The epidemiology of amyotrophic lateral sclerosis in Moscow (Russia)

被引:5
|
作者
Brylev, Lev [1 ,2 ,3 ]
Ataulina, Anastasia [1 ]
Fominykh, Vera [1 ,3 ]
Parshikov, Vadim [4 ,5 ]
Vorobyeva, Anna [6 ]
Istomina, Elena [7 ]
Shikhirimov, Rafiz [7 ]
Salikov, Alexandr [1 ]
Zakharova, Mariya [6 ]
Guekht, Alla [2 ,8 ]
Beghi, Ettore [9 ]
机构
[1] Bujanov Moscow City Clin Hosp, Moscow, Russia
[2] Healthcare Dept, Moscow Res & Clin Ctr Neuropsychiat, Moscow, Russia
[3] Russian Acad Sci, Inst Higher Nervous Act & Neurophysiol, Dept Funct Biochem Nervous Syst, Moscow, Russia
[4] St Alexis Hosp, Moscow, Russia
[5] Moscow Multiprofile Palliat Care Ctr, Moscow, Russia
[6] Res Ctr Neurol, Moscow, Russia
[7] Primary Care Multidisciplinary Clin 166 Healthcar, Dept Moscow, Moscow, Russia
[8] Russian Natl Res Med Univ, Moscow, Russia
[9] Ist Ric Farmacol Mario Negri IRCCS, Dept Neurosci, Milan, Italy
关键词
Amyotrophic lateral sclerosis; epidemiology; incidence; Russian Federation; MOTOR-NEURON DISEASE; DIAGNOSIS;
D O I
10.1080/21678421.2020.1752252
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To estimate the incidence of amyotrophic lateral sclerosis (ALS) in Moscow by investigating multiple sources of cases. Incidence rates from previous Russian studies ranged from 0.3 to 0.7 per 100,000/year.Methods: A retrospective study of the incidence of ALS was performed in the South district of Moscow (population, 1,760,000, 2015). Several data sources were investigated. The medical records of the calendar year 2015 were examined by an ALS expert who accepted only patients with definite or probable ALS according to the revised El Escorial criteria. Crude and standardized incidence rates were calculated, the latter adjusted to the Russian and the European population.Results: Twenty-two patients were found, accounting for a crude incidence of 1.25/100,000/year (95% CI 0.78-1.89) and a standardized incidence of 1.22 (Russia) and 1.28 (Europe). The sample included 11 men and 11 women aged 36-73 years (mean 56). Five patients (23%) had bulbar onset ALS. The mean diagnostic delay was 12.8 +/- 9.2 months (8.5 +/- 4.8 in men and 17.2 +/- 10.6 in women) (p = 0.02). Family history of ALS was present in two cases.Conclusion: The incidence of ALS in the Russian Federation is higher than previously reported but lower than in other countries. Poor diagnostic ascertainment, particularly in women, and the shorter life expectancy of the Russian population are possible explanations.
引用
收藏
页码:410 / 415
页数:6
相关论文
共 50 条
  • [41] An epidemiologic investigation of amyotrophic lateral sclerosis in Thrace, Turkey, 2006-2010*
    Turgut, Nilda
    Saracoglu, Gamze Varol
    Kat, Selahattin
    Balci, Kemal
    Guldiken, Baburhan
    Birgili, Ozlem
    Kabayel, Levent
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2019, 20 (1-2) : 100 - 106
  • [42] Diagnosis and management of amyotrophic lateral sclerosis
    Shin, Je-Young
    Lee, Kwang-Woo
    JOURNAL OF THE KOREAN MEDICAL ASSOCIATION, 2015, 58 (02): : 131 - 138
  • [43] Prognostic categories for amyotrophic lateral sclerosis
    Scotton, William J.
    Scott, Kirsten M.
    Moore, Dan H.
    Almedom, Leeza
    Wijesekera, Lokesh C.
    Janssen, Anna
    Nigro, Catherine
    Sakel, Mohammed
    Leigh, Peter N.
    Shaw, Chris
    Al-Chalabi, Ammar
    AMYOTROPHIC LATERAL SCLEROSIS, 2012, 13 (06): : 502 - 508
  • [44] AUTONOMIC SYSTEM AND AMYOTROPHIC LATERAL SCLEROSIS
    Piccione, Ezequiel A.
    Sletten, David M.
    Staff, Nathan P.
    Low, Phillip A.
    MUSCLE & NERVE, 2015, 51 (05) : 676 - 679
  • [45] What is amyotrophic lateral sclerosis prevalence?
    Vasta, Rosario
    Moglia, Cristina
    Manera, Umberto
    Canosa, Antonio
    Grassano, Maurizio
    Palumbo, Francesca
    Cugnasco, Paolo
    De Marchi, Fabiola
    Mazzini, Letizia
    Calvo, Andrea
    Chio, Adriano
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2022, 23 (3-4) : 203 - 208
  • [46] Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: a ten year follow up study
    Cabona, Corrado
    Ferraro, Pilar Maria
    Scialo, Carlo
    Di Poggio, Monica Bandettini
    Novi, Giovanni
    Gemelli, Chiara
    Vignolo, Manuela
    Rao, Fabrizio
    Capovilla, Marina
    Marogna, Maura
    Mandich, Paola
    Origone, Paola
    Schenone, Angelo
    Caponnetto, Claudia
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2024, 25 (1-2) : 104 - 111
  • [47] Incidence of amyotrophic lateral sclerosis in Sicily: A population based study
    Ragonese, Paolo
    Cellura, Eleonora
    Aridon, Paolo
    D'Amelio, Marco
    Spataro, Rossella
    Taiello, Alfonsa Claudia
    Maimone, Davide
    La Bella, Vincenzo
    Savettieri, Giovanni
    AMYOTROPHIC LATERAL SCLEROSIS, 2012, 13 (03): : 284 - 287
  • [48] Epidemiology and economic burden of amyotrophic lateral sclerosis in the United States: a literature review
    Berry, James D. D.
    Blanchard, Marie
    Bonar, Kerina
    Drane, Emma
    Murton, Molly
    Ploug, Uffe
    Ricchetti-Masterson, Kristen
    Savic, Natasa
    Worthington, Emma
    Heiman-Patterson, Terry
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2023, 24 (5-6) : 436 - 448
  • [49] Epidemiology and factors predicting survival of amyotrophic lateral sclerosis in a large Chinese cohort
    Gao Ming
    Liu Na
    Li Xue-Mei
    Chao Liu-Wen
    Lin Hong-Qi
    Wang Yan
    Sun Yan
    Huang Chen
    Li Xiao-Gang
    Deng Min
    中华医学杂志英文版, 2021, 134 (18) : 2231 - 2236
  • [50] The epidemiology of amyotrophic lateral sclerosis (ALS/MND) in people aged 80 or over
    Forbes, RB
    Colville, S
    Swingler, RJ
    AGE AND AGEING, 2004, 33 (02) : 131 - 134