» Articles » PMID: 39144119

Pharmacological Treatment of Cognitive Impairment Associated With Schizophrenia: State of the Art and Future Perspectives

Overview
Date 2024 Aug 15
PMID 39144119
Authors
Affiliations
Soon will be listed here.
Abstract

Cognitive Impairment Associated with Schizophrenia (CIAS) represents one of the core dimensions of Schizophrenia Spectrum Disorders (SSD), with an important negative impact on real-world functional outcomes of people living with SSD. Treatment of CIAS represents a therapeutic goal of considerable importance, and while cognition-oriented evidence-based psychosocial interventions are available, effective pharmacological treatment could represent a game-changer in the lives of people with SSD. The present critical review reports and discusses the evidence regarding the effects of several pharmacological agents that are available in clinical practice or are under study, commenting on both current and future perspectives of CIAS treatment. In particular, the effects on CIAS of antipsychotic medications, anticholinergic medications, benzodiazepines, which are currently commonly used in the treatment of SSD, and of iclepertin, d-serine, luvadaxistat, xanomeline-trospium, ulotaront, anti-inflammatory molecules, and oxytocin, which are undergoing regulatory trials or can be considered as experimental agents, will be reported and discussed. Currently, available pharmacological agents do not appear to provide substantial benefits on CIAS, but accurate management of antipsychotic medications and avoiding treatments that can further exacerbate CIAS represent important strategies. Some molecules that are currently being investigated in Phase 2 and Phase 3 trials have provided very promising preliminary results, but more information is currently required to assess their effectiveness in real-world contexts and to provide clear recommendations regarding their use in clinical practice. The results of ongoing and future studies will reveal whether any of these molecules represents the awaited pharmacological game-changer in the treatment of CIAS.

Citing Articles

The awareness, characterization, and burden of Cognitive Impairment Associated with Schizophrenia (CIAS) in clinical practice: Results from a nationwide survey in Italy.

Vita A, Barlati S, Cavallaro R, Cipelli R, Corrivetti G, Delmonte D Schizophr Res Cogn. 2025; 40:100352.

PMID: 40046087 PMC: 11880602. DOI: 10.1016/j.scog.2025.100352.


Interpretable machine learning to evaluate relationships between DAO/DAOA (pLG72) protein data and features in clinical assessments, functional outcome, and cognitive function in schizophrenia patients.

Lin C, Lin E, Lane H Schizophrenia (Heidelb). 2025; 11(1):27.

PMID: 39987274 PMC: 11846841. DOI: 10.1038/s41537-024-00548-z.


Cognitive rehabilitation in schizophrenia research: a bibliometric and visualization analysis.

Shu X, Dai Y, Tang J, Huang Y, Hu R, Lin Y Front Psychiatry. 2024; 15:1509539.

PMID: 39722848 PMC: 11668788. DOI: 10.3389/fpsyt.2024.1509539.


Feasibility and Acceptability of Providing Cognitive Remediation in a Large USA System of Coordinated Specialty Care for Early Psychosis.

Medalia A, Saperstein A, Wall M, Basaraba C, Bello I, Nossel I Early Interv Psychiatry. 2024; 19(1):e13624.

PMID: 39421910 PMC: 11732730. DOI: 10.1111/eip.13624.


Cognitive Impairment Associated With Schizophrenia: New Research Agenda.

Galderisi S, Marder S Schizophr Bull Open. 2024; 5(1):sgae023.

PMID: 39376222 PMC: 11457370. DOI: 10.1093/schizbullopen/sgae023.


References
1.
Dedic N, Dworak H, Zeni C, Rutigliano G, Howes O . Therapeutic Potential of TAAR1 Agonists in Schizophrenia: Evidence from Preclinical Models and Clinical Studies. Int J Mol Sci. 2021; 22(24). PMC: 8704992. DOI: 10.3390/ijms222413185. View

2.
Perry L, Ramson D, Stricklin S . Mirtazapine adjunct for people with schizophrenia. Cochrane Database Syst Rev. 2018; 5:CD011943. PMC: 6494505. DOI: 10.1002/14651858.CD011943.pub2. View

3.
Liu N, Daumit G, Dua T, Aquila R, Charlson F, Cuijpers P . Excess mortality in persons with severe mental disorders: a multilevel intervention framework and priorities for clinical practice, policy and research agendas. World Psychiatry. 2017; 16(1):30-40. PMC: 5269481. DOI: 10.1002/wps.20384. View

4.
Mailman R, Murthy V . Third generation antipsychotic drugs: partial agonism or receptor functional selectivity?. Curr Pharm Des. 2009; 16(5):488-501. PMC: 2958217. DOI: 10.2174/138161210790361461. View

5.
Ritsner M, Strous R . Neurocognitive deficits in schizophrenia are associated with alterations in blood levels of neurosteroids: a multiple regression analysis of findings from a double-blind, randomized, placebo-controlled, crossover trial with DHEA. J Psychiatr Res. 2009; 44(2):75-80. DOI: 10.1016/j.jpsychires.2009.07.002. View