Literature DB >> 17607412

A clinical epidemiological study of 251 cases of amyotrophic lateral sclerosis in the south of Brazil.

Lineu Cesar Werneck1, Ruth Bezerra, Octavio da Silveira Neto, Rosana Herminia Scola.   

Abstract

OBJECTIVE: To study the clinical forms of amyotrophic lateral sclerosis (ALS) and the possible presence of risk factors in order to verify if there is any difference between cases in Paraná, Brazil.
METHOD: We studied 251 cases, all of which fulfilled the diagnosis criteria proposed in El Escorial (WFN). Between 1977 and 2004, 157 male and 94 female patients were examined.
RESULTS: 220 cases were classified as ALS-Spinal Onset (ALS-SO), 24 as ALS-Bulbar Onset (ALS-BO) and 7 as Familial ALS. The mean age at time of evaluation was 54.4+/-12.3 years, and symptoms had started 17.9+/-15.7 months previously. In the group studied, statistical relationships were found between heavy occupations and males; previous surgeries and females; ALS-BO and dysphagia and dysarthria in females; and ALS-SO and males, cramps, weakness, muscle atrophy, hypertonia, increased deep tendon reflex and abnormal gait.
CONCLUSION: The average age at time of evaluation was lower than that registered in the literature but similar to the Brazilian series. Domestic work and heavy occupations appear to be related to precocious perception of the symptoms by interference with daily functions. The socioeconomically higher classes seek medical care early. There was no relationship with exposure to toxic agents or trauma.

Entities:  

Mesh:

Year:  2007        PMID: 17607412     DOI: 10.1590/s0004-282x2007000200001

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  6 in total

1.  Rural environment and risk factors of amyotrophic lateral sclerosis: a case-control study.

Authors:  Alain Furby; Katell Beauvais; Ivan Kolev; Jean-Gérard Rivain; Véronique Sébille
Journal:  J Neurol       Date:  2009-12-11       Impact factor: 4.849

Review 2.  Epidemiological evidence that physical activity is not a risk factor for ALS.

Authors:  Bello Hamidou; Philippe Couratier; Cyril Besançon; Marie Nicol; Pierre Marie Preux; Benoit Marin
Journal:  Eur J Epidemiol       Date:  2014-07-02       Impact factor: 8.082

3.  Epidemiology and surveillance of amyotrophic lateral sclerosis in two large metropolitan areas in California.

Authors:  Jhaqueline Valle; Eric Roberts; Susan Paulukonis; Natalie Collins; Paul English; Wendy Kaye
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2015-03-30       Impact factor: 4.092

4.  No association of GSTP1 rs1695 polymorphism with amyotrophic lateral sclerosis: A case-control study in the Brazilian population.

Authors:  Jéssica Barletto de Sousa Barros; Kamilla de Faria Santos; Rômulo Morais Azevedo; Rayana Pereira Dantas de Oliveira; Ana Carolina Dourado Leobas; Dhiogo da Cruz Pereira Bento; Rodrigo da Silva Santos; Angela Adamski da Silva Reis
Journal:  PLoS One       Date:  2021-02-19       Impact factor: 3.240

Review 5.  Dysphagia as a risk factor for mortality in Niemann-Pick disease type C: systematic literature review and evidence from studies with miglustat.

Authors:  Mark Walterfang; Yin-Hsiu Chien; Jackie Imrie; Derren Rushton; Danielle Schubiger; Marc C Patterson
Journal:  Orphanet J Rare Dis       Date:  2012-10-06       Impact factor: 4.123

6.  Distinct Phospho-TDP-43 brain distribution in two cases of FTD, one associated with ALS.

Authors:  Álvaro C B Guedes; Ricardo Santin; André S R Costa; Keli C Reiter; Arlete Hilbig; Liana L Fernandez
Journal:  Dement Neuropsychol       Date:  2017 Jul-Sep
  6 in total

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