Identification of cardiovascular risk components in urban Chinese with metabolic syndrome and application to coronary heart disease prediction: a longitudinal study
Metabolic syndrome (MetS) is proposed as a predictor for cardiovascular disease (CVD). It involves the mechanisms of insulin resistance, obesity, inflammation process of atherosclerosis, and their complex relationship in the metabolic network. Therefore, more cardiovascular risk-related biomarkers w...
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description | Metabolic syndrome (MetS) is proposed as a predictor for cardiovascular disease (CVD). It involves the mechanisms of insulin resistance, obesity, inflammation process of atherosclerosis, and their complex relationship in the metabolic network. Therefore, more cardiovascular risk-related biomarkers within this network should be considered as components of MetS in order to improve the prediction of CVD.
Factor analysis was performed in 5311 (4574 males and 737 females) Han Chinese subjects with MetS to extract CVD-related factors with specific clinical significance from 16 biomarkers tested in routine health check-up. Logistic regression model, based on an extreme case-control design with 445 coronary heart disease (CHD) patients and 890 controls, was performed to evaluate the extracted factors used to identify CHD. Then, Cox model, based on a cohort design with 1923 subjects followed up for 5 years, was conducted to validate their predictive effects. Finally, a synthetic predictor (SP) was created by weighting each factor with their risks for CHD to develop a risk matrix to predicting CHD.
Eight factors were obtained from both males and females with a similar pattern. The AUC to classify CHD under the extreme case-control suggested that SP might serve as a useful tool in identifying CHD with 0.994 (95%CI 0.984-0.998) for males and 0.998 (95%CI 0.982-1.000) for females respectively. In the cohort study, the AUC to predict CHD was 0.871 (95%CI 0.851-0.889) for males and 0.899 (95%CI 0.873-0.921) for females, highlighting that SP was a powerful predictor for CHD. The SP-based 5-year CHD risk matrix provided as convenient tool for CHD risk appraisal.
Eight factors were extracted from sixteen biomarkers in subjects with MetS and the SP adds to new insights into studies of prediction of CHD risk using data from routine health check-up. |
doi_str_mv | 10.1371/journal.pone.0084204 |
format | Article |
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Factor analysis was performed in 5311 (4574 males and 737 females) Han Chinese subjects with MetS to extract CVD-related factors with specific clinical significance from 16 biomarkers tested in routine health check-up. Logistic regression model, based on an extreme case-control design with 445 coronary heart disease (CHD) patients and 890 controls, was performed to evaluate the extracted factors used to identify CHD. Then, Cox model, based on a cohort design with 1923 subjects followed up for 5 years, was conducted to validate their predictive effects. Finally, a synthetic predictor (SP) was created by weighting each factor with their risks for CHD to develop a risk matrix to predicting CHD.
Eight factors were obtained from both males and females with a similar pattern. The AUC to classify CHD under the extreme case-control suggested that SP might serve as a useful tool in identifying CHD with 0.994 (95%CI 0.984-0.998) for males and 0.998 (95%CI 0.982-1.000) for females respectively. In the cohort study, the AUC to predict CHD was 0.871 (95%CI 0.851-0.889) for males and 0.899 (95%CI 0.873-0.921) for females, highlighting that SP was a powerful predictor for CHD. The SP-based 5-year CHD risk matrix provided as convenient tool for CHD risk appraisal.
