Mutating screening in the CHRNA7 gene resulted in the discovery of single nucleotide polymorphisms in the promoter and other abnormalities that have been associated with schizophrenia itself and also with the failure to inhibit P50 responses in schizophrenia (Figure 3). While the significance of all of these polymorphisms

is still being sorted out, the allele frequency of these polymorphisms is relatively high, Inhibitors,research,lifescience,medical as was predicted from the linkage data.9 Similarly high frequencies have been reported for most other putative candidate genes for schizophrenia.10 Taking all these genes into account, it would seem that the majority of the population has at least one of the genetic risk Inhibitors,research,lifescience,medical factors for schizophrenia. Figure 3. Effects of a single nucleotide polymorphism in the promoter of CHRNA7 on P50 sensory gating. The normal subject with more common alleles (-86 C/C) has normal suppression of P50, measured as a low P50 test to conditioning amplitude ratio. The subjects … Thus, the somewhat unexpected result

of genetic research to date is that genetic risk is much more wide-spread than initially posited. Identification of individuals at risk by genetic means alone Inhibitors,research,lifescience,medical is not likely to select individuals who have a high probability of actually developing schizophrenia. However, the situation is not as hopeless from the perspective of prevention. First, for CHRNA7 and for many of the other genes being discovered for schizophrenia, the neurobiological phenotypes are being elucidated. Most of the genes are associated with dysfunction in the mechanisms of neurotransmission.

For CHRNA7, there is an apparent link to an inhibitory dysfunction Inhibitors,research,lifescience,medical that can be measured physiologically, in both animal models and humans. To the extent that this dysfunction and similar dysfunctions can be traced through development, a biological developmental course of schizophrenia Inhibitors,research,lifescience,medical can be ascertained, so that the window for possible prevention can be determined. While this time course could have been established without the genetic information, the genetic associations and INK1197 mw linkages relate the physiological dysfunction, eg, diminished sensory gating, to a well-identified biological element, oxyclozanide eg, diminished activation of α7-nicotinic receptors. The dominant model with complete penetrance posited a model of pathophysiology in which a single genetic deficit produces a near catastrophic effect on brain function that results in schizophrenia. The more complex model posited here suggests that schizophrenia may be the coincidence in a single individual of multiple deficits, none of which in themselves are particularly problematic. Small changes in the pathophysiological effect of any one of these deficits could have significant effects on the development of illness.