Noninvasive prenatal diagnosis of Mendelian disorders for consanguineous couples by relative genotype dosage.

cell-free circulating DNA consanguinity fetal DNA monogenic disease noninvasive prenatal diagnosis

Journal

Clinical genetics
ISSN: 1399-0004
Titre abrégé: Clin Genet
Pays: Denmark
ID NLM: 0253664

Informations de publication

Date de publication:
11 2023
Historique:
revised: 20 06 2023
received: 29 03 2023
accepted: 21 06 2023
medline: 23 10 2023
pubmed: 12 7 2023
entrez: 12 7 2023
Statut: ppublish

Résumé

Noninvasive prenatal diagnosis relies on the presence in maternal blood of circulating cell-free fetal DNA released by apoptotic trophoblast cells. Widely used for aneuploidy screening, it can also be applied to monogenic diseases (NIPD-M) in case of known parental mutations. Due to the confounding effect of maternal DNA, detection of maternal or biparental mutations requires relative haplotype dosage (RHDO), a method relying on the presence of SNPs that are heterozygous in one parent and homozygous in the other. Unavoidably, there is a risk of test failure by lack of such informative SNPs, an event particularly likely for consanguineous couples who often share common haplotypes in regions of identity-by-descent. Here we present a novel approach, relative genotype dosage (RGDO) that bypasses this predicament by directly assessing fetal genotype with SNPs that are heterozygous in both parents (frequent in regions of identity-by-descent). We show that RGDO is as sensitive as RHDO and that it performs well over a large range of fetal fractions and DNA amounts, thereby opening NIPD-M to most consanguineous couples. We also report examples of couples, consanguineous or not, where combining RGDO and RHDO allowed a diagnosis that would not have been possible with only one approach.

Identifiants

pubmed: 37434539
doi: 10.1111/cge.14399
doi:

Substances chimiques

DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

505-515

Informations de copyright

© 2023 The Authors. Clinical Genetics published by John Wiley & Sons Ltd.

Références

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Auteurs

Siv Fokstuen (S)

Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Lina Quteineh (L)

Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.

Valérie M Schwitzgebel (VM)

Pediatric Endocrine and Diabetes Unit, Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals, Geneva, Switzerland.
Diabetes Center of the Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Bettina Köhler-Ballan (B)

Department of Infectious Disease, Geneva University Hospitals, Geneva, Switzerland.

Jean-Louis Blouin (JL)

Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Marc Abramowicz (M)

Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Thierry Nouspikel (T)

Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

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