Offspring number, pregnancy, and risk of a first clinical demyelinating event: the AusImmune Study.
Abstract
OBJECTIVE
To examine the association between past pregnancy, offspring number, and first clinical demyelination risk.
METHODS
Cases (n = 282) were aged 18-59 years with a first clinical diagnosis of CNS demyelination (first clinical demyelinating event
[FCD]) and resident within 1 of 4 Australian centers (from latitudes 27° south to 43° south) from 2003 to 2006. Controls (n
= 542) were matched to cases on age, sex, and study region, without first clinical diagnosis of CNS demyelination.
RESULTS
Higher offspring number was associated with FCD risk among women (p < 0.001) but not men (p = 0.71); difference in effect;
p = 0.001. Among women, higher parity was associated with reduced risk of FCD (adjusted odds ratio 0.51 [95% confidence interval
0.36, 0.72] per birth) with a similar magnitude of effect observed among classic first demyelinating events (adjusted odds
ratio 0.47 [95% confidence interval 0.29, 0.74]). The apparent beneficial effect of higher parity was also evident among parous
women only (p < 0.001). Among cases, a clear female excess was evident for those with low but not high (4 or more) offspring
number. Factors such as human leukocyte antigen DR15 genotype did not appear to modify the association between higher parity
and a reduced FCD risk among women.
CONCLUSIONS
These findings are consistent with a cumulative beneficial effect of pregnancy. Temporal changes toward an older maternal
age of parturition and reduced offspring number may partly underlie the increasing female excess among MS cases over time.
Links
Authors
Ponsonby AL, Lucas RM, van der Mei IA, Dear K, Valery PC, Pender MP, Taylor BV, Kilpatrick TJ, Coulthard A, Chapman C, Williams D, McMichael AJ, Dwyer T
Institution
Murdoch Childrens Research Institute, Melbourne, Australia. anne-louise.ponsonby@mcri.edu.au
Source
Neurology 78:12 2012 Mar 20 pg 867-74MeSH
Abortion, SpontaneousAdolescent
Adult
Australia
Autoimmune Diseases
Confidence Intervals
DNA
Data Interpretation, Statistical
Demyelinating Diseases
Female
Genotype
HLA-DR Antigens
Humans
Male
Menarche
Middle Aged
Odds Ratio
Parity
Pregnancy
Pregnancy Complications
Questionnaires
Risk Assessment
Risk Factors
Sex Factors
Young Adult
Pub Type(s)
Journal ArticleMulticenter Study
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22402857
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