Development and validation of an age-sex-ethnicity-specific metabolic syndrome score in the Chinese adults
Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethn...
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Published in | Nature communications Vol. 14; no. 1; pp. 6988 - 14 |
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01.11.2023
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Abstract | Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals.
Metabolic syndrome (MetS) could predict future risk for cardiovascular diseases (CVDs), but the traditionally defined dichotomous MetS cannot reflect MetS severity and demographic variations. Here, the authors develop a continuous, age-sex-ethnicity-specific MetS score to better identify CVD risk in a Chinese population. |
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AbstractList | Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals.
Metabolic syndrome (MetS) could predict future risk for cardiovascular diseases (CVDs), but the traditionally defined dichotomous MetS cannot reflect MetS severity and demographic variations. Here, the authors develop a continuous, age-sex-ethnicity-specific MetS score to better identify CVD risk in a Chinese population. Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals.Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals. Abstract Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals. Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals. Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the traditionally defined dichotomous MetS neither reflected MetS severity nor considered demographic variations. Here we develop a continuous, age-sex-ethnicity-specific MetS score based on continuous measures of the five metabolic dysfunctions (waist circumference [WC], triglycerides [TG], high-density lipoprotein cholesterol [HDL-C], mean arterial pressure [MAP], and fasting blood glucose [FBG]). We find that the weights of metabolic dysfunctions in the score vary across age-sex-ethnicity-specific subgroups, with higher weights for TG, HDL-C, and WC. Each unit increase in the score is associated with increased risks for hyperlipidemia, diabetes, and hypertension, and elevated levels of HbA1c, cholesterol, body mass index, and serum uric acid. The score shows high sensitivity and accuracy for detecting CVD-related risk factors and is validated in different geographical regions. Our study would advance early identification of CVD risks and, more broadly, preventive medicine and sustainable development goals.Metabolic syndrome (MetS) could predict future risk for cardiovascular diseases (CVDs), but the traditionally defined dichotomous MetS cannot reflect MetS severity and demographic variations. Here, the authors develop a continuous, age-sex-ethnicity-specific MetS score to better identify CVD risk in a Chinese population. |
ArticleNumber | 6988 |
Author | Feng, Chuanteng Shao, Ying Yang, Shujuan Yu, Wanqi Li, Xiaoqing Yu, Bin Jia, Peng Dai, Shaoqing Zhao, Xing He, Tianjing |
Author_xml | – sequence: 1 givenname: Shujuan orcidid: 0000-0002-6929-4823 surname: Yang fullname: Yang, Shujuan email: rekiny@126.com organization: West China School of Public Health and West China Fourth Hospital, Sichuan University, International Institute of Spatial Lifecourse Health (ISLE), Wuhan University – sequence: 2 givenname: Bin surname: Yu fullname: Yu, Bin organization: International Institute of Spatial Lifecourse Health (ISLE), Wuhan University, Institute for Disaster Management and Reconstruction, Sichuan University – sequence: 3 givenname: Wanqi surname: Yu fullname: Yu, Wanqi organization: International Institute of Spatial Lifecourse Health (ISLE), Wuhan University – sequence: 4 givenname: Shaoqing orcidid: 0000-0003-0858-4728 surname: Dai fullname: Dai, Shaoqing organization: International Institute of Spatial Lifecourse Health (ISLE), Wuhan University, Faculty of Geo-information Science and Earth Observation, University of Twente – sequence: 5 givenname: Chuanteng surname: Feng fullname: Feng, Chuanteng organization: International Institute of Spatial Lifecourse Health (ISLE), Wuhan University, Institute for Disaster Management and Reconstruction, Sichuan