Burden of Neurological Disorders Across the US From 1990-2017: A Global Burden of Disease Study

Key Points

Question  What is the current burden of neurological disorders in the US by states, and what are the temporal trends (from 1990 to 2017)?

Findings  Systematic analysis of the Global Burden of Disease study shows that, in 2017, the 3 most burdensome neurological disorders in the US were stroke, Alzheimer disease and other dementias, and migraine. The burden of individual neurological disorders varied moderately to widely by states (a 1.2-fold to 7.5-fold difference), and the absolute numbers of incident, prevalent, and fatal cases and disability-adjusted life-years of neurological disorders (except for traumatic brain injury incidence; spinal cord injury prevalence; meningitis prevalence, deaths, and disability-adjusted life-years; and encephalitis disability-adjusted life-years) across all US states increased from 1990 to 2017.

Meaning  A large and increasing number of people have various neurological disorders in the US, with significant variation in the burden of and trends in neurological disorders across the US states, and the reasons for these geographic variations need to be explored further.

Importance  Accurate and up-to-date estimates on incidence, prevalence, mortality, and disability-adjusted life-years (burden) of neurological disorders are the backbone of evidence-based health care planning and resource allocation for these disorders. It appears that no such estimates have been reported at the state level for the US.

Objective  To present burden estimates of major neurological disorders in the US states by age and sex from 1990 to 2017.

Design, Setting, and Participants  This is a systematic analysis of the Global Burden of Disease (GBD) 2017 study. Data on incidence, prevalence, mortality, and disability-adjusted life-years (DALYs) of major neurological disorders were derived from the GBD 2017 study of the 48 contiguous US states, Alaska, and Hawaii. Fourteen major neurological disorders were analyzed: stroke, Alzheimer disease and other dementias, Parkinson disease, epilepsy, multiple sclerosis, motor neuron disease, migraine, tension-type headache, traumatic brain injury, spinal cord injuries, brain and other nervous system cancers, meningitis, encephalitis, and tetanus.

Exposures  Any of the 14 listed neurological diseases.

Main Outcome and Measure  Absolute numbers in detail by age and sex and age-standardized rates (with 95% uncertainty intervals) were calculated.

Results  The 3 most burdensome neurological disorders in the US in terms of absolute number of DALYs were stroke (3.58 [95% uncertainty interval [UI], 3.25-3.92] million DALYs), Alzheimer disease and other dementias (2.55 [95% UI, 2.43-2.68] million DALYs), and migraine (2.40 [95% UI, 1.53-3.44] million DALYs). The burden of almost all neurological disorders (in terms of absolute number of incident, prevalent, and fatal cases, as well as DALYs) increased from 1990 to 2017, largely because of the aging of the population. Exceptions for this trend included traumatic brain injury incidence (−29.1% [95% UI, −32.4% to −25.8%]); spinal cord injury prevalence (−38.5% [95% UI, −43.1% to −34.0%]); meningitis prevalence (−44.8% [95% UI, −47.3% to −42.3%]), deaths (−64.4% [95% UI, −67.7% to −50.3%]), and DALYs (−66.9% [95% UI, −70.1% to −55.9%]); and encephalitis DALYs (−25.8% [95% UI, −30.7% to −5.8%]). The different metrics of age-standardized rates varied between the US states from a 1.2-fold difference for tension-type headache to 7.5-fold for tetanus; southeastern states and Arkansas had a relatively higher burden for stroke, while northern states had a relatively higher burden of multiple sclerosis and eastern states had higher rates of Parkinson disease, idiopathic epilepsy, migraine and tension-type headache, and meningitis, encephalitis, and tetanus.

Conclusions and Relevance  There is a large and increasing burden of noncommunicable neurological disorders in the US, with up to a 5-fold variation in the burden of and trends in particular neurological disorders across the US states. The information reported in this article can be used by health care professionals and policy makers at the national and state levels to advance their health care planning and resource allocation to prevent and reduce the burden of neurological disorders.

According to Gooch et al,¹ in 2011, nearly 100 million Americans were affected by at least 1 of the more than 1000 neurological disorders. This translates into an overall cost of $765 billion for the more prevalent conditions,¹ including Alzheimer disease (AD) and other dementias, chronic low back pain, stroke, migraine, epilepsy, traumatic brain injury (TBI), and Parkinson disease (PD). Although accurate data on incidence, prevalence, mortality, and disability from neurological disorders and their trends are important for evidence-based health care planning and resource allocation, there is a lack of national and state-level epidemiological data in the US, as well as their synthesis for use by health care planners.

Previous Global Burden of Diseases, Injuries, and Risk Factors (GBD) Study articles have reported burden of diseases, injuries, and risk factors among US states² and global, regional, and country-specific estimates of the burden from neurological disorders,^3,4 but no estimates for a comprehensive list of neurological disorders have been reported for the US states from this study. Globally, regionally, and at the country level of analysis, the burden of all noncommunicable neurological disorders, in terms of the absolute number of people who had, remained disabled by, or died from them, has increased significantly across all countries in the world, but the burden from communicable neurological disorders, such as tetanus, meningitis, and encephalitis, has decreased from 1990 to 2016.^5-14 This study provides estimates for noncommunicable and communicable neurological disorders at the state level from 1990 to 2017.

