Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study

Detalhes bibliográficos
Autor(a) principal: Miguel, I
Data de Publicação: 2021
Outros Autores: Rodrigues, F, Fragoso, S, Freixo, J, Clara, A, Luís, A, Bento, S, Fernandes, M, Bacelar, F, Câmara, S, Parreira, J, Duarte, T, Rodrigues, P, Santos, S, Vaz, F
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/153739
Resumo: Access to genetic testing and counselling in remote areas such as the Madeira archipelago, in the Northern Atlantic Ocean, may be complex. Different counselling methods, including telegenetics, should be explored. In this study, we characterise the Hereditary Breast/Ovarian Cancer (HBOC) families with Madeira ancestry enrolled in our programme. Of a total of 3, 566 index patients tested between January 2000 and June 2018, 68 had Madeira ancestry and 22 were diagnosed with a pathogenic germline variant (PV). As in the whole group, BRCA2 PV were more frequent in Madeira patients (68.4%: c.9382C>T (26.3%), c.658_659del (21%), c.156_157insAlu (10.5%), c.793+1G>A (5.3%) and c.298A>T (5.3%). However, the most frequently diagnosed PV in Madeira patients was the BRCA1 c.3331_3334del (31.6%). BRCA1/2 detection rates were 27.9% and 10.5% for Madeira and the whole group, respectively. This study is the first characterisation of HBOC patients with Madeira ancestry. A distinct pattern of BRCA1/2 variants was observed, and the geographic clustering of BRCA1 c.3331_3334del variant may support the possibility of a founder mutation previously described in Northern Portugal. The high detection rate observed reinforces the need to reduce gaps in access to genetic testing in Madeira and other remote areas. According to current guidelines, timely identification of HBOC patients can contribute to their ongoing care and treatment.
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spelling Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study Founder effect; Genetic testing; Hereditary breast and ovarian cancer syndrome; Pathogenic variantAccess to genetic testing and counselling in remote areas such as the Madeira archipelago, in the Northern Atlantic Ocean, may be complex. Different counselling methods, including telegenetics, should be explored. In this study, we characterise the Hereditary Breast/Ovarian Cancer (HBOC) families with Madeira ancestry enrolled in our programme. Of a total of 3, 566 index patients tested between January 2000 and June 2018, 68 had Madeira ancestry and 22 were diagnosed with a pathogenic germline variant (PV). As in the whole group, BRCA2 PV were more frequent in Madeira patients (68.4%: c.9382C>T (26.3%), c.658_659del (21%), c.156_157insAlu (10.5%), c.793+1G>A (5.3%) and c.298A>T (5.3%). However, the most frequently diagnosed PV in Madeira patients was the BRCA1 c.3331_3334del (31.6%). BRCA1/2 detection rates were 27.9% and 10.5% for Madeira and the whole group, respectively. This study is the first characterisation of HBOC patients with Madeira ancestry. A distinct pattern of BRCA1/2 variants was observed, and the geographic clustering of BRCA1 c.3331_3334del variant may support the possibility of a founder mutation previously described in Northern Portugal. The high detection rate observed reinforces the need to reduce gaps in access to genetic testing in Madeira and other remote areas. According to current guidelines, timely identification of HBOC patients can contribute to their ongoing care and treatment.ecancer20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/153739eng1754-660510.3332/ECANCER.2021.1261Miguel, IRodrigues, FFragoso, SFreixo, JClara, ALuís, ABento, SFernandes, MBacelar, FCâmara, SParreira, JDuarte, TRodrigues, PSantos, SVaz, Finfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T13:05:56Zoai:repositorio-aberto.up.pt:10216/153739Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:33:27.920200Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
title Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
spellingShingle Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
Miguel, I
 Founder effect; Genetic testing; Hereditary breast and ovarian cancer syndrome; Pathogenic variant
title_short Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
title_full Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
title_fullStr Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
title_full_unstemmed Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
title_sort Hereditary breast cancer and ancestry in the Madeira archipelago: An exploratory study
author Miguel, I
author_facet Miguel, I
Rodrigues, F
Fragoso, S
Freixo, J
Clara, A
Luís, A
Bento, S
Fernandes, M
Bacelar, F
Câmara, S
Parreira, J
Duarte, T
Rodrigues, P
Santos, S
Vaz, F
author_role author
author2 Rodrigues, F
Fragoso, S
Freixo, J
Clara, A
Luís, A
Bento, S
Fernandes, M
Bacelar, F
Câmara, S
Parreira, J
Duarte, T
Rodrigues, P
Santos, S
Vaz, F
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Miguel, I
Rodrigues, F
Fragoso, S
Freixo, J
Clara, A
Luís, A
Bento, S
Fernandes, M
Bacelar, F
Câmara, S
Parreira, J
Duarte, T
Rodrigues, P
Santos, S
Vaz, F
dc.subject.por.fl_str_mv  Founder effect; Genetic testing; Hereditary breast and ovarian cancer syndrome; Pathogenic variant
topic  Founder effect; Genetic testing; Hereditary breast and ovarian cancer syndrome; Pathogenic variant
description Access to genetic testing and counselling in remote areas such as the Madeira archipelago, in the Northern Atlantic Ocean, may be complex. Different counselling methods, including telegenetics, should be explored. In this study, we characterise the Hereditary Breast/Ovarian Cancer (HBOC) families with Madeira ancestry enrolled in our programme. Of a total of 3, 566 index patients tested between January 2000 and June 2018, 68 had Madeira ancestry and 22 were diagnosed with a pathogenic germline variant (PV). As in the whole group, BRCA2 PV were more frequent in Madeira patients (68.4%: c.9382C>T (26.3%), c.658_659del (21%), c.156_157insAlu (10.5%), c.793+1G>A (5.3%) and c.298A>T (5.3%). However, the most frequently diagnosed PV in Madeira patients was the BRCA1 c.3331_3334del (31.6%). BRCA1/2 detection rates were 27.9% and 10.5% for Madeira and the whole group, respectively. This study is the first characterisation of HBOC patients with Madeira ancestry. A distinct pattern of BRCA1/2 variants was observed, and the geographic clustering of BRCA1 c.3331_3334del variant may support the possibility of a founder mutation previously described in Northern Portugal. The high detection rate observed reinforces the need to reduce gaps in access to genetic testing in Madeira and other remote areas. According to current guidelines, timely identification of HBOC patients can contribute to their ongoing care and treatment.
publishDate 2021
dc.date.none.fl_str_mv 2021
2021-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/153739
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1754-6605
10.3332/ECANCER.2021.1261
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dc.publisher.none.fl_str_mv ecancer
publisher.none.fl_str_mv ecancer
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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