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Early biomarkers of psychosis
Authors:Freedman Robert  Ross Randal  Leonard Sherry  Myles-Worsley Marina  Adams Catherine E  Waldo Merilyne  Tregellas Jason  Martin Laura  Olincy Ann  Tanabe Jody  Kisley Michael A  Hunter Sharon  Stevens Karen E
Affiliation:Department of Psychiatry C-268-71, University of Colorado Health Sciences Center, Denver, CO 80262, USA. Robert.Freedman@UCHSC.edu
Abstract:Biological traits that are predictive of the later development of psychosis have not yet been identified. The complex, multidetermined nature of schizophrenia and other psychoses makes it unlikely that any single biomarker will be both sensitive and specific enough to unambiguously identify individuals who will later become psychotic. However, current genetic research has begun to identify genes associated with schizophrenia, some of which have phenotypes that appear early in life. While these phenotypes have low predictive power for identifying individuals who will become psychotic, they do serve as biomarkers for pathophysiological processes that can become the targets of prevention strategies. Examples are given from work on the role of the alpha(T)nicotinic receptor and its gene CHRNA7 on chromosome 15 in the neurobiology and genetic transmission of schizophrenia.
Keywords:schizophrenia   development   genetics   chromosome 15   nicotinic receptor   hippocampus   inhibition   auditory evoked potentials   eye movement
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