TY - JOUR
T1 - Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010
T2 - A systematic analysis for the Global Burden of Disease Study 2010
AU - Lozano, Rafael
AU - Naghavi, Mohsen
AU - Foreman, Kyle
AU - Lim, Stephen
AU - Shibuya, Kenji
AU - Aboyans, Victor
AU - Abraham, Jerry
AU - Adair, Timothy
AU - Aggarwal, Rakesh
AU - Ahn, Stephanie Y.
AU - AlMazroa, Mohammad A.
AU - Alvarado, Miriam
AU - Anderson, H. Ross
AU - Anderson, Laurie M.
AU - Andrews, Kathryn G.
AU - Atkinson, Charles
AU - Baddour, Larry M.
AU - Barker-Collo, Suzanne
AU - Bartels, David H.
AU - Bell, Michelle L.
AU - Benjamin, Emelia J.
AU - Bennett, Derrick
AU - Bhalla, Kavi
AU - Bikbov, Boris
AU - Bin Abdulhak, Aref
AU - Birbeck, Gretchen
AU - Blyth, Fiona
AU - Bolliger, Ian
AU - Boufous, Soufiane
AU - Bucello, Chiara
AU - Burch, Michael
AU - Burney, Peter
AU - Carapetis, Jonathan
AU - Chen, Honglei
AU - Chou, David
AU - Chugh, Sumeet S.
AU - Coffeng, Luc E.
AU - Colan, Steven D.
AU - Colquhoun, Samantha
AU - Colson, K. Ellicott
AU - Condon, John
AU - Connor, Myles D.
AU - Cooper, Leslie T.
AU - Corriere, Matthew
AU - Cortinovis, Monica
AU - Courville De Vaccaro, Karen
AU - Couser, William
AU - Cowie, Benjamin C.
AU - Criqui, Michael H.
AU - Cross, Marita
AU - Dabhadkar, Kaustubh C.
AU - Dahodwala, Nabila
AU - De Leo, Diego
AU - Degenhardt, Louisa
AU - Delossantos, Allyne
AU - Denenberg, Julie
AU - Des Jarlais, Don C.
AU - Dharmaratne, Samath D.
AU - Dorsey, E. Ray
AU - Driscoll, Tim
AU - Duber, Herbert
AU - Ebel, Beth
AU - Erwin, Patricia J.
AU - Espindola, Patricia
AU - Ezzati, Majid
AU - Feigin, Valery
AU - Flaxman, Abraham D.
AU - Forouzanfar, Mohammad H.
AU - Fowkes, Francis Gerry R.
AU - Franklin, Richard
AU - Fransen, Marlene
AU - Freeman, Michael K.
AU - Gabriel, Sherine E.
AU - Gakidou, Emmanuela
AU - Gaspari, Flavio
AU - Gillum, Richard F.
AU - Gonzalez-Medina, Diego
AU - Halasa, Yara A.
AU - Haring, Diana
AU - Harrison, James E.
AU - Havmoeller, Rasmus
AU - Hay, Roderick J.
AU - Hoen, Bruno
AU - Hotez, Peter J.
AU - Hoy, Damian
AU - Jacobsen, Kathryn H.
AU - James, Spencer L.
AU - Jasrasaria, Rashmi
AU - Jayaraman, Sudha
AU - Johns, Nicole
AU - Karthikeyan, Ganesan
AU - Kassebaum, Nicholas
AU - Keren, Andre
AU - Khoo, Jon Paul
AU - Knowlton, Lisa Marie
AU - Kobusingye, Olive
AU - Koranteng, Adofo
AU - Krishnamurthi, Rita
AU - Lipnick, Michael
AU - Lipshultz, Steven E.
AU - Lockett Ohno, Summer
AU - Mabweijano, Jacqueline
AU - MacIntyre, Michael F.
AU - Mallinger, Leslie
AU - March, Lyn
AU - Marks, Guy B.
