Accès ouvert déclaré
2022
article
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes
Catherine Schramm, Camille Charbonnier, Aline Zaréa, Morgane Lacour, David Wallon, Daniela Andriuta, Pierre Anthony, Sophie Auriacombe, Anna‐Chloé Balageas, Guillaume Ballan, Mélanie Barbay, É. Beaufils, Yannick Béjot, Serge Belliard, Marie Bénaiteau, Karim Bennys, Frédéric Blanc, Stéphanie Bombois, Claire Boutoleau Bretonnière, Pierre Branger, Jasmine Carlier, Leslie Cartz‐Piver, Pascaline Cassagnaud, Giovanni Castelnovo, Christine Champion, Annabelle Chaussenot, Mathieu Ceccaldi, Valérie Chauviré, Yaohua Chen, Julien Cogez, Emmanuel Cognat, Fabienne Contégal-Callier, Léa Corneille, Philippe Couratier, Hélène Courtemanche, Benjamin Cretin, C. Crinquette, Bernard Croisille, Benjamin Dauriat, Sophie Dautricourt, Vincent de La Sayette, Astrid De Liège, Marie De Verdal, Didier Deffond, Benoît Delpont, Florence Démurger, Vincent Deramecourt, Céline Derollez, Mira Didic, Giulia Diemert, Elsa Dionet, Philippe Diraison, Aude Doan, Martine Doco Fenzy, Boris Dufournet, Julien Dumurgier, Hélène Durand, Anaïs Dutray, Frédérique Etcharry‐Bouyx, Maïté Formaglio, Audrey Gabelle, Anne Gainche-Salmon, Jean‐Claude Getenet, Emmanuelle Ginglinger, Olivier Godefroy, Mathilde Graber, Chloé Gregoire, Stéphan Grimaldi, Julien Guéniat, Claude Guériot, Sophie Haffen, Lorraine Hamelin, Didier Hannequin, Cezara Hanta, Clémence Hardy, Geoffroy Hautecloque, Camille Heitz, Claire Hourrègue, Thérèse Jonveaux, Snejana Jurici, Catia Khoumri, Lejla Koric, Pierre Krolak‐Salmon, Pierre Labauge, Julien Lagarde, Hélène-Marie Lanoiselée, Brice Laurens, Isabelle Le Ber, Gwenaël Le Guyader, Amélie Leblanc, Thibaud Lebouvier, Anaïs Lippi, Marie‐Anne Mackowiak, Éloi Magnin, Cécilia Marelli, Olivier Martinaud, Aurélien Maureille, Emilie Milongo-Rigal, Sophie Mohr, Hélène Mollion, Olivier Moreaud, Alexandre Morin, Julia Nivelle, Camille Noiray, Elisabeth Ollagnon‐Roman, Claire Paquet, Jérémie Pariente, Florence Pasquier, Alexandre Perron, Nathalie Philippi, Virginie Pichon, Vincent Planche, Céline Poirsier, Marie Rafiq, Pauline Rod-Olivieri, Adeline Rollin‐Sillaire, Carole Roué-Jagot, Dario Saracino, Marie Sarazin, Mathilde Sauvée, François Sellal, Lila Sirven Villaros, Christel Thauvin, Camille Tisserand, Christophe Tomasino, Cédric Turpinat, Laurène Van Damme, Olivier Vercruysse, Alice Voilly, Nathalie Wagemann, Jean‐François Deleuze, Robert Olaso, Shahzad Ahmad, Philippe Amouyel, Claudine Berr, Paola Bossù, Femke H. Bouwman, José Brás, Dominique Campion, Jordi Clarimón, Antonio Daniele, Jean‐François Dartigues, Stéphanie Debette, Nicola Denning, Oriol Dols‐Icardo, Nick C. Fox, Daniela Galimberti, Emmanuelle Génin, Benjamin Grenier‐Boley, Detelina Grozeva, Rita Guerreiro, John J. Hardy, Clive Holmes, Henne Holstege, Marc Hulsman, Holger Hummerich, M. Arfan Ikram, M. Kamran Ikram, Iris E. Jansen, Amit Kawalia, Robert Kraaij, Jean‐Charles Lambert, M Lathrop, Afina W. Lemstra, Alberto Lleó, Lauren Luckcuck, Marcel M. A. M. Mannens, Iain Marshall, Carlo Masullo, Simon Mead, Patrizia Mecocci, Alun Meggy, Merel O. Mol, Kevin Morgan, Benedetta Nacmias, Penny J. Norsworthy, Pau Pástor, Olivier Quenez, Alfredo Ramı́rez, Rachel Raybould, Richard Redon, Marcel J. T. Reinders, Anne‐Claire Richard, Steffi G. Riedel‐Heller, Fernando Rivadeneira, Stéphane Rousseau, Natalie S. Ryan, Salha Saad, Pascual Sánchez‐Juan, Philip Scheltens, Jonathan M. Schott, Davide Seripa, Daoud Sie, Rebecca Sims, Erik A. Sistermans, Sandro Sorbi, Resie van Spaendonk, Gianfranco Spalleta, Niccoló Tesi, Betty M. Tijms, André G. Uitterlinden, Wiesje M. van der Flier, Sven J. van der Lee, Cornelia M. van Duijn, Jeroen van Rooij, John C. van Swieten, Pieter Jelle Visser, Michael Wagner, Julie Williams, Flora Alarcon, Grégory Nuel, Gaël Nicolas
25Citations signalées, ce qui n’est pas une note de qualité
12Institutions déclarées
1Pays d’affiliation déclarés
Rattachement africain : fr.
Niveau de preuve : code pays fourni par la source.
Le résumé fourni par la source
BACKGROUND: Alzheimer disease (AD) is a common complex disorder with a high genetic component. Loss-of-function (LoF) SORL1 variants are one of the strongest AD genetic risk factors. Estimating their age-related penetrance is essential before putative use for genetic counseling or preventive trials. However, relative rarity and co-occurrence with the main AD risk factor, APOE-ε4, make such estimations difficult. METHODS: We proposed to estimate the age-related penetrance of SORL1-LoF variants through a survival framework by estimating the conditional instantaneous risk combining (i) a baseline for non-carriers of SORL1-LoF variants, stratified by APOE-ε4, derived from the Rotterdam study (N = 12,255), and (ii) an age-dependent proportional hazard effect for SORL1-LoF variants estimated from 27 extended pedigrees (including 307 relatives ≥ 40 years old, 45 of them having genotyping information) recruited from the French reference center for young Alzheimer patients. We embedded this model into an expectation-maximization algorithm to accommodate for missing genotypes. To correct for ascertainment bias, proband phenotypes were omitted. Then, we assessed if our penetrance curves were concordant with age distributions of APOE-ε4-stratified SORL1-LoF variant carriers detected among sequencing data of 13,007 cases and 10,182 controls from European and American case-control study consortia. RESULTS: SORL1-LoF variants penetrance curves reached 100% (95% confidence interval [99-100%]) by age 70 among APOE-ε4ε4 carriers only, compared with 56% [40-72%] and 37% [26-51%] in ε4 heterozygous carriers and ε4 non-carriers, respectively. These estimates were fully consistent with observed age distributions of SORL1-LoF variant carriers in case-control study data. CONCLUSIONS: We conclude that SORL1-LoF variants should be interpreted in light of APOE genotypes for future clinical applications.
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Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes
- Date Crossref
- 28/06/2022
- Éditeur
- Springer Science and Business Media LLC
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Les institutions déclarées
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Les sujets associés
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchGenetics, Aging, and Longevity in Model Organisms