Details on the methodology of the GBD study overall¹⁵ and in association with the burden of neurological disorders have been published elsewhere.^5-14 In brief, using statistical modeling techniques, the GBD study allows use of all available epidemiological data (both published and unpublished) and routinely collected data (eg, vital registration, hospitalizations, medical claims) within and just outside of the country, region, or state of interest to provide the most accurate estimates of the disease burden, even for regions or states with no accurate epidemiological data.¹⁵ The burden estimates are presented in terms of age-adjusted annual rates per 100 000 people and numbers of prevalence, incidence, disability-adjusted life-years (DALYs), and deaths by cause (in millions), with corresponding 95% uncertainty intervals (UIs), and their trends or changes from 1990 to 2017.

Nonfatal estimates were obtained from systematic reviews, surveys, administrative health records, registries, and disease surveillance systems. We used available surveys and databases of claims information for US private and public insurance schemes, corrected for bias in health service encounters, as described elsewhere.^2,16,17 Data sources used for quantifying nonfatal outcomes are available online in the GBD results tool.¹⁸ Fatal estimates were obtained from vital registration data (death records from the National Center for Health Statistics and population counts from the US Census Bureau). The single cause of death was determined using the International Classification of Diseases, Ninth Revision, Ninth Revision, Clinical Modification; International Statistical Classification of Diseases and Related Health Problems, Tenth Revision; and International Statistical Classification of Diseases, Tenth Revision, Clinical Modification, with redistributions from less precise codes (such as ill-defined disease [R99] or injuries of undetermined intent [Y21-Y33]) to more specific diseases and injuries using regression methods of the subset of vital registration data for which we have multiple causes of death information. Under International Classification of Diseases rules, injury deaths are classified by the cause of injury (eg, fall or road injury) and not the nature of injury, such as TBI and spinal cord injuries (SCI). Thus, we report on incidence, prevalence, and years lived with disability for these causes, but not mortality. Causes of death data were analyzed using the Cause of Death Ensemble model (CODEm,¹⁹ with corrections for changes in coding practices for underlying causes of death as explained in detail elswhere²⁰), and nonfatal data were analyzed using DisMod-MR version 2.1 (World Health Organization),²¹ a bayesian meta-regression tool that adjusts data points for variations in study methods among different data sources and enforces consistency between prevalence, incidence, and mortality. For each disease and injury, years lived with disability for mutually exclusive sequelae (ie, disabling outcomes) were quantified as the product of prevalence and a weighting for severity (with the GBD disability weights). Values for disability weights have been derived from population surveys in 9 countries and an open-access internet survey.²² To account for co-occurrence of disease and injury outcomes, years lived with disability were corrected for comorbidity, assuming a multiplicative rather than additive function of disability weights.^23,24

To allow comparison with the GBD estimates on the global burden of neurological disorders,³ 14 neurological disorders that are quantified as part of GBD are included in this report. These are stroke, AD and other dementias, PD, idiopathic epilepsy (ie, epilepsy that is not secondary to any of the other GBD causes), multiple sclerosis (MS), motor neuron disease (MND), migraine, tension-type headache (TTH), TBI, SCI, brain and other central nervous system (CNS) cancers, meningitis, encephalitis, and tetanus.

Among the neurological disorders, the 5 most prevalent were TTH (121.6 [95% UI, 110-133] million people), migraine (68.5 [95% UI, 64-73] million people), stroke (7.8 [95% UI, 7.4-8.2] million people), AD and other dementias (2.9 [95% UI, 2.6-3.2] million people), and SCI (2.2 [95% UI, 2.0-2.3] million people) (Table 1), while the most burdensome in terms of DALYs were stroke (3.6 [95% UI, 3.3-3.9] million DALYs), AD and other dementias (2.6 [95% UI, 2.4-2.7] million DALYs), migraine (2.4 [95% UI, 1.5-3.4] million DALYs), idiopathic epilepsy (0.4 [95% UI, 0.3-0.6] million people), and PD (0.4 [95% UI, 0.3-0.4] million people). The 5 leading causes of death from neurological disorders were from AD and other dementias (258 600 [95% UI, 254 000-263 000] deaths), stroke (172 000 [95% UI, 166 000-178 000] deaths), PD (30 000 [95% UI, 24 000-31 000] deaths), MND (8400 [95% UI, 8000-9000] deaths), and MS (4000 [95% UI, 3000-4000] deaths). The highest incidence was of new-onset TTH (44.5 [95% UI, 40.0-48.8] million cases per year) followed by migraine (5.0 [95% UI, 4.6-5.5] million cases per year), TBI (0.96 [95% UI, 0.8-1.2] million cases per year), stroke (0.60 [95% UI, 0.55-0.65] million cases per year), and AD and other dementias (0.48 [0.47-0.57] million cases per year).

