Cargando…

A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population

BACKGROUND: Many MetS related biomarkers had been discovered, which provided the possibility for building the MetS prediction model. In this paper we aimed to develop a novel routine biomarker-based risk prediction model for MetS in urban Han Chinese population. METHODS: Exploring Factor analysis (E...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Wenchao, Chen, Qicai, Yuan, Zhongshang, Liu, Jing, Du, Zhaohui, Tang, Fang, Jia, Hongying, Xue, Fuzhong, Zhang, Chengqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320489/
https://www.ncbi.nlm.nih.gov/pubmed/25637138
http://dx.doi.org/10.1186/s12889-015-1424-z
_version_ 1782356124986507264
author Zhang, Wenchao
Chen, Qicai
Yuan, Zhongshang
Liu, Jing
Du, Zhaohui
Tang, Fang
Jia, Hongying
Xue, Fuzhong
Zhang, Chengqi
author_facet Zhang, Wenchao
Chen, Qicai
Yuan, Zhongshang
Liu, Jing
Du, Zhaohui
Tang, Fang
Jia, Hongying
Xue, Fuzhong
Zhang, Chengqi
author_sort Zhang, Wenchao
collection PubMed
description BACKGROUND: Many MetS related biomarkers had been discovered, which provided the possibility for building the MetS prediction model. In this paper we aimed to develop a novel routine biomarker-based risk prediction model for MetS in urban Han Chinese population. METHODS: Exploring Factor analysis (EFA) was firstly conducted in MetS positive 13,345 males and 3,212 females respectively for extracting synthetic latent predictors (SLPs) from 11 routine biomarkers. Then, depending on the cohort with 5 years follow-up in 1,565 subjects (male 1,020 and female 545), a Cox model for predicting 5 years MetS was built by using SLPs as predictor; Area under the ROC curves (AUC) with 10 fold cross validation was used to evaluate its power. Absolute risk (AR) and relative absolute risk (RAR) were calculated to develop a risk matrix for visualization of risk assessment. RESULTS: Six SLPs were extracted by EFA from 11 routine health check-up biomarkers. Each of them reflected the specific pathogenesis of MetS, with inflammatory factor (IF) contributed by WBC & LC & NGC, erythrocyte parameter factor (EPF) by Hb & HCT, blood pressure factor (BPF) by SBP & DBP, lipid metabolism factor (LMF) by TG & HDL-C, obesity condition factor (OCF) by BMI, and glucose metabolism factor (GMF) by FBG with the total contribution of 81.55% and 79.65% for males and females respectively. The proposed metabolic syndrome synthetic predictor (MSP) based predict model demonstrated good performance for predicting 5 years MetS with the AUC of 0.802 (95% CI 0.776-0.826) in males and 0.902 (95% CI 0.874-0.925) in females respectively, even after 10 fold cross validation, AUC was still enough high with 0.796 (95% CI 0.770-0.821) in males and 0.897 (95% CI 0.868-0.921) in females. More importantly, the MSP based risk matrix with a series of risk warning index provided a feasible and practical tool for visualization of risk assessment in the prediction of MetS. CONCLUSIONS: MetS could be explained by six SLPs in Chinese urban Han population. The proposed MSP based predict model demonstrated good performance for predicting 5 years MetS, and the MetS-based matrix provided a feasible and practical tool. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12889-015-1424-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4320489
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-43204892015-02-08 A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population Zhang, Wenchao Chen, Qicai Yuan, Zhongshang Liu, Jing Du, Zhaohui Tang, Fang Jia, Hongying Xue, Fuzhong Zhang, Chengqi BMC Public Health Research Article BACKGROUND: Many MetS related biomarkers had been discovered, which provided the possibility for building the MetS prediction model. In this paper we aimed to develop a novel routine biomarker-based risk prediction model for MetS in urban Han Chinese population. METHODS: Exploring Factor analysis (EFA) was firstly conducted in MetS positive 13,345 males and 3,212 females respectively for extracting synthetic latent predictors (SLPs) from 11 routine biomarkers. Then, depending on the cohort with 5 years follow-up in 1,565 subjects (male 1,020 and female 545), a Cox model for predicting 5 years MetS was built by using SLPs as predictor; Area under the ROC curves (AUC) with 10 fold cross validation was used to evaluate its power. Absolute risk (AR) and relative absolute risk (RAR) were calculated to develop a risk matrix for visualization of risk assessment. RESULTS: Six SLPs were extracted by EFA from 11 routine health check-up biomarkers. Each of them reflected the specific pathogenesis of MetS, with inflammatory factor (IF) contributed by WBC & LC & NGC, erythrocyte parameter factor (EPF) by Hb & HCT, blood pressure factor (BPF) by SBP & DBP, lipid metabolism factor (LMF) by TG & HDL-C, obesity condition factor (OCF) by BMI, and glucose metabolism factor (GMF) by FBG with the total contribution of 81.55% and 79.65% for males and females respectively. The proposed metabolic syndrome synthetic predictor (MSP) based predict model demonstrated good performance for predicting 5 years MetS with the AUC of 0.802 (95% CI 0.776-0.826) in males and 0.902 (95% CI 0.874-0.925) in females respectively, even after 10 fold cross validation, AUC was still enough high with 0.796 (95% CI 0.770-0.821) in males and 0.897 (95% CI 0.868-0.921) in females. More importantly, the MSP based risk matrix with a series of risk warning index provided a feasible and practical tool for visualization of risk assessment in the prediction of MetS. CONCLUSIONS: MetS could be explained by six SLPs in Chinese urban Han population. The proposed MSP based predict model demonstrated good performance for predicting 5 years MetS, and the MetS-based matrix provided a feasible and practical tool. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12889-015-1424-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-31 /pmc/articles/PMC4320489/ /pubmed/25637138 http://dx.doi.org/10.1186/s12889-015-1424-z Text en © Zhang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Wenchao
Chen, Qicai
Yuan, Zhongshang
Liu, Jing
Du, Zhaohui
Tang, Fang
Jia, Hongying
Xue, Fuzhong
Zhang, Chengqi
A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population
title A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population
title_full A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population
title_fullStr A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population
title_full_unstemmed A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population
title_short A routine biomarker-based risk prediction model for metabolic syndrome in urban Han Chinese population
title_sort routine biomarker-based risk prediction model for metabolic syndrome in urban han chinese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320489/
https://www.ncbi.nlm.nih.gov/pubmed/25637138
http://dx.doi.org/10.1186/s12889-015-1424-z
work_keys_str_mv AT zhangwenchao aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT chenqicai aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT yuanzhongshang aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT liujing aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT duzhaohui aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT tangfang aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT jiahongying aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT xuefuzhong aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT zhangchengqi aroutinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT zhangwenchao routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT chenqicai routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT yuanzhongshang routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT liujing routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT duzhaohui routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT tangfang routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT jiahongying routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT xuefuzhong routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation
AT zhangchengqi routinebiomarkerbasedriskpredictionmodelformetabolicsyndromeinurbanhanchinesepopulation