Literature DB >> 33757571

Increased detection of primary carnitine deficiency through second-tier newborn genetic screening.

Yiming Lin1, Weifeng Zhang2, Chenggang Huang3, Chunmei Lin1, Weihua Lin1, Weilin Peng1, Qingliu Fu4, Dongmei Chen5.   

Abstract

BACKGROUND: Newborn screening for primary carnitine deficiency (NBS) is commonly implemented worldwide; however, it has poor sensitivity. This study aimed to evaluate the feasibility of improving screening by including a second-tier genetic assay.
RESULTS: An Agena iPLEX assay was developed to identify 17 common SLC22A5 mutations in Chinese populations and was applied in NBS as a second-tier screening. From January 2017 to December 2018, 204,777 newborns were screened for PCD using tandem mass spectrometry. A total of 316 (0.15%) residual NBS-positive specimens with low free carnitine (C0) levels were subjected to this second-tier screening. The screening identified 20 screen-positive newborns who harboured biallelic mutations in theSLC22A5 gene, 99 carriers with one mutation, and 197 screen-negative newborns with no mutations. Among the 99 carriers, four newborns were found to have a second disease-causing SLC22A5mutation by further genetic analysis. Among the 197 screen-negatives were four newborns with persistently low C0 levels, and further genetic analysis revealed that one newborn had two novel SLC22A5 pathogenic variants. In total, 25 newborns were diagnosed with PCD, for a positive predictive value of 7.91% (25/316). Based on these data, we estimate the incidence of PCD in Quanzhou is estimated to be 1:8191.Thirteen distinct SLC22A5 variants were identified, and the most common was c.760C > T, with an allelic frequency of 32% (16/50), followed by c.1400C > G (7/50, 14%), and c.51C > G (7/50, 14%).
CONCLUSION: Data from this study revealed that 24% (6/25) of PCD cases would have been missed by conventional NBS. This high-throughput iPLEX assay is a powerful tool for PCD genotyping. The addition of this second-tier genetic screening to the current NBS program could identify missed PCD cases, thereby increasing PCD detection. However, further studies are needed to optimise the workflow of the new screening algorithm and to evaluate the cost-effectiveness of this screening approach.

Entities:  

Keywords:  Free carnitine; Newborn screening; Primary carnitine deficiency; Second-tier screening

Mesh:

Substances:

Year:  2021        PMID: 33757571      PMCID: PMC7988980          DOI: 10.1186/s13023-021-01785-6

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  30 in total

1.  Validation of dye-binding/high-resolution thermal denaturation for the identification of mutations in the SLC22A5 gene.

Authors:  Steven F Dobrowolski; Jason T McKinney; Cristina Amat di San Filippo; Keow Giak Sim; Bridget Wilcken; Nicola Longo
Journal:  Hum Mutat       Date:  2005-03       Impact factor: 4.878

2.  Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency.

Authors:  A Koizumi; J Nozaki; T Ohura; T Kayo; Y Wada; J Nezu; R Ohashi; I Tamai; Y Shoji; G Takada; S Kibira; T Matsuishi; A Tsuji
Journal:  Hum Mol Genet       Date:  1999-11       Impact factor: 6.150

3.  Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency.

Authors:  N L Tang; V Ganapathy; X Wu; J Hui; P Seth; P M Yuen; R J Wanders; T F Fok; N M Hjelm
Journal:  Hum Mol Genet       Date:  1999-04       Impact factor: 6.150

4.  Carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlation.

Authors:  Yi-Chen Chen; Yin-Hsiu Chien; Pin-Wen Chen; Nelson Leung-Sang Tang; Pao-Chin Chiu; Wuh-Liang Hwu; Ni-Chung Lee
Journal:  Hum Mutat       Date:  2013-04       Impact factor: 4.878

5.  Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency.

Authors:  Yiming Lin; Weilin Peng; Mengyi Jiang; Chunmei Lin; Weihua Lin; Zhenzhu Zheng; Min Li; Qingliu Fu
Journal:  Clin Chim Acta       Date:  2018-09-22       Impact factor: 3.786

6.  Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening.

Authors:  Kate C Verbeeten; Anne-Marie Lamhonwah; Dennis Bulman; Hanna Faghfoury; P Chakraborty; Ingrid Tein; Michael T Geraghty
Journal:  Mol Genet Metab       Date:  2019-12-10       Impact factor: 4.797

7.  Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects.

Authors:  Ayman W El-Hattab; Fang-Yuan Li; Joseph Shen; Berkley R Powell; Erawati V Bawle; Darius J Adams; Erica Wahl; Joyce A Kobori; Brett Graham; Fernando Scaglia; Lee-Jun Wong
Journal:  Genet Med       Date:  2010-01       Impact factor: 8.822

8.  Application of Next-Generation Sequencing Following Tandem Mass Spectrometry to Expand Newborn Screening for Inborn Errors of Metabolism: A Multicenter Study.

Authors:  Yuqi Yang; Leilei Wang; Benjing Wang; Shuang Liu; Bin Yu; Ting Wang
Journal:  Front Genet       Date:  2019-02-14       Impact factor: 4.599

9.  Molecular investigation in Chinese patients with primary carnitine deficiency.

Authors:  Yanghui Zhang; Haoxian Li; Jing Liu; Huiming Yan; Qin Liu; Xianda Wei; Hui Xi; Zhengjun Jia; Lingqian Wu; Hua Wang
Journal:  Mol Genet Genomic Med       Date:  2019-07-30       Impact factor: 2.183

10.  Newborn screening for citrin deficiency and carnitine uptake defect using second-tier molecular tests.

Authors:  Li-Yun Wang; Nien-I Chen; Pin-Wen Chen; Shu-Chuan Chiang; Wuh-Liang Hwu; Ni-Chung Lee; Yin-Hsiu Chien
Journal:  BMC Med Genet       Date:  2013-02-10       Impact factor: 2.103

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