The authors of this paper do not have any commercial associations that might pose a conflict of interest in connection with this manuscript.
Neonatal antibodies to infectious agents and risk of bipolar disorder: a population-based case–control study
Version of Record online: 15 NOV 2011
© 2011 John Wiley and Sons A/S
Volume 13, Issue 7-8, pages 624–629, November-December 2011
How to Cite
Mortensen, P. B., Pedersen, C. B., McGrath, J. J., Hougaard, D. M., Nørgaard-Petersen, B., Mors, O., Børglum, A. D. and Yolken, R. H. (2011), Neonatal antibodies to infectious agents and risk of bipolar disorder: a population-based case–control study. Bipolar Disorders, 13: 624–629. doi: 10.1111/j.1399-5618.2011.00962.x
- Issue online: 15 NOV 2011
- Version of Record online: 15 NOV 2011
- Received 26 July 2010, revised and accepted for publication 14 September 2011
- bipolar disorder;
- dried blood spots;
- herpes simplex virus type 1;
- herpes simplex virus type 2;
- Toxoplasma gondii
Mortensen PB, Pedersen CB, McGrath JJ, Hougaard DM, Nørgaard-Petersen B, Mors O, Børglum AD, Yolken RH. Neonatal antibodies to infectious agents and risk of bipolar disorder: a population-based case–control study. Bipolar Disord 2011: 13: 624–629. © 2011 The Authors. Journal compilation © 2011 John Wiley & Sons A/S.
Objective: There is a substantial evidence base linking prenatal exposure to infectious agents and an increased risk of schizophrenia. However, there has been less research examining the potential for these exposures to also contribute to risk for bipolar disorder. The aim of this study was to examine the association between neonatal markers of selected prenatal infections and risk for bipolar disorder.
Methods: Using population-based Danish registers, we examined 127 individuals with a diagnosis of bipolar disorder, and 127 sex and day-of-birth individually matched controls. Based on neonatal dried blood spots, we measured antibodies to herpes simplex virus type 1 (HSV-1) and 2 (HSV-2), cytomegalovirus (CMV), and Toxoplasma gondii. Relative risks were calculated for the matched pairs when examined for optical density units for antibodies to each of the infectious agents.
Results: There was no association between any of the neonatal markers of prenatal infection and risk of bipolar disorder.
Conclusions: In contrast with studies of schizophrenia, our analysis does not support maternal infection with HSV-1, HSV-2, CMV, or Toxoplasma gondii as risk factors for bipolar disorder. However, larger study samples are needed, and data on, for example, specific serotypes of Toxoplasma and indicators of the timing of maternal infection are still warranted.