AB034. Carrier frequency of inherited genetic disorders in Thai population: implication for designing expanded carrier screening panel
Population Genetics, Genetic Epidemiology, Statistics, Bioinformatics

AB034. Carrier frequency of inherited genetic disorders in Thai population: implication for designing expanded carrier screening panel

Sommon Klumsathian1, Woramon Lorlipiwong1, Nareenart Iemwimangsa1, Insee Sensorn1, Bhakbhoom Panthan1, Takol Chareonsirisuthigul2, Objoon Trachoo1, Wasun Chantratita1

1Center for Medical Genomics, 2Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University Bangkok, Bangkok, Thailand


Background: Expanded carrier screening (ECS) is the process of screening individuals for hundreds of autosomal recessive (AR) and X-linked recessive (XLR) diseases. ECS result is beneficial for couples who want to make an informed reproductive choice. Though next-generation sequencing allows thousands of genes to be sequenced at once, the ideal ECS gene panel should only include diseases that its carriers are common in the population (1% or higher), and the prenatal diagnosis of the disease is allowed. However, designing the ECS panel for Thais can be difficult because the carrier frequency for most genetic diseases is unknown. Therefore, we retrospectively review our exome sequencing data from Thai patient to get an estimation of the carrier frequency.

Methods: Variants in 540 genes associated with AR and XLR from exome sequencing data of 178 unrelated Thai patients are filtered and matched against known pathogenic mutations in reputable mutation databases (OMIM, Clinvar, and HGMD).

Results: Pathogenic mutations in SLC26A4 gene associated with Pendred syndrome have the highest carrier frequency of 2.81%. Usher syndrome (USH2A) is the second-most common with the carrier frequency of 2.25%. 1.69% of the patients also have pathogenic mutations in the gene related to impaired vision and impaired hearing such as OCA2, OTOF, CLCN1 BSND and AHI1. Only 1.12% or less is the carrier of severe diseases such as myotonia congenita (CLCN1), lactic acidosis (POLG) and molybdenum cofactor deficiency (MOCS1).

Conclusions: Inherited diseases that involved the impairment of hearing and vision are somewhat common among Thais. The ethical issue could arise when these diseases are included the ECS panel because they are not severe enough to allow for prenatal diagnosis. More discussion about ethics of ECS and more data on carrier frequency are needed to offer ECS ethically.

Keywords: Expanded carrier screening (ECS); ethical issue; next generation sequencing; carrier frequency; Thai population


doi: 10.21037/atm.2017.s034


Cite this article as: Klumsathian S, Lorlipiwong W, Iemwimangsa N, Sensorn I, Panthan B, Chareonsirisuthigul T, Trachoo O, Chantratita W. Carrier frequency of inherited genetic disorders in Thai population: implication for designing expanded carrier screening panel. Ann Transl Med 2017;5(Suppl 2):AB034. doi: 10.21037/atm.2017.s034

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