Assessing interactions between HLA-DRB1*15 and infectious mononucleosis on the risk of multiple sclerosis

被引:12
作者
Disanto, Giulio [1 ,2 ]
Hall, Carolina [3 ]
Lucas, Robyn [4 ]
Ponsonby, Anne-Louise [5 ]
Berlanga-Taylor, Antonio J. [1 ,2 ]
Giovannoni, Gavin [6 ]
Ramagopalan, Sreeram V. [1 ,2 ,6 ]
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, Oxford OX1 2JD, England
[2] Univ Oxford, MRC, Funct Genom Unit, Oxford OX1 2JD, England
[3] London Sch Hyg & Trop Med, Dept Epidemiol, London WC1, England
[4] Australian Natl Univ, Natl Ctr Epidemiol & Populat Hlth, Canberra, ACT, Australia
[5] Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[6] Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London E1 2AT, England
基金
英国医学研究理事会;
关键词
HLA-DRB1*15; infectious mononucleosis; interaction; multiple sclerosis;
D O I
10.1177/1352458513477231
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Gene-environment interactions may shed light on the mechanisms underlying multiple sclerosis (MS). We pooled data from two case-control studies on incident demyelination and used different methods to assess interaction between HLA-DRB1*15 (DRB1-15) and history of infectious mononucleosis (IM). Individuals exposed to both factors were at substantially increased risk of disease (OR=7.32, 95% CI=4.92-10.90). In logistic regression models, DRB1-15 and IM status were independent predictors of disease while their interaction term was not (DRB1-15*IM: OR=1.35, 95% CI=0.79-2.23). However, interaction on an additive scale was evident (Synergy index=2.09, 95% CI=1.59-2.59; excess risk due to interaction=3.30, 95%CI=0.47-6.12; attributable proportion due to interaction=45%, 95% CI=22-68%). This suggests, if the additive model is appropriate, the DRB1-15 and IM may be involved in the same causal process leading to MS and highlights the benefit of reporting gene-environment interactions on both a multiplicative and additive scale.
引用
收藏
页码:1355 / 1358
页数:4
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