Racial and ethnic differences among amyotrophic lateral sclerosis cases in the United States

被引:52
作者
Rechtman, Lindsay [1 ]
Jordan, Heather [1 ]
Wagner, Laurie [1 ]
Horton, D. Kevin [2 ]
Kaye, Wendy [1 ]
机构
[1] McKing Consulting Corp, Atlanta, GA USA
[2] Agcy Tox Subst & Dis Registry, Atlanta, GA USA
关键词
Amyotrophic lateral sclerosis; motor neuron disease; epidemiology; incidence studies; race; MOTOR-NEURON DISEASE; HONG-KONG; POPULATION; ALS; EPIDEMIOLOGY; HEALTH;
D O I
10.3109/21678421.2014.971813
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Our objective was to describe racial and ethnic differences of amyotrophic lateral sclerosis (ALS) in distinct geographic locations around the United States (U.S.). ALS cases for the period 2009-2011 were identified using active case surveillance in three states and eight metropolitan areas. Of the 5883 unique ALS cases identified, 74.8% were white, 9.3% were African-American/black, 3.6% were Asian, 12.0% were an unknown race, and 0.3% were marked as some other race. For ethnicity, 77.5% were defined as non-Hispanic, 10.8% Hispanic, and 11.7% were of unknown ethnicity. The overall crude average annual incidence rate was 1.52 per 100,000 person-years and the rate differed by race and ethnicity. The overall age-adjusted average annual incidence rate was 1.44 per 100,000 person-years and the age-adjusted average incidence rates also differed by race and ethnicity. Racial differences were also found in payer type, time from symptom onset to diagnosis, reported El Escorial criteria, and age at diagnosis. In conclusion, calculated incidence rates demonstrate that ALS occurs less frequently in African-American/blacks and Asians compared to whites, and less frequently in Hispanics compared to non-Hispanics in the U.S. A more precise understanding of racial and ethnic variations in ALS may help to reveal candidates for further studies of disease etiology and disease progression.
引用
收藏
页码:65 / 71
页数:7
相关论文
共 26 条
[1]  
Agency for Healthcare Research and Quality, 2011, DISP HEALTHC QUAL RA
[2]  
Antao VC, 2012, J ENVIRON HEALTH, V75, P28
[3]   The epidemiology of ALS and the role of population-based registries [J].
Beghi, Ettore ;
Logroscino, Giancarlo ;
Chio, Adriano ;
Hardiman, Orla ;
Mitchell, Douglas ;
Swingler, Robert ;
Traynor, Bryan J. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2006, 1762 (11-12) :1150-1157
[4]   El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis [J].
Brooks, BR ;
Miller, RG ;
Swash, M ;
Munsat, TL .
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05) :293-299
[5]   Global Epidemiology of Amyotrophic Lateral Sclerosis: A Systematic Review of the Published Literature [J].
Chio, A. ;
Logroscino, G. ;
Traynor, B. J. ;
Collins, J. ;
Simeone, J. C. ;
Goldstein, L. A. ;
White, L. A. .
NEUROEPIDEMIOLOGY, 2013, 41 (02) :118-130
[6]   Epidemiology of ALS in Italy A 10-year prospective population-based study [J].
Chio, A. ;
Mora, G. ;
Calvo, A. ;
Mazzini, L. ;
Bottacchi, E. ;
Mutani, R. .
NEUROLOGY, 2009, 72 (08) :725-731
[7]   Ethnic variation in the incidence of ALS - A systematic review [J].
Cronin, Simon ;
Hardiman, Orla ;
Traynor, Bryan J. .
NEUROLOGY, 2007, 68 (13) :1002-1007
[8]  
Fong GCY, 2005, AMYOTROPH LATERAL SC, V6, P164, DOI 10.1080/14660820510028412
[9]   Motor neuron disease in Hong Kong Chinese: Epidemiology and clinical picture [J].
Fong, KY ;
Yu, YL ;
Chan, YW ;
Kay, R ;
Chan, J ;
Yang, Z ;
Kwan, MC ;
Leung, KP ;
Li, PCK ;
Lam, TH ;
Cheung, RTF .
NEUROEPIDEMIOLOGY, 1996, 15 (05) :239-245
[10]   CONFIDENCE-INTERVALS RATHER THAN P-VALUES - ESTIMATION RATHER THAN HYPOTHESIS-TESTING [J].
GARDNER, MJ ;
ALTMAN, DG .
BMJ-BRITISH MEDICAL JOURNAL, 1986, 292 (6522) :746-750