Eight factors were extracted from sixteen biomarkers in subjects with MetS and the SP adds to new insights into studies of prediction of CHD risk using data from routine health check-up.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0084204</identifier><identifier>PMID: 24358344</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Aged ; Arteriosclerosis ; Atherosclerosis ; Biomarkers ; Blood pressure ; Body mass index ; Cardiovascular disease ; Cardiovascular diseases ; Cardiovascular Diseases - epidemiology ; Cardiovascular Diseases - etiology ; China - epidemiology ; Cholesterol ; Coronary artery disease ; Coronary Disease - epidemiology ; Coronary Disease - etiology ; Coronary heart disease ; Correlation analysis ; Data processing ; Development and progression ; Diabetes ; Disease control ; Epidemiology ; Factor analysis ; Family medical history ; Female ; Females ; Health risk assessment ; Health risks ; Heart ; Heart diseases ; Hospitals ; Humans ; Inflammation ; Insulin ; Insulin resistance ; Laboratories ; Liver diseases ; Longitudinal Studies ; Male ; Males ; Medical research ; Metabolic syndrome ; Metabolic Syndrome - complications ; Middle Aged ; Multivariate analysis ; Obesity ; Population ; Population Surveillance ; Predictions ; Prevalence ; Public health ; Regression analysis ; Regression models ; Researchers ; Risk ; Risk factors ; ROC Curve ; Sex Factors ; Studies ; Type 2 diabetes ; Urban Population ; Uric acid</subject><ispartof>PloS one, 2013-12, Vol.8 (12), p.e84204-e84204</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Zhu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Zhu et al 2013 Zhu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-33c9951e40329e14bb3dbf6ee0cabd82a497e1ed82efc68c58f05930eb6e73f53</citedby><cites>FETCH-LOGICAL-c692t-33c9951e40329e14bb3dbf6ee0cabd82a497e1ed82efc68c58f05930eb6e73f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866125/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866125/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23847,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24358344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Han, Weiqing</contributor><creatorcontrib>Zhu, Zhenxin</creatorcontrib><creatorcontrib>Liu, Yanxun</creatorcontrib><creatorcontrib>Zhang, Chengqi</creatorcontrib><creatorcontrib>Yuan, Zhongshang</creatorcontrib><creatorcontrib>Zhang, Qian</creatorcontrib><creatorcontrib>Tang, Fang</creatorcontrib><creatorcontrib>Lin, Haiyan</creatorcontrib><creatorcontrib>Zhang, Yongyuan</creatorcontrib><creatorcontrib>Liu, Longjian</creatorcontrib><creatorcontrib>Xue, Fuzhong</creatorcontrib><title>Identification of cardiovascular risk components in urban Chinese with metabolic syndrome and application to coronary heart disease prediction: a longitudinal study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Metabolic syndrome (MetS) is proposed as a predictor for cardiovascular disease (CVD). It involves the mechanisms of insulin resistance, obesity, inflammation process of atherosclerosis, and their complex relationship in the metabolic network. Therefore, more cardiovascular risk-related biomarkers within this network should be considered as components of MetS in order to improve the prediction of CVD.
Factor analysis was performed in 5311 (4574 males and 737 females) Han Chinese subjects with MetS to extract CVD-related factors with specific clinical significance from 16 biomarkers tested in routine health check-up. Logistic regression model, based on an extreme case-control design with 445 coronary heart disease (CHD) patients and 890 controls, was performed to evaluate the extracted factors used to identify CHD. Then, Cox model, based on a cohort design with 1923 subjects followed up for 5 years, was conducted to validate their predictive effects. Finally, a synthetic predictor (SP) was created by weighting each factor with their risks for CHD to develop a risk matrix to predicting CHD.
Eight factors were obtained from both males and females with a similar pattern. The AUC to classify CHD under the extreme case-control suggested that SP might serve as a useful tool in identifying CHD with 0.994 (95%CI 0.984-0.998) for males and 0.998 (95%CI 0.982-1.000) for females respectively. In the cohort study, the AUC to predict CHD was 0.871 (95%CI 0.851-0.889) for males and 0.899 (95%CI 0.873-0.921) for females, highlighting that SP was a powerful predictor for CHD. The SP-based 5-year CHD risk matrix provided as convenient tool for CHD risk appraisal.
