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BMJ 2006;332:76-80 (14 January), doi:10.1136/bmj.38668.616806.3A (published 6 January 2006)
Catherine S Gibson, postdoctoral research fellow, Department of Obstetrics and Gynaecology1, Alastair H MacLennan, professor, Department of Obstetrics and Gynaecology1, Paul N Goldwater, senior consultant clinical microbiologist, Department of Microbiology and Infectious Diseases1, Eric A Haan, clinical geneticist, Department of Genetic Medicine1, Kevin Priest, epidemiologist2, Gustaaf A Dekker, professor, Department of Obstetrics and Gynaecology1, South Australian Cerebral Palsy Research Group
1 University of Adelaide, Women's and Children's Hospital, 1st Floor Queen Victoria Building, 72 King William Road, Adelaide, SA 5006, Australia, 2 Epidemiology Branch, Department of Health, Adelaide, SA 5000, Australia
Correspondence to: C S Gibson catherine.s.gibson{at}adelaide.edu.au
Objective To investigate the association between cerebral palsy and direct evidence for perinatal exposure to neurotropic viruses.
Design Population based case-control study.
Setting Adelaide Women's and Children's Hospital Research Laboratory.
Participants and main outcome measures Newborn screening cards of 443 white case patients with cerebral palsy and 883 white controls were tested for viral nucleic acids from enteroviruses and herpes viruses by using polymerase chain reaction. Herpes group A viruses included herpes simplex viruses 1 and 2 (HSV-1 and HSV-2), Epstein-Barr virus (EBV), cytomegalovirus (CMV), and human herpes virus 8 (HHV-8), and herpes group B viruses included varicella zoster virus (VZV) and human herpes viruses 6 and 7 (HHV-6 and HHV-7).
Results The prevalence of viral nucleic acids in the control population was high: 39.8% of controls tested positive, and the prevalence was highest in preterm babies. The detection of herpes group B viral nucleic acids increased the risk of developing cerebral palsy (odds ratio 1.68, 95% confidence interval 1.09 to 2.59).
Conclusions Perinatal exposure to neurotropic viruses is associated with preterm delivery and cerebral palsy.
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