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Invited commentaries on: Signs of asphyxia at birth and risk of schizophrenia/Obstetric complications and risk of schizophrenia

More Large Studies Needed

Published online by Cambridge University Press:  02 January 2018

A. M. McIntosh
Affiliation:
Edinburgh University Department of Psychiatry, Kennedy Tower, Royal Edinburgh Hospital, Edinburgh E10 5HF UK
S. M. Lawrie
Affiliation:
Edinburgh University Department of Psychiatry, Kennedy Tower, Royal Edinburgh Hospital, Edinburgh E10 5HF UK
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Abstract

Type
Papers
Copyright
Copyright © Royal College of Psychiatrists, 2001 

MORE LARGE STUDIES NEEDED

We need more large studies and cumulative meta-analyses of individual obstetric complications and their effects on the neonate

Obstetric complications are ‘one’ of the few putative causes of schizophrenia for which there is relatively good evidence (Reference Geddes and LawrieGeddes & Lawrie, 1995), but only a few particular obstetric complications are likely to be important (Reference Geddes, Verdoux and lakeiGeddes et al, 1999) and they may have at most non-specific effects, for example in bringing forward the age at onset (Reference Verdoux, Geddes and TakeiVerdoux et al, 1997). The importance of the papers by Dalman et al (Reference Dalman, Thomas and David2001, this issue) and Thomas et al (Reference Thomas, Dalman and David2001, this issue) is that they attempt to relate obstetric complications to their effects on the neonate, and to the subsequent development of schizophrenia. They are a valuable contribution to the ongoing debate about the role of obstetric complications in schizophrenia, despite some inevitable methodological limitations.

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 (Reference Verdoux, Geddes and TakeiVerdoux 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.

References

Dalman, C., Thomas, H. V., David, A. S., et al (2001) Signs of asphyxia at birth and risk of schizophrenia. Population-based case–control study British Journal of Psychiatry, 179, 403408.Google Scholar
Geddes, J. R. & Lawrie, S. M. (1995) Obstetric complications and schizophrenia: a meta-analysis. British Journal of Psychiatry, 167, 786793.Google Scholar
Geddes, J. R., Verdoux, H., lakei, N., et al (1999) Schizophrenia and complications of pregnancy and labor: an individual patient data meta-analysis. Schizophrenia Bulletin, 25, 413423.Google Scholar
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, 409414.Google Scholar
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, 12201227.Google Scholar
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