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Christina M Hultman a Department of Neuroscience,
Psychiatry, Ulleråker, University of Uppsala, S-750 17 Uppsala 17, Sweden, b Stockholm Centre on Health of Societies in Transition,
Huddinge, Sweden, c Department of Psychiatry and Neurology, Hamamtsu University
School of Medicine, Hamamtsu, Japan, d Department of Psychological
Medicine, Institute of Psychiatry, London, e Department of Medical Epidemiology,
Karolinska Institute, Stockholm, Sweden
Correspondence to:
Christina M Hultman christina.hultman{at}ullpsyk.uu.se
Objective:
To examine prenatal and perinatal risk
factors for subsequent development of schizophrenia and affective and reactive psychosis.
Design:
Three population based, case-control studies conducted within a Sweden-wide cohort of all children born during 1973-9. This was done by linking individual data from the Swedish birth
register, which represents 99% of all births in Sweden, to the Swedish
inpatient register.
Subjects:
Patients listed in inpatient register as
having been first admitted to hospital aged 15-21 years with a
main diagnosis of schizophrenia (n=167), affective psychosis (n=198),
or reactive psychosis (n=292). For each case, five controls were selected.
Main outcome measures:
Risks of schizophrenia and
affective and reactive psychosis in relation to pregnancy and perinatal characteristics.
Results:
Schizophrenia was positively associated
with multiparity (odds ratio 2.0), maternal bleeding during
pregnancy (odds ratio 3.5), and birth in late winter (odds ratio 1.4).
Affective psychosis was associated with uterine atony (odds ratio 2.2)
and late winter birth (odds ratio 1.5). Reactive psychosis was
related to multiparity (odds ratio 2.1). An increased risk for
schizophrenia was found in boys who were small for their
gestational age at birth (odds ratio 3.2), who were number four or
more in birth order (odds ratio 3.6), and whose mothers had had
bleeding during late pregnancy (odds ratio 4.0).
Conclusions:
A few specific pregnancy and perinatal
factors were associated with the subsequent development of psychotic
disorder, particularly schizophrenia, in early adult life. The
association of small size for gestational age and bleeding during
pregnancy with increased risk of early onset schizophrenia among males
could reflect placental insufficiency.
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