Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.

ASD ASD risk genes Autism spectrum disorder BARAKA cohort De novo variants Middle Eastern population SNVs Whole genome sequencing

Journal

Genome medicine
ISSN: 1756-994X
Titre abrégé: Genome Med
Pays: England
ID NLM: 101475844

Informations de publication

Date de publication:
07 10 2023
Historique:
received: 02 03 2023
accepted: 04 09 2023
medline: 9 10 2023
pubmed: 8 10 2023
entrez: 7 10 2023
Statut: epublish

Résumé

Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by impaired social and communication skills, restricted interests, and repetitive behaviors. The prevalence of ASD among children in Qatar was recently estimated to be 1.1%, though the genetic architecture underlying ASD both in Qatar and the greater Middle East has been largely unexplored. Here, we describe the first genomic data release from the BARAKA-Qatar Study-a nationwide program building a broadly consented biorepository of individuals with ASD and their families available for sample and data sharing and multi-omics research. In this first release, we present a comprehensive analysis of whole-genome sequencing (WGS) data of the first 100 families (372 individuals), investigating the genetic architecture, including single-nucleotide variants (SNVs), copy number variants (CNVs), tandem repeat expansions (TREs), as well as mitochondrial DNA variants (mtDNA) segregating with ASD in local families. Overall, we identify potentially pathogenic variants in known genes or regions in 27 out of 100 families (27%), of which 11 variants (40.7%) were classified as pathogenic or likely-pathogenic based on American College of Medical Genetics (ACMG) guidelines. Dominant variants, including de novo and inherited, contributed to 15 (55.6%) of these families, consisting of SNVs/indels (66.7%), CNVs (13.3%), TREs (13.3%), and mtDNA variants (6.7%). Moreover, homozygous variants were found in 7 families (25.9%), with a sixfold increase in homozygous burden in consanguineous versus non-consanguineous families (13.6% and 1.8%, respectively). Furthermore, 28 novel ASD candidate genes were identified in 20 families, 23 of which had recurrent hits in MSSNG and SSC cohorts. This study illustrates the value of ASD studies in under-represented populations and the importance of WGS as a comprehensive tool for establishing a molecular diagnosis for families with ASD. Moreover, it uncovers a significant role for recessive variation in ASD architecture in consanguineous settings and provides a unique resource of Middle Eastern genomes for future research to the global ASD community.

Sections du résumé

BACKGROUND
Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by impaired social and communication skills, restricted interests, and repetitive behaviors. The prevalence of ASD among children in Qatar was recently estimated to be 1.1%, though the genetic architecture underlying ASD both in Qatar and the greater Middle East has been largely unexplored. Here, we describe the first genomic data release from the BARAKA-Qatar Study-a nationwide program building a broadly consented biorepository of individuals with ASD and their families available for sample and data sharing and multi-omics research.
METHODS
In this first release, we present a comprehensive analysis of whole-genome sequencing (WGS) data of the first 100 families (372 individuals), investigating the genetic architecture, including single-nucleotide variants (SNVs), copy number variants (CNVs), tandem repeat expansions (TREs), as well as mitochondrial DNA variants (mtDNA) segregating with ASD in local families.
RESULTS
Overall, we identify potentially pathogenic variants in known genes or regions in 27 out of 100 families (27%), of which 11 variants (40.7%) were classified as pathogenic or likely-pathogenic based on American College of Medical Genetics (ACMG) guidelines. Dominant variants, including de novo and inherited, contributed to 15 (55.6%) of these families, consisting of SNVs/indels (66.7%), CNVs (13.3%), TREs (13.3%), and mtDNA variants (6.7%). Moreover, homozygous variants were found in 7 families (25.9%), with a sixfold increase in homozygous burden in consanguineous versus non-consanguineous families (13.6% and 1.8%, respectively). Furthermore, 28 novel ASD candidate genes were identified in 20 families, 23 of which had recurrent hits in MSSNG and SSC cohorts.
CONCLUSIONS
This study illustrates the value of ASD studies in under-represented populations and the importance of WGS as a comprehensive tool for establishing a molecular diagnosis for families with ASD. Moreover, it uncovers a significant role for recessive variation in ASD architecture in consanguineous settings and provides a unique resource of Middle Eastern genomes for future research to the global ASD community.

Identifiants

pubmed: 37805537
doi: 10.1186/s13073-023-01228-w
pii: 10.1186/s13073-023-01228-w
pmc: PMC10560429
doi:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

81

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Mona Abdi (M)

College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
Department of Genetics, Sidra Medicine, Doha, Qatar.

Elbay Aliyev (E)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Brett Trost (B)

The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

Muhammad Kohailan (M)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Waleed Aamer (W)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Najeeb Syed (N)

Genomics Data Science Core, Sidra Medicine, Doha, Qatar.

Rulan Shaath (R)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Geethanjali Devadoss Gandhi (GD)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Worrawat Engchuan (W)

The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

Jennifer Howe (J)

The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

Bhooma Thiruvahindrapuram (B)

The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

Melissa Geng (M)

Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.

Joe Whitney (J)

The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

Amira Syed (A)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Jyothi Lakshmi (J)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Sura Hussein (S)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Najwa Albashir (N)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Amal Hussein (A)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Ilaria Poggiolini (I)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Saba F Elhag (SF)

Department of Genetics, Sidra Medicine, Doha, Qatar.
Hamad Medical Corporation, Doha, Qatar.

Sasirekha Palaniswamy (S)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Marios Kambouris (M)

Pathology and Laboratory Medicine Department, Genetics Division, Sidra Medicine, Doha, Qatar.

Maria de Fatima Janjua (M)

Department of Pediatrics, Sidra Medicine, Doha, Qatar.

Mohamed O El Tahir (MOE)

Hamad Medical Corporation, Doha, Qatar.

Ahsan Nazeer (A)

Department of Psychiatry, Sidra Medicine, Doha, Qatar.
Weill Cornell Medicine, Doha, Qatar.

Durre Shahwar (D)

Department of Psychiatry, Sidra Medicine, Doha, Qatar.
Weill Cornell Medicine, Doha, Qatar.

Muhammad Waqar Azeem (MW)

Department of Psychiatry, Sidra Medicine, Doha, Qatar.
Weill Cornell Medicine, Doha, Qatar.

Younes Mokrab (Y)

Department of Genetics, Sidra Medicine, Doha, Qatar.
Department of Genetic Medicine, Weill Cornell Medicine, Doha, Qatar.
Qatar University, Doha, Qatar.

Nazim Abdel Aati (NA)

Hamad Medical Corporation, Doha, Qatar.

Ammira Akil (A)

Department of Genetics, Sidra Medicine, Doha, Qatar.

Stephen W Scherer (SW)

The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
McLaughlin Centre, University of Toronto, Toronto, ON, Canada.

Madeeha Kamal (M)

Department of Pediatrics, Sidra Medicine, Doha, Qatar.

Khalid A Fakhro (KA)

College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar. kfakhro@sidra.org.
Department of Genetics, Sidra Medicine, Doha, Qatar. kfakhro@sidra.org.
Department of Genetic Medicine, Weill Cornell Medicine, Doha, Qatar. kfakhro@sidra.org.

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