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Carrier screening for spinal muscular atrophy with a simple test based on melting analysis.
Xia, Zhongmin; Zhou, Yulin; Fu, Dongmei; Wang, Zengge; Ge, Yunsheng; Ren, Jun; Guo, Qiwei.
Afiliação
  • Xia Z; United Diagnostic and Research Center for Clinical Genetics, School of Public Health of Xiamen University & Xiamen Maternal and Child Health Hospital, 361003, Xiamen, Fujian, China.
  • Zhou Y; United Diagnostic and Research Center for Clinical Genetics, School of Public Health of Xiamen University & Xiamen Maternal and Child Health Hospital, 361003, Xiamen, Fujian, China.
  • Fu D; United Diagnostic and Research Center for Clinical Genetics, School of Public Health of Xiamen University & Xiamen Maternal and Child Health Hospital, 361003, Xiamen, Fujian, China.
  • Wang Z; United Diagnostic and Research Center for Clinical Genetics, School of Public Health of Xiamen University & Xiamen Maternal and Child Health Hospital, 361003, Xiamen, Fujian, China.
  • Ge Y; United Diagnostic and Research Center for Clinical Genetics, School of Public Health of Xiamen University & Xiamen Maternal and Child Health Hospital, 361003, Xiamen, Fujian, China.
  • Ren J; United Diagnostic and Research Center for Clinical Genetics, School of Public Health of Xiamen University & Xiamen Maternal and Child Health Hospital, 361003, Xiamen, Fujian, China. renjun666@126.com.
  • Guo Q; Department of Dermatology, Zhongshan Hospital Xiamen University, 361004, Xiamen, Fujian, China. renjun666@126.com.
J Hum Genet ; 64(5): 387-396, 2019 May.
Article em En | MEDLINE | ID: mdl-30765868
ABSTRACT
Carrier screening of spinal muscular atrophy (SMA) can provide reproductive options for carriers and prevent the birth defects. Here, we developed a simple screening test based on melting analysis. The test comprises a duplex PCR with two primer pairs and three probes to simultaneous amplify SMN1, SMN2, and CFTR. By analyzing the melting profiles, we were able to determine the SMN1/SMN2 ratio and SMN1 + SMN2 copy number to subsequently determine the copy number of SMN1. Samples with one copy of SMN1 were considered as "high risk for carrier," while samples with ≥2 copies of SMN1 were considered as "low risk for carrier." We evaluated the clinical performance of this test using 215 clinical samples with various genotypes that had been previously confirmed by multiplex ligation-dependent probe amplification (MLPA). The test showed high sensitivity (100%) and specificity (97.1%) as well as high positive (97.3%) and negative (100%) predictive value, and was in perfect agreement with the gold standard test, MLPA (k = 0.97). Moreover, it is rapid, inexpensive, and easy to perform and automate, with high reproducibility and capacity. Therefore, we expect this test will advance carrier screening for SMA.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Regulador de Condutância Transmembrana em Fibrose Cística / Proteína 1 de Sobrevivência do Neurônio Motor / Triagem de Portadores Genéticos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Female / Humans / Male Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Regulador de Condutância Transmembrana em Fibrose Cística / Proteína 1 de Sobrevivência do Neurônio Motor / Triagem de Portadores Genéticos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Female / Humans / Male Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China