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A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit

Inborn errors of metabolism (IEMs) have great repercussions in neonatal intensive care units (NICUs). However, the integrative analysis of the incidence for full-term and premature neonates of IEMs in NICUs have not been reported. In this study, we aimed to estimate the incidence of IEMs in the NICU...

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Autores principales: Zhang, Wanqiao, Yang, Yao, Peng, Wei, Chang, Juan, Mei, Yabo, Yan, Lei, Chen, Yuhan, Wei, Xiujuan, Liu, Yabin, Wang, Yan, Feng, Zhichun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967400/
https://www.ncbi.nlm.nih.gov/pubmed/31998365
http://dx.doi.org/10.3389/fgene.2019.01302
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author Zhang, Wanqiao
Yang, Yao
Peng, Wei
Chang, Juan
Mei, Yabo
Yan, Lei
Chen, Yuhan
Wei, Xiujuan
Liu, Yabin
Wang, Yan
Feng, Zhichun
author_facet Zhang, Wanqiao
Yang, Yao
Peng, Wei
Chang, Juan
Mei, Yabo
Yan, Lei
Chen, Yuhan
Wei, Xiujuan
Liu, Yabin
Wang, Yan
Feng, Zhichun
author_sort Zhang, Wanqiao
collection PubMed
description Inborn errors of metabolism (IEMs) have great repercussions in neonatal intensive care units (NICUs). However, the integrative analysis of the incidence for full-term and premature neonates of IEMs in NICUs have not been reported. In this study, we aimed to estimate the incidence of IEMs in the NICU population so as to better evaluate the impact of IEMs on Chinese NICUs. A total of 42,257 newborns (proportion of premature as 36.7%) enrolled to the largest Chinese NICU center for a sequential 7 years screen, and 66 were diagnosed with IEMs. The prevalence of IEMs in total, full-term, and premature infants was 1:640, 1:446, and 1:2,584, respectively. In spectrum of our NICU, diseases that cause endogenous intoxication like methylmalonic acidemia accounted for 93.9% (62/66), and this ratio was higher in full-term infants with 98.3% (59/60), while the most prevalent disease in premature newborn was hyperphenylalaninemia (50%, 3/6), respectively. The genetic analysis of 49 cases revealed 62 potentially pathogenic mutations in 10 well-documented pathogenic genes of IEMs, among which 21 were novel. In conclusion, differences in incidence and spectrum of full-term and premature births we obtained in NICU will provide diagnostic guidelines and therapeutic clues of neonatal IEMs for pediatricians.
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spelling pubmed-69674002020-01-29 A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit Zhang, Wanqiao Yang, Yao Peng, Wei Chang, Juan Mei, Yabo Yan, Lei Chen, Yuhan Wei, Xiujuan Liu, Yabin Wang, Yan Feng, Zhichun Front Genet Genetics Inborn errors of metabolism (IEMs) have great repercussions in neonatal intensive care units (NICUs). However, the integrative analysis of the incidence for full-term and premature neonates of IEMs in NICUs have not been reported. In this study, we aimed to estimate the incidence of IEMs in the NICU population so as to better evaluate the impact of IEMs on Chinese NICUs. A total of 42,257 newborns (proportion of premature as 36.7%) enrolled to the largest Chinese NICU center for a sequential 7 years screen, and 66 were diagnosed with IEMs. The prevalence of IEMs in total, full-term, and premature infants was 1:640, 1:446, and 1:2,584, respectively. In spectrum of our NICU, diseases that cause endogenous intoxication like methylmalonic acidemia accounted for 93.9% (62/66), and this ratio was higher in full-term infants with 98.3% (59/60), while the most prevalent disease in premature newborn was hyperphenylalaninemia (50%, 3/6), respectively. The genetic analysis of 49 cases revealed 62 potentially pathogenic mutations in 10 well-documented pathogenic genes of IEMs, among which 21 were novel. In conclusion, differences in incidence and spectrum of full-term and premature births we obtained in NICU will provide diagnostic guidelines and therapeutic clues of neonatal IEMs for pediatricians. Frontiers Media S.A. 2020-01-10 /pmc/articles/PMC6967400/ /pubmed/31998365 http://dx.doi.org/10.3389/fgene.2019.01302 Text en Copyright © 2020 Zhang, Yang, Peng, Chang, Mei, Yan, Chen, Wei, Liu, Wang and Feng http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Zhang, Wanqiao
Yang, Yao
Peng, Wei
Chang, Juan
Mei, Yabo
Yan, Lei
Chen, Yuhan
Wei, Xiujuan
Liu, Yabin
Wang, Yan
Feng, Zhichun
A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
title A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
title_full A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
title_fullStr A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
title_full_unstemmed A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
title_short A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
title_sort 7-year report of spectrum of inborn errors of metabolism on full-term and premature infants in a chinese neonatal intensive care unit
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967400/
https://www.ncbi.nlm.nih.gov/pubmed/31998365
http://dx.doi.org/10.3389/fgene.2019.01302
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