Journal Article

Noninvasive prenatal diagnosis of duchenne muscular dystrophy in five Chinese families based on relative mutation dosage approach

Zhao, Ganye, Dai, Peng, Wang, Xiaofeng, Liu, Lina, Kong, Xiangdong

2021

Overview

Background Relative haplotype dosage (RHDO) approach has been applied in noninvasive prenatal diagnosis (NIPD) of Duchenne muscular dystrophy (DMD). However, the RHDO procedure is relatively complicated and the parental haplotypes need to be constructed. Furthermore, it is not suitable for the diagnosis of de novo mutations or mosaicism in germ cells. Here, we investigated NIPD of DMD using a relative mutation dosage (RMD)-based approach—cell-free DNA Barcode-Enabled Single-Molecule Test (cfBEST), which has not previously been applied in the diagnosis of exon deletion. Methods Five DMD families caused by DMD gene point mutations or exon deletion were recruited for this study. After the breakpoints of exon deletion were precisely mapped with multiple PCR, the genotypes of the fetuses from the five DMD families were inferred using cfBEST, and were further validated by invasive prenatal diagnosis. Results The cfBEST results of the five families indicated that one fetus was female and did not carry the familial molecular alteration, three fetuses were carriers and one was male without the familial mutation. The invasive prenatal diagnosis results were consistent with those of the cfBEST procedure. Conclusion This is the first report of NIPD of DMD using the RMD-based approach. We extended the application of cfBEST from point mutation to exon deletion mutation. The results showed that cfBEST would be suitable for NIPD of DMD caused by different kinds of mutation types.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Biomedical and Life Sciences / Biomedicine / Breakpoints / Cell free DNA / cfBEST / China / Diagnosis / Diagnosis, Noninvasive / Disease / Dosage / Duchenne muscular dystrophy / Duchenne's muscular dystrophy / Dystrophin / Dystrophin - genetics / Female / Fetuses / Gene deletion / Gene Expression / Gene mutations / Genetic screening / Genotypes / Germ cells / Haplotypes / Health aspects / Human Genetics / Humans / Male / Methods / Microarrays / Mosaicism / Muscular dystrophy / Muscular Dystrophy, Duchenne - diagnosis / Muscular Dystrophy, Duchenne - genetics / Mutation / Noninvasive prenatal diagnosis / Noninvasive Prenatal Testing / Plasma / Point mutation / Pregnancy / Prenatal diagnosis / Relative mutation dosage / Womens health