Highlights
- •There is no evidence regarding the potential link between heterogeneity in parental ethnicity and MS development.
- •We investigated the heterogeneity in parental ethnicity and MS risk in the setting of a population-based case-control study.
- •Heterogeneity in parental ethnicity of common ethnic groups was significantly associated with increased risk of MS.
- •MS was unequally distributed in the ethnicities with overrepresentation of one specific background, Lor of Caucasian origin.
Abstract
Background
The epidemiology of multiple sclerosis (MS) includes a consideration of geography
and population ethnicity. To determine whether there is any association between ethnicity
and risk of MS in a multiethnic, population-based case–control study.
Methods
We conducted a population-based case–control of 547 incident MS cases and 1057 healthy
controls between August 2013 and February 2015, Tehran, a multi-ethnic city. The patients
were identified and enrolled through the Iranian MS Society. Case status was confirmed
by a panel of MS specialists beside of 2010 McDonald criteria. Controls were selected
through random digit dialing. A logistic regression model was applied to estimate
the odds ratios (95%CI) adjusted for age, sex, tobacco smoking and socioeconomic status.
Results
The risk of MS for Kurd, Turk and Fars ethnicities was apparently smaller compared
to one specific ethnic background (Lor); OR 0.36 (0.15–0.86) for Kurd, OR 0.42 (0.24–0.74)
for Turk and OR 0.53 (0.31–0.89) for Fars. Heterogeneity in parental ethnicity of
common ethnic groups was significantly associated with increased risk of MS OR 1.61
(1.13–2.29). All associations remained after adjustment for relevant confounders.
Conclusions
MS was unequally distributed in the ethnic groups. Moreover, heterogeneity in parental
ethnicity seems to be a risk factor for MS.
Abbreviations:
IMSS (Iranian multiple sclerosis society), RDD (random digit dialing)Keywords
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Article info
Publication history
Published online: January 16, 2018
Accepted:
January 12,
2018
Received in revised form:
December 17,
2017
Received:
September 12,
2017
Identification
Copyright
© 2018 Elsevier B.V. All rights reserved.