AU - Marks, Robin
AU - Matsumori, Akira
AU - Matzopoulos, Richard
AU - Mayosi, Bongani M.
AU - McAnulty, John H.
AU - McDermott, Mary M.
AU - McGrath, John
AU - Memish, Ziad A.
AU - Mensah, George A.
AU - Merriman, Tony R.
AU - Michaud, Catherine
AU - Miller, Matthew
AU - Miller, Ted R.
AU - Mock, Charles
AU - Mocumbi, Ana Olga
AU - Mokdad, Ali A.
AU - Moran, Andrew
AU - Mulholland, Kim
AU - Nair, M. Nathan
AU - Naldi, Luigi
AU - Narayan, K. M.Venkat
AU - Nasseri, Kiumarss
AU - Norman, Paul
AU - O'Donnell, Martin
AU - Omer, Saad B.
AU - Ortblad, Katrina
AU - Osborne, Richard
AU - Ozgediz, Doruk
AU - Pahari, Bishnu
AU - Pandian, Jeyaraj Durai
AU - Panozo Rivero, Andrea
AU - Perez Padilla, Rogelio
AU - Perez-Ruiz, Fernando
AU - Perico, Norberto
AU - Phillips, David
AU - Pierce, Kelsey
AU - Pope, C. Arden
AU - Porrini, Esteban
AU - Pourmalek, Farshad
AU - Raju, Murugesan
AU - Ranganathan, Dharani
AU - Rehm, Jürgen T.
AU - Rein, David B.
AU - Remuzzi, Guiseppe
AU - Rivara, Frederick P.
AU - Roberts, Thomas
AU - Rodriguez De León, Felipe
AU - Rosenfeld, Lisa C.
AU - Rushton, Lesley
AU - Sacco, Ralph L.
AU - Salomon, Joshua A.
AU - Sampson, Uchechukwu
AU - Sanman, Ella
AU - Schwebel, David C.
AU - Segui-Gomez, Maria
AU - Shepard, Donald S.
AU - Singh, David
AU - Singleton, Jessica
AU - Sliwa, Karen
AU - Smith, Emma
AU - Steer, Andrew
AU - Taylor, Jennifer A.
AU - Thomas, Bernadette
AU - Tleyjeh, Imad M.
AU - Towbin, Jeffrey A.
AU - Truelsen, Thomas
AU - Undurraga, Eduardo A.
AU - Venketasubramanian, N.
AU - Vijayakumar, Lakshmi
AU - Vos, Theo
AU - Wagner, Gregory R.
AU - Wang, Mengru
AU - Wang, Wenzhi
AU - Watt, Kerrianne
AU - Weinstock, Martin A.
AU - Weintraub, Robert
AU - Wilkinson, James D.
AU - Woolf, Anthony D.
AU - Wulf, Sarah
AU - Yeh, Pon Hsiu
AU - Yip, Paul
AU - Zabetian, Azadeh
AU - Zheng, Zhi Jie
AU - Lopez, Alan D.
AU - Murray, Christopher J.L.
N1 - Funding Information:
E R Dorsey has received consulting fees from Medtronic and Lundbeck and research support from Lundbeck and Prana Biotechnology. M Ezzati chaired a session and gave a talk at the World Cardiology Congress (WCC), with travel cost reimbursed by the World Heart Federation. At the WCC, he also gave a talk at a session organised by PepsiCo with no financial or other renumeration. P J Hotez reports holding several positions: Dean, National School of Tropical Medicine, Baylor College of Medicine; Director, Sabin Vaccine Institute Texas Children's Hospital Center for Vaccine Development; and President, Sabin Vaccine Institute. He also is an inventor on several patents: 5,527,937 “Hookworm Anticoagulant”; 5,753,787 “Nucleic Acids for Ancylostoma Secreted Proteins”; 7,303,752 B2 “Hookworm vaccine”; 12/492,734 “Human Hookworm Vaccine”; 61/077,256 “Multivalent Anthelminthic Vaccine”; and PCT-20100701/0.20.5.18 “Malaria Transmission blocking vaccine”. G A Mensah is a former employee of PepsiCo. F Perez-Ruiz was an adviser for Ardea, Menarini, Novartis, and Metabolex; was a member of the Speaker's Bureau for Menarini, Novartis; an adviser for educational issues for Savient; led an investigation grants for the Spanish Health Ministry, Hospital de Cruces Rheumatology Association; and was principal investigator in clinical trials for Ardea.