Eight factors were extracted from sixteen biomarkers in subjects with MetS and the SP adds to new insights into studies of prediction of CHD risk using data from routine health check-up.</description><subject>Adult</subject><subject>Aged</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Biomarkers</subject><subject>Blood pressure</subject><subject>Body mass index</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - etiology</subject><subject>China - epidemiology</subject><subject>Cholesterol</subject><subject>Coronary artery disease</subject><subject>Coronary Disease - epidemiology</subject><subject>Coronary Disease - etiology</subject><subject>Coronary heart disease</subject><subject>Correlation analysis</subject><subject>Data processing</subject><subject>Development and progression</subject><subject>Diabetes</subject><subject>Disease control</subject><subject>Epidemiology</subject><subject>Factor analysis</subject><subject>Family medical history</subject><subject>Female</subject><subject>Females</subject><subject>Health risk assessment</subject><subject>Health risks</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Laboratories</subject><subject>Liver diseases</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Males</subject><subject>Medical research</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - complications</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Obesity</subject><subject>Population</subject><subject>Population Surveillance</subject><subject>Predictions</subject><subject>Prevalence</subject><subject>Public health</subject><subject>Regression analysis</subject><subject>Regression models</subject><subject>Researchers</subject><subject>Risk</subject><subject>Risk factors</subject><subject>ROC Curve</subject><subject>Sex Factors</subject><subject>Studies</subject><subject>Type 2 diabetes</subject><subject>Urban Population</subject><subject>Uric acid</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9tu1DAQhiMEolB4AwSWkBBc7OLYzokLpKrisFKlSpxurYk92XVx7MV2Cn0fHhSHbqsu6gXKRUbON__kH88UxZOSLkvelK_P_BQc2OXWO1xS2gpGxZ3iQdlxtqgZ5XdvxAfFwxjPKK14W9f3iwMmeNVyIR4Uv1caXTKDUZCMd8QPREHQxp9DVJOFQIKJ34ny41zHpUiMI1PowZHjjXEYkfw0aUNGTNB7axSJF04HPyIBpwlst_ZKOvksE7yDcEE2CCERbSJCVtgG1EbN0BsCxHq3NmnSJrsjMQcXj4p7A9iIj3fvw-Lr-3dfjj8uTk4_rI6PThaq7lhacK66ripRUM46LEXfc90PNSJV0OuWgegaLDFHOKi6VVU70KrjFPsaGz5U_LB4dqm7tT7KXYOjLEXdtm3NxUysLgnt4UxugxmzG-nByL8HPqxlNmaURVkjdIyzhvZ9J5qmh0pAz4BxQakeqlnr7a7a1I-oVe5uALsnuv_FmY1c-3M5X2LJZoGXO4Hgf0wYkxxNVGgtOPTT_N8dbXjd1Tyjz_9Bb3e3o9aQDRg3-FxXzaLySDQtE6yrmkwtb6Hyo3E0Kk_JYPL5XsKrvYTMJPyV1jDFKFefP_0_e_ptn31xg80jZdMmejvNgxT3QXEJquBjDDhcN7mkcl6mq27Iecjlbply2tObF3SddLU9_A-ijB5c</recordid><startdate>20131217</startdate><enddate>20131217</enddate><creator>Zhu, Zhenxin</creator><creator>Liu, Yanxun</creator><creator>Zhang, Chengqi</creator><creator>Yuan, Zhongshang</creator><creator>Zhang, Qian</creator><creator>Tang, Fang</creator><creator>Lin, Haiyan</creator><creator>Zhang, Yongyuan</creator><creator>Liu, Longjian</creator><creator>Xue, Fuzhong</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20131217</creationdate><title>Identification of cardiovascular risk components in urban Chinese with metabolic syndrome and application to coronary heart disease prediction: a longitudinal study</title><author>Zhu, Zhenxin ; Liu, Yanxun ; Zhang, Chengqi ; Yuan, Zhongshang ; Zhang, Qian ; Tang, Fang ; Lin, Haiyan ; Zhang, Yongyuan ; Liu, Longjian ; Xue, Fuzhong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-33c9951e40329e14bb3dbf6ee0cabd82a497e1ed82efc68c58f05930eb6e73f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Biomarkers</topic><topic>Blood pressure</topic><topic>Body mass index</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>Cardiovascular Diseases - etiology</topic><topic>China - epidemiology</topic><topic>Cholesterol</topic><topic>Coronary artery disease</topic><topic>Coronary Disease - epidemiology</topic><topic>Coronary Disease - etiology</topic><topic>Coronary heart disease</topic><topic>Correlation analysis</topic><topic>Data processing</topic><topic>Development and progression</topic><topic>Diabetes</topic><topic>Disease control</topic><topic>Epidemiology</topic><topic>Factor analysis</topic><topic>Family medical history</topic><topic>Female</topic><topic>Females</topic><topic>Health risk assessment</topic><topic>Health