Expanded targeted preconception screening panel in Israel: findings and insights.

Genetic Carrier Screening Genetic Counseling Inborn Genetic Diseases

Journal

Journal of medical genetics
ISSN: 1468-6244
Titre abrégé: J Med Genet
Pays: England
ID NLM: 2985087R

Informations de publication

Date de publication:
06 May 2024
Historique:
received: 10 09 2023
accepted: 25 04 2024
medline: 9 5 2024
pubmed: 9 5 2024
entrez: 8 5 2024
Statut: aheadofprint

Résumé

We aimed to analyse the efficacy and added value of a targeted Israeli expanded carrier screening panel (IL-ECSP), beyond the first-tier test covered by the Israeli Ministry of Health (IMOH) and the second-tier covered by the Health Maintenance Organisations (HMOs). A curated variant-based IL-ECSP, tailored to the uniquely diverse Israeli population, was offered at two tertiary hospitals and a major genetics laboratory. The panel includes 1487 variants in 357 autosomal recessive and X-linked genes. We analysed 10 115 Israeli samples during an 18-month period. Of these, 6036 (59.7%) were tested as couples and 4079 (40.3%) were singles. Carriers were most frequently identified with mutations in the following genes: This is the largest cohort of targeted ECSP testing, tailored to the diverse Israeli population. The IL-ECSP expands the identification of couples at risk and empowers their reproductive choices. We recommend endorsing an expanded targeted panel to the National Genetic Carrier Screening programme.

Sections du résumé

BACKGROUND BACKGROUND
We aimed to analyse the efficacy and added value of a targeted Israeli expanded carrier screening panel (IL-ECSP), beyond the first-tier test covered by the Israeli Ministry of Health (IMOH) and the second-tier covered by the Health Maintenance Organisations (HMOs).
METHODS METHODS
A curated variant-based IL-ECSP, tailored to the uniquely diverse Israeli population, was offered at two tertiary hospitals and a major genetics laboratory. The panel includes 1487 variants in 357 autosomal recessive and X-linked genes.
RESULTS RESULTS
We analysed 10 115 Israeli samples during an 18-month period. Of these, 6036 (59.7%) were tested as couples and 4079 (40.3%) were singles. Carriers were most frequently identified with mutations in the following genes:
CONCLUSION CONCLUSIONS
This is the largest cohort of targeted ECSP testing, tailored to the diverse Israeli population. The IL-ECSP expands the identification of couples at risk and empowers their reproductive choices. We recommend endorsing an expanded targeted panel to the National Genetic Carrier Screening programme.

Identifiants

pubmed: 38719349
pii: jmg-2023-109629
doi: 10.1136/jmg-2023-109629
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: DMB was involved in the design of the CarrierScan array and is entitled to certain royalties.

Auteurs

Adi Reches (A)

The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Department of Obstetrics and Gynecology, Lis Maternity Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Vered Ofen Glassner (V)

The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Nurit Goldstein (N)

The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel.

Josepha Yeshaya (J)

American Medical Genetics (AMG) Laboratory, Herzliya, Israel.

Galit Delmar (G)

Igentify, Caesarea, Israel.

Ellie Portugali (E)

Igentify, Caesarea, Israel.

Tova Hallas (T)

Igentify, Caesarea, Israel.

Amit Weinstein (A)

The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Alina Kurolap (A)

The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Michal Berkenstadt (M)

The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel.
Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Tal Mantsour (T)

American Medical Genetics (AMG) Laboratory, Herzliya, Israel.

Liat Abu-Gutstein (L)

The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel.

Liat Ries-Levavi (L)

The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel.

Haike Reznik-Wolf (H)

The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel.
Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Doron Moshe Behar (DM)

Igentify, Caesarea, Israel.

Yuval Yaron (Y)

The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Elon Pras (E)

The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel.
Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Hagit Baris Feldman (H)

The Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel hagitbf@tlvmc.gov.il.
Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Classifications MeSH