PY - 2012/12/1
Y1 - 2012/12/1
N2 - Background: Reliable and timely information on the leading causes of death in populations, and how these are changing, is a crucial input into health policy debates. In the Global Burden of Diseases, Injuries, and Risk Factors Study 2010 (GBD 2010), we aimed to estimate annual deaths for the world and 21 regions between 1980 and 2010 for 235 causes, with uncertainty intervals (UIs), separately by age and sex. Methods: We attempted to identify all available data on causes of death for 187 countries from 1980 to 2010 from vital registration, verbal autopsy, mortality surveillance, censuses, surveys, hospitals, police records, and mortuaries. We assessed data quality for completeness, diagnostic accuracy, missing data, stochastic variations, and probable causes of death. We applied six different modelling strategies to estimate cause-specific mortality trends depending on the strength of the data. For 133 causes and three special aggregates we used the Cause of Death Ensemble model (CODEm) approach, which uses four families of statistical models testing a large set of different models using different permutations of covariates. Model ensembles were developed from these component models. We assessed model performance with rigorous out-of-sample testing of prediction error and the validity of 95% UIs. For 13 causes with low observed numbers of deaths, we developed negative binomial models with plausible covariates. For 27 causes for which death is rare, we modelled the higher level cause in the cause hierarchy of the GBD 2010 and then allocated deaths across component causes proportionately, estimated from all available data in the database. For selected causes (African trypanosomiasis, congenital syphilis, whooping cough, measles, typhoid and parathyroid, leishmaniasis, acute hepatitis E, and HIV/AIDS), we used natural history models based on information on incidence, prevalence, and case-fatality. We separately estimated cause fractions by aetiology for diarrhoea, lower respiratory infections, and meningitis, as well as disaggregations by subcause for chronic kidney disease, maternal disorders, cirrhosis, and liver cancer. For deaths due to collective violence and natural disasters, we used mortality shock regressions. For every cause, we estimated 95% UIs that captured both parameter estimation uncertainty and uncertainty due to model specification where CODEm was used. We constrained cause-specific fractions within every age-sex group to sum to total mortality based on draws from the uncertainty distributions. Findings: In 2010, there were 52·8 million deaths globally. At the most aggregate level, communicable, maternal, neonatal, and nutritional causes were 24·9% of deaths worldwide in 2010, down from 15·9 million (34·1%) of 46·5 million in 1990. This decrease was largely due to decreases in mortality from diarrhoeal disease (from 2·5 to 1·4 million), lower respiratory infections (from 3·4 to 2·8 million), neonatal disorders (from 3·1 to 2·2 million), measles (from 0·63 to 0·13 million), and tetanus (from 0·27 to 0·06 million). Deaths from HIV/AIDS increased from 0·30 million in 1990 to 1·5 million in 2010, reaching a peak of 1·7 million in 2006. Malaria mortality also rose by an estimated 19·9% since 1990 to 1·17 million deaths in 2010. Tuberculosis killed 1·2 million people in 2010. Deaths from non-communicable diseases rose by just under 8 million between 1990 and 2010, accounting for two of every three deaths (34·5 million) worldwide by 2010. 8 million people died from cancer in 2010, 38% more than two decades ago; of these, 1·5 million (19%) were from trachea, bronchus, and lung cancer. Ischaemic heart disease and stroke collectively killed 12·9 million people in 2010, or one in four deaths worldwide, compared with one in five in 1990; 1·3 million deaths were due to diabetes, twice as many as in 1990. The fraction of global deaths due to injuries (5·1 million deaths) was marginally higher in 2010 (9·6%) compared with two decades earlier (8·8%). This was driven by a 46% rise in deaths worldwide due to road traffic accidents (1·3 million in 2010) and a rise in deaths from falls. Ischaemic heart disease, stroke, chronic