamar, Melissa Wassertheil-Smoller, Sylvia Cai, Jianwen DeCarli, Charles S. Gonzalez, Hector M. Fornage, Myriam |
author_facet | Sofer, Tamar Kurniansyah, Nuzulul Granot-Hershkovitz, Einat Goodman, Matthew O. Tarraf, Wassim Broce, Iris Lipton, Richard B. Daviglus, Martha Lamar, Melissa Wassertheil-Smoller, Sylvia Cai, Jianwen DeCarli, Charles S. Gonzalez, Hector M. Fornage, Myriam |
author_sort | Sofer, Tamar |
collection | PubMed |
description | INTRODUCTION: Polygenic Risk Scores (PRSs) are summaries of genetic risk alleles for an outcome. METHODS: We used summary statistics from five GWASs of AD to construct PRSs in 4,189 diverse Hispanics/Latinos (mean age 63 years) from the Study of Latinos-Investigation of Neurocognitive Aging (SOL-INCA). We assessed the PRS associations with MCI in the combined set of people and in diverse subgroups, and when including and excluding the APOE gene region. We also assessed PRS associations with MCI in an independent dataset from the Mass General Brigham Biobank. RESULTS: A simple sum of 5 PRSs (“PRSsum”), each constructed based on a different AD GWAS, was associated with MCI (OR = 1.28, 95% CI [1.14, 1.41]) in a model adjusted for counts of the APOE-[Formula: see text] and APOE-[Formula: see text] alleles. Associations of single-GWAS PRSs were weaker. When removing SNPs from the APOE region from the PRSs, the association of PRSsum with MCI was weaker (OR = 1.17, 95% CI [1.04,1.31] with adjustment for APOE alleles). In all association analyses, APOE-[Formula: see text] and APOE-[Formula: see text] alleles were not associated with MCI. DISCUSSION: A sum of AD PRSs is associated with MCI in Hispanic/Latino older adults. Despite no association of APOE-[Formula: see text] and APOE-[Formula: see text] alleles with MCI, the association of the AD PRS with MCI is stronger when including the APOE region. Thus, APOE variants different than the classic APOE alleles may be important predictors of MCI in Hispanic/Latino adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-023-01298-3. |
format | Online Article Text |
id | pubmed-10469805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104698052023-09-01 A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. Sofer, Tamar Kurniansyah, Nuzulul Granot-Hershkovitz, Einat Goodman, Matthew O. Tarraf, Wassim Broce, Iris Lipton, Richard B. Daviglus, Martha Lamar, Melissa Wassertheil-Smoller, Sylvia Cai, Jianwen DeCarli, Charles S. Gonzalez, Hector M. Fornage, Myriam Alzheimers Res Ther Research INTRODUCTION: Polygenic Risk Scores (PRSs) are summaries of genetic risk alleles for an outcome. METHODS: We used summary statistics from five GWASs of AD to construct PRSs in 4,189 diverse Hispanics/Latinos (mean age 63 years) from the Study of Latinos-Investigation of Neurocognitive Aging (SOL-INCA). We assessed the PRS associations with MCI in the combined set of people and in diverse subgroups, and when including and excluding the APOE gene region. We also assessed PRS associations with MCI in an independent dataset from the Mass General Brigham Biobank. RESULTS: A simple sum of 5 PRSs (“PRSsum”), each constructed based on a different AD GWAS, was associated with MCI (OR = 1.28, 95% CI [1.14, 1.41]) in a model adjusted for counts of the APOE-[Formula: see text] and APOE-[Formula: see text] alleles. Associations of single-GWAS PRSs were weaker. When removing SNPs from the APOE region from the PRSs, the association of PRSsum with MCI was weaker (OR = 1.17, 95% CI [1.04,1.31] with adjustment for APOE alleles). In all association analyses, APOE-[Formula: see text] and APOE-[Formula: see text] alleles were not associated with MCI. DISCUSSION: A sum of AD PRSs is associated with MCI in Hispanic/Latino older adults. Despite no association of APOE-[Formula: see text] and APOE-[Formula: see text] alleles with MCI, the association of the AD PRS with MCI is stronger when including the APOE region. Thus, APOE variants different than the classic APOE alleles may be important predictors of MCI in Hispanic/Latino adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-023-01298-3. BioMed Central 2023-08-30 /pmc/articles/PMC10469805/ /pubmed/37649099 http://dx.doi.org/10.1186/s13195-023-01298-3 Text en © The Author(s) 2023 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/) . 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 Sofer, Tamar Kurniansyah, Nuzulul Granot-Hershkovitz, Einat Goodman, Matthew O. Tarraf, Wassim Broce, Iris Lipton, Richard B. Daviglus, Martha Lamar, Melissa Wassertheil-Smoller, Sylvia Cai, Jianwen DeCarli, Charles S. Gonzalez, Hector M. Fornage, Myriam A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. |
title | A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. |
title_full | A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. |
title_fullStr | A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. |
title_full_unstemmed | A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. |
title_short | A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. |
title_sort | polygenic risk score for alzheimer’s disease constructed using apoe-region variants has stronger association than apoe alleles with mild cognitive impairment in hispanic/latino adults in the u.s. |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469805/ https://www.ncbi.nlm.nih.gov/pubmed/37649099 http://dx.doi.org/10.1186/s13195-023-01298-3 |
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