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Published on: October 13, 2016
Finding diseases associated with amyotrophic lateral sclerosis: a total population-based case-control study.
Ching-Piao Tsai1,2, Chenyu Hu3, Charles Tzu-Chi Lee3
1a Department of Biotechnology , Asia University , Taichung , Taiwan.
Prior diseases impact amyotrophic lateral sclerosis (ALS) risk. Hypermetabolic disorders like metabolic syndrome and infections increase ALS risk, while hypometabolic disorders, such as diabetes mellitus, may offer protection.
Area of Science:
- Neurology
- Epidemiology
- Metabolic Disorders
Background:
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease.
- Understanding pre-existing conditions associated with ALS is crucial for pathogenesis research.
- Population-based studies are essential for identifying disease risk factors.
Purpose of the Study:
- To investigate diseases associated with amyotrophic lateral sclerosis (ALS).
- To identify potential risk and protective factors for ALS using a large-scale medical database.
- To explore the relationship between prior diseases and ALS incidence.
Main Methods:
- A population-based case-control study utilizing Taiwan's National Health Insurance Research Database (NHIRD) and Serious Disabling Diseases (SDD) database.
- Inclusion of 705 ALS patients and 14,100 matched controls, analyzing diseases diagnosed up to 9 years prior to ALS diagnosis.
- Application of conditional logistic regression and path analysis to evaluate disease associations and pathways with ALS risk.
Main Results:
- Twenty-eight diseases showed significant associations with ALS (17 positive, 11 negative).
- Positive associations included metabolic syndrome, neuroinflammation, head trauma, infections, and comorbidities.
- Negative associations were linked to diabetes mellitus and its comorbidities.
Conclusions:
- Prior diseases associated with ALS support the hypothesis of hypermetabolic disorders.
- Hypometabolic disorders, like diabetes, may have a protective effect on ALS incidence.
- Defective energy metabolism is implicated in the pathogenesis of ALS.
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