While the US-wide age-standardized incidence, prevalence, mortality, and DALY rates of most neurological disorders declined or remained flat from 1990 through 2017 (Table 2), the absolute number of incident cases, prevalent cases, mortality, and DALYs increased, except for meningitis and encephalitis (Table 1). In 2017, the 5 highest incidence rates were for TTH (13 014 [95% UI, 11 602-14 432] cases per 100 000 people), migraine (1722 [95% UI, 1578-1865] cases per 100 000 people), TBI (285 [95% UI, 238-341] cases per 100 000 people), stroke (115 [95% UI, 107-125] cases per 100 000 people), and AD and other dementias (85 [95% UI, 78-93] cases per 100 000 people). Prevalence was highest for TTH (34 642 [95% UI, 31 341-38 113] cases per 100 000 people), migraine (20 188 [95% UI, 18 678-21 750] cases per 100 000 people), stroke (1536 [95% UI, 1461-1621] cases per 100 000 people), SCI (541 [95% UI, 502-583] cases per 100 000 people), and TBI (502 [95% UI, 478-525] cases per 100 000 people). The 2 leading causes of mortality were AD and other dementias (38 [95% UI, 38-39] per 100 000 population per year) and stroke (29 [95% UI, 28-30] per 100 000 population per year). The 5 leading causes of DALYs (rates) were migraine (705 [95% UI, 446-1021] per 100 000 population per year), stroke (692 [95% UI, 625-759] per 100 000 population per year), AD and other dementias (419 [95% UI, 399-439] per 100 000 population per year), idiopathic epilepsy (124 [95% UI, 75-187] per 100 000 population per year), and brain and other nervous system cancers (120 [95% UI, 111-138] per 100 000 population per year).

For stroke, from 1990 to 2017, there were significant reductions in age-standardized incidence (−16.3% [95% UI, −19.1% to −13.8%]), mortality (−32.0% [95% UI, −34.5% to −29.8%]), and DALY (−24.0% [95% UI, −26.9% to −21.3]) rates, but no significant change in age-standardized prevalence (0.2% [95% UI, −3.8% to 3.3%]) (Table 2). Age-standardized DALY rates of stroke stopped declining and plateaued around 2010, with some nonsignificant trends to increase since 2015 (Figure 1; eFigure in the Supplement). Age-standardized incidence and prevalence of AD and other dementias decreased (−12.4% [95% UI, −19.2% to −5.2%] and −13.4% [95% UI, −20.6% to −5.1%], respectively), but mortality and DALY rates increased by 9.8% (95% UI, 7.3%-12.2%) and 1.2% (95% UI, −1.9% to 4.2%), respectively. For TBI and SCI, there were also significant decreases in age-standardized incidence (−29.1% [95% UI, −32.4% to −25.8%] and −30.5% [95% UI, −34.8% to −26.2%], respectively) and prevalence (−28.3% [95% UI, −29.7% to −26.9%] and −38.5% [95% UI, −43.1% to −34.0%], respectively). Although age-standardized mortality and DALY rates from brain and other CNS cancers decreased (−3.4% [95% UI, −9.2% to 6.8%] and −8.6% [95% UI, −15.5% to 5.4%], respectively), incidence and prevalence rates increased significantly (24.1% [95% UI, 12.4%-41.4%] and 52.2% [95% UI, 36.7%-76.5%], respectively). In meningitis, there were significant reductions in the age-standardized rates of incidence (−28.7% [95% UI, −32.9% to −24.4%]), prevalence (−44.8% [95% UI, −47.3% to −42.3%]), mortality (−64.4% [95% UI, −67.7% to −50.3%]), and DALY (−66.9% [95% UI, −70.1% to −55.9%]). In encephalitis, rates of incidence (−0.1% [95% UI, −0.7% to 0.6%]), prevalence (−10.1% [95% UI, −12% to −8.1%]), mortality (−20.6% [95% UI, −24.9% to −1.7%]), and DALY (−25.8% [95% UI, −30.7% to −5.8%]) also decreased. In PD, there were small but significant increases in the age-standardized rates of incidence (21.9% [95% UI, 11.2%-14.6%]), prevalence (16.2% [95% UI, 2.7%-31%]), mortality (33.1% [95% UI, −4.6% to 41.7%]), and DALY (24.8% [95% UI, −5.2% to 32.9%]) of PD. Age-standardized incidence (17.4% [95% UI, −6% to 45.1%]), prevalence (15.2% [95% UI, −7.5% to 43.3%]), and DALY (5.5% [95% UI, −18.4% to 33.2%]) rates of epilepsy increased, but mortality rates decreased (−2.7% [95% UI, −7.8% to 1.5%]). There was an increase in the age-standardized incidence, prevalence, mortality, and DALY rates of MS (13.2% [95% UI, 7.3%-18.9%], 14.7% [95% UI, 8.1%-21.3%], 32.8% [95% UI, −20.1% to 56.1%], and 16.6% [95% UI, −1.4% to 26.2%], respectively) and MND (12.5% [95% UI, 9.8%-15.3%], 0.3% [95% UI, −4.4% to 5.6%], 38.3% [95% UI, 30%-45.6%], and 20.9% [95% UI, 13.9%-27.6%], respectively). There were small increases in the incidence, prevalence, and DALY age-standardized rates of migraine (1.6% [95% UI, −0.8% to 4.2%], 1.4% [95% UI, −0.8% to 4%], and 1.5% [95% UI, −0.8% to 4%], respectively) and TTH (0.4% [95% UI, −2.1% to 2.9%], 0.5% [95% UI, −2% to 3.3%], and 0.1% [95% UI, −1.5% to 1.9%], respectively).

However, the absolute numbers of people affected by noncommunicable neurological disorders (Table 1) in terms of incident, prevalent, and fatal cases, as well as DALYs, have increased substantially from 1990 to 2017 (except with respect to TBI incident and SCI prevalent cases, where small, nonsignificant reductions were observed). The largest increases were observed for (in order of increase) PD, MND, AD and other dementias, brain and other CNS cancers, and stroke.

