The global burden of metabolic disease: Data from 2000 to 2019
Global estimates of prevalence, deaths, and disability-adjusted life years (DALYs) from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 were examined for metabolic diseases (type 2 diabetes mellitus [T2DM], hypertension, and non-alcoholic fatty liver disease [NAFLD]). For metabo...
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Published in | Cell metabolism Vol. 35; no. 3; pp. 414 - 428.e3 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
07.03.2023
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Subjects | |
Online Access | Get full text |
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Abstract | Global estimates of prevalence, deaths, and disability-adjusted life years (DALYs) from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 were examined for metabolic diseases (type 2 diabetes mellitus [T2DM], hypertension, and non-alcoholic fatty liver disease [NAFLD]). For metabolic risk factors (hyperlipidemia and obesity), estimates were limited to mortality and DALYs. From 2000 to 2019, prevalence rates increased for all metabolic diseases, with the greatest increase in high socio-demographic index (SDI) countries. Mortality rates decreased over time in hyperlipidemia, hypertension, and NAFLD, but not in T2DM and obesity. The highest mortality was found in the World Health Organization Eastern Mediterranean region, and low to low-middle SDI countries. The global prevalence of metabolic diseases has risen over the past two decades regardless of SDI. Urgent attention is needed to address the unchanging mortality rates attributed to metabolic disease and the entrenched sex-regional-socioeconomic disparities in mortality.
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•Global estimates from the GBD Study 2019 were examined for metabolic diseases•Mortality rates decreased over time for hyperlipidemia, hypertension, and NAFLD•Mortality rates remained unchanged over time for diabetes and obesity•The highest mortality was in the Eastern Mediterranean and low-income countries
Global estimates from the GBD Study 2019 reveal decreasing mortality rates between 2000 and 2019 for hyperlipidemia, hypertension, and NAFLD, but not for T2DM and obesity. The highest mortality rate due to metabolic disease was found in the Eastern Mediterranean, and in low- to low-middle-income countries. Urgent attention is needed to address high and unchanging mortality rates as well as entrenched sex-regional-socioeconomic disparities in death related to metabolic disease. |
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AbstractList | Global estimates of prevalence, deaths, and disability-adjusted life years (DALYs) from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 were examined for metabolic diseases (type 2 diabetes mellitus [T2DM], hypertension, and non-alcoholic fatty liver disease [NAFLD]). For metabolic risk factors (hyperlipidemia and obesity), estimates were limited to mortality and DALYs. From 2000 to 2019, prevalence rates increased for all metabolic diseases, with the greatest increase in high socio-demographic index (SDI) countries. Mortality rates decreased over time in hyperlipidemia, hypertension, and NAFLD, but not in T2DM and obesity. The highest mortality was found in the World Health Organization Eastern Mediterranean region, and low to low-middle SDI countries. The global prevalence of metabolic diseases has risen over the past two decades regardless of SDI. Urgent attention is needed to address the unchanging mortality rates attributed to metabolic disease and the entrenched sex-regional-socioeconomic disparities in mortality. Global estimates of prevalence, deaths, and disability-adjusted life years (DALYs) from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 were examined for metabolic diseases (type 2 diabetes mellitus [T2DM], hypertension, and non-alcoholic fatty liver disease [NAFLD]). For metabolic risk factors (hyperlipidemia and obesity), estimates were limited to mortality and DALYs. From 2000 to 2019, prevalence rates increased for all metabolic diseases, with the greatest increase in high socio-demographic index (SDI) countries. Mortality rates decreased over time in hyperlipidemia, hypertension, and NAFLD, but not in T2DM and obesity. The highest mortality was found in the World Health Organization Eastern Mediterranean region, and low to low-middle