Clinical application value of pre-pregnancy carrier screening in Chinese Han childbearing population.

Autor: Tan L; Department of Reproductive Medical Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Qi Y; Department of Medical Imaging, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Zhao P; Department of Reproductive Genetics, Pingdingshan Maternal and Child Health Hospital, Pingdingshan, China., Cheng L; Department of Reproductive Medical Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Yu G; Department of Reproductive Medical Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Zhao D; Department of Reproductive Medical Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Song YX; Department of Reproductive Medical Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Xiang YG; Department of Reproductive Medical Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jazyk: angličtina
Zdroj: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Apr; Vol. 12 (4), pp. e2425.
DOI: 10.1002/mgg3.2425
Abstrakt: Background: To explore the clinical application value of pre-conception expanded carrier screening (PECS) in the Chinese Han ethnicity population of childbearing age.
Methods: The results of genetic testing of infertile parents who underwent PECS in the Reproductive Medicine Center of the Second Affiliated Hospital of Zhengzhou University, China, from September 2019 to December 2021, were retrospectively analyzed. The carrier rate of single gene disease, the detection rate of high-risk parents, and the clinical outcome of high-risk parents were statistically analyzed.
Results: A total of 1372 Chinese Han ethnicity patients underwent PECS, among which 458 patients underwent the extended 108-gene test, their overall carrier rate was 31.7%, and the detection rate of high-risk parents was 0.3%. The highest carrier rates were SLC22A (2.4%), ATP7B (2.4%), MMACHC (2.2%), PAH (1.8%), GALC (1.8%), MLC1 (1.3%), UNC13D (1.1%), CAPN3 (1.1%), and PKHD1 (1.1%). There were 488 women with fragile X syndrome-FMR1 gene detection, and 6 patients (1.2%) had FMR1 gene mutation. A total of 426 patients were screened for spinal muscular atrophy-SMN1, and the carrier rate was 3.5%, and the detection rate of parents' co-carrier was 0.5%.
Conclusion: Monogenic recessive hereditary diseases had a high carrier rate in the population. Pre-pregnancy screening could provide good prenatal and postnatal care guidance for patients and preimplantation genetic testing for monogenic/single gene disorders (PGT-M) and prenatal diagnosis could provide more precise reproductive choices for high-risk parents.
(© 2024 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC.)
Databáze: MEDLINE
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