Figure 2 and Figure 3 show age-standardized incidence, prevalence, mortality, and DALY rates of the selected neurological disorders in the US states in 2017. Age-standardized prevalence, incidence, mortality, and DALY rates for specific neurological disorders in the US states and changes in the rates from 1990 to 2017 and the US states’ ranking based on the 2017 estimates are described and shown in eTables 1 through 13 in the Supplement.

The different metrics of age-standardized rates varied between the US states from a 1.2-fold difference for TTH to 7.5-fold for tetanus. Southeastern states and Arkansas had a relatively higher burden for stroke, northern states had a relatively higher burden of MS, and eastern states had higher rates of PD, idiopathic epilepsy, migraine, TTH, and meningitis, encephalitis, and tetanus (eFigure, eAppendix, and eTables 1 through 12 in the Supplement).

From 1990 to 2017, the direction of trends in changes in the age-standardized incidence, prevalence, mortality, and DALY rates across US states mirrored those for the country as a whole. Over that period of time, there were very few changes in any of the states in the rates of migraine and TTH.

To our knowledge, this is the first comprehensive report on incidence, prevalence, mortality, and DALY estimates and their trends from 1990 to 2017 for 14 neurological disorders for the individual 50 US states and the country overall. The study showed reductions in the age-adjusted rates of most burden metrics of stroke, AD and other dementias, TBI, SCI, meningitis, and encephalitis, but increasing numbers of people affected by various neurological disorders in the US, with a significant (up to 5-fold) variation in the burden of and trends in particular neurological disorders across the US states. Falling rates of stroke, AD and other dementias, TBI, SCI, meningitis, and encephalitis might suggest that primary prevention of these disorders are beginning to show an influence, while between-state variations may be associated with differences in the case ascertainment, as well as access to health care; racial/ethnic, genetic, and socioeconomic diversity; quality and comprehensiveness of preventive strategies; and risk factor distribution. For dementia, improving educational levels of cohort reaching the age groups at greatest risk of disease may also be contributing to a modest decline over time.²⁵ While globally, 6 neurological disorders (AD and other dementias, PD, epilepsy, MS, MND, and headache disorders) in 2017 constituted 4.4% (95% UI, 3.7%-5.3%)²⁶ of total DALYs and ranked ninth among the leading causes of DALYs, in the US, they constituted 6.7% (95% UI, 6.0%-7.6%) and ranked fifth. In 2017, deaths from these neurological disorders were ranked fifth (5.5% [95% UI, 5.4%-5.6%]) among all causes of death globally and third (10.8% [95% UI, 10.6%-10.9%]) in the US.²⁶ Similar findings were observed for neurological disorders in Western European countries.³ Given the association of prevalent disorders, such as AD, stroke, PD, and MND with older age, the higher rank of neurological disorders in the US can be explained by the longer life expectancy in the US compared with the world overall. In addition, it may also be attributable to better case ascertainment in the US, including improved diagnosis, surveillance or reporting, and health care access.

The exact causes for significant between-state variations in the age-standardized rates of some neurological disorders are unknown, but these may be associated with between-state differences in the completeness of medical examinations and accuracy of diagnosis, completeness and accuracy of data from medical claims, and referral patterns to specialized centers (eg, seeking medical advice for brain tumors outside of the place of residence), despite corrections for these measurement biases during data analysis. The highest between-state variations were observed for tetanus, but the number of tetanus cases was very low, and thus large relative variation reflected variation by just 1 or a few cases. However, our data on between-state variations in the burden from neurological disorders concur with previous GBD observations of large differences in the burden of disease among US states² and significant geographical variations in the burden of neurological disorders in the world.³ For example, for stroke, there is a strong increasing gradient from north to south, while for MS, the gradient is decreasing from north to south. Both gradients might have been expected based on our understanding of the epidemiology of both diseases.^27-29 While confirming previous observations of the so-called stroke belt mortality in the southeastern United States, unlike previous estimates that identified North Carolina, South Carolina, and Georgia with a higher stroke mortality rate than the other states of the stroke belt,^30,31 our 2017 GBD stroke mortality estimates show that the stroke belt is now in Alabama, Mississippi, and South Carolina. Our dementia mortality estimates also showed a higher percentage change (increase) in the stroke belt states compared with the other states, likely attributable to the reciprocal association between stroke and dementia.³² These findings can be used to set research priorities (eg, identifying causes of between-state variations in the burden of neurological disorders). These data will also allow health care professionals and policy makers on national and state levels to allocate resources (eg, number of hospital beds, specialists, services) and give priorities for improving care for people with some major neurological disorders in each US state.

