Month of birth as a risk factor for multiple
sclerosis: an update
Torkildsen Ø, Grytten N, Aarseth J, Myhr K-M, Kampman MT.
Month of birth as a risk factor for multiple sclerosis: an update.
Acta Neurol Scand: 2012: 126 (Suppl. 195): 58–62.
© 2012 John Wiley & Sons A/S.
Background – Several studies have indicated month of birth as a risk
factor for multiple sclerosis (MS) susceptibility and disease
progression. Methods – We performed a systematic search on PubMed
and Medline up to May 2012 using the search string ‘multiple
sclerosis’ and ‘month of birth’ or ‘season of birth’. In addition,
congress abstracts and the reference lists of the publications identified
were examined for further citations of relevance. Results – A total of
fifteen published studies and two congress abstracts were found on the
effect of month or season of birth on MS risk (sixteen in the northern
and one in the southern hemisphere). Most studies in the northern
hemisphere detected an excess of MS births in spring and a decrease
in autumn. In the southern hemisphere, a reverse pattern was
detected, with an excess in November and a decrease in April. Only
three studies did not report any month of birth effect, all in low-risk
areas for MS. Five studies have analysed a possible effect on disease
course by month of birth. Of these, two studies reported an
association between month of birth and age at onset of relapsing-
remitting MS, with a younger disease onset for those born in the
winter months. No consistent findings have been detected on the
association between month of birth and disease progression.
Discussion – The month of birth effect is consistently found to
influence the risk of MS, and the effect seems to be most prominent in
high-risk areas of the disease, especially in areas with low sunlight
exposure. There seems to be little or no month of birth effects in
areas with high sunlight exposure. These findings indicate a possible
role for vitamin D concentrations during pregnancy or early life of
the newborn. A possible effect of vitamin D supplementation needs to
be further investigated.
Ø. Torkildsen
1,2
, N. Grytten
1,2
,
J. Aarseth
1,2
, K.-M. Myhr
1,2
,
M. T. Kampman
3,4
1
Norwegian Multiple Sclerosis Competence Centre,
Department of Neurology, Haukeland University
Hospital, Bergen, Norway;
2
Kristian Gerhard Jebsen
MS Research Centre, Department of Clinical Medicine,
University of Bergen, Bergen, Norway;
3
Institute of
Clinical Medicine, University of Tromsø, Tromsø,
Norway;
4
Centre for clinical research and education,
UNN, Tromsø, Norway
Key words: multiple sclerosis; epidemiology; month of
birth; season of birth
Ø. Torkildsen, Department of Neurology, Haukeland
University Hospital, N-5021 Bergen, Norway
Tel.: +47 55 97 70 39
Fax: +47 55 97 59 01
e-mail: oivind.torkildsen@gmail.com
Accepted for publication June 4, 2012
Introduction
Multiple sclerosis (MS) is a chronic, demyelinat-
ing disease of the central nervous system (CNS),
which is thought to be caused by a complex inter-
play between genetic and environmental risk fac-
tors. A number of studies have indicated that the
risk of MS is strongly associated with place of
residence in early life (1). Further, early life and
gestational events have frequently been suggested
to contribute to MS susceptibility. Findings of
seasonal birth patterns that differ significantly
from the general population suggest that environ-
mental factors acting in early life or in the intra-
uterine period are important for disease
susceptibility (2). We have reviewed the current
literature on month and season of birth in MS
and whether they can indicate possible risk fac-
tors for the disease.
Methods
We searched PubMed and Medline up to May
2012, using the search string ‘multiple sclerosis’
and ‘month of birth’ or ‘season of birth’. Addi-
tionally, we searched abstract books and abstract
CDs for relevant abstracts presented in the past
3 years at meetings or congresses held by the
European Committee for Treatment and
Research in Multiple Sclerosis (ECTRIMS), the
58
Acta Neurol Scand 2012: 126 (Suppl. 195): 58–62 DOI: 10.1111/ane.12040 Ó 2012 John Wiley & Sons A/S
ACTA NEUROLOGICA
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