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Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010

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机构: [1]Univ Washington, Inst Hlth Metr & Evaluat, Seattle, WA 98121 USA; [2]Univ Washington, Dept Anesthesiol & Pain Med, Seattle, WA 98121 USA; [3]Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98121 USA; [4]Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, London, England; [5]Univ Tokyo, Dept Global Hlth, Tokyo, Japan; [6]Dupuytren Univ Hosp, Dept Cardiol, Limoges, France; [7]Univ Texas San Antonio, Sch Med, San Antonio, TX USA; [8]Univ Queensland, Queensland Brain Inst, Sch Populat Hlth, Brisbane, Qld, Australia; [9]Univ Queensland, Queensland Brain Inst, Queensland Ctr Mental Hlth Res, Brisbane, Qld, Australia; [10]Sanjay Gandhi Postgrad Inst Med Sci, Lucknow, Uttar Pradesh, India; [11]Univ London, London, England; [12]Mayo Clin, Rochester, MN USA; [13]Univ Auckland, Auckland 1, New Zealand; [14]Harvard Univ, Brigham & Womens Hosp, Boston, MA 02115 USA; [15]Harvard Univ, Harvard Med Sch, Boston, MA 02115 USA; [16]Harvard Univ, Harvard Humanitarian Initiat, Boston, MA 02115 USA; [17]Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA; [18]Yale Univ, Global Partners Anesthesia & Surg, New Haven, CT USA; [19]Boston Univ, Boston, MA 02215 USA; [20]Univ Oxford, Clin Trial Serv Unit, Oxford, England; [21]Univ Oxford, Epidemiol Studies Unit, Oxford, England; [22]Moscow State Univ Med & Dent, Res Inst Transplantol & Artificial Organs, Moscow, Russia; [23]King Fahad Med City, Riyadh, Saudi Arabia; [24]Michigan State Univ, E Lansing, MI 48824 USA; [25]Univ Sydney, Sch Publ Hlth, Sydney, NSW 2006, Australia; [26]Univ Sydney, Fac Hlth Sci, Sydney, NSW 2006, Australia; [27]Univ Sydney, Dept Rheumatol, No Clin Sch, Sydney, NSW 2006, Australia; [28]Univ Sydney, Inst Bone & Joint Res, Sydney, NSW 2006, Australia; [29]Univ New S Wales, Natl Drug & Alcohol Res Ctr, Sydney, NSW, Australia; [30]Great Ormond St Hosp Sick Children, London WC1N 3JH, England; [31]Univ Western Australia, Telethon Inst Child Hlth Res, Ctr Child Hlth Res, Perth, WA 6009, Australia; [32]NIEHS, Res Triangle Pk, NC 27709 USA; [33]Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA; [34]Univ Med Ctr Rotterdam, Erasmus MC, Rotterdam, Netherlands; [35]Menzies Sch Hlth Res, Darwin, NT, Australia; [36]Natl Hlth Serv, Edinburgh, Midlothian, Scotland; [37]Univ Edinburgh, Edinburgh, Midlothian, Scotland; [38]Univ Witwatersrand, Johannesburg, South Africa; [39]Loyola Univ, Sch Med, Chicago, IL 60611 USA; [40]Wake Forest Univ, Sch Publ Hlth Sci, Dept Epidemiol, Winston Salem, NC 27109 USA; [41]Mario Negri Inst Pharmacol Res, I-24100 Bergamo, Italy; [42]Hosp Dr Gustavo N Collado, Puerto Chitre, Panama; [43]Victorian Infect Dis Reference Lab, Melbourne, Vic, Australia; [44]Univ Calif San Diego, San Diego, CA 92103 USA; [45]Emory Univ, Sch Publ Hlth, Atlanta, GA USA; [46]Emory Univ, Sch Med, Atlanta, GA USA; [47]Univ Penn, Philadelphia, PA 19104 USA; [48]Griffith Univ, Brisbane, Qld 4111, Australia; [49]Beth Israel Deaconess Med Ctr, New York, NY 10003 USA; [50]Univ Peradeniya, Peradeniya, Sri Lanka; [51]Johns Hopkins Univ, Baltimore, MD USA; [52]Hosp Maciel, Montevideo, Uruguay; [53]MRC HPA Ctr Environm & Hlth, London, England; [54]Auckland Tech Univ, Natl Inst Stroke & Appl Neurosci, Auckland, New Zealand; [55]Royal Life Saving Soc, Sydney, NSW, Australia; [56]James Cook Univ, Townsville, Qld 4811, Australia; [57]Howard Univ, Coll Med, Washington, DC USA; [58]Brandeis Univ, Waltham, MA USA; [59]Flinders Univ S Australia, Adelaide, SA 5001, Australia; [60]Karolinska Univ Hosp, Stockholm, Sweden; [61]Kings Coll London, Kings Coll Hosp NHS Trust, London, England; [62]Baylor Coll Med, Natl Sch Trop Med, Waco, TX USA; [63]Monash