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Global, Regional, and National Burden of Neurological Disorders, 1990–2016: A Systematic Analysis for the Global Burden of Disease Study 2016 Publisher Pubmed



Feigin VL1, 3, 4 ; Nichols E4 ; Alam T4 ; Bannick MS4 ; Beghi E12 ; Blake N13 ; Culpepper WJ14, 15 ; Dorsey ER17 ; Elbaz A18 ; Ellenbogen RG5, 19 ; Fisher JL21 ; Fitzmaurice C4, 7 ; Giussani G12 ; Glennie L13 Show All Authors
Authors
  1. Feigin VL1, 3, 4
  2. Nichols E4
  3. Alam T4
  4. Bannick MS4
  5. Beghi E12
  6. Blake N13
  7. Culpepper WJ14, 15
  8. Dorsey ER17
  9. Elbaz A18
  10. Ellenbogen RG5, 19
  11. Fisher JL21
  12. Fitzmaurice C4, 7
  13. Giussani G12
  14. Glennie L13
  15. James SL4
  16. Johnson CO4
  17. Kassebaum NJ4, 20
  18. Logroscino G25, 26
  19. Marin B27
  20. Mountjoyvenning WC4
  21. Nguyen M4
  22. Oforiasenso R28, 31
  23. Patel AP32
  24. Piccininni M23, 24
  25. Roth GA4, 6
  26. Steiner TJ33, 34
  27. Stovner LJ33, 37
  28. Szoeke CEI38, 41
  29. Theadom A1, 3
  30. Vollset SE4, 8
  31. Wallin MT16, 43
  32. Wright C13
  33. Zunt JR5
  34. Abbasi N44, 60
  35. Abdallah F62
  36. Abdelalim A62
  37. Abdollahpour I63, 64
  38. Aboyans V65, 66
  39. Abraha HN67
  40. Acharya D75, 76
  41. Adamu AA77, 80
  42. Adebayo OM82
  43. Adeoye AM83, 85
  44. Adsuar JC86
  45. Afarideh M45
  46. Agrawal S88, 89
  47. Ahmadi A90
  48. Ahmed MB104
  49. Aichour AN107
  50. Aichour I107
  51. Aichour MTE108
  52. Akinyemi RO84
  53. Akseer N109
  54. Aleyadhy A112
  55. Alshahi Salman R115
  56. Alahdab F117
  57. Alene KA118, 121
  58. Aljunid SM123, 124
  59. Altirkawi K114
  60. Alvisguzman N125, 126
  61. Anber NH127
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  223. Khan EA361
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  225. Khazaie H93
  226. Kiadaliri AA364
  227. Kiirithio DN366, 367
  228. Kim AS368
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  231. Kim YJ371
  232. Kisa A372, 374
  233. Kokubo Y375
  234. Koyanagi A308
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  241. Lansingh VC382, 383
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  244. Li S29
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  247. Lo WD22, 390
  248. Lopez JCF130
  249. Lorkowski S391, 393
  250. Lotufo PA183
  251. Lucas RM122, 304
  252. Lunevicius R394, 395
  253. Mackay MT39, 396
  254. Mahotra NB397
  255. Majdan M398
  256. Majdzadeh R50, 58
  257. Majeed A35
  258. Malekzadeh R51, 399
  259. Malta DC400
  260. Manafi N401, 402
  261. Mansournia MA48
  262. Mantovani LG238
  263. Marz W334, 403
  264. Mashambathompson TP404
  265. Massenburg BB9
  266. Mate KKV61
  267. Mcalinden C405
  268. Mcgrath JJ406, 408
  269. Mehta V409
  270. Meier T392, 410
  271. Meles HG74
  272. Melese A412
  273. Memiah PTN413
  274. Memish ZA228, 414
  275. Mendoza W415
  276. Mengistu DT73
  277. Mengistu G416, 417
  278. Meretoja A38, 418
  279. Meretoja TJ419, 420
  280. Mestrovic T421, 422
  281. Miazgowski B424
  282. Miazgowski T423
  283. Miller TR426, 427
  284. Mini GK428, 431
  285. Mirrakhimov EM432, 433
  286. Moazen B335, 434
  287. Mohajer B44, 46
  288. Mohammad Gholi Mezerji N347
  289. Mohammadi M244
  290. Mohammadikhanaposhtani M199
  291. Mohammadibakhsh R348, 435
  292. Mohammadniaafrouzi M200
  293. Mohammed S335, 436
  294. Mohebi F44, 52
  295. Mokdad AH4, 8
  296. Monasta L438
  297. Mondello S439, 440
  298. Moodley Y404
  299. Moosazadeh M245
  300. Moradi G441, 442
  301. Moradilakeh M133
  302. Moradinazar M94
  303. Moraga P443
  304. Moreno Velasquez I224
  305. Morrison SD10
  306. Mousavi SM53
  307. Muhammed OS188
  308. Muruet W444
  309. Musa KI446
  310. Mustafa G447, 448
  311. Naderi M95
  312. Nagel G449
  313. Naheed A450
  314. Naik G452
  315. Najafi F96
  316. Nangia V456
  317. Negoi I192
  318. Negoi RI193, 457
  319. Newton CRJ180, 458
  320. Ngunjiri JW459
  321. Nguyen CT460
  322. Nguyen LH316
  323. Ningrum DNA461, 462
  324. Nirayo YL67
  325. Nixon MR4
  326. Norrving B365
  327. Noubiap JJ463
  328. Nourollahpour Shiadeh M250
  329. Nyasulu PS78
  330. Ogbo FA465
  331. Oh IH466
  332. Olagunju AT287, 467
  333. Olagunju TO468
  334. Olivares PR280
  335. Onwujekwe OE469
  336. Oren E11, 470
  337. Owolabi MO84
  338. A MP471
  339. Pakpour AH472
  340. Pan WH473
  341. Pandajonas S336
  342. Pandian JD235
  343. Patel SK474, 475
  344. Pereira DM216, 476
  345. Petzold M477, 478
  346. Pillay JD479
  347. Piradov MA288
  348. Polanczyk GV184
  349. Polinder S295
  350. Postma MJ480, 481
  351. Poulton R482
  352. Poustchi H51
  353. Prakash S484
  354. Prakash V485
  355. Qorbani M486
  356. Radfar A273, 487
  357. Rafay A488
  358. Rafiei A246, 249
  359. Rahim F358
  360. Rahimimovaghar V54
  361. Rahman M151
  362. Rahman MHU325
  363. Rahman MA489, 490
  364. Rajati F97
  365. Ram U491
  366. Ranta A483, 492
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  374. Rezai MS247
  375. Rios Gonzalez CM220, 499
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  377. Roever L500
  378. Ronfani L438
  379. Roro EM189, 265
  380. Roshandel G51, 501
  381. Rostami A201
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  383. Sacco RL332
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Source: The Lancet Neurology Published:2019


Abstract

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% [9·0–12·1]), 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. Funding: Bill & Melinda Gates Foundation. © 2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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