risks</topic><topic>Heart</topic><topic>Heart diseases</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Laboratories</topic><topic>Liver diseases</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Males</topic><topic>Medical research</topic><topic>Metabolic syndrome</topic><topic>Metabolic Syndrome - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>TestCollectionTL3OpenAccess</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Zhenxin</au><au>Liu, Yanxun</au><au>Zhang, Chengqi</au><au>Yuan, Zhongshang</au><au>Zhang, Qian</au><au>Tang, Fang</au><au>Lin, Haiyan</au><au>Zhang, Yongyuan</au><au>Liu, Longjian</au><au>Xue, Fuzhong</au><au>Han, Weiqing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of cardiovascular risk components in urban Chinese with metabolic syndrome and application to coronary heart disease prediction: a longitudinal study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-12-17</date><risdate>2013</risdate><volume>8</volume><issue>12</issue><spage>e84204</spage><epage>e84204</epage><pages>e84204-e84204</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Metabolic syndrome (MetS) is proposed as a predictor for cardiovascular disease (CVD). It involves the mechanisms of insulin resistance, obesity, inflammation process of atherosclerosis, and their complex relationship in the metabolic network. Therefore, more cardiovascular risk-related biomarkers within this network should be considered as components of MetS in order to improve the prediction of CVD.
Factor analysis was performed in 5311 (4574 males and 737 females) Han Chinese subjects with MetS to extract CVD-related factors with specific clinical significance from 16 biomarkers tested in routine health check-up. Logistic regression model, based on an extreme case-control design with 445 coronary heart disease (CHD) patients and 890 controls, was performed to evaluate the extracted factors used to identify CHD. Then, Cox model, based on a cohort design with 1923 subjects followed up for 5 years, was conducted to validate their predictive effects. Finally, a synthetic predictor (SP) was created by weighting each factor with their risks for CHD to develop a risk matrix to predicting CHD.
Eight factors were obtained from both males and females with a similar pattern. The AUC to classify CHD under the extreme case-control suggested that SP might serve as a useful tool in identifying CHD with 0.994 (95%CI 0.984-0.998) for males and 0.998 (95%CI 0.982-1.000) for females respectively. In the cohort study, the AUC to predict CHD was 0.871 (95%CI 0.851-0.889) for males and 0.899 (95%CI 0.873-0.921) for females, highlighting that SP was a powerful predictor for CHD. The SP-based 5-year CHD risk matrix provided as convenient tool for CHD risk appraisal.
Eight factors were extracted from sixteen biomarkers in subjects with MetS and the SP adds to new insights into studies of prediction of CHD risk using data from routine health check-up.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24358344</pmid><doi>10.1371/journal.pone.0084204</doi><tpages>e84204</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Arteriosclerosis Atherosclerosis Biomarkers Blood pressure Body mass index Cardiovascular disease Cardiovascular diseases Cardiovascular Diseases - epidemiology Cardiovascular Diseases - etiology China - epidemiology Cholesterol Coronary artery disease Coronary Disease - epidemiology Coronary Disease - etiology Coronary heart disease Correlation analysis Data processing Development and progression Diabetes Disease control Epidemiology Factor analysis Family medical history Female Females Health risk assessment Health risks Heart Heart diseases Hospitals Humans Inflammation Insulin Insulin resistance Laboratories Liver diseases Longitudinal Studies Male Males Medical research Metabolic syndrome Metabolic Syndrome - complications Middle Aged Multivariate analysis Obesity Population Population Surveillance Predictions Prevalence Public health Regression analysis Regression models Researchers Risk Risk factors ROC Curve Sex Factors Studies Type 2 diabetes Urban Population Uric acid |
title | Identification of cardiovascular risk components in urban Chinese with metabolic syndrome and application to coronary heart disease prediction: a longitudinal study |
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