SDI countries. The global prevalence of metabolic diseases has risen over the past two decades regardless of SDI. Urgent attention is needed to address the unchanging mortality rates attributed to metabolic disease and the entrenched sex-regional-socioeconomic disparities in mortality.Global estimates of prevalence, deaths, and disability-adjusted life years (DALYs) from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 were examined for metabolic diseases (type 2 diabetes mellitus [T2DM], hypertension, and non-alcoholic fatty liver disease [NAFLD]). For metabolic risk factors (hyperlipidemia and obesity), estimates were limited to mortality and DALYs. From 2000 to 2019, prevalence rates increased for all metabolic diseases, with the greatest increase in high socio-demographic index (SDI) countries. Mortality rates decreased over time in hyperlipidemia, hypertension, and NAFLD, but not in T2DM and obesity. The highest mortality was found in the World Health Organization Eastern Mediterranean region, and low to low-middle SDI countries. The global prevalence of metabolic diseases has risen over the past two decades regardless of SDI. Urgent attention is needed to address the unchanging mortality rates attributed to metabolic disease and the entrenched sex-regional-socioeconomic disparities in mortality. Global estimates of prevalence, deaths, and disability-adjusted life years (DALYs) from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 were examined for metabolic diseases (type 2 diabetes mellitus [T2DM], hypertension, and non-alcoholic fatty liver disease [NAFLD]). For metabolic risk factors (hyperlipidemia and obesity), estimates were limited to mortality and DALYs. From 2000 to 2019, prevalence rates increased for all metabolic diseases, with the greatest increase in high socio-demographic index (SDI) countries. Mortality rates decreased over time in hyperlipidemia, hypertension, and NAFLD, but not in T2DM and obesity. The highest mortality was found in the World Health Organization Eastern Mediterranean region, and low to low-middle SDI countries. The global prevalence of metabolic diseases has risen over the past two decades regardless of SDI. Urgent attention is needed to address the unchanging mortality rates attributed to metabolic disease and the entrenched sex-regional-socioeconomic disparities in mortality. [Display omitted] •Global estimates from the GBD Study 2019 were examined for metabolic diseases•Mortality rates decreased over time for hyperlipidemia, hypertension, and NAFLD•Mortality rates remained unchanged over time for diabetes and obesity•The highest mortality was in the Eastern Mediterranean and low-income countries Global estimates from the GBD Study 2019 reveal decreasing mortality rates between 2000 and 2019 for hyperlipidemia, hypertension, and NAFLD, but not for T2DM and obesity. The highest mortality rate due to metabolic disease was found in the Eastern Mediterranean, and in low- to low-middle-income countries. Urgent attention is needed to address high and unchanging mortality rates as well as entrenched sex-regional-socioeconomic disparities in death related to metabolic disease. |
Author | Xiao, Jieling Lin, Chaoxing Muthiah, Mark Dhinesh Young, Dan Yock Cummings, David E. Tan, Darren Jun Hao Sanyal, Arun Khoo, Chin Meng Dimitriadis, Georgios K. Figtree, Gemma A. Chin, Yip Han Mantzoros, Christos S. Fu, Clarissa Elysia Syn, Nicholas Ma, Ronald Ching Wan Wong, Vincent Wai-Sun Chew, Nicholas W.S. Quek, Jingxuan Kong, Gwyneth Huang, Daniel Q. Ng, Cheng Han Wang, Jiong-Wei Lam, Carolyn S.P. Siddiqui, Mohammad Shadab Chan, Mark Y. Wang, Yibin Lim, Wen Hui Foo, Roger Noureddin, Mazen |
Author_xml | – sequence: 1 givenname: Nicholas W.S. surname: Chew fullname: Chew, Nicholas W.S. email: nicholas_ws_chew@nuhs.edu.sg organization: Department of Cardiology, National University Heart Centre, National University Health System, Singapore, Singapore – sequence: 2 givenname: Cheng Han orcidid: 0000-0002-8297-1569 surname: Ng fullname: Ng, Cheng Han email: chenhanng@gmail.com organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 3 givenname: Darren Jun Hao surname: Tan fullname: Tan, Darren Jun Hao organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 4 givenname: Gwyneth surname: Kong fullname: Kong, Gwyneth organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 5 givenname: Chaoxing surname: Lin fullname: