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China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases

BACKGROUND: Inherited metabolic disorders (IMDs) usually occurs at young age and hence it severely threatening the health and life of young people. While so far there lacks a comprehensive study which can reveals China’s nationwide landscape of IMDs. This study aimed to evaluate IMDs incidence and r...

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Autores principales: Zhao, Beibei, Chen, Peichun, She, Xuhui, Chen, Xiuru, Ni, Zhou, Zhou, Duo, Yu, Zinan, Liu, Chang, Huang, Xinwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398906/
https://www.ncbi.nlm.nih.gov/pubmed/37537594
http://dx.doi.org/10.1186/s13023-023-02834-y
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author Zhao, Beibei
Chen, Peichun
She, Xuhui
Chen, Xiuru
Ni, Zhou
Zhou, Duo
Yu, Zinan
Liu, Chang
Huang, Xinwen
author_facet Zhao, Beibei
Chen, Peichun
She, Xuhui
Chen, Xiuru
Ni, Zhou
Zhou, Duo
Yu, Zinan
Liu, Chang
Huang, Xinwen
author_sort Zhao, Beibei
collection PubMed
description BACKGROUND: Inherited metabolic disorders (IMDs) usually occurs at young age and hence it severely threatening the health and life of young people. While so far there lacks a comprehensive study which can reveals China’s nationwide landscape of IMDs. This study aimed to evaluate IMDs incidence and regional distributions in China at a national and province level to guide clinicians and policy makers. METHODS: The retrospective study conducted from January 2012 to March 2021, we analyzed and characterized 372255 cases’ clinical test information and diagnostic data from KingMed Diagnostics Laboratory. The samples were from 32 provincial regions of China, the urine organic acids were detected by gas chromatography-mass spectrometry (GC–MS), amino acids and acylcarnitines in dried blood spots were detected by liquid chromatography-tandem mass spectrometry (LC–MS/MS). We did a statistical analysis of the distribution of the 16 most common IMDs in amino acid disorders and organic acidemias, and then paid special attention to analyze the age and regional distributions of different IMDs. The statistical analyses and visualization analysis were performed with the programming language R (version 4.2.1). RESULTS: There were 4911 positive cases diagnosed, which was 1.32% of the total sample during the ten-year study period. Most diseases tended to occur at ages younger than 18 year-old. The Ornithine Transcarbamylase Deficiency tended to progress on male infants who were less than 28 days old. While the peak of the positive case number of Citrin Deficiency disease (CD) was at 1–6 months. Different IMDs’ had different distribution patterns in China’s provinces. Methylmalonic Acidemias and Hyperphenylalaninemia had an imbalanced distribution pattern in China and its positive rate was significantly higher in North China than South China. Conversely, the positive rate of CD was significantly higher in South China than North China. CONCLUSIONS: Results of this work, such as the differences in distribution pattern of different diseases in terms of age, region, etc. provide important insights and references for clinicians, researchers and healthcare policy makers. The policy makers could optimize the better health screening programs for covering children and infants in specific ages and regions based on our findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02834-y.
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spelling pubmed-103989062023-08-04 China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases Zhao, Beibei Chen, Peichun She, Xuhui Chen, Xiuru Ni, Zhou Zhou, Duo Yu, Zinan Liu, Chang Huang, Xinwen Orphanet J Rare Dis Research BACKGROUND: Inherited metabolic disorders (IMDs) usually occurs at young age and hence it severely threatening the health and life of young people. While so far there lacks a comprehensive study which can reveals China’s nationwide landscape of IMDs. This study aimed to evaluate IMDs incidence and regional distributions in China at a national and province level to guide clinicians and policy makers. METHODS: The retrospective study conducted from January 2012 to March 2021, we analyzed and characterized 372255 cases’ clinical test information and diagnostic data from KingMed Diagnostics Laboratory. The samples were from 32 provincial regions of China, the urine organic acids were detected by gas chromatography-mass spectrometry (GC–MS), amino acids and acylcarnitines in dried blood spots were detected by liquid chromatography-tandem mass spectrometry (LC–MS/MS). We did a statistical analysis of the distribution of the 16 most common IMDs in amino acid disorders and organic acidemias, and then paid special attention to analyze the age and regional distributions of different IMDs. The statistical analyses and visualization analysis were performed with the programming language R (version 4.2.1). RESULTS: There were 4911 positive cases diagnosed, which was 1.32% of the total sample during the ten-year study period. Most diseases tended to occur at ages younger than 18 year-old. The Ornithine Transcarbamylase Deficiency tended to progress on male infants who were less than 28 days old. While the peak of the positive case number of Citrin Deficiency disease (CD) was at 1–6 months. Different IMDs’ had different distribution patterns in China’s provinces. Methylmalonic Acidemias and Hyperphenylalaninemia had an imbalanced distribution pattern in China and its positive rate was significantly higher in North China than South China. Conversely, the positive rate of CD was significantly higher in South China than North China. CONCLUSIONS: Results of this work, such as the differences in distribution pattern of different diseases in terms of age, region, etc. provide important insights and references for clinicians, researchers and healthcare policy makers. The policy makers could optimize the better health screening programs for covering children and infants in specific ages and regions based on our findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02834-y. BioMed Central 2023-08-03 /pmc/articles/PMC10398906/ /pubmed/37537594 http://dx.doi.org/10.1186/s13023-023-02834-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhao, Beibei
Chen, Peichun
She, Xuhui
Chen, Xiuru
Ni, Zhou
Zhou, Duo
Yu, Zinan
Liu, Chang
Huang, Xinwen
China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
title China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
title_full China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
title_fullStr China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
title_full_unstemmed China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
title_short China nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
title_sort china nationwide landscape of 16 types inherited metabolic disorders: a retrospective analysis on 372,255 clinical cases
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398906/
https://www.ncbi.nlm.nih.gov/pubmed/37537594
http://dx.doi.org/10.1186/s13023-023-02834-y
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