4.5 Article

Early-life hygiene-related factors affect risk of central nervous system demyelination and asthma differentially

期刊

CLINICAL AND EXPERIMENTAL IMMUNOLOGY
卷 172, 期 3, 页码 466-474

出版社

OXFORD UNIV PRESS
DOI: 10.1111/cei.12077

关键词

allergy; asthma; autoimmunity; hygiene; multiple sclerosis; siblings

资金

  1. National Multiple Sclerosis Society of the United States of America
  2. National Health and Medical Research Council of Australia
  3. Multiple Sclerosis Research Australia
  4. MS Research Australia Fellowship
  5. Royal Australasian College of Physicians Cottrell Fellowship
  6. NHMRC

向作者/读者索取更多资源

The increasing prevalence of immune-related diseases, including multiple sclerosis, may be partly explained by reduced microbial burden during childhood. Within a multi-centre casecontrol study population, we examined: (i) the co-morbid immune diseases profile of adults with a first clinical diagnosis of central nervous system demyelination (FCD) and (ii) sibship structure in relation to an autoimmune (FCD) and an allergic (asthma) disease. FCD cases (n=282) were aged 1859 years; controls (n=558) were matched on age, sex and region. Measures include: history of doctor-diagnosed asthma; sibling profile (number; dates of birth); and regular childcare attendance. FCD cases did not differ from controls with regard to personal or family history of allergy, but had a greater likelihood of chronic fatigue syndrome [odds ratio (OR)=3 center dot 11; 95% confidence interval (CI) 1 center dot 11, 8 center dot 71]. Having any younger siblings showed reduced odds of FCD (OR=0 center dot 68; 95% CI: 0 center dot 49, 0 center dot 95) but not asthma (OR=1 center dot 47; 95% CI: 0 center dot 91, 2 center dot 38). In contrast, an increasing number of older siblings was associated with reduced risk of asthma (P trend=0 center dot 04) but not FCD (P trend=0 center dot 66). Allergies were not over-represented among people presenting with FCD. Sibship characteristics influence both FCD and asthma risk but the underlying mechanisms differ, possibly due to the timing of the putative sibling effect'.

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