4.7 Article

Smoking and Risk for Amyotrophic Lateral Sclerosis: Analysis of the EPIC Cohort

期刊

ANNALS OF NEUROLOGY
卷 65, 期 4, 页码 378-385

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WILEY-LISS
DOI: 10.1002/ana.21653

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资金

  1. British Heart Foundation Funding Source: Medline
  2. Cancer Research UK Funding Source: Medline
  3. Medical Research Council [G0401527] Funding Source: Medline
  4. Wellcome Trust Funding Source: Medline
  5. Department of Health Funding Source: Medline
  6. Medical Research Council [G0401527] Funding Source: researchfish
  7. Associazione Italiana per la Ricerca sul Cancro Funding Source: Custom

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Objective: Cigarette smoking has been reported as probable risk factor for Amyotrophic Lateral Sclerosis (ALS), a poorly understood disease in terms of aetiology. The extensive longitudinal data of the European Prospective Investigation into Cancer and Nutrition (EPIC) were used to evaluate age-specific mortality rates from ALS and the role of cigarette smoking on the risk of dying from ALS. Methods: A total of 517,890 healthy subjects were included, resulting in 4,591,325 person-years. ALS cases were ascertained through death certificates. Cox hazard models were built to investigate the role of smoking on the risk of ALS, using packs/years and smoking duration to study dose-response. Results: A total of 118 subjects died from ALS, resulting in a crude mortality rate of 2.69 per 100,000/year. Current smokers at recruitment had an almost two-fold increased risk of dying from ALS compared to never smokers (HR = 1.89, 95% C.I. 1.14-3.14), while former smokers at the time of enrolment had a 50% increased risk (HR = 1.48, 95% C.I. 0.94-2-32). The number of years spent smoking increased the risk of ALS (p for trend = 0.002). Those who smoked more than 33 years had more than a two-fold increased risk of ALS compared with never smokers (HR = 2.16, 95% C.I. 1.33-3.53). Conversely, the number of years since quitting smoking was associated with a decreased risk of ALS compared with continuing smoking. Interpretation: These results strongly support the hypothesis of a role of cigarette smoking in aetiology of ALS. We hypothesize that this could occur through lipid peroxidation via formaldehyde exposure. Ann Neurol 2009;65:378-385

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