Lin, Chaoxing organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 6 givenname: Yip Han surname: Chin fullname: Chin, Yip Han organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 7 givenname: Wen Hui surname: Lim fullname: Lim, Wen Hui organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 8 givenname: Daniel Q. surname: Huang fullname: Huang, Daniel Q. organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 9 givenname: Jingxuan surname: Quek fullname: Quek, Jingxuan organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 10 givenname: Clarissa Elysia surname: Fu fullname: Fu, Clarissa Elysia organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 11 givenname: Jieling surname: Xiao fullname: Xiao, Jieling organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 12 givenname: Nicholas surname: Syn fullname: Syn, Nicholas organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 13 givenname: Roger surname: Foo fullname: Foo, Roger organization: Department of Cardiology, National University Heart Centre, National University Health System, Singapore, Singapore – sequence: 14 givenname: Chin Meng surname: Khoo fullname: Khoo, Chin Meng organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 15 givenname: Jiong-Wei surname: Wang fullname: Wang, Jiong-Wei organization: Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 16 givenname: Georgios K. surname: Dimitriadis fullname: Dimitriadis, Georgios K. organization: Department of Endocrinology ASO/Easo COM, King's College Hospital NHS Foundation Trust, Denmark Hill, London, UK – sequence: 17 givenname: Dan Yock surname: Young fullname: Young, Dan Yock organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore – sequence: 18 givenname: Mohammad Shadab surname: Siddiqui fullname: Siddiqui, Mohammad Shadab organization: Division of Gastroenterology, Hepatology and Nutrition, Department of Internal Medicine, Virginia Commonwealth University, Richmond, VA, USA – sequence: 19 givenname: Carolyn S.P. surname: Lam fullname: Lam, Carolyn S.P. organization: National Heart Centre Singapore, Singapore, Singapore – sequence: 20 givenname: Yibin surname: Wang fullname: Wang, Yibin organization: Duke-NUS Medical School, Singapore, Singapore – sequence: 21 givenname: Gemma A. surname: Figtree fullname: Figtree, Gemma A. organization: Northern Clinical School, Kolling Institute of Medical Research, University of Sydney, Sydney, NSW, Australia – sequence: 22 givenname: Mark Y. surname: Chan fullname: Chan, Mark Y. organization: Department of Cardiology, National University Heart Centre, National University Health System, Singapore, Singapore – sequence: 23 givenname: David E. surname: Cummings fullname: Cummings, David E. organization: UW Medicine Diabetes Institute, VA Puget Sound Health Care System, University of Washington, Seattle, WA, USA – sequence: 24 givenname: Mazen surname: Noureddin fullname: Noureddin, Mazen organization: Houston Research Institute, Houston, TX, USA – sequence: 25 givenname: Vincent Wai-Sun surname: Wong fullname: Wong, Vincent Wai-Sun organization: Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong, China – sequence: 26 givenname: Ronald Ching Wan surname: Ma fullname: Ma, Ronald Ching Wan organization: Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong, China – sequence: 27 givenname: Christos S. surname: Mantzoros fullname: Mantzoros, Christos S. organization: Section of Endocrinology, Boston VA Healthcare System, Boston, MA, USA – sequence: 28 givenname: Arun surname: Sanyal fullname: Sanyal, Arun organization: Division of Gastroenterology, Hepatology and Nutrition, Department of Internal Medicine, Virginia Commonwealth University, Richmond, VA, USA – sequence: 29 givenname: Mark Dhinesh surname: Muthiah fullname: Muthiah, Mark Dhinesh organization: Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36889281$$D View this record in MEDLINE/PubMed |
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SubjectTerms | diabetes mellitus Diabetes Mellitus, Type 2 - epidemiology disability-adjusted life years disparity global burden Global Burden of Disease Humans Hypertension metabolic disease Metabolic Diseases - epidemiology mortality Non-alcoholic Fatty Liver Disease obesity Obesity - epidemiology Quality-Adjusted Life Years Risk Factors |
Title | The global burden of metabolic disease: Data from 2000 to 2019 |
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