Table 4.
Timing of prenatal infection and risk of schizophrenia and other psychotic disorders in adult offspring
| Time of exposure | Infectious agent | Effect sizea | Study | Cohort |
|---|---|---|---|---|
| Around conception | Genital/reproductive infection | 5 | Babulas et al. 2006 | PDS |
| First trimester | Influenza | 7 | Brown et al. 2004a | PDS |
| Bacterial infection | 2 | Sorensen et al. 2009 | Copenhagen perinatal cohort |
|
| Second trimester | Influenzab | 3 | Brown et al. 2004a | PDS |
| Respiratory infection | 2 | Brown et al. 2000 | ||
| Third trimester or at delivery |
HSV-2 | 1.5 |
Buka et al. 2001, 2008 and Xiao et al. 2009 |
NCPP |
| Toxoplasma gondii | 2 | Brown et al. 2005 | PDS | |
| Mortensen et al. 2007, 2010 | Danish cohorts |
NCPP, National Collaborative Perinatal Project ; PDS, Prenatal Determinants of Schizophrenia ; HSV-2, herpes simplex virus type 2.
Only studies that reported an increase in risk in relation to prenatal infection were included in this table ; approximate point estimates shown for guide purpose only ; heterogeneity in exposure measurement, case definition, analysis and measure of risk exists between individual studies, refer to Table 1 for individual study details and results.
Early second-trimester exposure.