The finding that the 3 most burdensome neurological disorders in the US in terms of the absolute numbers of DALYs are stroke, AD and other dementias, and migraine is in line with ranking of age-standardized DALY rates for neurological disorders found in other high-income countries in 2016.³ There were diverse changes in the rates of all neurological disorders in the country overall (eg, decreased incidence rates of stroke, AD and other dementias, TBI, SCI, and meningitis, and increased incidence rates of PD, MS, MND, and brain and other nervous system cancers) and across all US states from 1990 to 2017. However, the absolute number of people who are affected by noncommunicable neurological disorders over that period has increased substantially and is likely to continue increasing because of aging of the US population and population growth. Unfavorable trends in some lifestyle factors (eg, overweight, fasting plasma glucose level)² in the US are also likely additional contributing factors for the increasing burden from some neurological disorders (eg, stroke, dementia).³³ These developments are consistent with the global trends³ and support the call to action to reduce the burden of neurological disorders in the United States, as outlined by Gooch et al.¹

Although we understand that individuals may have more than 1 neurological condition, assuming no overlap between stroke, TBI, SCI, brain and other CNS cancers, meningitis, encephalitis, tetanus, and other neurological disorders (AD and other dementias, PD, idiopathic epilepsy, MS, MND, migraine, TTH, and other neurological disorders), it can be estimated that in 2017 more than 200 million Americans (60% of the population) were afflicted by at least 1 neurological disorder, ranging from TTH and migraine to stroke and dementia. This is twice the estimate by Gooch et al¹ and 9 times the estimate by Borlongan et al.³⁴ The greater than previously reported overall prevalence of neurological disorders in the US may be explained by at least 3 factors. First, we included many disorders in this study that Gooch et al¹ did not, such as TTH (the most prevalent of all neurological disorders analyzed in the GBD study), brain and other CNS cancers, tetanus, meningitis, and encephalitis, although they¹ did include chronic low back pain, which we did not. The selection of neurological disorders included in this analysis was largely based on 2 factors: (1) the GBD study currently provides estimates of the burden of only these specific neurological disorders, and (2) these neurological disorders are considered by the GBD study as conditions for which neurologists play a particular important role in care and diagnosis (as opposed to, for example, low back pain, for which the role of a neurologist is less dominant). Second, Gooch et al¹ based their analysis on previously published articles only, while the GBD study analyses also included administrative data and modeling, thus allowing estimates for US states with no epidemiological data on a particular neurological disorder. Differences in the methodologies may explain differences in the estimates of stroke prevalence (7.8 million in the GBD study vs 6.8 million in the Gooch et al study¹), AD and other dementias (2.9 million vs 5.3 million), epilepsy (1.4 million vs 2.8 million), TBI (2.1 million vs 1.4 million), and SCI (2.2 million vs 0.3 million). The large difference in SCI cases may reflect a weakness in GBD methods, which rely on sparse data on the association between the incidence of a cause of injury (eg, falls and road injury) and the nature of the injury (eg, fall or SCI), which should be examined in future rounds of GBD. Our GBD estimates of PD (0.6 million), migraine (69 million), MS (0.4 million), and MND (38 000) are close to those reported by Gooch et al (0.6 million, 72 million, 0.4 million, and 18 000-30 000, respectively).¹ Third, the Gooch et al¹ study was based on articles published prior to 2017, with many of them referring to the data collected 5 to 10 years ago; thus, ongoing aging of the population and population growth may partly explain the greater prevalence of selected neurological disorders in our study.

General limitations of the GBD study discussed elsewhere³ fully apply to this report and may account for differences between these data and those collected by other governmental or disease-specific organizations. Specifically, for this report, we were not able to provide burden estimates for all neurological disorders combined, or burden estimates by age and sex, because these estimates will be the subjects of separate reports. In addition, some very prevalent neurological disorders (eg, restless leg syndrome and peripheral neuropathy are not currently estimated by GBD) and some common disorders (eg, low back and neck pain) are not regarded as neurological disorders in this article, although they are at least partly within the realm of neurology. Inclusion of these currently unaccounted disorders would increase the estimates of the burden of neurological disorders. Other limitations specific to this report include (1) difficulty in determining death from dementia because coding practices have changed by orders of magnitude over the last 30 years; (2) lack of data to quantify headaches in the US; and (3) accuracy of medical claims and hospitalization data and potential inaccuracies in the adjustments of administrative data to those reported in epidemiological studies. Because GBD study estimates are updated annually, the current limitations can be addressed, and with an increasing amount of data being added year to year, a more accurate picture of the burden of neurological disorders in the US can be made.

In summary, this report showed that, while there were reductions in the rates of most burden metrics of stroke, Alzheimer and other dementias, TBI, SCI, meningitis, and encephalitis, there was a large and increasing number of people affected by various neurological disorders in the US, with a significant variation of the burden of and trends in particular neurological disorders across the US states. The reasons for geographic variations among different US states need to be explored further. Health care professionals and policy makers at the national and state levels can use the information reported in this article to advance their health care planning and resource allocation, including research funding, to prevent and reduce the morbidity and mortality of neurological disorders.

Accepted for Publication: July 30, 2020.

Corresponding Author: Valery L. Feigin, MD, PhD, National Institute for Stroke and Applied Neurosciences, Faculty of Health and Environmental Sciences, Auckland University of Technology School of Public Health and Psychosocial Studies, 90 Akoranga Dr, Northcote, Auckland 0627, New Zealand (valery.feigin@aut.ac.nz) and Theo Vos, MD, PhD, Institute for Health Metrics and Evaluation, University of Washington, Population Health Building, Hans Rosling Center, 3980 15th Ave NE, Seattle, WA 98195 (tvos@uw.edu).

