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Edinburgh University Department of Psychiatry, Kennedy Tower, Royal Edinburgh Hospital, Edinburgh E10 5HF, UK
See pp. 403–414, this
issue. 
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 TOP MORE LARGE STUDIES NEEDED REFERENCES |
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The investigators identified the obstetric records of 524 cases and 1043 controls ascertained from the Stockholm County In-Patient Register, thus avoiding the potential pitfalls of maternal recall bias. Apgar scores were recorded at the time of delivery in only 20.5% of the sample and the majority of the scores were therefore calculated retrospectively, albeit blind to case/control status. An Apgar score of 6 or less at 1, 5 or 10 minutes was taken as evidence of asphyxia and found in 44 obstetric records. These ‘positive’ records were then scrutinised by experienced paediatricians, although negative records were not subject to the same scrutiny. Interrater reliability was high. The methodological limitations may have resulted in some bias but are unlikely to have lead to a false positive result.
Sample characteristics for cases and controls differed in a few important respects. A higher proportion of cases were unmarried or divorced, many received inadequate antenatal care and cases were more likely to have a history of maternal psychotic illness. The risk each complication contributed to the development of schizophrenia was calculated using the odds ratio (OR) by conditional logistic regression.
Most obstetric complications were not found to contribute any additional risk, with the exception of signs of asphyxia which were found significantly to increase the odds of the subsequent development of schizophrenia (OR 2.7, 95% CI 1.5-4.8). This result remained significant and was in fact strengthened once potential confounders (maternal history of psychotic illness, maternal age, socio-economic class, marital status, attendance at antenatal care) were taken into account (OR 4.4, 95% CI 1.9-10.3). Notably, however, no dose—response relationship was found between the severity of asphyxia and the risk of schizophrenia. This does not support an aetiological relationship, but one could argue that collapsing Apgar scores of less than seven over three time points (presumably to increase statistical power) added ‘noise’. A large or consistent effect of gender, age at diagnosis or maternal history of psychosis was not found.
These results are in keeping with the results of meta-analyses suggesting that obstetric complications are not simply a manifestation of genetic risk and may be pathogenic via a potential final common pathway of hypoxic brain damage (Verdoux et al, 1997). Although the age at onset effect was not significant, the results are in the expected direction. Single studies are often underpowered, frequently fail to find significant differences between cases and controls and tend to rely on summary scales of mainly maternal complications. The current studies avoid the problems of summary scales and their uncertain interpretation. It is, however, sobering to realise that despite a total sample of over 1500 they may have been too small to detect some important effects. More large studies of specific complications, and cumulative meta-analyses of them, are required before the case for or against the potential role of obstetric complications in schizophrenia is conclusive.
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TOPMORE LARGE STUDIES NEEDEDREFERENCES |
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Geddes, J. R. & Lawrie, S. M. (1995)
Obstetric complications and schizophrenia: a meta-analysis. British
Journal of Psychiatry, 167,
786-793.
Geddes, J. R., Verdoux, H., Takei, N., et al (1999) Schizophrenia and complications of pregnancy and labor: an individual patient data meta-analysis. Schizophrenia Bulletin, 25, 413-423.
Thomas, H. V., Dalman, C., David, A. S., et al
(2001) Obstetric complications and risk of schizophrenia.
Effect of gender, age at diagnosis and maternal history of psychosis.
British Journal of Psychiatry,
179,
409-414.
Verdoux, H., Geddes, J. R., Takei, N., et al (1997) Obstetric complications and age at onset in schizophrenia: an international collaborative meta-analysis of individual patient data. American Journal of Psychiatry, 154, 1220-1227.[Abstract]
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