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The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.

Diagnosis of hereditary non-polyposis colorectal cancer (HNPCC) is currently based on phenotypical analysis of an expanded pedigree. Diagnostic guidelines ('Amsterdam criteria') proposed by the International Collaborative Group on HNPCC are often too stringent for use with small families....

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Autores principales: Percesepe, A., Anti, M., Roncucci, L., Armelao, F., Marra, G., Pahor, M., Coco, C., Gasbarrini, G., Ponz de Leon, M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033924/
https://www.ncbi.nlm.nih.gov/pubmed/7577490
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author Percesepe, A.
Anti, M.
Roncucci, L.
Armelao, F.
Marra, G.
Pahor, M.
Coco, C.
Gasbarrini, G.
Ponz de Leon, M.
author_facet Percesepe, A.
Anti, M.
Roncucci, L.
Armelao, F.
Marra, G.
Pahor, M.
Coco, C.
Gasbarrini, G.
Ponz de Leon, M.
author_sort Percesepe, A.
collection PubMed
description Diagnosis of hereditary non-polyposis colorectal cancer (HNPCC) is currently based on phenotypical analysis of an expanded pedigree. Diagnostic guidelines ('Amsterdam criteria') proposed by the International Collaborative Group on HNPCC are often too stringent for use with small families. There is also the possibility of false-positive diagnosis in large pedigrees that may contain chance clusters of tumours. This study was conducted to determine the effect of family size on the probability of diagnosing HNPCC according to the Amsterdam criteria. A total of 1052 patients with colorectal cancer were classified as HNPCC or non-HNPCC according to the Amsterdam criteria. Associations between this diagnosis and the size of the first-degree pedigree were evaluated in logistic regression and linear discriminant analyses. Logistic regression showed a significant association for family size with the Amsterdam-criteria-based HNPCC diagnosis. Linear discriminant analysis showed that HNPCC diagnosis was most likely to occur when first-degree pedigrees contained more than seven relatives. Failure to consider family size in phenotypic diagnosis of HNPCC can lead to both under- and overestimation of the frequency of this disease. Small pedigrees must be expanded to reliably exclude HNPCC. Positive diagnoses based on assessment of eight or more first-degree relatives should be supported by other clinical features.
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spelling pubmed-20339242009-09-10 The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer. Percesepe, A. Anti, M. Roncucci, L. Armelao, F. Marra, G. Pahor, M. Coco, C. Gasbarrini, G. Ponz de Leon, M. Br J Cancer Research Article Diagnosis of hereditary non-polyposis colorectal cancer (HNPCC) is currently based on phenotypical analysis of an expanded pedigree. Diagnostic guidelines ('Amsterdam criteria') proposed by the International Collaborative Group on HNPCC are often too stringent for use with small families. There is also the possibility of false-positive diagnosis in large pedigrees that may contain chance clusters of tumours. This study was conducted to determine the effect of family size on the probability of diagnosing HNPCC according to the Amsterdam criteria. A total of 1052 patients with colorectal cancer were classified as HNPCC or non-HNPCC according to the Amsterdam criteria. Associations between this diagnosis and the size of the first-degree pedigree were evaluated in logistic regression and linear discriminant analyses. Logistic regression showed a significant association for family size with the Amsterdam-criteria-based HNPCC diagnosis. Linear discriminant analysis showed that HNPCC diagnosis was most likely to occur when first-degree pedigrees contained more than seven relatives. Failure to consider family size in phenotypic diagnosis of HNPCC can lead to both under- and overestimation of the frequency of this disease. Small pedigrees must be expanded to reliably exclude HNPCC. Positive diagnoses based on assessment of eight or more first-degree relatives should be supported by other clinical features. Nature Publishing Group 1995-11 /pmc/articles/PMC2033924/ /pubmed/7577490 Text en 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 Research Article
Percesepe, A.
Anti, M.
Roncucci, L.
Armelao, F.
Marra, G.
Pahor, M.
Coco, C.
Gasbarrini, G.
Ponz de Leon, M.
The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
title The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
title_full The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
title_fullStr The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
title_full_unstemmed The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
title_short The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
title_sort effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033924/
https://www.ncbi.nlm.nih.gov/pubmed/7577490
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