Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers

Lynch syndrome is mostly characterized by early-onset colorectal and endometrial adenocarcinomas. Over 90% of the causal mutations occur in two mismatch repair genes, MSH2 and MLH1. The aim of this study was to evaluate the age-dependent cancer risk in MSH2 or MLH1 mutation carriers from data of DNA...

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Main Authors: Sylviane Olschwang, Kai Yu, Christine Lasset, Stéphanie Baert-Desurmont, Marie-Pierre Buisine, Qing Wang, Pierre Hutter, Etienne Rouleau, Olivier Caron, Violaine Bourdon, Gilles Thomas
Format: Article
Language:English
Published: Hindawi Limited 2009-01-01
Series:Journal of Cancer Epidemiology
Online Access:http://dx.doi.org/10.1155/2009/791754
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spelling doaj-5e0f1bef701642f89e129fe61fa8440e2020-11-25T00:08:59ZengHindawi LimitedJournal of Cancer Epidemiology1687-85581687-85662009-01-01200910.1155/2009/791754791754Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation CarriersSylviane Olschwang0Kai Yu1Christine Lasset2Stéphanie Baert-Desurmont3Marie-Pierre Buisine4Qing Wang5Pierre Hutter6Etienne Rouleau7Olivier Caron8Violaine Bourdon9Gilles Thomas10Institut National de la Santé et de la Recherche Médicale (INSERM), Unité 891, Centre de Recherches en Cancérologie de Marseille, 13009 Marseille, FranceDivision of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH), Gaithersburg, MD 20877, USAOncogenetics Department, Centre Léon Bérard, 69003 Lyon, FranceMedical Genetics Department, Hôpital Charles-Nicolle, 76000 Rouen, FranceMolecular Biology Laboratory, Hôpital Claude Huriez, 59000 Lille, FranceOncogenetics Department, Centre Léon Bérard, 69003 Lyon, FranceInstitut Central des Hépitaux Valaisans, 1951 Sion, SwitzerlandOncogenetics Department, Centre René Huguenin, 92210 Saint-Cloud, FranceGenetics Department, Hospices Civils, 67000 Strasbourg, FranceDepartment of Oncogenetics, Institut Paoli-Calmettes, 13009 Marseille, FranceFondation Synergie Lyon Cancer, 69008 Lyon, FranceLynch syndrome is mostly characterized by early-onset colorectal and endometrial adenocarcinomas. Over 90% of the causal mutations occur in two mismatch repair genes, MSH2 and MLH1. The aim of this study was to evaluate the age-dependent cancer risk in MSH2 or MLH1 mutation carriers from data of DNA diagnostic laboratories. To avoid overestimation, evaluation was based on the age-dependent proportion of mutation carriers in asymptomatic first-degree relatives of identified mutation carriers. Data from 859 such eligible relatives were collected from 8 centers; 387 were found to have inherited the mutation from their relatives. Age-dependent risks were calculated either using a nonparametric approach for four discrete age groups or assuming a modified Weibull distribution for the dependence of risk on age. Cancer risk was estimated starting at 28 (25–32 0.68 confidence interval) and to reach near 0.70 at 70 years. The risks were very similar for MSH2 and MLH1 mutation carriers. Although not statistically significant, the risk in males appeared to precede that for females by ten years. This difference needs to be investigated on a larger dataset. If confirmed, this would indicate that the onset of the colonoscopic surveillance may be different in male and female mutation carriers.http://dx.doi.org/10.1155/2009/791754
collection DOAJ
language English
format Article
sources DOAJ
author Sylviane Olschwang
Kai Yu
Christine Lasset
Stéphanie Baert-Desurmont
Marie-Pierre Buisine
Qing Wang
Pierre Hutter
Etienne Rouleau
Olivier Caron
Violaine Bourdon
Gilles Thomas
spellingShingle Sylviane Olschwang
Kai Yu
Christine Lasset
Stéphanie Baert-Desurmont
Marie-Pierre Buisine
Qing Wang
Pierre Hutter
Etienne Rouleau
Olivier Caron
Violaine Bourdon
Gilles Thomas
Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers
Journal of Cancer Epidemiology
author_facet Sylviane Olschwang
Kai Yu
Christine Lasset
Stéphanie Baert-Desurmont
Marie-Pierre Buisine
Qing Wang
Pierre Hutter
Etienne Rouleau
Olivier Caron
Violaine Bourdon
Gilles Thomas
author_sort Sylviane Olschwang
title Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers
title_short Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers
title_full Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers
title_fullStr Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers
title_full_unstemmed Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers
title_sort age-dependent cancer risk is not different in between msh2 and mlh1 mutation carriers
publisher Hindawi Limited
series Journal of Cancer Epidemiology
issn 1687-8558
1687-8566
publishDate 2009-01-01
description Lynch syndrome is mostly characterized by early-onset colorectal and endometrial adenocarcinomas. Over 90% of the causal mutations occur in two mismatch repair genes, MSH2 and MLH1. The aim of this study was to evaluate the age-dependent cancer risk in MSH2 or MLH1 mutation carriers from data of DNA diagnostic laboratories. To avoid overestimation, evaluation was based on the age-dependent proportion of mutation carriers in asymptomatic first-degree relatives of identified mutation carriers. Data from 859 such eligible relatives were collected from 8 centers; 387 were found to have inherited the mutation from their relatives. Age-dependent risks were calculated either using a nonparametric approach for four discrete age groups or assuming a modified Weibull distribution for the dependence of risk on age. Cancer risk was estimated starting at 28 (25–32 0.68 confidence interval) and to reach near 0.70 at 70 years. The risks were very similar for MSH2 and MLH1 mutation carriers. Although not statistically significant, the risk in males appeared to precede that for females by ten years. This difference needs to be investigated on a larger dataset. If confirmed, this would indicate that the onset of the colonoscopic surveillance may be different in male and female mutation carriers.
url http://dx.doi.org/10.1155/2009/791754
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