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Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability

Bchetnia Mbarka, Bouchard Luigi, Mathieu Jean, Campeau Philippe M, Morin Charles, Brisson Diane, Laberge Anne-Marie, Vézina Hélène, Gaudet Daniel et Laprise Catherine. (2021). Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability. Journal of Medical Genetics, 58, (10), p. 653-665.

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URL officielle: http://dx.doi.org/doi:10.1136/jmedgenet-2021-10780...

Résumé

The Saguenay–Lac-Saint-Jean (SLSJ) region located in the province of Quebec was settled in the 19th century by pioneers issued from successive migration waves starting in France in the 17th century and continuing within Quebec until the beginning of the 20th century. The genetic structure of the SLSJ population is considered to be the product of a triple founder effect and is characterised by a higher prevalence of some rare genetic diseases. Several studies were performed to elucidate the historical, demographic and genetic background of current SLSJ inhabitants to assess the origins of these rare disorders and their distribution in the population. Thanks to the development of new sequencing technologies, the genes and the variants responsible for the most prevalent conditions were identified. Combined with other resources such as the BALSAC population database, identifying the causal genes and the pathogenic variants allowed to assess the impacts of some of these founder mutations on the population health and to design precision medicine public health strategies based on carrier testing. Furthermore, it stimulated the establishment of many public programmes. We report here a review and an update of a subset of inherited disorders and founder mutations in the SLSJ region. Data were collected from published scientific sources. This work expands the knowledge about the current frequencies of these rare disorders, the frequencies of other rare genetic diseases in this population, the relevance of the carrier tests offered to the population, as well as the current available treatments and research about future therapeutic avenues for these inherited disorders.

Type de document:Article publié dans une revue avec comité d'évaluation
ISSN:0022-2593
Volume:58
Numéro:10
Pages:p. 653-665
Version évaluée par les pairs:Oui
Date:2021
Identifiant unique:10.1136/jmedgenet-2021-107809
Sujets:Sciences de la santé > Sciences médicales > Génétique
Département, module, service et unité de recherche:Départements et modules > Département des sciences fondamentales
Départements et modules > Département des sciences humaines
Mots-clés:neonatal diseases and abnormalities, community medicine, congenital, genetic background, genetic counselling, genetic load, hereditary, founder effect
Déposé le:09 mai 2022 18:25
Dernière modification:09 mai 2022 18:25
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Creative Commons LicenseSauf indication contraire, les documents archivés dans Constellation sont rendus disponibles selon les termes de la licence Creative Commons "Paternité, pas d'utilisation commerciale, pas de modification" 2.5 Canada.

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