obstructive pulmonary disease (COPD), lower respiratory infections, lung cancer, and HIV/AIDS were the leading causes of death in 2010. Ischaemic heart disease, lower respiratory infections, stroke, diarrhoeal disease, malaria, and HIV/AIDS were the leading causes of years of life lost due to premature mortality (YLLs) in 2010, similar to what was estimated for 1990, except for HIV/AIDS and preterm birth complications. YLLs from lower respiratory infections and diarrhoea decreased by 45-54% since 1990; ischaemic heart disease and stroke YLLs increased by 17-28%. Regional variations in leading causes of death were substantial. Communicable, maternal, neonatal, and nutritional causes still accounted for 76% of premature mortality in sub-Saharan Africa in 2010. Age standardised death rates from some key disorders rose (HIV/AIDS, Alzheimer's disease, diabetes mellitus, and chronic kidney disease in particular), but for most diseases, death rates fell in the past two decades; including major vascular diseases, COPD, most forms of cancer, liver cirrhosis, and maternal disorders. For other conditions, notably malaria, prostate cancer, and injuries, little change was noted. Interpretation: Population growth, increased average age of the world's population, and largely decreasing age-specific, sex-specific, and cause-specific death rates combine to drive a broad shift from communicable, maternal, neonatal, and nutritional causes towards non-communicable diseases. Nevertheless, communicable, maternal, neonatal, and nutritional causes remain the dominant causes of YLLs in sub-Saharan Africa. Overlaid on this general pattern of the epidemiological transition, marked regional variation exists in many causes, such as interpersonal violence, suicide, liver cancer, diabetes, cirrhosis, Chagas disease, African trypanosomiasis, melanoma, and others. Regional heterogeneity highlights the importance of sound epidemiological assessments of the causes of death on a regular basis.
AB - Background: Reliable and timely information on the leading causes of death in populations, and how these are changing, is a crucial input into health policy debates. In the Global Burden of Diseases, Injuries, and Risk Factors Study 2010 (GBD 2010), we aimed to estimate annual deaths for the world and 21 regions between 1980 and 2010 for 235 causes, with uncertainty intervals (UIs), separately by age and sex. Methods: We attempted to identify all available data on causes of death for 187 countries from 1980 to 2010 from vital registration, verbal autopsy, mortality surveillance, censuses, surveys, hospitals, police records, and mortuaries. We assessed data quality for completeness, diagnostic accuracy, missing data, stochastic variations, and probable causes of death. We applied six different modelling strategies to estimate cause-specific mortality trends depending on the strength of the data. For 133 causes and three special aggregates we used the Cause of Death Ensemble model (CODEm) approach, which uses four families of statistical models testing a large set of different models using different permutations of covariates. Model ensembles were developed from these component models. We assessed model performance with rigorous out-of-sample testing of prediction error and the validity of 95% UIs. For 13 causes with low observed numbers of deaths, we developed negative binomial models with plausible covariates. For 27 causes for which death is rare, we modelled the higher level cause in the cause hierarchy of the GBD 2010 and then allocated deaths across component causes proportionately, estimated from all available data in the database. For selected causes (African trypanosomiasis, congenital syphilis, whooping cough, measles, typhoid and parathyroid, leishmaniasis, acute hepatitis E, and HIV/AIDS), we used natural history models based on information on incidence, prevalence, and case-fatality. We separately estimated cause fractions by aetiology for diarrhoea, lower respiratory infections, and meningitis, as well as disaggregations by subcause for chronic kidney disease, maternal disorders, cirrhosis, and liver cancer. For deaths due to collective violence and natural disasters, we used