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Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients

BACKGROUND: Breast cancer patients from the indigenous Arab population present much earlier than patients from Western countries and have traditionally been underrepresented in cancer genomics studies. The contribution of polygenic and Mendelian risk toward the earlier onset of breast cancer in the...

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Autores principales: Al-Jumaan, Mohammed, Chu, Hoyin, Alsulaiman, Abdullah, Camp, Sabrina Y., Han, Seunghun, Gillani, Riaz, Al Marzooq, Yousef, Almulhim, Fatmah, Vatte, Chittibabu, Al Nemer, Areej, Almuhanna, Afnan, Van Allen, Eliezer M., Al-Ali, Amein, AlDubayan, Saud H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474689/
https://www.ncbi.nlm.nih.gov/pubmed/37658461
http://dx.doi.org/10.1186/s13073-023-01220-4
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author Al-Jumaan, Mohammed
Chu, Hoyin
Alsulaiman, Abdullah
Camp, Sabrina Y.
Han, Seunghun
Gillani, Riaz
Al Marzooq, Yousef
Almulhim, Fatmah
Vatte, Chittibabu
Al Nemer, Areej
Almuhanna, Afnan
Van Allen, Eliezer M.
Al-Ali, Amein
AlDubayan, Saud H.
author_facet Al-Jumaan, Mohammed
Chu, Hoyin
Alsulaiman, Abdullah
Camp, Sabrina Y.
Han, Seunghun
Gillani, Riaz
Al Marzooq, Yousef
Almulhim, Fatmah
Vatte, Chittibabu
Al Nemer, Areej
Almuhanna, Afnan
Van Allen, Eliezer M.
Al-Ali, Amein
AlDubayan, Saud H.
author_sort Al-Jumaan, Mohammed
collection PubMed
description BACKGROUND: Breast cancer patients from the indigenous Arab population present much earlier than patients from Western countries and have traditionally been underrepresented in cancer genomics studies. The contribution of polygenic and Mendelian risk toward the earlier onset of breast cancer in the population remains elusive. METHODS: We performed low-pass whole genome sequencing (lpWGS) and whole-exome sequencing (WES) from 220 female breast cancer patients unselected for positive family history from the indigenous Arab population. Using publicly available resources, we imputed population-specific variants and calculated breast cancer burden-sensitive polygenic risk scores (PRS). Variant pathogenicity was also evaluated on exome variants with high coverage. RESULTS: Variants imputed from lpWGS showed high concordance with paired exome (median dosage correlation: 0.9459, Interquartile range: 0.9410–0.9490). After adjusting the PRS to the Arab population, we found significant associations between PRS performance in risk prediction and first-degree relative breast cancer history prediction (Spearman rho=0.43, p = 0.03), where breast cancer patients in the top PRS decile are 5.53 (95% CI 1.76–17.97, p = 0.003) times more likely also to have a first-degree relative diagnosed with breast cancer compared to those in the middle deciles. In addition, we found evidence for the genetic liability threshold model of breast cancer where among patients with a family history of breast cancer, pathogenic rare variant carriers had significantly lower PRS than non-carriers (p = 0.0205, Mann-Whitney U test) while for non-carriers every standard deviation increase in PRS corresponded to 4.52 years (95% CI 8.88–0.17, p = 0.042) earlier age of presentation. CONCLUSIONS: Overall, our study provides a framework to assess polygenic risk in an understudied population using lpWGS and identifies common variant risk as a factor independent of pathogenic variant carrier status for earlier age of onset of breast cancer among indigenous Arab breast cancer patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-023-01220-4.
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spelling pubmed-104746892023-09-03 Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients Al-Jumaan, Mohammed Chu, Hoyin Alsulaiman, Abdullah Camp, Sabrina Y. Han, Seunghun Gillani, Riaz Al Marzooq, Yousef Almulhim, Fatmah Vatte, Chittibabu Al Nemer, Areej Almuhanna, Afnan Van Allen, Eliezer M. Al-Ali, Amein AlDubayan, Saud H. Genome Med Research BACKGROUND: Breast cancer patients from the indigenous Arab population present much earlier than patients from Western countries and have traditionally been underrepresented in cancer genomics studies. The contribution of polygenic and Mendelian risk toward the earlier onset of breast cancer in the population remains elusive. METHODS: We performed low-pass whole genome sequencing (lpWGS) and whole-exome sequencing (WES) from 220 female breast cancer patients unselected for positive family history from the indigenous Arab population. Using publicly available resources, we imputed population-specific variants and calculated breast cancer burden-sensitive polygenic risk scores (PRS). Variant pathogenicity was also evaluated on exome variants with high coverage. RESULTS: Variants imputed from lpWGS showed high concordance with paired exome (median dosage correlation: 0.9459, Interquartile range: 0.9410–0.9490). After adjusting the PRS to the Arab population, we found significant associations between PRS performance in risk prediction and first-degree relative breast cancer history prediction (Spearman rho=0.43, p = 0.03), where breast cancer patients in the top PRS decile are 5.53 (95% CI 1.76–17.97, p = 0.003) times more likely also to have a first-degree relative diagnosed with breast cancer compared to those in the middle deciles. In addition, we found evidence for the genetic liability threshold model of breast cancer where among patients with a family history of breast cancer, pathogenic rare variant carriers had significantly lower PRS than non-carriers (p = 0.0205, Mann-Whitney U test) while for non-carriers every standard deviation increase in PRS corresponded to 4.52 years (95% CI 8.88–0.17, p = 0.042) earlier age of presentation. CONCLUSIONS: Overall, our study provides a framework to assess polygenic risk in an understudied population using lpWGS and identifies common variant risk as a factor independent of pathogenic variant carrier status for earlier age of onset of breast cancer among indigenous Arab breast cancer patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-023-01220-4. BioMed Central 2023-09-01 /pmc/articles/PMC10474689/ /pubmed/37658461 http://dx.doi.org/10.1186/s13073-023-01220-4 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
Al-Jumaan, Mohammed
Chu, Hoyin
Alsulaiman, Abdullah
Camp, Sabrina Y.
Han, Seunghun
Gillani, Riaz
Al Marzooq, Yousef
Almulhim, Fatmah
Vatte, Chittibabu
Al Nemer, Areej
Almuhanna, Afnan
Van Allen, Eliezer M.
Al-Ali, Amein
AlDubayan, Saud H.
Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients
title Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients
title_full Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients
title_fullStr Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients
title_full_unstemmed Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients
title_short Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients
title_sort interplay of mendelian and polygenic risk factors in arab breast cancer patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474689/
https://www.ncbi.nlm.nih.gov/pubmed/37658461
http://dx.doi.org/10.1186/s13073-023-01220-4
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