Amyotrophic lateral sclerosis in Catalonia: A population based study

被引:40
|
作者
Pradas, Jesus [1 ,4 ]
Puig, Teresa [2 ]
Rojas-Garcia, Ricard [1 ,4 ]
Luisa Viguera, Maria [1 ]
Gich, Ignasi [2 ]
Logroscino, Giancarlo [3 ]
机构
[1] Univ Autonoma Barcelona, Hosp Santa Cruz & St Pau, Dept Neurol, E-08193 Barcelona, Spain
[2] Univ Autonoma Barcelona, IIB St Pau, Hosp Santa Creu & St Pau, Dept Epidemiol, E-08193 Barcelona, Spain
[3] Univ Bari, Dept Neurol & Psychiat, Bari, Italy
[4] Ctr Invest Biomed Red Neurodegenrac CIBERNED, Barcelona, Spain
关键词
Amyotrophic lateral sclerosis; epidemiology; population based study; incidence; Catalonia; MOTOR-NEURON-DISEASE; CLINICAL-FEATURES; ALS; EPIDEMIOLOGY; MORTALITY; IRELAND; METHODOLOGY; PREVALENCE; FREQUENCY; REGISTER;
D O I
10.3109/21678421.2012.749915
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 determine the incidence and clinical-epidemiological characteristics of an ALS cohort patient in Catalonia (Spain). We conducted a population based registry for a three-year period (1999-2001) in Catalonia (6,361,365 inhabitants) using several sources of information. The original El Escorial diagnostic criteria (1994) for ALS were applied for the classification of patients. New cases diagnosed between 1 January 1999 and 31 December 2001 were 215 (118 males and 97 females), with an annual crude incidence rate of 1.4/100,000 (95% CI 1.3-1.8). This rate showed a peak age between 75 and 79 years. The incidence rate was 1.6 (95% CI 1.5-2.2) in males and 1.2 (95% CI 1.1-1.7) in females. Prevalence at the end of the period was 5.4/100,000 of the total population. Median age at onset was 64.3 years. Onset of symptoms was bulbar or generalized in 38% of cases. Mean disease duration at diagnosis was 11.0 months. Median time of survival from onset was 30.8 months. In conclusion, ALS incidence in Catalonia is within the range of other countries across Europe with different geographic, environmental and socioeconomic situations. However, as in other studies conducted in the Mediterranean area, Catalonia incidence is in the lower range of rates in Europe.
引用
收藏
页码:278 / 283
页数:6
相关论文
共 50 条
  • [41] Amyotrophic lateral sclerosis surveillance in Baltimore and Philadelphia
    Jordan, Heather
    Rechtman, Lindsay
    Wagner, Laurie
    Kaye, Wendy E.
    MUSCLE & NERVE, 2015, 51 (06) : 815 - 821
  • [42] Association of fractures with the incidence of amyotrophic lateral sclerosis
    Peters, Tracy L.
    Weibull, Caroline E.
    Fang, Fang
    Sandler, Dale P.
    Lambert, Paul C.
    Ye, Weimin
    Kamel, Freya
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2017, 18 (5-6) : 419 - 425
  • [43] The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study
    Phukan, Julie
    Elamin, Marwa
    Bede, Peter
    Jordan, Norah
    Gallagher, Laura
    Byrne, Susan
    Lynch, Catherine
    Pender, Niall
    Hardiman, Orla
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2012, 83 (01) : 102 - 108
  • [44] Trauma and amyotrophic lateral sclerosis: a european population-based case-control study from the EURALS consortium
    Pupillo, Elisabetta
    Poloni, Marco
    Bianchi, Elisa
    Giussani, Giorgia
    Logroscino, Giancarlo
    Zoccolella, Stefano
    Chio, Adriano
    Calvo, Andrea
    Corbo, Massimo
    Lunetta, Christian
    Marin, Benoit
    Mitchell, Douglas
    Hardiman, Orla
    Rooney, James
    Stevic, Zorica
    di Poggio, Monica Bandettini
    Filosto, Massimiliano
    Cotelli, Maria Sofia
    Perini, Michele
    Riva, Nilo
    Tremolizzo, Lucio
    Vitelli, Eugenio
    Damiani, Danira
    Beghi, Ettore
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2018, 19 (1-2) : 118 - 125
  • [45] Amyotrophic Lateral Sclerosis in Southwestern and Eastern Finland
    Hanhisuanto, Mirka
    Solje, Eino
    Jokela, Manu
    Sipila, Jussi O. T.
    NEUROEPIDEMIOLOGY, 2023, 57 (04) : 238 - 245
  • [46] Hypothesis: amyotrophic lateral sclerosis and environmental pollutants
    Swash, Michael
    Eisen, Andrew
    MUSCLE & NERVE, 2020, 62 (02) : 187 - 191
  • [47] Population-Based Evidence that Survival in Amyotrophic Lateral Sclerosis Is Related to Weight Loss at Diagnosis
    Marin, Benoit
    Arcuti, Simona
    Jesus, Pierre
    Logroscino, Giancarlo
    Copetti, Massimiliano
    Fontana, Andrea
    Nicol, Marie
    Raynnondeau, Marie
    Desport, Jean Claude
    Preux, Pierre Marie
    Couratier, Philippe
    NEURODEGENERATIVE DISEASES, 2016, 16 (3-4) : 225 - 234
  • [48] Five-Year Incidence of Amyotrophic Lateral Sclerosis in British Columbia (2010-2015)
    Golby, Riley
    Poirier, Brigitte
    Fabros, Marife
    Cragg, Jacquelyn J.
    Yousefi, Masoud
    Cashman, Neil
    CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 2016, 43 (06) : 791 - 795
  • [49] Incidence and prevalence of Amyotrophic Lateral Sclerosis in three Italian Regions: a study based on health administrative databases
    Bacigalupo, Ilaria
    Finocchietti, Marco
    Paoletti, Olga
    Bargagli, Anna Maria
    Brunori, Paola
    Lombardi, Niccolo
    Sciancalepore, Francesco
    Agabiti, Nera
    Kirchmayer, Ursula
    EPIDEMIOLOGIA & PREVENZIONE, 2024, 48 (03): : 201 - 209
  • [50] Prevalence and Incidence of Amyotrophic Lateral Sclerosis in Japan
    Doi, Yuriko
    Atsuta, Naoki
    Sobue, Gen
    Morita, Mitsuya
    Nakano, Imaharu
    JOURNAL OF EPIDEMIOLOGY, 2014, 24 (06) : 494 - 499