Conference Agenda

Overview and details of the sessions of this conference. Please select a date or location to show only sessions at that day or location. Please select a single session for detailed view (with abstracts and downloads if available).

 
 
Session Overview
Session
Symposium 1_1: Cognitive deficits in neuropsychiatric disorders: from neural networks to function
Time:
Friday, 15/Sept/2023:
8:30am - 9:45am

Session Chair: Paolo Calabresi, Fondazione Policlinico Universitario A. Gemelli
Session Chair: Alfonso Tortorella, University of Perugia
Location: Sala Cinquecento

476 seats

SIPB – SINS joint Symposium

Session Abstract

Cognitive functioning represents an excellent opportunity to better characterize psychiatric disorders, since cognitive impairment is present in individuals with putatively “distinct” conditions that share the feature of psychosis. Alterations of cognitive function have a fundamental role in modulating recovery and quality of life in patients with severe psychiatric disorders. Ongoing research has focused on the impact that cognition might have on functioning and quality of life parameters. However, there is paucity of data on the extent to which cognition predicts remission and recovery and on the predictive role of biological and clinical markers in modulating illness outcomes.


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Presentations
8:30am - 8:50am

Cognitive deficits in schizophrenia: impact on functioning and new treatment options

Armida Mucci, Paola Bucci, Giulia Maria Giordano, Silvana Galderisi

University of Campania Luigi Vanvitelli, Italy

Cognitive impairment represents a core dimension of schizophrenia that can be considered a cognitive disorder.

In fact, neurocognitive and social cognitive deficits are documented in all phases of the disorder, as well as in subjects at risk to develop psychosis.

These deficits are the strongest predictors of poor outcome in different functional domains, but still remain a major therapeutic challenge.

Second-generation antipsychotics are recommended for their favorable cognitive profile compared to first generation antipsychotics. Anticholinergic and benzodiazepine burden should be kept to a minimum, considering the negative impact on cognitive functioning.

Among psychosocial interventions, cognitive remediation and physical exercise are recommended for the treatment of cognitive impairment in schizophrenia. The presence of metabolic syndrome hampers the capacity of cognitive remediation to restore cognitive deficits and should be addressed carefully before initiating cognitive remediation. Non-invasive brain stimulation techniques can be offered as add on therapy.

Individualized integrated interventions combining cognitive remediation with other approaches already changed the pessimistic view of schizophrenia as a stable or deteriorating cognitive disorder.

New treatment strategies are under development and might be available in the near future.



8:50am - 9:05am

A new animal model of Gaming Disorder: sexual differences in behavior and reward sistem

Antonino Casile1,2,3, Brigitta Bonaldo2,3, Sofia Nasini4, Martina Bettarelli2, Marilena Marraudino2, Maria Vittoria Micioni Di Bonaventura1, Carlo Cifani1, Stefano Gotti1,2,3

1University of Camerino, School of Pharmacy, Pharmacology Unit, Via Madonna delle Carceri, 9, 62032 Camerino (MC), Italy.; 2Neuroscience Institute Cavalieri Ottolenghi (NICO), Regione Gonzole, 10, Orbassano (TO), University of Turin, 10043 Turin, Italy; 3Department of Neuroscience “Rita Levi-Montalcini”, Via Cherasco 15, 10126 Turin (TO), Italy.; 4Laboratory of Molecular and Cellular Pharmacology, Department of Pharmacology, University of Padua, Largo Egidio Meneghetti, 2, 35131 Padua, Italy

In 2018 International Classification of Diseases (ICD-11) classified Gaming Disorder (GD) as a mental disorder. GD mainly occurs among adolescents, who after developing addiction, show psychopathological traits such as social anxiety, depressive disorder, social isolation, and attention deficit. However, the different studies conducted in humans so far show several limitations, such as exposure period, duration, and gender. Trying to address the lack of an experimental model for such a disorder, in the present work we proposed a GD rat model to investigate some peculiar tracts of the disorder. GD-rats showed a significant increase in frequency and duration of play, and time spent in front of the screen compared to both controls and rats trained but did not GD. In addition, GD females showed greater interaction and duration of play, which was maintained even in the presence of sexual or social stimuli compared to GD-males, and reduced interaction time to CON-females. Quantitative analysis of immunoreactivity of Dopamine in the Ventral Tegmental Area and Substantia Nigra, and Serotonin in Dorsal Raphe showed a significative reduction in GD animals compared to control groups.

In conclusion, we propose the first animal model of GD in rats, with great translational potential that exhibits characteristics also found in GD patients. The use of our animal model of GD will allow us to further investigate the neurological basis of the disorder also considering the sex differences.



9:05am - 9:25am

Cognition and clinical outcomes in severe psychiatric disorders: trans-diagnostic approaches

Mirko Manchia1,2

1University of Cagliari, Italy; 2Dalhousie University, Canada

Cognitive deficits are common symptoms during the course of severe mental disorders (SMD). Their manifestation can antecede or follow the onset of full-blown psychopathological symptoms with varying degree of severity. In general, cognitive impairment appears to influence the trajectory of SMD even when remission is achieved impacting on the quality of life and functioning of patients. Here I will focus on the results of two longitudinal prospective studies in cohorts of patients with SMD (bipolar disorders and psychotic disorders) followed at the Unit of Psychiatry of the University of Cagliari. We found that in 105 patients with schizophrenia spectrum disorder the higher the level of cognitive functioning and in particular verbal functioning (letter fluency) as measured with the Brief Assessment for Cognitive Symptoms in schizophrenia (BACS) the higher the lifetime suicide risk. Further, in a cohort of 45 patients with bipolar disorders and lifetime suicidality we found a statistically significant difference for the Color Naming and the Neutral words (NW) subtasks of the of the Brief Assessment of Cognition for Affective Disorder (BACA) with higher scores compared to those without lifetime suicidality. These data show
that cognitive testing can be useful in the formulation of lifetime suicide risk, albeit with a different meaning for impairment or retained cognition depending on the clinical diagnosis (e.g., in mood disorders, lower performances in certain cognitive tasks may instead be associated with a higher suicide risk).



 
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