Incidence of ALS in Lombardy, Italy

被引:118
作者
Beghi, E.
Millul, A.
Micheli, A.
Vitelli, E.
Logroscino, G.
机构
[1] Ist Ric Farmacol Mario Negri, I-20157 Milan, Italy
[2] Univ Milano Bicocca, Neurol Clin, Monza, Italy
[3] Fdn S Maugeri, Clin Lavoro Riabil, Gussago, Italy
[4] AO Prov Lodi, Dipartimento Neurol, Lodi, Italy
[5] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
D O I
10.1212/01.wnl.0000250339.14392.bb
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To assess the incidence and trends of ALS in a large population at risk. Methods: This study was performed in nine provinces of Lombardy in Northern Italy (population 4,947,554). Patients with newly diagnosed ALS were enrolled during the period 1998 to 2002 through a prospective regional register. For each patient, the main demographic and clinical information was collected by the caring physicians and reviewed by a panel of experts according to the original and revised El Escorial diagnostic criteria. Overall, age- and sex-specific and standardized annual incidence rates were calculated for the entire population and for each year and province separately. Results: We studied 517 patients (M:F ratio 1.3) aged 18 to 92 years (mean 63.6). Onset of symptoms was bulbar in 29% of cases. ALS was definite in 45%, probable in 27%, probable laboratory supported in 3.5%, possible in 15%, and suspected in 10%. Mean disease duration at diagnosis was 10.6 months. The standardized incidence rate was 2.09 per 100,000/year (95% CI: 1.17 to 3.18). The rate, which was 2.43 in men and 1.76 in women, tended to increase up to ages 65 to 74 and to decrease thereafter. The rate was unchanged over time and presented moderate variations across provinces. The incidence rate of definite ALS was 0.93 (spinal-onset ALS 1.35; bulbar-onset ALS 0.74) and was consistently higher in men with spinal-onset ALS vs men with bulbar-onset ALS and women. Conclusions: The incidence of ALS varied according to age, sex, and site of onset. No temporal and geographic clusters were detected over a 5-year period.
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页码:141 / 145
页数:5
相关论文
共 21 条
[1]   Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia [J].
Andersen, PM ;
Nilsson, P ;
Keranen, ML ;
Forsgren, L ;
Hagglund, J ;
Karlsborg, M ;
Ronnevi, LO ;
Gredal, O ;
Marklund, SL .
BRAIN, 1997, 120 :1723-1737
[2]   An evidence-based medicine approach to the evaluation of the role of exogenous risk factors in sporadic amyotrophic lateral sclerosis [J].
Armon, C .
NEUROEPIDEMIOLOGY, 2003, 22 (04) :217-228
[3]  
Beghi E, 2001, AMYOTROPH LATERAL SC, V2, P99
[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
[6]   Severely increased risk of amyotrophic lateral sclerosis among Italian professional football players [J].
Chiò, A ;
Benzi, G ;
Dossena, M ;
Mutani, R ;
Mora, G .
BRAIN, 2005, 128 :472-476
[7]  
Chiò A, 2001, NEUROLOGY, V56, P239
[8]   Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene [J].
Cudkowicz, ME ;
McKenna-Yasek, D ;
Chen, C ;
Hedley-Whyte, ET ;
Brown, RH .
ANNALS OF NEUROLOGY, 1998, 43 (06) :703-710
[9]   Prognosis in amyotrophic lateral sclerosis - A population-based study [J].
del Aguila, MA ;
Longstreth, WT ;
McGuire, V ;
Koepsell, TD ;
van Belle, G .
NEUROLOGY, 2003, 60 (05) :813-819
[10]   The epidemiology of amyotrophic lateral sclerosis (ALS/MND) in people aged 80 or over [J].
Forbes, RB ;
Colville, S ;
Swingler, RJ .
AGE AND AGEING, 2004, 33 (02) :131-134