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Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease
The incidence of Alzheimer’s Disease in females is almost double that of males. To search for sex-specific gene associations, we build a machine learning approach focused on functionally impactful coding variants. This method can detect differences between sequenced cases and controls in small cohor...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183026/ https://www.ncbi.nlm.nih.gov/pubmed/37179358 http://dx.doi.org/10.1038/s41467-023-38374-z |
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author | Bourquard, Thomas Lee, Kwanghyuk Al-Ramahi, Ismael Pham, Minh Shapiro, Dillon Lagisetty, Yashwanth Soleimani, Shirin Mota, Samantha Wilhelm, Kevin Samieinasab, Maryam Kim, Young Won Huh, Eunna Asmussen, Jennifer Katsonis, Panagiotis Botas, Juan Lichtarge, Olivier |
author_facet | Bourquard, Thomas Lee, Kwanghyuk Al-Ramahi, Ismael Pham, Minh Shapiro, Dillon Lagisetty, Yashwanth Soleimani, Shirin Mota, Samantha Wilhelm, Kevin Samieinasab, Maryam Kim, Young Won Huh, Eunna Asmussen, Jennifer Katsonis, Panagiotis Botas, Juan Lichtarge, Olivier |
author_sort | Bourquard, Thomas |
collection | PubMed |
description | The incidence of Alzheimer’s Disease in females is almost double that of males. To search for sex-specific gene associations, we build a machine learning approach focused on functionally impactful coding variants. This method can detect differences between sequenced cases and controls in small cohorts. In the Alzheimer’s Disease Sequencing Project with mixed sexes, this approach identified genes enriched for immune response pathways. After sex-separation, genes become specifically enriched for stress-response pathways in male and cell-cycle pathways in female. These genes improve disease risk prediction in silico and modulate Drosophila neurodegeneration in vivo. Thus, a general approach for machine learning on functionally impactful variants can uncover sex-specific candidates towards diagnostic biomarkers and therapeutic targets. |
format | Online Article Text |
id | pubmed-10183026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101830262023-05-15 Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease Bourquard, Thomas Lee, Kwanghyuk Al-Ramahi, Ismael Pham, Minh Shapiro, Dillon Lagisetty, Yashwanth Soleimani, Shirin Mota, Samantha Wilhelm, Kevin Samieinasab, Maryam Kim, Young Won Huh, Eunna Asmussen, Jennifer Katsonis, Panagiotis Botas, Juan Lichtarge, Olivier Nat Commun Article The incidence of Alzheimer’s Disease in females is almost double that of males. To search for sex-specific gene associations, we build a machine learning approach focused on functionally impactful coding variants. This method can detect differences between sequenced cases and controls in small cohorts. In the Alzheimer’s Disease Sequencing Project with mixed sexes, this approach identified genes enriched for immune response pathways. After sex-separation, genes become specifically enriched for stress-response pathways in male and cell-cycle pathways in female. These genes improve disease risk prediction in silico and modulate Drosophila neurodegeneration in vivo. Thus, a general approach for machine learning on functionally impactful variants can uncover sex-specific candidates towards diagnostic biomarkers and therapeutic targets. Nature Publishing Group UK 2023-05-13 /pmc/articles/PMC10183026/ /pubmed/37179358 http://dx.doi.org/10.1038/s41467-023-38374-z 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bourquard, Thomas Lee, Kwanghyuk Al-Ramahi, Ismael Pham, Minh Shapiro, Dillon Lagisetty, Yashwanth Soleimani, Shirin Mota, Samantha Wilhelm, Kevin Samieinasab, Maryam Kim, Young Won Huh, Eunna Asmussen, Jennifer Katsonis, Panagiotis Botas, Juan Lichtarge, Olivier Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease |
title | Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease |
title_full | Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease |
title_fullStr | Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease |
title_full_unstemmed | Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease |
title_short | Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease |
title_sort | functional variants identify sex-specific genes and pathways in alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183026/ https://www.ncbi.nlm.nih.gov/pubmed/37179358 http://dx.doi.org/10.1038/s41467-023-38374-z |
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