Published Online: November 2, 2020. doi:10.1001/jamaneurol.2020.4152

GBD 2017 US Neurological Disorders Authors: Valery L. Feigin, PhD; Theo Vos, PhD; Fares Alahdab, MSc; Arianna Maever L. Amit, BS; Till Winfried Bärnighausen, MD; Ettore Beghi, MD; Mahya Beheshti, MD; Prachi P. Chavan, PhD; Michael H. Criqui, MD; Rupak Desai, MBBS; Samath Dhamminda Dharmaratne, MD; E. Ray Dorsey, MD; Arielle Wilder Eagan, MSW; Islam Y. Elgendy, MD; Irina Filip, MD; Simona Giampaoli, MD; Giorgia Giussani, PhD; Nima Hafezi-Nejad, MD; Michael K. Hole, MD; Takayoshi Ikeda, PhD; Catherine Owens Johnson, PhD; Rizwan Kalani, MD; Khaled Khatab, PhD; Jagdish Khubchandani, PhD; Daniel Kim, DrPH; Walter J. Koroshetz, MD; Vijay Krishnamoorthy, MD; Rita V. Krishnamurthi, PhD; Xuefeng Liu, PhD; Warren David Lo, MD; Giancarlo Logroscino, PhD; George A. Mensah, MD; Ted R. Miller, PhD; Salahuddin Mohammed, MSc; Ali H. Mokdad, PhD; Maziar Moradi-Lakeh, MD; Shane Douglas Morrison, MD; Veeresh Kumar N. Shivamurthy, MD; Mohsen Naghavi, MD; Emma Nichols, MPH; Bo Norrving, PhD; Christopher M. Odell, MPP; Elisabetta Pupillo, PharmD; Amir Radfar, MD; Gregory A. Roth, MD; Azadeh Shafieesabet, MD; Aziz Sheikh, MD; Sara Sheikhbahaei, MD; Jae Il Shin, MD; Jasvinder A. Singh, MD; Timothy J. Steiner, PhD; Lars Jacob Stovner, PhD; Mitchell Taylor Wallin, MD; Jordan Weiss, MA; Chenkai Wu, PhD; Joseph Raymond Zunt, MD; Jaimie D. Adelson, PhD; Christopher J. L. Murray, PhD.