mortality shock regressions. For every cause, we estimated 95% UIs that captured both parameter estimation uncertainty and uncertainty due to model specification where CODEm was used. We constrained cause-specific fractions within every age-sex group to sum to total mortality based on draws from the uncertainty distributions. Findings: In 2010, there were 52·8 million deaths globally. At the most aggregate level, communicable, maternal, neonatal, and nutritional causes were 24·9% of deaths worldwide in 2010, down from 15·9 million (34·1%) of 46·5 million in 1990. This decrease was largely due to decreases in mortality from diarrhoeal disease (from 2·5 to 1·4 million), lower respiratory infections (from 3·4 to 2·8 million), neonatal disorders (from 3·1 to 2·2 million), measles (from 0·63 to 0·13 million), and tetanus (from 0·27 to 0·06 million). Deaths from HIV/AIDS increased from 0·30 million in 1990 to 1·5 million in 2010, reaching a peak of 1·7 million in 2006. Malaria mortality also rose by an estimated 19·9% since 1990 to 1·17 million deaths in 2010. Tuberculosis killed 1·2 million people in 2010. Deaths from non-communicable diseases rose by just under 8 million between 1990 and 2010, accounting for two of every three deaths (34·5 million) worldwide by 2010. 8 million people died from cancer in 2010, 38% more than two decades ago; of these, 1·5 million (19%) were from trachea, bronchus, and lung cancer. Ischaemic heart disease and stroke collectively killed 12·9 million people in 2010, or one in four deaths worldwide, compared with one in five in 1990; 1·3 million deaths were due to diabetes, twice as many as in 1990. The fraction of global deaths due to injuries (5·1 million deaths) was marginally higher in 2010 (9·6%) compared with two decades earlier (8·8%). This was driven by a 46% rise in deaths worldwide due to road traffic accidents (1·3 million in 2010) and a rise in deaths from falls. Ischaemic heart disease, stroke, chronic obstructive pulmonary disease (COPD), lower respiratory infections, lung cancer, and HIV/AIDS were the leading causes of death in 2010. Ischaemic heart disease, lower respiratory infections, stroke, diarrhoeal disease, malaria, and HIV/AIDS were the leading causes of years of life lost due to premature mortality (YLLs) in 2010, similar to what was estimated for 1990, except for HIV/AIDS and preterm birth complications. YLLs from lower respiratory infections and diarrhoea decreased by 45-54% since 1990; ischaemic heart disease and stroke YLLs increased by 17-28%. Regional variations in leading causes of death were substantial. Communicable, maternal, neonatal, and nutritional causes still accounted for 76% of premature mortality in sub-Saharan Africa in 2010. Age standardised death rates from some key disorders rose (HIV/AIDS, Alzheimer's disease, diabetes mellitus, and chronic kidney disease in particular), but for most diseases, death rates fell in the past two decades; including major vascular diseases, COPD, most forms of cancer, liver cirrhosis, and maternal disorders. For other conditions, notably malaria, prostate cancer, and injuries, little change was noted. Interpretation: Population growth, increased average age of the world's population, and largely decreasing age-specific, sex-specific, and cause-specific death rates combine to drive a broad shift from communicable, maternal, neonatal, and nutritional causes towards non-communicable diseases. Nevertheless, communicable, maternal, neonatal, and nutritional causes remain the dominant causes of YLLs in sub-Saharan Africa. Overlaid on this general pattern of the epidemiological transition, marked regional variation exists in many causes, such as interpersonal violence, suicide, liver cancer, diabetes, cirrhosis, Chagas disease, African trypanosomiasis, melanoma, and others. Regional heterogeneity highlights the importance of sound epidemiological assessments of the causes of death on a regular basis.
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U2 - 10.1016/S0140-6736(12)61728-0
DO - 10.1016/S0140-6736(12)61728-0
M3 - Article
C2 - 23245604
AN - SCOPUS:84871036375
SN - 0140-6736
VL - 380
SP - 2095
EP - 2128
JO - The Lancet
JF - The Lancet
IS - 9859
ER -