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

Author:

Hughes A-M1,Lucas R M1,McMichael A J1,Dwyer T2,Pender M P3,van der Mei I4,Taylor B V4,Valery P5,Chapman C6,Coulthard A3,Dear K1,Kilpatrick T J7,Williams D8,Ponsonby A-L2

Affiliation:

1. National Centre for Epidemiology and Population Health, Australian National University,, Canberra

2. Murdoch Childrens Research Institute, Melbourne

3. University of Queensland and Royal Brisbane and Women's Hospital, Brisbane

4. Menzies Research Institute, Hobart

5. Menzies School of Health Research, Brisbane

6. Barwon Health, Geelong

7. Centre for Neuroscience, University of Melbourne, Melbourne

8. John Hunter Hospital, Newcastle, Australia

Abstract

Summary The increasing prevalence of immune-related diseases, including multiple sclerosis, may be partly explained by reduced microbial burden during childhood. Within a multi-centre case–control 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 18–59 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) = 3·11; 95% confidence interval (CI) 1·11, 8·71]. Having any younger siblings showed reduced odds of FCD (OR = 0·68; 95% CI: 0·49, 0·95) but not asthma (OR = 1·47; 95% CI: 0·91, 2·38). In contrast, an increasing number of older siblings was associated with reduced risk of asthma (P trend = 0·04) but not FCD (P trend = 0·66). 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’.

Funder

National Multiple Sclerosis Society of the United States of America

National Health and Medical Research Council of Australia

Multiple Sclerosis Research Australia

MS Research Australia Fellowship

Royal Australasian College of Physicians Cottrell Fellowship

NHMRC Capacity Building Grant

NHMRC Training Fellowship

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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