Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 9 de 9
Filter
1.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 44(1): 26-34, Jan.-Feb. 2022. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1360175

ABSTRACT

Objective: To test the hypothesis that genetic variations of cannabinoid receptors contribute to the pathophysiology of cognitive deficits in schizophrenia. Methods: In this genetic association case-control study, cannabinoid receptor polymorphisms CNR1 rs12720071 and CNR2 rs2229579 were tested for association with neurocognitive performance in 69 patients with schizophrenia and 45 healthy controls. Neurocognition was assessed by the Brief Assessment of Cognition in Schizophrenia (BACS). Results: We found a consistent association between CNR1 rs12720071 polymorphism and the cognitive performance of patients in several cognitive domains. Patients with C/C polymorphism presented significantly worse performance in motor speed, verbal fluency, attention/processing speed and reasoning/problem solving. Conclusion: Although limited, our data support the hypothesis that CNR1 variations may be associated with the pathogenesis of cognitive deficits of schizophrenia.

2.
Braz J Psychiatry ; 44(1): 26-34, 2022.
Article in English | MEDLINE | ID: mdl-34190825

ABSTRACT

OBJECTIVE: To test the hypothesis that genetic variations of cannabinoid receptors contribute to the pathophysiology of cognitive deficits in schizophrenia. METHODS: In this genetic association case-control study, cannabinoid receptor polymorphisms CNR1 rs12720071 and CNR2 rs2229579 were tested for association with neurocognitive performance in 69 patients with schizophrenia and 45 healthy controls. Neurocognition was assessed by the Brief Assessment of Cognition in Schizophrenia (BACS). RESULTS: We found a consistent association between CNR1 rs12720071 polymorphism and the cognitive performance of patients in several cognitive domains. Patients with C/C polymorphism presented significantly worse performance in motor speed, verbal fluency, attention/processing speed and reasoning/problem solving. CONCLUSION: Although limited, our data support the hypothesis that CNR1 variations may be associated with the pathogenesis of cognitive deficits of schizophrenia.


Subject(s)
Receptor, Cannabinoid, CB1/genetics , Receptor, Cannabinoid, CB2/genetics , Schizophrenia , Case-Control Studies , Cognition , Humans , Neuropsychological Tests , Polymorphism, Genetic , Schizophrenia/genetics
3.
Nord J Psychiatry ; 74(3): 187-193, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31738648

ABSTRACT

Aims: Recent findings suggest that cognitive impairment can be associated with inflammation and immune changes in schizophrenia. We aimed to study possible associations between cytokine levels and cognitive performance in a sample of patients with schizophrenia.Methods: Cognition was assessed with the brief assessment of cognition in schizophrenia in 63 clinically stable outpatients with schizophrenia. Blood was collected and cytokines (IL-2, IL-4, IL-6, IL-10, IL-17A, TNF-α, IFN-γ) were measured by cytometric bead array method. Psychopathological scales were also applied.Results: IL-6 correlated negatively with general cognitive performance (rho = -0.395, p = .017) and positively with antipsychotic dose (rho = 0.412, p = .004). Multiple regression analysis showed that cognitive performance is associated with age and antipsychotic dose (p = .000 and p = .033).Conclusion: The association between IL-6 levels and cognitive performance is dependent on age and antipsychotic dose.


Subject(s)
Antipsychotic Agents/therapeutic use , Cognition/drug effects , Interleukin-6/blood , Mental Status and Dementia Tests , Schizophrenia/blood , Schizophrenia/drug therapy , Adult , Age Factors , Antipsychotic Agents/pharmacology , Biomarkers/blood , Cognition/physiology , Cross-Sectional Studies , Cytokines/blood , Female , Humans , Male , Middle Aged , Schizophrenic Psychology , Treatment Outcome , Tumor Necrosis Factor-alpha/blood
4.
J Psychiatr Res ; 87: 44-52, 2017 04.
Article in English | MEDLINE | ID: mdl-28011441

ABSTRACT

OBJECTIVES: to evaluate cannabinoid receptors (CBRs) expression on peripheral immune cells, i.e., blood monocytes, neutrophils, lymphocytes, and NK cells, and their relationship to a wide range of serum cytokine levels in subjects with schizophrenia and controls. METHODS: A sample of 55 people with chronic schizophrenia and 48 controls were enrolled in the study. The expression of the cannabinoid receptors CB1R and CB2R was evaluated in peripheral blood leukocytes by flow cytometry. Serum levels of cytokines/chemokines were simultaneously analyzed by cytometric bead array. RESULTS: We found higher expression of cannabinoid receptors on cells of the innate immune system in subjects with schizophrenia when compared with controls. Serum levels of interleukin-4 (IL-4), IL-6, IL-10, IL-17, interferon (IFN-γ), and (C-X-C motif) ligand 10/interferon gamma-induced protein 10 (CXCL10/IP10) were decreased, while levels of the chemokine (C-C motif) ligand 2/monocyte chemoattractant protein-1 (CCL2/MCP-1) were increased in the schizophrenia group in comparison with controls. Patients with schizophrenia showed simpler correlation network between cytokines and CBRs expression than controls. CONCLUSION: Patients with schizophrenia showed increased CBRs expression in cells of the innate immune system and simpler correlation network between cytokines and CBRs expression when compared with controls. These results suggest a defective endocannabinoid system-mediated immunomodulation in patients with schizophrenia.


