Carrier burden of over 300 diseases in Han Chinese identified by expanded carrier testing of 300 couples using assisted reproductive technology
- 14 July 2023
- journal article
- research article
- Published by Springer Nature in Journal of Assisted Reproduction and Genetics
- Vol. 40 (9) , 2157-2173
Abstract
Background Expanded carrier screening (ECS) has become a common practice for identifying carriers of monogenic diseases. However, existing large gene panels are not well-tailored to Chinese populations. In this study, ECS testing for pathogenic variants of both single-nucleotide variants (SNVs) and copy number variants (CNVs) in 330 genes implicated in 342 autosomal recessive (AR) or X-linked diseases was carried out. We assessed the differences in allele frequencies specific to the Chinese population who have used assisted reproductive technology (ART) and the important genes to screen for in this population. Methodology A total of 300 heterosexual couples were screened by our ECS panel using next-generation sequencing. A customed bioinformatic algorithm was used to analyze SNVs and CNVs. Guidelines from the American College of Medical Genetics and Genomics and the Association for Molecular Pathology were adapted for variant interpretation. Pathogenic or likely pathogenic (P/LP) SNVs located in high homology regions/deletions and duplications of one or more exons in length were independently verified with other methods. Results 64.83% of the patients were identified to be carriers of at least one of 342 hereditary conditions. We identified 622 P/LP variants, 4.18% of which were flagged as CNVs. The rate of at-risk couples was 3%. A total of 149 AR diseases accounted for 64.05% of the cumulative carrier rate, and 48 diseases had a carrier rate above 1/200 in the test. Conclusion An expanded screening of inherited diseases by incorporating different variant types, especially CNVs, has the potential to reduce the occurrence of severe monogenic diseases in the offspring of patients using ART in China.Keywords
Funding Information
- National Key R&D Program of China (21YFC2701002, 2018YFC1004900)
- National Natural Science Foundation of China (81971344, 81771638 and 81901495)
- Shanghai Municipal Health Commission (202140110, GW-10.1-XK07)
- Shanghai “Rising Stars of Medical Talent” Youth Development Program Clinical Laboratory Practitioners Program (201972)
- Shanghai Municipal Commission of Health and Family Planning (202140110, 20215Y0216)
This publication has 71 references indexed in Scilit:
- Involvement of and Interaction between WNT10A and EDA Mutations in Tooth Agenesis Cases in the Chinese PopulationPLOS ONE, 2013
- Carrier screening of 8,500 IVF patients utilizing next generation DNA sequencing detects common, rare and otherwise undetectable mutations across society-recommended diseasesFertility and Sterility, 2013
- SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in ChinaPLOS ONE, 2013
- The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing ageBMC Medical Genetics, 2013
- An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individualsGenetics in Medicine, 2013
- Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for citrin deficiencyGene, 2012
- Functional Studies of MLC1 Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical CystsPLOS ONE, 2012
- Carrier screening for Beta-thalassaemia: a review of international practiceEuropean Journal of Human Genetics, 2010
- Carrier screening for spinal muscular atrophyGenetics in Medicine, 2008
- Carrier screening in individuals of Ashkenazi Jewish descentGenetics in Medicine, 2008