Literature DB >> 30824524

The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect.

Sanne W Ten Broeke1, Mar Rodríguez-Girondo2, Manon Suerink3, Stefan Aretz4,5, Inge Bernstein6,7, Gabriel Capellá8, Christoph Engel9, Encarna B Gomez-Garcia10, Liselot P van Hest11, Magnus von Knebel Doeberitz12,13, Kristina Lagerstedt-Robinson14, Tom G W Letteboer15, Pal Moller16,17,18, Theo A van Os19, Marta Pineda8, Nils Rahner20, Maran J W Olderode-Berends21, Jenny von Salomé14, Hans K Schackert22, Liesbeth Spruijt23, Verena Steinke-Lange24, Anja Wagner25, Carli M J Tops3, Maartje Nielsen3.   

Abstract

BACKGROUND: PMS2-associated Lynch syndrome is characterized by a relatively low colorectal cancer penetrance compared with other Lynch syndromes. However, age at colorectal cancer diagnosis varies widely, and a strong genetic anticipation effect has been suggested for PMS2 families. In this study, we examined proposed genetic anticipation in a sample of 152 European PMS2 families.
METHODS: The 152 families (637 family members) that were eligible for analysis were mainly clinically ascertained via clinical genetics centers. We used weighted Cox-type random effects model, adjusted by birth cohort and sex, to estimate the generational effect on the age of onset of colorectal cancer. Probands and young birth cohorts were excluded from the analyses. Weights represented mutation probabilities based on kinship coefficients, thus avoiding testing bias.
RESULTS: Family data across three generations, including 123 colorectal cancers, were analyzed. When compared with the first generation, the crude HR for anticipation was 2.242 [95% confidence interval (CI), 1.162-4.328] for the second generation and 2.644 (95% CI, 1.082-6.464) for the third generation. However, after correction for birth cohort and sex, the effect vanished [HR = 1.302 (95% CI, 0.648-2.619) and HR = 1.074 (95% CI, 0.406-2.842) for second and third generations, respectively].
CONCLUSIONS: Our study did not confirm previous reports of genetic anticipation in PMS2-associated Lynch syndrome. Birth-cohort effect seems the most likely explanation for observed younger colorectal cancer diagnosis in subsequent generations, particularly because there is currently no commonly accepted biological mechanism that could explain genetic anticipation in Lynch syndrome. IMPACT: This new model for studying genetic anticipation provides a standard for rigorous analysis of families with dominantly inherited cancer predisposition. ©2019 American Association for Cancer Research.

Entities:  

Year:  2019        PMID: 30824524     DOI: 10.1158/1055-9965.EPI-18-0576

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.254


  2 in total

1.  Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.

Authors:  Pål Møller; Toni Seppälä; James G Dowty; Saskia Haupt; Mev Dominguez-Valentin; Lone Sunde; Inge Bernstein; Christoph Engel; Stefan Aretz; Maartje Nielsen; Gabriel Capella; Dafydd Gareth Evans; John Burn; Elke Holinski-Feder; Lucio Bertario; Bernardo Bonanni; Annika Lindblom; Zohar Levi; Finlay Macrae; Ingrid Winship; John-Paul Plazzer; Rolf Sijmons; Luigi Laghi; Adriana Della Valle; Karl Heinimann; Elizabeth Half; Francisco Lopez-Koestner; Karin Alvarez-Valenzuela; Rodney J Scott; Lior Katz; Ido Laish; Elez Vainer; Carlos Alberto Vaccaro; Dirce Maria Carraro; Nathan Gluck; Naim Abu-Freha; Aine Stakelum; Rory Kennelly; Des Winter; Benedito Mauro Rossi; Marc Greenblatt; Mabel Bohorquez; Harsh Sheth; Maria Grazia Tibiletti; Leonardo S Lino-Silva; Karoline Horisberger; Carmen Portenkirchner; Ivana Nascimento; Norma Teresa Rossi; Leandro Apolinário da Silva; Huw Thomas; Attila Zaránd; Jukka-Pekka Mecklin; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; Anna Lepisto; Päivi Peltomäki; Christina Therkildsen; Lars Joachim Lindberg; Ole Thorlacius-Ussing; Magnus von Knebel Doeberitz; Markus Loeffler; Nils Rahner; Verena Steinke-Lange; Wolff Schmiegel; Deepak Vangala; Claudia Perne; Robert Hüneburg; Aída Falcón de Vargas; Andrew Latchford; Anne-Marie Gerdes; Ann-Sofie Backman; Carmen Guillén-Ponce; Carrie Snyder; Charlotte K Lautrup; David Amor; Edenir Palmero; Elena Stoffel; Floor Duijkers; Michael J Hall; Heather Hampel; Heinric Williams; Henrik Okkels; Jan Lubiński; Jeanette Reece; Joanne Ngeow; Jose G Guillem; Julie Arnold; Karin Wadt; Kevin Monahan; Leigha Senter; Lene J Rasmussen; Liselotte P van Hest; Luigi Ricciardiello; Maija R J Kohonen-Corish; Marjolijn J L Ligtenberg; Melissa Southey; Melyssa Aronson; Mohd N Zahary; N Jewel Samadder; Nicola Poplawski; Nicoline Hoogerbrugge; Patrick J Morrison; Paul James; Grant Lee; Rakefet Chen-Shtoyerman; Ravindran Ankathil; Rish Pai; Robyn Ward; Susan Parry; Tadeusz Dębniak; Thomas John; Thomas van Overeem Hansen; Trinidad Caldés; Tatsuro Yamaguchi; Verónica Barca-Tierno; Pilar Garre; Giulia Martina Cavestro; Jürgen Weitz; Silke Redler; Reinhard Büttner; Vincent Heuveline; John L Hopper; Aung Ko Win; Noralane Lindor; Steven Gallinger; Loïc Le Marchand; Polly A Newcomb; Jane Figueiredo; Daniel D Buchanan; Stephen N Thibodeau; Sanne W Ten Broeke; Eivind Hovig; Sigve Nakken; Marta Pineda; Nuria Dueñas; Joan Brunet; Kate Green; Fiona Lalloo; Katie Newton; Emma J Crosbie; Miriam Mints; Douglas Tjandra; Florencia Neffa; Patricia Esperon; Revital Kariv; Guy Rosner; Walter Hernán Pavicic; Pablo Kalfayan; Giovana Tardin Torrezan; Thiago Bassaneze; Claudia Martin; Gabriela Moslein; Aysel Ahadova; Matthias Kloor; Julian R Sampson; Mark A Jenkins
Journal:  Hered Cancer Clin Pract       Date:  2022-10-01       Impact factor: 2.164

2.  Telomere Instability in Lynch Syndrome Families Leads to Some Shorter Telomeres in MSH2+/- Carriers.

Authors:  M Carmen Garrido-Navas; Frances Tippins; Julian Barwell; Jonathan Hoffman; Veryan Codd; Nicola J Royle
Journal:  Life (Basel)       Date:  2020-10-31
  2 in total

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