Global Epidemiology of Amyotrophic Lateral Sclerosis: A Systematic Review of the Published Literature

被引:569
|
作者
Chio, A. [1 ]
Logroscino, G. [2 ]
Traynor, B. J. [3 ]
Collins, J. [4 ]
Simeone, J. C. [4 ]
Goldstein, L. A. [5 ]
White, L. A. [6 ]
机构
[1] Univ Turin, Rita Levi Montalcini Dept Neurosci, IT-10126 Turin, Italy
[2] Univ Bari, Bari, Italy
[3] NIA, NIH, Bethesda, MD 20892 USA
[4] United BioSource Corp, Lexington, MA USA
[5] Sci Solut, United BioSource Corp Envis Grp, Southport, CT USA
[6] Biogen Idec Inc, Weston, MA USA
关键词
Amyotrophic lateral sclerosis; Case ascertainment; Demographics; Diagnostic criteria; Epidemiology; Incidence; Prevalence; Temporal and age-related trends; MOTOR-NEURON DISEASE; SOUTH-EAST ENGLAND; HEXANUCLEOTIDE REPEAT; CLINICAL-FEATURES; REGGIO-EMILIA; KII PENINSULA; ALS INCIDENCE; PREVALENCE; COUNTY; MORTALITY;
D O I
10.1159/000351153
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Amyotrophic lateral sclerosis (ALS) is relatively rare, yet the economic and social burden is substantial. Having accurate incidence and prevalence estimates would facilitate efficient allocation of healthcare resources. Objective: To provide a comprehensive and critical review of the epidemiological literature on ALS. Methods: MEDLINE and EMBASE (1995-2011) databases of population-based studies on ALS incidence and prevalence reporting quantitative data were analyzed. Data extracted included study location and time, design and data sources, case ascertainment methods and incidence and/or prevalence rates. Medians and interquartile ranges (IQRs) were calculated, and ALS case estimates were derived using 2010 population estimates. Results: In all, 37 articles met the inclusion criteria. In Europe, the median incidence rate (/100,000 population) was 2.08 (IQR 1.47-2.43), corresponding to an estimated 15,355 (10,852-17,938) cases. Median prevalence (/100,000 population) was 5.40 (IQR 4.06-7.89), or 39,863 (29,971-58,244) prevalent cases. Conclusions: Disparity in rates among ALS incidence and prevalence studies may be due to differences in study design or true variations in population demographics such as age and geography, including environmental factors and genetic predisposition. Additional large-scale studies that use standardized case ascertainment methods are needed to more accurately assess the true global burden of ALS. copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:118 / 130
页数:13
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