Affiliations of GBD 2017 US Neurological Disorders Authors: Faculty of Health and Environmental Sciences, Auckland University of Technology School of Public Health and Psychosocial Studies, Auckland, New Zealand (Feigin, Krishnamurthi); Institute for Health Metrics and Evaluation, University of Washington, Seattle (Feigin, Vos, Dhamminda Dharmaratne, Owens Johnson, Mokdad, Naghavi, Nichols, Odell, Roth, Adelson, Murray); Research Center of Neurology, Moscow, Russia (Feigin); Department of Health Metrics Sciences, University of Washington School of Medicine, Seattle (Vos, Dhamminda Dharmaratne, Mokdad, Naghavi, Roth, Murray); Mayo Evidence-Based Practice Center, Mayo Clinic Foundation for Medical Education and Research, Rochester, Minnesota (Alahdab); Department of Epidemiology and Biostatistics, University of the Philippines Manila, Manila, Philippines (Amit); Johns Hopkins University School of Public Health, Baltimore, Maryland (Amit); Heidelberg Institute of Global Health, Heidelberg University, Heidelberg, Germany (Bärnighausen); Harvard University T.H. Chan School of Public Health, Boston, Massachusetts (Bärnighausen); Department of Neuroscience, Mario Negri Institute for Pharmacological Research, Milan, Italy (Beghi, Pupillo); Department of Physical Medicine and Rehabilitation, New York University, New York (Beheshti); Department of Epidemiology and Environmental Health, the University of Buffalo, Buffalo, New York (Chavan); Department of Family Medicine and Public Health, University of California, San Diego, La Jolla (Criqui); Division of Cardiology, Atlanta Veterans Affairs Medical Center, Decatur, Georgia (Desai); Department of Community Medicine, University of Peradeniya, Peradeniya, Sri Lanka (Dhamminda Dharmaratne); University of Rochester, Rochester, New York (Dorsey); Department of Global Health and Social Medicine, Harvard University, Boston, Massachusetts (Wilder Eagan); Department of Social Services, Tufts Medical Center, Boston, Massachusetts (Wilder Eagan); Division of Cardiology, Massachusetts General Hospital, Boston (Elgendy); Division of Cardiology, Harvard University, Boston, Massachusetts (Elgendy); Psychiatry Department, Kaiser Permanente, Fontana, California (Filip); A.T. Still University School of Osteopathic Medicine in Arizona, Arizona School of Health Sciences, Mesa, Arizona (Filip); Department of Cardiovascular Endocrine-Metabolic Diseases and Aging, Istituto Superiore di Sanità (Italian National Institute of Health), Rome, Italy (Giampaoli); Laboratory of Neurological Disorders, Mario Negri Institute for Pharmacological Research, Milan, Italy (Giussani); Department of Radiology and Radiological Science, Johns Hopkins University, Baltimore, Maryland (Hafezi-Nejad, Sheikhbahaei); Tehran University of Medical Sciences School of Medicine, Tehran, Iran (Hafezi-Nejad); Department of Pediatrics, The University of Texas, Austin, Austin (Hole); Department of Biostatistics and Epidemiology, Auckland University of Technology, Auckland, New Zealand (Ikeda); Department of Neurology, University of Washington, Seattle (Kalani, Zunt); Faculty of Health and Wellbeing, Sheffield Hallam University, Sheffield, United Kingdom (Khatab); Ohio University College of Arts and Sciences, Zanesville (Khatab); Department of Nutrition and Health Science, Ball State University, Muncie, Indiana (Khubchandani); Department of Health Sciences, Northeastern University, Boston, Massachusetts (Kim); National Institutes of Neurological Disorders and Stroke, National Institute of Health, Bethesda, Maryland (Koroshetz); Department of Anesthesiology, Duke University, Durham, North Carolina (Krishnamoorthy); Department of Anesthesiology, University of Washington, Seattle (Krishnamoorthy); Department of Systems, Populations, and Leadership, University of Michigan, Ann Arbor (Liu); Department of Pediatrics, Ohio State University, Columbus (Lo); Department of Pediatric Neurology, Nationwide Children’s Hospital, Columbus, Ohio (Lo); Department of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari Aldo Moro, Bari, Italy (Logroscino); Department of Clinical Research in Neurology, Fondazione Cardinale Giovanni Panico Hospital, Tricase, Italy (Logroscino); Center for Translation Research and Implementation Science, National Institutes of Health, Bethesda, Maryland (Mensah); Department of Medicine, University of Cape Town, Cape Town, South Africa (Mensah); Pacific Institute for Research & Evaluation, Calverton, Maryland (Miller); School of Public Health, Curtin University, Perth, Australia (Miller); Department of Biomolecular Sciences, University of Mississippi, Oxford (Mohammed); Department of Pharmacy, Mizan-Tepi University, Mizan, Ethiopia (Mohammed); Preventive Medicine and Public Health Research Center, Iran University of Medical Sciences, Tehran, Iran (Moradi-Lakeh); Section of Plastic Surgery, University of Michigan, Ann Arbor (Morrison); Department of Neurology, Emory University, Atlanta, Georgia (Shivamurthy); Department of Clinical Sciences, Lund University, Lund, Sweden (Norrving); University of Central Florida College of Medicine, Orlando (Radfar); Division of Cardiology, University of Washington, Seattle (Roth); Department of Cardiology, Charité Medical University Berlin, Berlin, Germany (Shafieesabet); Center for Stroke Research Berlin, Berlin, Germany (Shafieesabet); Centre for Medical Informatics, University of Edinburgh, Edinburgh, United Kingdom (Sheikh); Division of General Internal Medicine, Harvard University, Boston, Massachusetts (Sheikh); Yonsei University College of Medicine, Seoul, South Korea (Shin); The University of Alabama at Birmingham School of Medicine, Birmingham (Singh); Medicine Service, US Department of Veterans Affairs, Birmingham, Alabama (Singh); Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway (Steiner, Stovner); Division of Brain Sciences, Imperial College London, London, United Kingdom (Steiner); Department of Neurology and Clinical Neurophysiology, St Olavs Hospital, Trondheim, Norway (Stovner); Department of Neurology, George Washington University, Washington, DC (Wallin); University of Maryland School of Medicine, Baltimore (Wallin); Department of Demography, University of California, Berkeley, Berkeley (Weiss); Global Health Research Center, Duke Kunshan University, Kunshan, China (Wu); Duke Global Health Institute, Duke University, Durham, North Carolina (Wu).

Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2020 GBD 2017 US Neurological Disorders Collaborators. JAMA Neurology.

Author Contributions: Dr Vos had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: Feigin, Vos, Bärnighausen, Dorsey, Kalani, Krishnamurthi, Salahuddin, Mokdad, Naghavi, Roth.

Acquisition, analysis, or interpretation of data: Feigin, Vos, Alahdab, Amit, Beghi, Beheshti, Chavan, Criqui, Desai, Dharmaratne, Eagan, Elgendy, Filip, Giampaoli, Giussani, Hafezi-Nejad, Hole, Ikeda, Johnson, Kalani, Khatab, Khubchandani, Kim, Koroshetz, Krishnamoorthy, Liu, Lo, Logroscino, Mensah, Miller, Salahuddin, Mokdad, Moradi-Lakeh, Morrison, N. Shivamurthy, Naghavi, Nichols, Norrving, Odell, Pupillo, Radfar, Roth, Shafieesabet, Sheikh, Sheikhbahaei, Shin, Singh, Steiner, Stovner, Wallin, Weiss, Wu, Zunt, Adelson, Murray.

Drafting of the manuscript: Feigin, Vos, Salahuddin, Mokdad, Wallin.

Critical revision of the manuscript for important intellectual content: Feigin, Vos, Alahdab, Amit, Bärnighausen, Beghi, Beheshti, Chavan, Criqui, Desai, Dharmaratne, Dorsey, Eagan, Elgendy, Filip, Giampaoli, Giussani, Hafezi-Nejad, Hole, Ikeda, Johnson, Kalani, Khatab, Khubchandani, Kim, Koroshetz, Krishnamoorthy, Krishnamurthi, Liu, Lo, Logroscino, Mensah, Miller, Salahuddin, Mokdad, Moradi-Lakeh, Morrison, N. Shivamurthy, Naghavi, Nichols, Norrving, Odell, Pupillo, Radfar, Roth, Shafieesabet, Sheikh, Sheikhbahaei, Shin, Singh, Steiner, Stovner, Weiss, Wu, Zunt, Adelson, Murray.

