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Familial risks in nervous system tumours: joint Nordic study
BACKGROUND: Familial nervous system cancers are rare and limited data on familial aspects are available particularly on site-specific tumours. METHODS: Data from five Nordic countries were used to analyse familial risks of nervous system tumours. Standardised incidence ratios (SIRs) were calculated...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883707/ https://www.ncbi.nlm.nih.gov/pubmed/20502456 http://dx.doi.org/10.1038/sj.bjc.6605708 |
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author | Hemminki, K Tretli, S Olsen, J H Tryggvadottir, L Pukkala, E Sundquist, J Granström, C |
author_facet | Hemminki, K Tretli, S Olsen, J H Tryggvadottir, L Pukkala, E Sundquist, J Granström, C |
author_sort | Hemminki, K |
collection | PubMed |
description | BACKGROUND: Familial nervous system cancers are rare and limited data on familial aspects are available particularly on site-specific tumours. METHODS: Data from five Nordic countries were used to analyse familial risks of nervous system tumours. Standardised incidence ratios (SIRs) were calculated for offspring of affected relatives compared with offspring of non-affected relatives. RESULTS: The total number of patients with nervous system tumour was 63 307, of whom 32 347 belonged to the offspring generation. Of 851 familial patients (2.6%) in the offspring generation, 42 (4.7%) belonged to the families of a parent and at least two siblings affected. The SIR of brain tumours was 1.7 in offspring of affected parents; it was 2.0 in siblings and 9.4 in families with a parent and sibling affected. For spinal tumours, the SIRs were much higher for offspring of early onset tumours, 14.0 for offspring of affected parents and 22.7 for siblings. The SIRs for peripheral nerve tumours were 16.3 in offspring of affected parents, 27.7 in siblings and 943.9 in multiplex families. CONCLUSION: The results of this population-based study on medically diagnosed tumours show site-, proband- and age-specific risks for familial tumours, with implications for clinical genetic counselling and identification of the underlying genes. |
format | Text |
id | pubmed-2883707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-28837072011-06-08 Familial risks in nervous system tumours: joint Nordic study Hemminki, K Tretli, S Olsen, J H Tryggvadottir, L Pukkala, E Sundquist, J Granström, C Br J Cancer Genetics and Genomics BACKGROUND: Familial nervous system cancers are rare and limited data on familial aspects are available particularly on site-specific tumours. METHODS: Data from five Nordic countries were used to analyse familial risks of nervous system tumours. Standardised incidence ratios (SIRs) were calculated for offspring of affected relatives compared with offspring of non-affected relatives. RESULTS: The total number of patients with nervous system tumour was 63 307, of whom 32 347 belonged to the offspring generation. Of 851 familial patients (2.6%) in the offspring generation, 42 (4.7%) belonged to the families of a parent and at least two siblings affected. The SIR of brain tumours was 1.7 in offspring of affected parents; it was 2.0 in siblings and 9.4 in families with a parent and sibling affected. For spinal tumours, the SIRs were much higher for offspring of early onset tumours, 14.0 for offspring of affected parents and 22.7 for siblings. The SIRs for peripheral nerve tumours were 16.3 in offspring of affected parents, 27.7 in siblings and 943.9 in multiplex families. CONCLUSION: The results of this population-based study on medically diagnosed tumours show site-, proband- and age-specific risks for familial tumours, with implications for clinical genetic counselling and identification of the underlying genes. Nature Publishing Group 2010-06-08 2010-05-25 /pmc/articles/PMC2883707/ /pubmed/20502456 http://dx.doi.org/10.1038/sj.bjc.6605708 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genetics and Genomics Hemminki, K Tretli, S Olsen, J H Tryggvadottir, L Pukkala, E Sundquist, J Granström, C Familial risks in nervous system tumours: joint Nordic study |
title | Familial risks in nervous system tumours: joint Nordic study |
title_full | Familial risks in nervous system tumours: joint Nordic study |
title_fullStr | Familial risks in nervous system tumours: joint Nordic study |
title_full_unstemmed | Familial risks in nervous system tumours: joint Nordic study |
title_short | Familial risks in nervous system tumours: joint Nordic study |
title_sort | familial risks in nervous system tumours: joint nordic study |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883707/ https://www.ncbi.nlm.nih.gov/pubmed/20502456 http://dx.doi.org/10.1038/sj.bjc.6605708 |
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