University – sequence: 6 givenname: Ying surname: Shao fullname: Shao, Ying organization: Yunnan Center for Disease Control and Prevention – sequence: 7 givenname: Xing surname: Zhao fullname: Zhao, Xing organization: West China School of Public Health and West China Fourth Hospital, Sichuan University – sequence: 8 givenname: Xiaoqing surname: Li fullname: Li, Xiaoqing organization: Fujian Provincial Center for Disease Control and Prevention – sequence: 9 givenname: Tianjing surname: He fullname: He, Tianjing organization: Hubei Provincial Center for Disease Control and Prevention – sequence: 10 givenname: Peng orcidid: 0000-0003-0110-3637 surname: Jia fullname: Jia, Peng email: jiapengff@hotmail.com organization: International Institute of Spatial Lifecourse Health (ISLE), Wuhan University, School of Resource and Environmental Sciences, Wuhan University, Hubei Luojia Laboratory, School of Public Health, Wuhan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37914709$$D View this record in MEDLINE/PubMed |
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Diabetes201632623627 GurkaMJIndependent associations between a metabolic syndrome severity score and future diabetes by sex and race: the Atherosclerosis Risk In Communities Study and Jackson Heart StudyDiabetologia2017601261127028378033548178310.1007/s00125-017-4267-6 RochlaniYPothineniNVKovelamudiSMehtaJLMetabolic syndrome: pathophysiology, management, and modulation by natural compoundsTher. Adv. Cardiovasc Dis.2017112152251:CAS:528:DC%2BC1cXhvVSgsL8%3D28639538593358010.1177/1753944717711379 Zhang, X. et al. Geographic Variation in Prevalence of Adult Obesity in China: Results From the 2013–2014 National Chronic Disease and Risk Factor Surveillance. Annals of internal medicine, https://doi.org/10.7326/M19-0477 (2019). JiaPSpatial lifecourse epidemiologyLancet Planet. Health20193e57e593079740610.1016/S2542-5196(18)30245-6 HuangQAssociation between metabolic syndrome and microvascular complications in Chinese adults with Type 1 Diabetes MellitusDiabetes Metab. J.202246931033446501610.4093/dmj.2020.0240 ZhaoDLiuJWangMZhangXZhouMEpidemiology of cardiovascular disease in China: current features and implicationsNat. Rev. Cardiol.2019162032123046732910.1038/s41569-018- BF Dele-Ojo (42423_CR41) 2021; 39 42423_CR13 42423_CR50 CS Endocrinology (42423_CR48) 2016; 32 F Abbasi (42423_CR23) 2016; 120 American Diabetes, A. (42423_CR44) 2019; 42 MJ Gurka (42423_CR7) 2014; 63 MJ Gurka (42423_CR14) 2012; 11 B Yang (42423_CR5) 2018; 164 JM Dekker (42423_CR4) 2005; 112 J Kaur (42423_CR22) 2014; 2014 42423_CR25 T Unger (42423_CR37) 2020; 38 KG Alberti (42423_CR49) 2006; 23 X Xiao (42423_CR16) 2021; 15 Q Huang (42423_CR40) 2022; 46 I Jialal (42423_CR17) 2022; 36 MJ Gurka (42423_CR30) 2017; 60 Joint committee for guideline, r. (42423_CR39) 2018; 15 BM Cheung (42423_CR20) 2008; 68 P Jia (42423_CR27) 2019; 3 ER DeLong (42423_CR51) 1988; 44 42423_CR34 SD Pierdomenico (42423_CR21) 2007; 20 42423_CR33 42423_CR31 X Zhang (42423_CR29) 2020; 15 S Low (42423_CR15) 2019; 65 P Jia (42423_CR26) 2021; 22 K Bunsawat (42423_CR12) 2022; 71 B Zhou (42423_CR46) 2002; 15 Y Rochlani (42423_CR36) 2017; 11 J Mikolaityte (42423_CR43) 2022; 58 MD DeBoer (42423_CR8) 2018; 41 D Zhao (42423_CR9) 2019; 16 LT Hu (42423_CR35) 1999; 6 42423_CR45 42423_CR1 42423_CR2 JB Buse (42423_CR38) 2020; 43 SJ Kim-Dorner (42423_CR18) 2010; 59 S Yang (42423_CR10) 2022; 838 X Li (42423_CR11) 2022; 10 J Ke (42423_CR19) 2022; 183 P Jia (42423_CR28) 2021; 22 H Pham (42423_CR42) 2022; 19 K Qin (42423_CR6) 2023; 11 CH Hsu (42423_CR32) 2015; 72 AJ Hanley (42423_CR3) 2005; 112 B Song (42423_CR24) 2022; 13 X Sui (42423_CR47) 2008; 57 38519510 - Nat Commun. 2024 Mar 22;15(1):2589 |
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Snippet | Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the... Abstract Metabolic syndrome (MetS) is characterized by metabolic dysfunctions and could predict future risk for cardiovascular diseases (CVDs). However, the... |
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Title | Development and validation of an age-sex-ethnicity-specific metabolic syndrome score in the Chinese adults |
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