Literature DB >> 25102806

Inborn Error of Metabolism (IEM) screening in Singapore by electrospray ionization-tandem mass spectrometry (ESI/MS/MS): An 8 year journey from pilot to current program.

J S Lim1, E S Tan2, C M John1, S Poh1, S J Yeo1, J S M Ang1, P Adakalaisamy1, R A Rozalli1, C Hart1, E T H Tan1, E Ranieri3, V S Rajadurai4, M A Cleary2, D L M Goh5.   

Abstract

IEM screening by ESI/MS/MS was introduced in Singapore in 2006. There were two phases; a pilot study followed by implementation of the current program. The pilot study was over a 4 year period. During the pilot study, a total of 61,313 newborns were screened, and 20 cases of IEM were diagnosed (detection rate of 1:3065; positive predictive value (PPV) of 11%). Regular self-review, participation in external quality assessment and the Region 4 Genetic collaborative programs (http://www.region4genetics.org/) had led to the robust development of our current NBS MS/MS program. Overall, from July 2006 to April 2014, we screened a total of 177,267 newborns. The mean age at the time of sampling was 47.9h. Transportation of samples to the testing laboratory averaged 0.92 day. Upon receipt of sample, the NBS result was available within 1.64 days and within 3.8 days if a second tier test was required. Using absolute cut-off values in place of the initial 99th percentile reference range for the analyte markers and the introduction of two 2nd tier tests (MMA and Succinylacetone) had significantly reduced the high recall rate from an initial 1.5% during the period 2006-07 to 0.12% in 2013. The NBS MS/MS program was supported by a centralized confirmatory/diagnostic testing laboratory and a rapid response team of metabolic specialists. The detection rate was 1: 3165 (1:2727 if maternal conditions were also included). There were 23 newborns affected with organic acidemias (incidence: 1:6565), 23 with fatty acid oxidation disorders (incidence: 1:6565), and 10 with amino acidopathies (incidence 1:17,726). The performance metrics for the screening test were acceptable (sensitivity: 95.59%, specificity: 99.85%, PPV: 20%, FPR: 0.15). Participation in the NBS MS/MS program by hospitals was voluntary, and in 2013, the uptake rate was 71% of the annual births. We hope that newborn screening by MS/MS will become a standard of care for all babies in Singapore.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  FAOD; Inborn Error of Metabolism; MS/MS; Newborn screening; Tandem mass spectrometry

Mesh:

Year:  2014        PMID: 25102806     DOI: 10.1016/j.ymgme.2014.07.018

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  22 in total

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Authors:  Chandra Shekar R Ambati; Furong Yuan; Lutfi A Abu-Elheiga; Yiqing Zhang; Vivekananda Shetty
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Authors:  Chiju Yang; Caihong Shi; Cheng Zhou; Qiuhua Wan; Yanbin Zhou; Xigui Chen; Xianlian Jin; Chenggang Huang; Peng Xu
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Review 4.  Genetic etiology and clinical challenges of phenylketonuria.

Authors:  Nasser A Elhawary; Imad A AlJahdali; Iman S Abumansour; Ezzeldin N Elhawary; Nagwa Gaboon; Mohammed Dandini; Abdulelah Madkhali; Wafaa Alosaimi; Abdulmajeed Alzahrani; Fawzia Aljohani; Ehab M Melibary; Osama A Kensara
Journal:  Hum Genomics       Date:  2022-07-19       Impact factor: 6.481

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Authors:  Fatma A Al-Jasmi; Aisha Al-Shamsi; Jozef L Hertecant; Sania M Al-Hamad; Abdul-Kader Souid
Journal:  JIMD Rep       Date:  2015-11-21

Review 6.  Impact of newborn screening on the reported incidence and clinical outcomes associated with medium- and long-chain fatty acid oxidation disorders.

Authors:  Deborah Marsden; Camille L Bedrosian; Jerry Vockley
Journal:  Genet Med       Date:  2021-01-25       Impact factor: 8.822

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8.  Simultaneous determination of 3-hydroxypropionic acid, methylmalonic acid and methylcitric acid in dried blood spots: Second-tier LC-MS/MS assay for newborn screening of propionic acidemia, methylmalonic acidemias and combined remethylation disorders.

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Journal:  PLoS One       Date:  2017-09-15       Impact factor: 3.240

9.  Diagnosis and therapeutic monitoring of inborn errors of metabolism in 100,077 newborns from Jining city in China.

Authors:  Chi-Ju Yang; Na Wei; Ming Li; Kun Xie; Jian-Qiu Li; Cheng-Gang Huang; Yong-Sheng Xiao; Wen-Hua Liu; Xi-Gui Chen
Journal:  BMC Pediatr       Date:  2018-03-13       Impact factor: 2.125

10.  Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.

Authors:  Yasmin Bylstra; Jyn Ling Kuan; Weng Khong Lim; Jaydutt Digambar Bhalshankar; Jing Xian Teo; Sonia Davila; Bin Tean Teh; Steve Rozen; Ene-Choo Tan; Wendy Kein Meng Liew; Khung Keong Yeo; Patrick Tan; Seang Mei Saw; Ching-Yu Cheng; Stuart Cook; Roger Foo; Saumya Shekhar Jamuar
Journal:  Genet Med       Date:  2018-07-02       Impact factor: 8.822

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