Literature DB >> 30252892

Non-parametric estimation of survival in age-dependent genetic disease and application to the transthyretin-related hereditary amyloidosis.

Flora Alarcon1, Violaine Planté-Bordeneuve2,3, Malin Olsson4, Grégory Nuel5,6.   

Abstract

In genetic diseases with variable age of onset, survival function estimation for the mutation carriers as well as estimation of the modifying factors effects are essential to provide individual risk assessment, both for mutation carriers management and prevention strategies. In practice, this survival function is classically estimated from pedigrees data where most genotypes are unobserved. In this article, we present a unifying Expectation-Maximization (EM) framework combining probabilistic computations in Bayesian networks with standard statistical survival procedures in order to provide mutation carrier survival estimates. The proposed approach allows to obtain previously published parametric estimates (e.g. Weibull survival) as particular cases as well as more general Kaplan-Meier non-parametric estimates, which is the main contribution. Note that covariates can also be taken into account using a proportional hazard model. The whole methodology is both validated on simulated data and applied to family samples with transthyretin-related hereditary amyloidosis (a rare autosomal dominant disease with highly variable age of onset), showing very promising results.

Entities:  

Mesh:

Year:  2018        PMID: 30252892      PMCID: PMC6155453          DOI: 10.1371/journal.pone.0203860

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


  23 in total

1.  Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families.

Authors:  V Planté-Bordeneuve; J Carayol; A Ferreira; D Adams; F Clerget-Darpoux; M Misrahi; G Said; C Bonaïti-Pellié
Journal:  J Med Genet       Date:  2003-11       Impact factor: 6.318

2.  Exact genetic linkage computations for general pedigrees.

Authors:  M Fishelson; D Geiger
Journal:  Bioinformatics       Date:  2002       Impact factor: 6.937

3.  The Elston-Stewart algorithm for continuous genotypes and environmental factors.

Authors:  R C Elston; V T George; F Severtson
Journal:  Hum Hered       Date:  1992       Impact factor: 0.444

4.  GMCheck: Bayesian error checking for pedigree genotypes and phenotypes.

Authors:  Alun Thomas
Journal:  Bioinformatics       Date:  2005-05-06       Impact factor: 6.937

5.  PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history.

Authors:  F Alarcon; C Bourgain; M Gauthier-Villars; V Planté-Bordeneuve; D Stoppa-Lyonnet; C Bonaïti-Pellié
Journal:  Genet Epidemiol       Date:  2009-07       Impact factor: 2.135

6.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

7.  A general model for the genetic analysis of pedigree data.

Authors:  R C Elston; J Stewart
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

8.  Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.

Authors:  D F Easton; D T Bishop; D Ford; G P Crockford
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

9.  ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data.

Authors:  C Le Bihan; C Moutou; L Brugières; J Feunteun; C Bonaïti-Pellié
Journal:  Genet Epidemiol       Date:  1995       Impact factor: 2.135

10.  Kerfdr: a semi-parametric kernel-based approach to local false discovery rate estimation.

Authors:  Mickael Guedj; Stephane Robin; Alain Celisse; Gregory Nuel
Journal:  BMC Bioinformatics       Date:  2009-03-16       Impact factor: 3.169

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