Evidence map›Paper›PMID 35348702›Full record

ArticleHuman molecular genetics2022

Analysis of incidental findings in Qatar genome participants reveals novel functional variants in LMNA and DSP.

Amal Elfatih, Sahar I Da'as, Doua Abdelrahman, Hamdi Mbarek, Idris Mohammed, Waseem Hasan, Khalid A Fakhro, The Qatar Genome Program Research Consortium, Xavier Estivill, Borbala Mifsud

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Article in Human molecular genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Amal ElfatihCollege of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
Sahar I Da'asCollege of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
Doua AbdelrahmanDepartment of Human Genetics, Sidra Medicine, Doha, Qatar.
Hamdi MbarekQatar Genome Programme, Qatar Foundation Research, Development and Innovation, Qatar Foundation, Doha, Qatar.
Idris MohammedCollege of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
Waseem HasanDepartment of Human Genetics, Sidra Medicine, Doha, Qatar.
Khalid A FakhroCollege of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
The Qatar Genome Program Research Consortium
Xavier EstivillQuantitative Genomic Medicine Laboratories (qGenomics), Barcelona, Spain.
Borbala MifsudCollege of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.ORCID 0000-0003-3429-3094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to report clinically actionable incidental findings in genetic testing, the American College of Medical Genetics and Genomics (ACMG) recommended the evaluation of variants in 59 genes associated with highly penetrant mutations. However, there is a lack of epidemiological data on medically actionable rare variants in these genes in Arab populations. We used whole genome sequencing data from 6045 participants from the Qatar Genome Programme and integrated it with phenotypic data collected by the Qatar Biobank. We identified novel putative pathogenic variants in the 59 ACMG genes by filtering previously unrecorded variants based on computational prediction of pathogenicity, variant rarity and segregation evidence. We assessed the phenotypic associations of candidate variants in genes linked to cardiovascular diseases. Finally, we used a zebrafish knockdown and synthetic human mRNA co-injection assay to functionally characterize two of these novel variants. We assessed the zebrafish cardiac function in terms of heart rate, rhythm and hemodynamics, as well as the heart structure. We identified 52 492 novel variants, which have not been reported in global and disease-specific databases. A total of 74 novel variants were selected with potentially pathogenic effect. We prioritized two novel cardiovascular variants, DSP c.1841A > G (p.Asp614Gly) and LMNA c.326 T > G (p.Val109Gly) for functional characterization. Our results showed that both variants resulted in abnormal zebrafish heart rate, rhythm and structure. This study highlights medically actionable variants that are specific to the Middle Eastern Qatari population.

Indexed as

Incidental FindingsLamin Type AAnimalsDesmoplakinsGenetic Predisposition to DiseaseGenetic TestingHumansQatarZebrafishDesmoplakinsDSP protein, humanLamin Type ALMNA protein, human

Identifiers

PMID35348702
PMCPMC9402234

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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.