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A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns
BACKGROUND: Newborn screening (NBS) in China is mainly aimed at detecting biochemical levels of metabolites in the blood, which may generate false-positive/negative results. Current biochemical NBS includes tandem mass spectrometry (MS/MS) screening for metabolites as well as phenylalanine (Phe), th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575988/ https://www.ncbi.nlm.nih.gov/pubmed/33145277 http://dx.doi.org/10.21037/atm-20-1147 |
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author | Luo, Xiaomei Sun, Yu Xu, Feng Guo, Jun Li, Lin Lin, Zhiwei Ye, Jun Gu, Xuefan Yu, Yongguo |
author_facet | Luo, Xiaomei Sun, Yu Xu, Feng Guo, Jun Li, Lin Lin, Zhiwei Ye, Jun Gu, Xuefan Yu, Yongguo |
author_sort | Luo, Xiaomei |
collection | PubMed |
description | BACKGROUND: Newborn screening (NBS) in China is mainly aimed at detecting biochemical levels of metabolites in the blood, which may generate false-positive/negative results. Current biochemical NBS includes tandem mass spectrometry (MS/MS) screening for metabolites as well as phenylalanine (Phe), thyroid-stimulating hormone (TSH), 17-α-hydroxyprogesterone (17-OHP), and glucose-6-phosphate dehydrogenase (G6PD) test. This study intended to explore whether next-generation sequencing (NGS) for dried blood spots combining with biochemical screening could improve the current screening efficiency and to investigate the carrier frequencies of mutations in causative genes related to amino acid metabolism, organic acid metabolism, and fatty acid oxidation in this cohort. METHODS: We designed a panel of 573 genes related to severe inherited disorders and performed NGS in 1,127 individuals who had undergone biochemical NBS. The NGS screening results of neonates were used to compare with the biochemical results. RESULTS: NGS screening results revealed that all the four newborns with abnormal G6PD values carried hemizygous G6PD mutations, which were consistent with the decreased G6PD enzymatic activity. The NGS results revealed an individual with compound heterozygous mutations of SLC22A5, who was biochemically negative in 2016. The MS/MS screening results in 2019 showed free carnitine deficiency, which was consistent with the genetic findings. The top five genes with the highest carrier frequencies of mutations in these newborns were PAH (1:56, 1.79%), ETFDH (1:81, 1.23%), MMACHC (1:87, 1.15%), SLC25A13 (1:102, 0.98%), and GCDH (1:125, 0.80%). CONCLUSIONS: Our study highlighted that combining NGS screening with biochemical screening could improve the current NBS efficiency. This is the first study to investigate carrier frequencies of mutations in 77 genes causing inherited metabolic diseases (IMDs) in China. |
format | Online Article Text |
id | pubmed-7575988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-75759882020-11-02 A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns Luo, Xiaomei Sun, Yu Xu, Feng Guo, Jun Li, Lin Lin, Zhiwei Ye, Jun Gu, Xuefan Yu, Yongguo Ann Transl Med Original Article BACKGROUND: Newborn screening (NBS) in China is mainly aimed at detecting biochemical levels of metabolites in the blood, which may generate false-positive/negative results. Current biochemical NBS includes tandem mass spectrometry (MS/MS) screening for metabolites as well as phenylalanine (Phe), thyroid-stimulating hormone (TSH), 17-α-hydroxyprogesterone (17-OHP), and glucose-6-phosphate dehydrogenase (G6PD) test. This study intended to explore whether next-generation sequencing (NGS) for dried blood spots combining with biochemical screening could improve the current screening efficiency and to investigate the carrier frequencies of mutations in causative genes related to amino acid metabolism, organic acid metabolism, and fatty acid oxidation in this cohort. METHODS: We designed a panel of 573 genes related to severe inherited disorders and performed NGS in 1,127 individuals who had undergone biochemical NBS. The NGS screening results of neonates were used to compare with the biochemical results. RESULTS: NGS screening results revealed that all the four newborns with abnormal G6PD values carried hemizygous G6PD mutations, which were consistent with the decreased G6PD enzymatic activity. The NGS results revealed an individual with compound heterozygous mutations of SLC22A5, who was biochemically negative in 2016. The MS/MS screening results in 2019 showed free carnitine deficiency, which was consistent with the genetic findings. The top five genes with the highest carrier frequencies of mutations in these newborns were PAH (1:56, 1.79%), ETFDH (1:81, 1.23%), MMACHC (1:87, 1.15%), SLC25A13 (1:102, 0.98%), and GCDH (1:125, 0.80%). CONCLUSIONS: Our study highlighted that combining NGS screening with biochemical screening could improve the current NBS efficiency. This is the first study to investigate carrier frequencies of mutations in 77 genes causing inherited metabolic diseases (IMDs) in China. AME Publishing Company 2020-09 /pmc/articles/PMC7575988/ /pubmed/33145277 http://dx.doi.org/10.21037/atm-20-1147 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Luo, Xiaomei Sun, Yu Xu, Feng Guo, Jun Li, Lin Lin, Zhiwei Ye, Jun Gu, Xuefan Yu, Yongguo A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns |
title | A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns |
title_full | A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns |
title_fullStr | A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns |
title_full_unstemmed | A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns |
title_short | A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns |
title_sort | pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in china: results from 1,127 newborns |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575988/ https://www.ncbi.nlm.nih.gov/pubmed/33145277 http://dx.doi.org/10.21037/atm-20-1147 |
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