Evidence map›Paper›PMID 31880204›Full record

ArticleStatistical methods in medical research2020

Estimating the age at onset distribution of the asymptomatic stage of a genetic disease based on pedigree data.

Marianne A Jonker, Priya Vart, Mar Rodriguez Girondo

Abstract read
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Article in Statistical methods in medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Marianne A JonkerDepartment for Health Evidence, Section Biostatistics, Radboud University Medical Center, Nijmegen, the Netherlands.
Priya VartDepartment for Health Evidence, Section Biostatistics, Radboud University Medical Center, Nijmegen, the Netherlands.
Mar Rodriguez GirondoDepartment of Biomedical Data Sciences, Leiden University Medical Center, Leiden, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Information on the age at onset distribution of the asymptomatic stage of a disease can be of paramount importance in early detection and timely management of that disease. However, accurately estimating this distribution is challenging, because the asymptomatic stage is difficult to recognize for the patient and is often detected as an incidental finding or in case of recommended screening; the age at onset is often interval-censored. In this paper, we propose a method for the estimation of the age at onset distribution of the asymptomatic stage of a genetic disease based on ascertained pedigree data that take into account the way the data are ascertained to overcome selection bias. Simulation studies show that the estimates seem to be asymptotically unbiased. Our work is motivated by the analysis of data on facioscapulohumeral muscular dystrophy, a genetic muscle disorder. In our application, carriers of the genetic causal variant are identified through genetic screening of the relatives of symptomatic carriers and their disease status is determined by a medical examination. The estimates reveal an early age at onset of the asymptomatic stage of facioscapulohumeral muscular dystrophy.

Indexed as

Muscular Dystrophy, FacioscapulohumeralAge of OnsetHumansPedigreeSelection BiasAge at onsetascertainmentcurrent status datafamily dataoutcome-dependent sampling

Identifiers

PMID31880204
PMCPMC7391479

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.