The Self-Defense Skill Linked To PR-171
Further investigation is required. Genetic trait Not only do patients with psychotic disorders exhibit abnormalities in olfactory processing, but their unaffected first-degree relatives also demonstrate mildly abnormal brain activation patterns when contrasted to non-related controls[27]. When presented with an unpleasant odour, patients�� unaffected brothers demonstrated reduced frontal activation (relative to the healthy control group) and increased activation in anterior cingulate, but during the presentation of a pleasant odorant, no differences were noted. This group suggested that hypofrontality YES1 may be a genetic trait that is expressed to a lesser degree in the non-affected brothers. Age Despite age being considered an important factor to consider in olfactory neuroimaging research[71], to date, no studies have examined the difference in olfactory neural processing between young and older patients with psychotic disorders. In all studies presented in this literature review, the age of the patients and that of control subject have been well matched and also relatively young (Mean ages AZD9291 male patients were examined PR 171 in the studies published by Schneider et al[27], Clark et al[73], and Plailly et al[25] and investigations by Crespo-Facorro et al[72] and Malaspina et al[33] contained samples that were predominantly male. Only Turetsky et al[20] (not described) and Good et al (under review) examined almost equal numbers of males and female subjects. The data on sex differences in olfactory processing is not fully developed; however, in patients with psychotic disorders, the overwhelming number of sex differences is a very important aspect of the disorder and is likely overlooked in neuroimaging studies of this population. Not all patients with psychotic disorder are impaired on olfactory testing. Some of the data provided herein suggest that may be subgroups within the heterogenous diagnostic category ��schizophrenia��. Not only are there potential differences in brain activation, but there are within diagnostic group differences in symptomatology and outcome[8,9]. Further investigations are needed to tease out the differences within schizophrenia. A further limitation on the data that were presented is that patients and controls differ on many variables that are related to brain activation patterns.