Statistical analysis: Vos, Bärnighausen, Hafezi-Nejad, Ikeda, Johnson, Khatab, Liu, Salahuddin, Mokdad, Naghavi, Nichols, Roth, Sheikhbahaei, Wallin, Wu, Adelson.

Administrative, technical, or material support: Alahdab, Criqui, Eagan, Salahuddin, Mokdad, Odell.

Supervision: Feigin, Vos, Bärnighausen, Elgendy, Khatab, Salahuddin, Mokdad, N. Shivamurthy, Naghavi, Shin.

Other—Review and approval of the final version to be published: Radfar.

Other—Reviewing plausibility of statistical models, and model outputs: Moradi-Lakeh.

Other—data sources and feedback: Alahdab.

Other— Member of the Global Burden of Disease Scientific Council: Mensah.

Other—Review manuscript: N. Shivamurthy.

Other—Review and approval of the final version to be published: Filip, Khubchandani, Liu.

Conflict of Interest Disclosures: Dr Beghi reports grants from Italian Ministry of Health, Italian Ministry of Health, American ALS Association, and SOBI and personal fees from Arvelle Therapeutics and Eisai, outside the submitted work. Dr Dorsey reports personal fees from American Academy of Neurology courses, American Neurological Association, University of Michigan, 23andMe, Abbott, AbbVie, American Well, Biogen, BrainNeuroBio, Clintrex, Curasen Therapeutics, DeciBio, Denali Therapeutics, GlaxoSmithKline, Grand Rounds, Karger, Lundbeck, MC10, MedAvante, Medical-Legal services, Mednick Associates, National Institute of Neurological Disorders and Stroke, Olson Research Group, Optio, Origent Data Sciences Inc, Otsuka, Prilenia, Putnam Associates, Roche, Sanofi, Shire, Spark, Sunovion Pharma, Teva, Theravance, UCB, and Voyager Therapeutics; grants from AbbVie, Acadia Pharmaceuticals, AMC Health, Biosensics, Burroughs Wellcome Fund, Davis Phinney Foundation, Duke University, Food and Drug Administration, GlaxoSmithKline, Greater Rochester Health Foundation, Huntington Study Group, Michael J. Fox Foundation, National Institutes of Health/National Institute of Neurological Disorders and Stroke, National Science Foundation, Nuredis Pharmaceuticals, Patient-Centered Outcomes Research Institute, Pfizer, Prana Biotechnology, Raptor Pharmaceuticals, Roche, Safra Foundation, Teva Pharmaceuticals, and University of California, Irvine; editorial services from Karger Publications; and an ownership interest in Grand Rounds (a second-opinion service), outside the submitted work. Dr Norrving reports personal fees from AstraZeneca and Bayer, outside the submitted work. Dr Pupillo reports grants from American Amyotrophic Lateral Sclerosis Association and other support from Revalesio Corporation outside the submitted work. Dr Sheikh reports grants from Health Data Research UK, outside the submitted work; personal fees from Crealta/Horizon, Medisys, Fidia, UBM LLC, Trio Health, Medscape, WebMD, Clinical Care Options, Clearview Healthcare Partners, Putnam Associates, Focus Forward, Navigant Consulting, Spherix, Practice Point Communications, the National Institutes of Health, the American College of Rheumatology, and Simply Speaking; ownership in stock options from Amarin Pharmaceuticals and Viking Pharmaceuticals; other support from Vaxart Pharmaceuticals; and nonfinancial support from the US Food and Drug Administration Arthritis Advisory Committee, the steering committee of OMERACT, an international organization that develops measures for clinical trials and receives arm’s length funding from 12 pharmaceutical companies, and Veterans Affairs Rheumatology Field Advisory Committee, the UAB Cochrane Musculoskeletal Group Satellite Center on Network Meta-analysis, outside the submitted work. In addition, Dr Singh is the chair of the Veterans Affairs Rheumatology Field Advisory Committee, the editor and director of the UAB Cochrane Musculoskeletal Group Satellite Center on Network Meta-analysis, and a former member of the following committees: the American College of Rheumatology's Annual Meeting Planning Committee and Quality of Care Committees, the Chair of the American College of Rheumatology Meet the Professor, Workshop and Study Group Subcommittee and the cochair of the American College of Rheumatology Criteria and Response Criteria subcommittee. Dr Steiner reports personal fees from Eli Lilly outside the submitted work. Dr Stovner reports grants and personal fees from Allergan, Teva, and Novartis and personal fees from Lundbeck, Lilly, and Springer Publisher, outside the submitted work. Dr Wu reports personal fees from Health Keepers and grants from Suzhou Science and Technology Bureau, Kunshan Government, and Duke Kunshan University, outside the submitted work. Dr Roth reported grants from the Bill and Melinda Gates Foundation and Cardiovascular Medical Research and Education Foundation during the conduct of the study. No other disclosures were reported.

Funding/Support: This study was supported by the Bill & Melinda Gates Foundation. Dr Sheikh acknowledges support from Health Data Research UK. Dr Bärnighausen acknowledges support from the Alexander von Humboldt Foundation through the Alexander von Humboldt Professor Award, funded by the German Federal Ministry of Education and Research.

Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.