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Smoking may be considered an established risk factor for sporadic ALS
1Division of Neurology, Tufts University School of Medicine/Baystate Medical Center, Springfield, MA 01199, USA. carmel.armon@bhs.org
Neurology
|November 18, 2009
Summary
Smoking is an established risk factor for amyotrophic lateral sclerosis (ALS). This review confirms that smoking increases ALS risk, with evidence showing a dose-response relationship and reduced risk after quitting.
Area of Science:
- Neurology
- Epidemiology
Background:
- A 2003 review identified smoking as a probable risk factor for sporadic amyotrophic lateral sclerosis (ALS).
- The review was based on limited class II evidence.
Purpose of the Study:
- To update the evidence-based review of exogenous risk factors for sporadic ALS.
- To determine if the 2003 conclusion regarding smoking as a risk factor needed modification based on newer studies.
Main Methods:
- A systematic literature search of Medline was performed for studies published between 2003 and April 2009.
- Search terms included "smoking" and variations of "amyotrophic lateral sclerosis" (ALS, MND).
- Primary articles were assessed for evidence class (II-V) to evaluate study quality.
Main Results:
- Seven articles met the inclusion criteria from 28 identified titles.
- One class II study and one class III study demonstrated an increased risk of ALS associated with smoking.
- The class II study indicated a dose-response effect and a decrease in risk with time since smoking cessation.
Conclusions:
- Smoking is confirmed as an established risk factor for sporadic amyotrophic lateral sclerosis (ALS) with a Level A rating.
- The updated evidence, including 3 class II and 1 class III studies, supports a consistent link between smoking and ALS.
- Analysis of high-quality epidemiologic data reinforces the conclusion that smoking contributes to ALS development.
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