Literature DB >> 23094606

Prevalence and prognostic impact of comorbidities in amyotrophic lateral sclerosis.

S Körner1, K Kollewe, J Ilsemann, A Müller-Heine, R Dengler, K Krampfl, S Petri.   

Abstract

BACKGROUND AND
PURPOSE: Amyotrophic lateral sclerosis (ALS) is characterized by rapidly progressive paralysis of striated muscles due to the loss of upper and lower motor neurons. The disease leads to death within 2-5 years, mainly due to respiratory failure. The pathogenesis of ALS is still unexplained for the most part. In this study, we aimed to determine the prevalence of different cardiovascular, metabolic, and neuropsychiatric comorbidities in a large ALS cohort and to evaluate their influence on the disease course.
METHODS: A cohort of 514 patients with ALS of our ALS outpatient clinic was investigated retrospectively with reference to known prognostic factors and comorbidities. The prevalence of concomitant diseases was compared with the data from the German general population. Uni- and multivariate survival analyses were performed using the Cox proportional hazards model and Kaplan-Meier analysis.
RESULTS: The prevalence of cardiovascular diseases and cardiovascular risk factors was significantly lower in patients with ALS compared to the German general population, whilst the prevalence of dementia, parkinsonism, and depressive symptoms was significantly higher in the ALS cohort. None of the investigated comorbidities had an influence on the disease course or on the survival of patients.
CONCLUSIONS: Persons with cardiovascular diseases or risk factors seem to be at lower risk of ALS. Although these diseases are apparently somehow protective regarding ALS susceptibility, their presence did not modify disease progression and survival in patients with ALS. Our study further confirms the well-known continuum between ALS and dementia. It also suggests a link with other neurodegenerative diseases such as Parkinson's disease.
© 2012 The Author(s) European Journal of Neurology © 2012 EFNS.

Entities:  

Mesh:

Year:  2012        PMID: 23094606     DOI: 10.1111/ene.12015

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  32 in total

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2.  Depression in amyotrophic lateral sclerosis.

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Review 4.  Comorbidities in Neurology: Is adenosine the common link?

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5.  Association between depression and survival in Chinese amyotrophic lateral sclerosis patients.

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7.  Network Analysis Identifies Disease-Specific Pathways for Parkinson's Disease.

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8.  An exploratory study of serum creatinine levels in patients with amyotrophic lateral sclerosis.

Authors:  Xueping Chen; Xiaoyan Guo; Rui Huang; Zhenzhen Zheng; Yongping Chen; Hui-Fang Shang
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Review 9.  Advances in cellular models to explore the pathophysiology of amyotrophic lateral sclerosis.

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10.  Case-control study of occupational exposure to electric shocks and magnetic fields and mortality from amyotrophic lateral sclerosis in the US, 1991-1999.

Authors:  Ximena Vergara; Gabor Mezei; Leeka Kheifets
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