Global, regional, and national burden of neurological disorders, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016

被引:1671
作者
Feigin, Valery L. [1 ,4 ]
Nichols, Emma [4 ]
Alam, Tahiya [4 ]
Bannick, Marlena S. [4 ]
Beghi, Ettore [12 ]
Blake, Natacha [13 ]
Culpepper, William J. [14 ,15 ]
Dorsey, E. Ray [17 ]
Elbaz, Alexis [18 ]
Ellenbogen, Richard G. [5 ,19 ]
Fisher, James L. [21 ]
Fitzmaurice, Christina [4 ,7 ]
Giussani, Giorgia [12 ]
Glennie, Linda [13 ]
James, Spencer L. [4 ]
Johnson, Catherine Owens [4 ]
Kassebaum, Nicholas J. [4 ,20 ]
Logroscino, Giancarlo [25 ,26 ]
Marin, Benoit [27 ]
Mountjoy-Venning, W. Cliff [4 ]
Minh Nguyen [4 ]
Ofori-Asenso, Richard [28 ]
Patel, Anoop P. [31 ]
Piccininni, Marco [23 ,24 ]
Roth, Gregory A. [4 ,6 ]
Steiner, Timothy J. [32 ,33 ]
Stovner, Lars Jacob [32 ,36 ]
Szoeke, Cassandra E. I. [37 ,40 ]
Theadom, Alice [1 ]
Vollset, Stein Emil [4 ,8 ]
Wallin, Mitchell Taylor [16 ,42 ]
Wright, Claire [13 ]
Zunt, Joseph Raymond [5 ]
Abbasi, Nooshin [43 ,59 ]
Abd-Allah, Foad [61 ]
Abdelalim, Ahmed [61 ]
Abdollahpour, Ibrahim [62 ,63 ]
Aboyans, Victor [64 ,65 ]
Abraha, Haftom Niguse [66 ]
Acharya, Dilaram [74 ,75 ]
Adamu, Abdu A. [76 ,79 ]
Adebayo, Oladimeji M. [81 ]
Adeoye, Abiodun Moshood [82 ,84 ]
Adsuar, Jose C. [85 ]
Afarideh, Mohsen [44 ]
Agrawal, Sutapa [87 ]
Ahmadi, Alireza [88 ]
Ahmed, Muktar Beshir [102 ]
Aichour, Amani Nidhal [105 ]
Aichour, Ibtihel [105 ]
机构
[1] Auckland Univ Technol, Natl Inst Stroke & Appl Neurosci, Auckland, New Zealand
[2] Auckland Univ Technol, Sch Publ Hlth, Auckland, New Zealand
[3] Auckland Univ Technol, Natl Inst Stroke & Appl Neurosci, Auckland, New Zealand
[4] Univ Washington, Inst Hlth Metr & Evaluat, Seattle, WA 98195 USA
[5] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[6] Univ Washington, Dept Med, Div Cardiol, Seattle, WA USA
[7] Univ Washington, Div Hematol, Seattle, WA 98195 USA
[8] Univ Washington, Dept Hlth Metr Sci, Seattle, WA 98195 USA
[9] Univ Washington, Div Plast Surg, Seattle, WA 98195 USA
[10] Univ Washington, Dept Surg, Seattle, WA 98195 USA
[11] Univ Washington, Seattle, WA 98195 USA
[12] Mario Negri Inst Pharmacol Res, Dept Neurosci, Milan, Italy
[13] Meningitis Res Fdn, Res Evidence & Policy Dept, Bristol, Avon, England
[14] US Dept Vet Affairs, Multiple Sclerosis Ctr Excellence, Baltimore, MD USA
[15] Univ Maryland, Sch Med, Dept Neurol, Baltimore, MD 21201 USA
[16] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[17] Univ Rochester, Rochester, NY USA
[18] Natl Inst Hlth & Med Res, Ctr Res Epidemiol & Populat Hlth, Paris, France
[19] Seattle Childrens Hosp, Dept Surg, Seattle, WA USA
[20] Seattle Childrens Hosp, Dept Anesthesiol & Pain Med, Seattle, WA USA
[21] Ohio State Univ, James Canc Hosp, Columbus, OH 43210 USA
[22] Ohio State Univ, Dept Pediat, Columbus, OH 43210 USA
[23] Univ Bari Aldo Moro, Dept Basic Med Sci Neurosci & Sense Organs, Bari, Italy
[24] Univ Bari Aldo Moro, Unit Neurodegenerat Dis, Dept Clin Res Neurol, Bari, Italy
[25] Univ Bari Aldo Moro, Bari, Italy
[26] Fdn Cardinale Giovanni Panico Hosp, Dept Clin Res Neurol, Tricase, Italy
[27] Univ Limoges, Inst Neurol Epidemiol & Trop Neurol, Limoges, France
[28] Monash Univ, Ctr Cardiovasc Res & Educ Therapeut, Melbourne, Vic, Australia
[29] Monash Univ, Sch Publ Hlth & Prevent Med, Melbourne, Vic, Australia
[30] Monash Univ, Melbourne, Vic, Australia
[31] Univ Washington, Med Ctr, Neurosurg, Seattle, WA 98195 USA
[32] Norwegian Univ Sci & Technol, Dept Neuromed & Movement Sci, Trondheim, Norway
[33] Imperial Coll London, Div Brain Sci, London, England
[34] Imperial Coll London, Dept Primary Care & Publ Hlth, London, England
[35] Imperial Coll London, WHO Collaborating Ctr Publ Hlth Educ & Training, London, England
[36] St Olavs Hosp, Neuro Ctr, Trondheim, Norway
[37] Univ Melbourne, Sch Hlth Sci, Melbourne, Vic, Australia
[38] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[39] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[40] Australian Catholic Univ, Inst Brain, Melbourne, Vic, Australia
[41] Australian Catholic Univ, Mary MacKillop Inst Hlth Res, Melbourne, Vic, Australia
[42] George Washington Univ, Dept Neurol, Washington, DC USA
[43] Univ Tehran Med Sci, Noncommunicable Dis Res Ctr, Tehran, Iran
