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Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method
BACKGROUND: Reference interval (RI) research is to make it a concise, effective, and practical diagnostic tool. This study aimed to establish sex- and age-specific RI for myocardial enzyme activity in population aged 1–<18 years old in Changchun, China. METHODS: Healthy subjects (n = 6,322, 1–<...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150721/ https://www.ncbi.nlm.nih.gov/pubmed/32328149 http://dx.doi.org/10.1155/2020/2013148 |
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author | Guo, Wenjia Zhou, Qi Jia, Yanan Xu, Jiancheng |
author_facet | Guo, Wenjia Zhou, Qi Jia, Yanan Xu, Jiancheng |
author_sort | Guo, Wenjia |
collection | PubMed |
description | BACKGROUND: Reference interval (RI) research is to make it a concise, effective, and practical diagnostic tool. This study aimed to establish sex- and age-specific RI for myocardial enzyme activity in population aged 1–<18 years old in Changchun, China. METHODS: Healthy subjects (n = 6,322, 1–<18 years old) were recruited from communities and schools. Aspartate aminotransferase (AST), lactate dehydrogenase (LDH), creatine kinase (CK), and creatine kinase isoenzyme (CKMB) were measured using an automatic biochemical analyzer. Fisher's optimal segmentation method was used to partition by including percentiles as impact factors, aiming at minimizing the sum of the squares of the total dispersion into groups as splitting sequence of ordered data. RESULTS: AST decreased gradually and was partitioned as 1, 2∼<10 and 10∼<18 years old. LDH presented disparate descending rate among 1∼<4, 4∼<12, and 12∼<18 years old. CK stood quite stable with the same RI in all ages. CKMB began to differ at 6 years of age sexually and then remained stable during 6∼<14 years old for male while it continued to decline in female. Cardiac development was partitioned as 1∼<6, 6∼<13, and 13∼<18 years old using multiple percentiles from massive data that reflect characteristics of totality as impact factors. CONCLUSIONS: Fisher's optimal segmentation method excelled for multidimensionality, continuity, and loop calculating as dealing with RIs for myocardial enzymes activity and cardiac development process despite limitations. In future, impact of partition on the overall interval should be delved into. |
format | Online Article Text |
id | pubmed-7150721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-71507212020-04-23 Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method Guo, Wenjia Zhou, Qi Jia, Yanan Xu, Jiancheng Comput Math Methods Med Research Article BACKGROUND: Reference interval (RI) research is to make it a concise, effective, and practical diagnostic tool. This study aimed to establish sex- and age-specific RI for myocardial enzyme activity in population aged 1–<18 years old in Changchun, China. METHODS: Healthy subjects (n = 6,322, 1–<18 years old) were recruited from communities and schools. Aspartate aminotransferase (AST), lactate dehydrogenase (LDH), creatine kinase (CK), and creatine kinase isoenzyme (CKMB) were measured using an automatic biochemical analyzer. Fisher's optimal segmentation method was used to partition by including percentiles as impact factors, aiming at minimizing the sum of the squares of the total dispersion into groups as splitting sequence of ordered data. RESULTS: AST decreased gradually and was partitioned as 1, 2∼<10 and 10∼<18 years old. LDH presented disparate descending rate among 1∼<4, 4∼<12, and 12∼<18 years old. CK stood quite stable with the same RI in all ages. CKMB began to differ at 6 years of age sexually and then remained stable during 6∼<14 years old for male while it continued to decline in female. Cardiac development was partitioned as 1∼<6, 6∼<13, and 13∼<18 years old using multiple percentiles from massive data that reflect characteristics of totality as impact factors. CONCLUSIONS: Fisher's optimal segmentation method excelled for multidimensionality, continuity, and loop calculating as dealing with RIs for myocardial enzymes activity and cardiac development process despite limitations. In future, impact of partition on the overall interval should be delved into. Hindawi 2020-03-31 /pmc/articles/PMC7150721/ /pubmed/32328149 http://dx.doi.org/10.1155/2020/2013148 Text en Copyright © 2020 Wenjia Guo et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Guo, Wenjia Zhou, Qi Jia, Yanan Xu, Jiancheng Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method |
title | Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method |
title_full | Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method |
title_fullStr | Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method |
title_full_unstemmed | Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method |
title_short | Division of Myocardial Enzyme Reference Intervals in Population Aged 1 to <18 Years Old Based on Fisher's Optimal Segmentation Method |
title_sort | division of myocardial enzyme reference intervals in population aged 1 to <18 years old based on fisher's optimal segmentation method |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150721/ https://www.ncbi.nlm.nih.gov/pubmed/32328149 http://dx.doi.org/10.1155/2020/2013148 |
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