Univ, Melbourne, Vic 3004, Australia; [64]George Mason Univ, Fairfax, VA 22030 USA; [65]All India Inst Med Sci, New Delhi, India; [66]Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Cardiol, IL-91010 Jerusalem, Israel; [67]Makerere Univ, Sch Publ Hlth, Kampala, Uganda; [68]Univ S Africa, Johannesburg, South Africa; [69]Kwame Nkrumah Univ Sci & Technol, Kumasi, Ghana; [70]Univ Calif San Francisco, San Francisco, CA 94143 USA; [71]Univ Miami, Miller Sch Med, Miami, FL 33136 USA; [72]Mulago Hosp, Kampala, Uganda; [73]Univ Melbourne, Ctr Int Child Hlth, Melbourne, Vic, Australia; [74]Univ Melbourne, Royal Childrens Hosp, Dept Paediat, Melbourne, Vic, Australia; [75]Asian Pacific Soc Cardiol, Kyoto, Japan; [76]MRC, Tygerberg, South Africa; [77]Univ Cape Town, Hatter Inst, ZA-7925 Cape Town, South Africa; [78]Univ Cape Town, Dept Med, ZA-7925 Cape Town, South Africa; [79]Legacy Hlth Syst, Portland, OR USA; [80]Northwestern Univ, Feinberg Sch Med, Evanston, IL USA; [81]Univ Otago, Dunedin, New Zealand; [82]China Med Board, Boston, MA USA; [83]Pacific Inst Res & Evaluat, Calverton, MD USA; [84]Natl Inst Hlth, Maputo, Mozambique; [85]Univ Eduardo Mondlane, Maputo, Mozambique; [86]Columbia Univ, New York, NY USA; [87]London Sch Hyg & Trop Med, London WC1, England; [88]Centro Studi GISED, Bergamo, Italy; [89]Univ Liverpool, Sch Publ Hlth, Liverpool L69 3BX, Merseyside, England; [90]Natl Univ Ireland Galway, HRB Clin Res Facil, Galway, Ireland; [91]Deakin Univ, Melbourne, Vic, Australia; [92]BP Koirala Inst Hlth Sci, Dharan, Nepal; [93]Betty Cowan Res & Innovat Ctr, Ludhiana, Punjab, India; [94]Hosp Joan 23, La Paz, Bolivia; [95]Inst Nacl Enfermedades Resp, Mexico City, DF, Mexico; [96]Hosp Univ Cruces, Baracaldo, Spain; [97]Brigham Young Univ, Provo, UT 84602 USA; [98]Hosp Univ Canarias, Tenerife, Spain; [99]Univ British Columbia, Fac Med, Sch Populat & Publ Hlth, Vancouver, BC, Canada; [100]Univ Missouri, Mason Eye Inst, Columbia, MO USA; [101]Ctr Addict & Mental Hlth, Toronto, ON, Canada; [102]Univ Chicago, Natl Opin Res Ctr, Chicago, IL 60637 USA; [103]Complejo Hosp Caja Seguro Social, Panama City, Panama; [104]Vanderbilt Univ, Nashville, TN USA; [105]Univ Alabama Birmingham, Birmingham, AL USA; [106]Minist Interior, Madrid, Spain; [107]Queens Med Ctr, Honolulu, HI USA; [108]Drexel Univ, Sch Publ Hlth, Philadelphia, PA 19104 USA; [109]Cincinnati Childrens Hosp, Cincinnati, OH USA; [110]Copenhagen Univ Hosp, Dept Neurol, Herlev, Denmark; [111]Natl Univ Singapore, Singapore 117548, Singapore; [112]Voluntary Hlth Serv, Chennai, Tamil Nadu, India; [113]NIOSH, Baltimore, MD USA; [114]Capital Med Univ, Beijing Neurosurg Inst, Beijing, Peoples R China; [115]Brown Univ, Providence, RI 02912 USA; [116]Royal Cornwall Hosp, Truro, England; [117]London Sch Econ, London WC2A 2AE, England; [118]Univ Hong Kong, Ctr Suicide Res & Prevent, Hong Kong, Hong Kong, Peoples R China; [119]Shanghai Jiao Tong Univ, Sch Publ Hlth, Shanghai 200030, Peoples R China; [120]Univ Washington, Inst Hlth Metr & Evaluat, 2301 5th Ave,Suite 600, Seattle, WA 98121 USA
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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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出版当年[2011]版:
大类 | 1 区 医学
小类 | 1 区 医学:内科
最新[2023]版:
大类 | 1 区 医学
小类 | 1 区 医学:内科
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出版当年[2010]版:
Q1 MEDICINE, GENERAL & INTERNAL
最新[2023]版:
Q1 MEDICINE, GENERAL & INTERNAL

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第一作者机构: [1]Univ Washington, Inst Hlth Metr & Evaluat, Seattle, WA 98121 USA;
通讯作者:
通讯机构: [1]Univ Washington, Inst Hlth Metr & Evaluat, Seattle, WA 98121 USA; [120]Univ Washington, Inst Hlth Metr & Evaluat, 2301 5th Ave,Suite 600, Seattle, WA 98121 USA
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