Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-22T07:07:54.563Z Has data issue: false hasContentIssue false

The Search for the Psychosis Gene

Published online by Cambridge University Press:  02 January 2018

T. J. Crow*
Affiliation:
Division of Psychiatry, Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ

Extract

The major psychoses remain an enigma. Affective and schizophrenic psychoses are apparently present (probably at about the same lifetime prevalence of approximately 2%) in all human societies. Yet their aetiology is obscure. While a genetic contribution is acknowledged by most authorities, few accept that genes are a sufficient explanation of causation because: onset is in adult life; psychosis – particularly schizophrenia – is associated with a substantial fertility disadvantage; and most cases lack a family history of illness. But genetic determination has to be considered because onset is determined by chronological age rather than environmental insult (Crow & Done, 1986), adoption away from a family with schizophrenia does not reduce risk of illness, and no plausible environmental precipitant of psychosis has been identified. The fact that psychosis occurs across widely differing climatic, industrial, and social environments without obvious variations in incidence suggests that the disease is relatively independent of the external milieu. The suggestion that birth injury is relevant has been tested in a prospective study (the National Child Development Study) and found wanting (Done et al, 1991).

Type
Molecular Biology Symposium
Copyright
Copyright © Royal College of Psychiatrists, 1991 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Angst, J., Scharfetter, C. & Stasen, H. H. (1983) Classification of schizoaffective patients by multidimensional scaling and cluster analysis. Psychiatria Clinica, 16, 254264.Google ScholarPubMed
Angst, J., Scharfetter, C. (1990) Schizoaffective psychoses. Ein Nosologischer Aergernis. In Affective Psychosen (ed. R. J. Witowski). Stuttgart: Schattauer.Google Scholar
Annett, M. (1985) Left, Right, Hand and Brain: The Right Shift Theory. London: Erlbaum.Google Scholar
Baker, H. F., Ridley, R. M. & Crow, T. J. (1985) Experimental transmission of an autosomal dominant spongiform encephalopathy: does the infectious agent originate in the human genome? British Medical Journal, 291, 299302.Google Scholar
Crow, T. J. (1986) The continuum of psychosis and its implication for the structure of the gene. British Journal of Psychiatry, 149, 419429.CrossRefGoogle ScholarPubMed
Crow, T. J. (1988) Sex chromosomes and psychosis: the case for a pseudoautosomal locus. British Journal of Psychiatry, 153, 675683.Google Scholar
Crow, T. J. (1989) Pseudoautosomal locus for the cerebral dominance gene. Lancet, ii, 339340.Google Scholar
Crow, T. J. (1990) Temporal lobe asymmetries as the key to the aetiology of schizophrenia. Schizophrenia Bulletin, 16, 433443.Google Scholar
Crow, T. J. & Done, D. J. (1986) Age of onset of schizophrenia in siblings: a test of the contagion hypothesis. Psychiatry Research, 18, 107117.Google Scholar
Crow, T. J., DeLisi, L. E. & Johnstone, E. C. (1989a) Concordance by sex in sibling pairs with schizophrenia is paternally inherited. Evidence for a pseudoautosomal locus. British Journal of Psychiatry, 155, 9297.CrossRefGoogle ScholarPubMed
Crow, T. J., Ball, J., Bloom, S. R., et al (1989b) Schizophrenia as an anomaly of development of cerebral asymmetry. Archives of General Psychiatry, 46, 11451150.Google Scholar
Done, D. J., Johnstone, E. C., Frith, C. D., et al (1991) Complications of pregnancy and delivery in relation to psychosis in adult life: a study using the British Perinatal Mortality Survey. Schizophrenia Research, 3, 91.CrossRefGoogle Scholar
Egeland, J. A., Gerhard, D. S., Pauls, D. L., et al (1987) Bipolar affective disorders linked to DNA markers on chromosome 11. Nature, 325, 783787.CrossRefGoogle ScholarPubMed
Farde, L., Wiesel, F. A., Stone-Elanders, , et al (1990) D2 dopamine emission tomography study with C-raclopride. Archives of General Psychiatry, 47, 213219.Google Scholar
Gershon, E. S., Hamovit, J., Guroff, J. J., et al (1982) A family study of schizoaffective, bipolar I, bipolar II, unipolar and normal control patients. Archives of General Psychiatry, 39, 1571167.Google Scholar
Gershon, E. S., DeLisi, L. E. & Hamovit, J., et al (1988) A controlled family study of chronic psychoses: schizophrenia and schizoaffective disorder. Archives of General Psychiatry, 45, 328336.Google Scholar
Gurling, H. D. M., Sherrington, R. P., Brynjolfsson, J., et al (1989) Recent and future molecular genetic research into schizophrenia. Schizophrenia Bulletin, 15, 373382.CrossRefGoogle ScholarPubMed
Hsiao, K., Baker, H. F., Crow, T. J., et al (1989) Linkage of a prion protein missense variant to Gerstmann–Straussler syndrome. Nature, 388, 342345.Google Scholar
Kelsoe, J. R., Ginns, E. I., Egeland, J. A., et al (1989) Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish. Nature, 342, 238243.Google Scholar
Kennedy, J. L., Giuffra, L. A., Moises, H. E., et al (1988) Evidence against linkage of schizophrenia to markers on chromosome 5 in a Northern Swedish pedigree. Nature, 336, 167170.Google Scholar
Moises, H. W., Gelernter, J., Grandy, D. K., et al (1989) Exclusion of the D2 dopamine receptor gene as candidate gene for schizophrenia in a large pedigree from Sweden. In Abstracts for the First World Congress on Psychiatric Genetics (Cambridge). Nottingham: Bell-Howe Conferences.Google Scholar
Ødegaard, O. (1972) The multifactorial inheritance of predisposition to schizophrenia. In Genetic Factors in “Schizophrenia” (ed. A. R. Kaplan), pp. 256275. Springfield, Illinois: Thomas.Google Scholar
Owen, F., Poulter, M., Shah, T., et al (1990) An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease. Molecular Brain Research, 7, 273276.Google Scholar
Prusiner, S. B. (1989) Scrapie prions. Annual Review of Microbiology, 43, 345374.CrossRefGoogle ScholarPubMed
Sherrington, R., Brynjolfsson, J., Pertursson, H., et al (1988) Localisation of a susceptibility locus for schizophrenia on chromosome 5. Nature, 336, 164167.Google Scholar
St Clair, D. M., Blackwood, D., Muir, W., et al (1989) No linkage of chromosome 11q-q13 markers to schizophrenia in Scottish families. Nature, 339, 305309.Google Scholar
Stewart, J., Debray, Q. & Caillard, V. (1980) Schizophrenia: the testing of genetic models by pedigree analysis. American Journal of Human Genetics, 32, 5563.Google Scholar
Submit a response

eLetters

No eLetters have been published for this article.