Literature DB >> 30765868

Carrier screening for spinal muscular atrophy with a simple test based on melting analysis.

Zhongmin Xia1, Yulin Zhou1, Dongmei Fu1, Zengge Wang1, Yunsheng Ge1, Jun Ren2,3, Qiwei Guo4.   

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.

Entities:  

Mesh:

Substances:

Year:  2019        PMID: 30765868     DOI: 10.1038/s10038-019-0576-6

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  29 in total

1.  Multiplex digital PCR: breaking the one target per color barrier of quantitative PCR.

Authors:  Qun Zhong; Smiti Bhattacharya; Steven Kotsopoulos; Jeff Olson; Valérie Taly; Andrew D Griffiths; Darren R Link; Jonathan W Larson
Journal:  Lab Chip       Date:  2011-05-17       Impact factor: 6.799

Review 2.  SMA carrier testing: a meta-analysis of differences in test performance by ethnic group.

Authors:  William Kim MacDonald; David Hamilton; Stefan Kuhle
Journal:  Prenat Diagn       Date:  2014-08-06       Impact factor: 3.050

3.  Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy.

Authors:  Eva L Arkblad; Niklas Darin; Kerstin Berg; Eva Kimber; Göran Brandberg; Christopher Lindberg; Eva Holmberg; Mar Tulinius; Margareta Nordling
Journal:  Neuromuscul Disord       Date:  2006-10-17       Impact factor: 4.296

4.  Newborn and carrier screening for spinal muscular atrophy.

Authors:  Thomas W Prior; Pamela J Snyder; Britton D Rink; Dennis K Pearl; Robert E Pyatt; David C Mihal; Todd Conlan; Betsy Schmalz; Laura Montgomery; Katie Ziegler; Carolee Noonan; Sayaka Hashimoto; Shannon Garner
Journal:  Am J Med Genet A       Date:  2010-07       Impact factor: 2.802

5.  Evaluation and characterization of a high-resolution melting analysis kit for rapid carrier-screening test of spinal muscular atrophy.

Authors:  Kai Chen Wang; Chi Chang Chang; Yu-Fen Chang; Szu-Hsien Wang; Chien-Kuan Chiang; Ching-Piao Tsai
Journal:  J Neurogenet       Date:  2015-04-20       Impact factor: 1.250

6.  Establishing a reference dataset for the authentication of spinal muscular atrophy cell lines using STR profiling and digital PCR.

Authors:  Deborah L Stabley; Jennifer Holbrook; Ashlee W Harris; Kathryn J Swoboda; Thomas O Crawford; Katia Sol-Church; Matthew E R Butchbach
Journal:  Neuromuscul Disord       Date:  2017-02-06       Impact factor: 4.296

7.  A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy.

Authors:  Tsuyoshi Kashima; James L Manley
Journal:  Nat Genet       Date:  2003-08       Impact factor: 38.330

8.  Assessment of liquid microbead arrays for the screening of newborns for spinal muscular atrophy.

Authors:  Robert E Pyatt; David C Mihal; Thomas W Prior
Journal:  Clin Chem       Date:  2007-09-21       Impact factor: 8.327

9.  Validation of a high resolution NGS method for detecting spinal muscular atrophy carriers among phase 3 participants in the 1000 Genomes Project.

Authors:  Jessica L Larson; Ari J Silver; Dalin Chan; Carlos Borroto; Brett Spurrier; Lee M Silver
Journal:  BMC Med Genet       Date:  2015-10-29       Impact factor: 2.103

10.  SMN1 and SMN2 copy numbers in cell lines derived from patients with spinal muscular atrophy as measured by array digital PCR.

Authors:  Deborah L Stabley; Ashlee W Harris; Jennifer Holbrook; Nicholas J Chubbs; Kevin W Lozo; Thomas O Crawford; Kathryn J Swoboda; Vicky L Funanage; Wenlan Wang; William Mackenzie; Mena Scavina; Katia Sol-Church; Matthew E R Butchbach
Journal:  Mol Genet Genomic Med       Date:  2015-03-21       Impact factor: 2.183

View more
  2 in total

1.  Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants.

Authors:  John N Milligan; Jessica L Larson; Stela Filipovic-Sadic; Walairat Laosinchai-Wolf; Ya-Wen Huang; Tsang-Ming Ko; Kristin M Abbott; Henny H Lemmink; Minna Toivonen; Johanna Schleutker; Caren Gentile; Vivianna M Van Deerlin; Huiping Zhu; Gary J Latham
Journal:  J Mol Diagn       Date:  2021-03-30       Impact factor: 5.341

2.  Polymerase chain reaction-based assays facilitate the breeding and study of mouse models of Klinefelter syndrome.

Authors:  Hai-Xia Zhang; Yu-Lin Zhou; Wen-Yan Xu; Xiao-Lu Chen; Jia-Yang Jiang; Xiao-Man Zhou; Zeng-Ge Wang; Rong-Qin Ke; Qi-Wei Guo
Journal:  Asian J Androl       Date:  2022 Jan-Feb       Impact factor: 3.285

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.