Evidence map›Paper›PMID 42441689›Full record

ArticlePLoS genetics2026

Age-based risk estimates for C9orf72RE-related diseases: Theoretical developments and added value for genetic counseling.

Dominique de Vienne, Damien M de Vienne

Abstract read
In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Dominique de VienneUniversité Paris-Saclay, Institute for the Diversity, Ecology and Evolution of the Living World, Gif-sur-Yvette, France.ORCID https://orcid.org/0000-0003-3395-7901
Damien M de VienneUniversité Lyon 1-CNRS, Laboratoire de Biométrie et Biologie Évolutive, Villeurbanne, France.ORCID https://orcid.org/0000-0001-9532-5251

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The C9orf72 hexanucleotide repeat expansion is the most common genetic cause of amyotrophic lateral sclerosis (ALS) or frontotemporal dementia (FTD). In genetic counseling, children of mutation carriers are often told that they have a 50% risk of carrying the mutation, but this figure does not take into account the fact that penetrance is age-related, with a unimodal distribution of disease onset around 58 years of age. Using a Bayesian approach, we developed a theory to calculate the probability of carrying the mutation for asymptomatic relatives (children/siblings and grandchildren/niblings) as well as the probability of developing ALS/FDT within a given time frame, based on their age. Using published data on age-related penetrance, we then calculated these probabilities and developed an online simulator that makes it easy to calculate them on a case-by-case basis. The conditional probabilities obtained can be very different from Mendelian values. For example, a 70-year-old asymptomatic child born to a carrier has approximately a 6% risk of being a carrier, which is far from 50%. For grandchildren, taking into account both their age and that of their parents also leads to figures that are much lower than those obtained if only their age were considered. For consultands, the decision to undergo testing is based in part on risk estimates. In this regard, the refined estimates and simulator we propose may prove to be valuable tools for genetic counseling for families affected by ALS/FTD linked to the C9orf72RE mutation. In addition, the formulas used in this study could also be used to calculate risk estimates for other diseases caused by autosomal dominant mutations with age-dependent penetrance.

Indexed as

Amyotrophic Lateral SclerosisFrontotemporal DementiaGenetic CounselingProteinsAgedBayes TheoremC9orf72 ProteinDNA Repeat ExpansionHumansMutationPenetranceC9orf72 ProteinC9orf72 protein, humanProteins

Identifiers

PMID42441689
PMCPMC13379100

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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.