4.4 Article

Stressful life events and the risk of initial central nervous system demyelination

期刊

MULTIPLE SCLEROSIS JOURNAL
卷 23, 期 7, 页码 1000-1007

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458516667566

关键词

First demyelinating event; first clinical diagnosis; stress; stressful life events; multiple sclerosis; risk factors

资金

  1. Australian Research Council [100100511]
  2. National Health and Medical Research Council of Australia
  3. Multiple Sclerosis Research Australia
  4. Royal Australasian College of Physicians
  5. MS Research Australia
  6. US National Multiple Sclerosis Society
  7. Poola Foundation
  8. Health Research Council of New Zealand
  9. MS Society of Tasmania
  10. Bayer Schering Pharma
  11. Biogen Idec, Inc.
  12. Australian National Health and Medical Research Council Career Development Fellowships
  13. Australian Research Council Future Fellowship

向作者/读者索取更多资源

Background: There is substantial evidence that stress increases multiple sclerosis disease activity, but limited evidence on its association with the onset of multiple sclerosis. Objective: To examine the association between stressful life events and risk of first demyelinating event (FDE). Methods: This was a multicentre incident case-control study. Cases (n=282 with first diagnosis of central nervous system (CNS) demyelination, including n=216 with classic FDE') were aged 18-59years. Controls without CNS demyelination (n=558) were matched to cases on age, sex and study region. Stressful life events were assessed using a questionnaire based on the Social Readjustment Rating Scale. Results: Those who suffered from a serious illness in the previous 12months were more likely to have an FDE (odds ratio (OR)=2.35 (1.36, 4.06), p=0.002), and when we limited our reference group to those who had no stressful life events, the magnitude of effect became stronger (OR=5.41 (1.80, 16.28)). The total stress number and stress load were not convincingly associated with the risk of an FDE. Conclusion: Cases were more likely to report a serious illness in the previous 12months, which could suggest that a non-specific illness provides an additional strain to an already predisposed immune system.

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