Abstract:Objective-Patients affected by schizophrenia show deficits in both visual perception and working memory. The authors tested early-stage vision and working memory in subjects with schizotypal personality disorder, which has been biologically associated with schizophrenia.Method-Eleven subjects who met DSM-III-R criteria for schizotypal personality disorder and 12 normal comparison subjects were evaluated. Performance thresholds were obtained for tests of visual discrimination and working memory. Both form and t… Show more
“…parents, siblings, children) demonstrate deficits on tasks designed to measure working memory function (Park et al 1995a;Callicott et al 2003). In addition, individuals who score high on measures of psychosis proneness and individuals diagnosed with schizotypal personality disorder (Barch et al, unpublished data;Park et al 1995b;Park and McTigue 1997;Farmer et al 2000;Lenzenweger and Gold 2000;Roitman et al 2000;Mitropoulou et al 2002) also display deficits on working memory tasks.…”
Section: Pharmacological Manipulation Of Human Working Memorymentioning
Compounds geared towards enhancing the dopamine system and the acetycholine system remain promising avenues for the development of pro-cognitive drugs, though further work is clearly needed on developing agents that may more selectively target specific receptors.
“…parents, siblings, children) demonstrate deficits on tasks designed to measure working memory function (Park et al 1995a;Callicott et al 2003). In addition, individuals who score high on measures of psychosis proneness and individuals diagnosed with schizotypal personality disorder (Barch et al, unpublished data;Park et al 1995b;Park and McTigue 1997;Farmer et al 2000;Lenzenweger and Gold 2000;Roitman et al 2000;Mitropoulou et al 2002) also display deficits on working memory tasks.…”
Section: Pharmacological Manipulation Of Human Working Memorymentioning
Compounds geared towards enhancing the dopamine system and the acetycholine system remain promising avenues for the development of pro-cognitive drugs, though further work is clearly needed on developing agents that may more selectively target specific receptors.
“…Individuals with SPD, for example, show deficits in nonverbal learning, and especially in verbal learning (51), in working memory (52), and in several executive functions, including concept formation, abstraction, and mental flexibility (53). Similarly, relatives of patients who do not have SPD show dysfunction in several cognitive domains, including motor and perceptual-motor ability, short-term memory, working memory, learning and recall, verbal and language skills, sustained attention, and executive function (2).…”
Objective: Early intervention to prevent schizophrenia is one of the most important goals of schizophrenia research. However, the field is not yet ready to initiate trials to prevent prodromal or psychotic symptoms in people who are at risk for developing the disorder. In this paper, we consider some of the major obstacles that must be studied before prevention strategies become feasible.
Method and Results:One of the most important hurdles is the identification of a syndrome or set of traits that reflects a predisposition to schizophrenia and that might provide potential targets for intervention. In a recent reformulation of Paul Meehl's concept of schizotaxia, we integrate research findings obtained over the last 4 decades to propose a syndrome with meaningful clinical manifestations. We review the conceptualization of this syndrome and consider its multidimensional clinical expression. We then describe preliminary research diagnostic criteria for use in adult, nonpsychotic, first-degree relatives of patients diagnosed with schizophrenia, based on negative symptoms and neuropsychological deficits. We follow this with evidence supporting the validity of the proposed syndrome, which mainly includes social dysfunction and response to a low dosage of one of the newer antipsychotic medications.
Conclusions:Continued progress toward the eventual initiation of prevention strategies for schizophrenia will include sustained efforts to validate the traits reflecting a predisposition to develop the disorder (for example, schizotaxia), follow-up studies to confirm initial findings, and the identification of potentially useful preventive interventions. (Can J Psychiatry 2002;47:518-526) See page 524 for research funding and support and page 525 for author affiliations.Clinical Implications · The predisposition to develop schizophrenia in nonprodromal, nonpsychotic adult relatives of patients with schizophrenia may be expressed as a meaningful, diagnosable, clinical syndrome or set of traits, called schizotaxia. · In adults, at least some schizotaxia symptoms may be attenuated with interventions. · Interventions that attenuate schizotaxia symptoms in adults may eventually be useful in strategies aimed at preventing schizophrenia.Limitations · Double-blind intervention studies of schizotaxia are needed. · Longitudinal neuroimaging data are needed for children at high risk for developing schizophrenia. · Molecular-genetic studies of schizotaxia are needed to extend and validate the syndrome.
“…Studies of monozygotic and dizygotic twins pairs discordant for schizophrenia (Cannon et al 2000 ;Glahn et al 2005) indicate that SWM deficits are associated with increased genetic risk for schizophrenia, and it has been suggested that a higher genetic loading for disease-related traits is linked to greater cognitive impairment (Saperstein et al 2006). Impaired spatial memory performance has also been reported in subjects with high levels of schizotypy (Park et al 1995) or schizotypal personality disorder (Farmer et al 2000), and in those with a history of very preterm birth (Narberhaus et al 2009). …”
Background. Impaired spatial working memory (SWM) is a robust feature of schizophrenia and has been linked to the risk of developing psychosis in people with an at-risk mental state (ARMS). We used functional magnetic resonance imaging (fMRI) to examine the neural substrate of SWM in the ARMS and in patients who had just developed schizophrenia.Method. fMRI was used to study 17 patients with an ARMS, 10 patients with a first episode of psychosis and 15 agematched healthy comparison subjects. The blood oxygen level-dependent (BOLD) response was measured while subjects performed an object-location paired-associate memory task, with experimental manipulation of mnemonic load.Results. In all groups, increasing mnemonic load was associated with activation in the medial frontal and medial posterior parietal cortex. Significant between-group differences in activation were evident in a cluster spanning the medial frontal cortex and right precuneus, with the ARMS groups showing less activation than controls but greater activation than first-episode psychosis (FEP) patients. These group differences were more evident at the most demanding levels of the task than at the easy level. In all groups, task performance improved with repetition of the conditions. However, there was a significant group difference in the response of the right precuneus across repeated trials, with an attenuation of activation in controls but increased activation in FEP and little change in the ARMS.
Conclusions.Abnormal neural activity in the medial frontal cortex and posterior parietal cortex during an SWM task may be a neural correlate of increased vulnerability to psychosis.
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