[44] Univ Tehran Med Sci, Endocrinol & Metab Res Ctr, Tehran, Iran
[45] Univ Tehran Med Sci, Multiple Sclerosis Res Ctr, Tehran, Iran
[46] Univ Tehran Med Sci, Dept Pharmacol, Tehran, Iran
[47] Univ Tehran Med Sci, Dept Epidemiol & Biostat, Tehran, Iran
[48] Univ Tehran Med Sci, Hematol Malignancies Res Ctr, Tehran, Iran
[49] Univ Tehran Med Sci, Knowledge Utilizat Res Ctr, Tehran, Iran
[50] Univ Tehran Med Sci, Digest Dis Res Inst, Tehran, Iran
基金
新加坡国家研究基金会; 英国医学研究理事会; 澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会; 英国惠康基金; 美国国家卫生研究院; 中国国家自然科学基金;
关键词
D O I
10.1016/S1474-4422(18)30499-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background Neurological disorders are increasingly recognised as major causes of death and disability worldwide. The aim of this analysis from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2016 is to provide the most comprehensive and up-to-date estimates of the global, regional, and national burden from neurological disorders. Methods We estimated prevalence, incidence, deaths, and disability-adjusted life-years (DALYs; the sum of years of life lost [YLLs] and years lived with disability [YLDs]) by age and sex for 15 neurological disorder categories (tetanus, meningitis, encephalitis, stroke, brain and other CNS cancers, traumatic brain injury, spinal cord injury, Alzheimer's disease and other dementias, Parkinson's disease, multiple sclerosis, motor neuron diseases, idiopathic epilepsy, migraine, tension-type headache, and a residual category for other less common neurological disorders) in 195 countries from 1990 to 2016. DisMod-MR 2.1, a Bayesian meta-regression tool, was the main method of estimation of prevalence and incidence, and the Cause of Death Ensemble model (CODEm) was used for mortality estimation. We quantified the contribution of 84 risks and combinations of risk to the disease estimates for the 15 neurological disorder categories using the GBD comparative risk assessment approach. Findings Globally, in 2016, neurological disorders were the leading cause of DALYs (276 million [95% UI 247-308]) and second leading cause of deaths (9.0 million [8.8-9.4]). The absolute number of deaths and DALYs from all neurological disorders combined increased (deaths by 39% [34-44] and DALYs by 15% [9-21]) whereas their age-standardised rates decreased (deaths by 28% [26-30] and DALYs by 27% [24-31]) between 1990 and 2016. The only neurological disorders that had a decrease in rates and absolute numbers of deaths and DALYs were tetanus, meningitis, and encephalitis. The four largest contributors of neurological DALYs were stroke (42.2% [38.6-46.1]), migraine (16.3% [11.7-20.8]), Alzheimer's and other dementias (10.4% [9.0-124]), and meningitis (7.9% [6.6-10.4]). For the combined neurological disorders, age-standardised DALY rates were significantly higher in males than in females (male-to-female ratio 1.12 [1.05-1.20]), but migraine, multiple sclerosis, and tension-type headache were more common and caused more burden in females, with male-to-female ratios of less than 0.7. The 84 risks quantified in GBD explain less than 10% of neurological disorder DALY burdens, except stroke, for which 88.8% (86.5-90.9) of DALYs are attributable to risk factors, and to a lesser extent Alzheimer's disease and other dementias (22.3% [11.8-35.1] of DALYs are risk attributable) and idiopathic epilepsy (14.1% [10.8-17.5] of DALYs are risk attributable). Interpretation Globally, the burden of neurological disorders, as measured by the absolute number of DALYs, continues to increase. As populations are growing and ageing, and the prevalence of major disabling neurological disorders steeply increases with age, governments will face increasing demand for treatment, rehabilitation, and support services for neurological disorders. The scarcity of established modifiable risks for most of the neurological burden demonstrates that new knowledge is required to develop effective prevention and treatment strategies. Copyright (C) The Author(s). Published by Elsevier Ltd.
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收藏
页码:459 / 480
页数:22
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