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A Review of Risk Factors for Schizophrenia. Joy Welham Sukanta Saha John McGrath. Schizophrenia is a group of imperfectly understood brain disorders characterized by alterations in higher functions related to perception, cognition, communication, planning and motivation.
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A Review of Risk Factors for Schizophrenia Joy Welham Sukanta SahaJohn McGrath
Schizophrenia is a group of imperfectly understood brain disorders characterized by alterations in higher functions related to perception, cognition, communication, planning and motivation. Signs and symptoms are hallucinations, delusions, thought disorder, and negative symptoms - eg blunted affect and reduced speech. These usually emerge in early adulthood. While many affected individuals recover, others have intermittent/persistent symptoms. Although advances in biological and psychosocial treatments are improving outcomes, schizophrenia is still a leading contributor to the global burden of disease. This keeps research focused on finding the causes of schizophrenia.
Aims To examine risk indicators, proxy variables and risk factors in relation to the developmental hypothesis. These may operate: Prenatally Perinatally Post natally - early childhood - later childhood - adolescence/adulthood
Outline • Defining risk factors • Risk indicators • Risk proxies • Putative risk factors • Caveats and conclusions
Developmental models of schizophrenia Schizophrenia as a neurodevelopmental disorder - results from early (pre- or perinatal) events - possibly modified by later events - manifests in late adolescent/early adulthood
Risk indicators throughout development Early childhood Developmental delays Later childhood Neurological/cognitive anomalies Psycho-social deficits Brain anomalies Structural Functional Minor physical anomalies Dermatoglyphic anomalies
Proxy variables • Season-of-birth • Place-of-birth • Migration
Proxy variables (1) Perinatal Season-of-birth Estimated effect size 5-15% winter/spring excess eg • relative risk =1.11 • but population attributable fraction (PAF) about 10.5%
Risk proxy (2) Perinatal Place-of-birth; Urban vs rural birth Estimated effect size = 1.5 – 4.2 Relative risk 2.4 but PAF about 30%
Risk proxy (3) Migration Estimated effect size 4 - 14
Other genetic Non-hereditary genetic risk factors • Paternal age/mutation (no estimated effect size available)
Environmental exposures: prenatal (1) • Prenatal nutrition • Macro-nutrition; eg calories/kilojoules • Micro-nutrition; eg specific vitamins • Estimated effect size for prenatal famine = 2.0
Environmental exposures: prenatal (2) Prenatal Infections • Influenza (estimated effect size =2.0) • Poliomyelitis (estimated effect size = 1.05) • Respiratory infection (estimated effect size = 2.1) • Rubella (estimated effect size = 5.2) • Toxoplasmosis (uncertain effect size)
Environmental exposures: prenatal (3) Maternal stress • death of spouse (estimated effect size = 6.2) • flood (estimated effect size =1.8) • ‘unwanted’ child (estimated effect size = 2.4) • depression (estimated effect size = 1.8)
Environmental exposures: adolescence/adulthood (1) • Adverse life events • Social isolation • Stress • Estimated effect size =1.5 - 6
Environmental exposures: perinatal Pregnancy & Birth Complications eg • prematurity, high & low birth weight, high & low body mass index, diminished head circumference • fetal distress and hypoxia-related PBCs • pre-eclampsia, prolonged labour, multiparity • Rhesus incompatibility (estimated effect size =2.8) Estimated effect size≈ 2
Environmental exposures: childhood Infections Estimated effect size =4.0 Brain injury No estimated effect size available
Environmental exposures: adolescence/adulthood (1) • Adverse life events • social isolation • stress • other • Estimated effect size = 1.5 – 6.0
Environmental exposures: adolescence/adulthood (2) • Drug use • Alcohol • Marihuana • Other • Estimated effect size =2.0
Sex differences • Sex is an example of a fixed risk factor • Sex modifies the effects of other risk factors • Male–female differences in schizophrenia: • familial transmission. • age at onset • symptomatology • neurobiological factors • (eg brain abnormalities & cognitive function) • course of illness • treatment response • incidence
Risk factors and Age-at-onset • Variable age-at-onset • – wide range from childhood to older ages • Different risk indicators/RFs may be involved • Earlier onset seems to be associated with • male sex • positive family history • greater history of developmental deviance
Caveats • Many possible risk factors identified; some RFs have substantial if inconclusive evidence (eg genes, obstetric complications), other RFs have been studied less • Mostly ecological studies • Risk factors and indicators lack specificity • Determining caseness • More than one syndrome? • Cause versus effect can be difficult to establish
Conclusions (1) Some/many risk factors may interact Risk factors may be modified by time, place or person Heterogeneity can lead to further hypotheses & studies
Conclusions (2) • Improved fetal and infant growth may be a means to improve adult health. • Non-specific environmental risk factors may lead to universal prevention • Epidemiology has discovered interesting leads …..more studies needed • ….epidemiological • ….laboratory, and • ….clinical