Subject(s)
Leukocytes, Mononuclear/metabolism , Receptors, Cannabinoid/metabolism , Schizophrenia/blood , Adult , Cytokines/blood , Female , Flow Cytometry , Humans , Killer Cells, Natural/metabolism , Lymphocytes/metabolism , Male , Middle Aged , Monocytes/metabolism , Neutrophils/metabolism , Psychiatric Status Rating Scales , Schizophrenia/pathology
5.
Trends Psychiatry Psychother ; 38(2): 96-9, 2016.
Article in English | MEDLINE | ID: mdl-27409135

ABSTRACT

OBJECTIVES: To investigate the determinants of family burden in a sample of patients with schizophrenia and their caregivers. METHODS: Thirty-one stable patients with schizophrenia and their main caregivers were recruited. Sociodemographic variables were assessed in a semi-structured interview, and positive and negative symptoms were assessed with the Positive and Negative Syndrome Scale (PANSS). Cognitive performance was assessed with the Schizophrenia Cognition Rating Scale (SCoRS). Levels of burden on caregivers were assessed with the Family Burden Interview Schedule (FBIS). Interactions among variables were analyzed using Pearson correlations and linear regression analysis. RESULTS: Objective and subjective FBIS scores were 1.9 (standard deviation [SD] = 0.5) and 2.4 (SD = 0.6) respectively. Objective burden correlated positively with positive and negative symptoms, and cognitive impairment. Subjective burden correlated positively with positive symptoms and negatively with mean age of disease onset. Positive, negative and cognitive symptoms accounted for 47.6% of the variance of objective burden, with negative symptoms accounting independently for 30.3%. Age of onset, parents as caregivers and positive symptoms accounted for 28% of the variance of subjective burden, with age of onset independently explaining 20.3%. CONCLUSION: Patients' clinical and sociodemographic variables are important determinants of family burden in schizophrenia. Objective burden is predicted by symptoms, particularly negative ones. Subjective burden is predicted by symptoms and sociodemographic variables, particularly age of disease onset.


Subject(s)
Caregivers/psychology , Cost of Illness , Schizophrenia/therapy , Adult , Age of Onset , Cognition , Female , Humans , Interview, Psychological , Linear Models , Male , Psychiatric Status Rating Scales , Schizophrenia/diagnosis , Schizophrenic Psychology , Socioeconomic Factors
7.
Schizophr Res ; 156(2-3): 254-60, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24853061

ABSTRACT

Schizophrenia is a chronic psychiatric syndrome characterized by generalized cognitive deficits that are associated with functional impairment. The endocannabinoid system (ECS) modulates neurotransmission and neuronal plasticity and is important for cognitive functioning. Evidence points to the involvement of this neuromodulatory system in the pathophysiology of schizophrenia and that alteration of the ECS on peripheral lymphocytes could reflect central changes. The objective of this study was to compare levels of peripheral endocannabinoid receptor expression in patients with schizophrenia and healthy subjects and find evidence of association between peripheral expression of those receptors and cognitive performance. Patients with stabilized schizophrenia (N=53) and controls (N=22) underwent clinical and cognitive evaluation, and assessment of cannabinoid receptor expression on the surface of peripheral immune cells (lymphocytes, natural killer cells and monocytes) by flow cytometry. Patients with schizophrenia had lower levels of cannabinoid receptor expression on total T lymphocytes, but after controlling for possible confounders this difference did not remain significant. In patients, increased cannabinoid receptor expression on lymphocytes and monocytes was significantly correlated with worst cognitive performance. These data provide additional evidence of the involvement of the ECS in the pathophysiology of cognitive deficits in schizophrenia.


Subject(s)
Cognition/physiology , Leukocytes, Mononuclear/metabolism , Receptor, Cannabinoid, CB1/metabolism , Receptor, Cannabinoid, CB2/metabolism , Schizophrenia/blood , Schizophrenic Psychology , Adult , Antipsychotic Agents/therapeutic use , Female , Flow Cytometry , Humans , Killer Cells, Natural/metabolism , Lymphocytes/metabolism , Male , Monocytes/metabolism , Neuropsychological Tests , Schizophrenia/drug therapy , T-Lymphocytes/metabolism
8.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 34(supl.2): s163-s177, Oct. 2012. ilus, tab
Article in English | LILACS | ID: lil-662766

ABSTRACT

OBJECTIVE: Schizophrenia is a psychiatric disorder whose mechanisms have remained only partially elucidated. The current proposals regarding its biological basis, such as the dopaminergic hypothesis, do not fully explain the diversity of its symptoms, indicating that other processes may be involved. This paper aims to review evidence supporting the involvement of the endocannabinoid system (ECS), a neurotransmitter group that is the target of Cannabis sativa compounds, in this disorder. METHODS: A systematic review of original papers, published in English, indexed in PubMed up to April, 2012. RESULTS: Most studies employed genetics and histological, neuroimaging or neurochemical methods - either in vivo or post-mortem - to investigate whether components of the ECS are compromised in patients. Overall, the data show changes in cannabinoid receptors in certain brain regions as well as altered levels in endocannabinoid levels in cerebrospinal fluid and/or blood. CONCLUSIONS: Although a dysfunction of the ECS has been described, results are not entirely consistent across studies. Further data are warrant to better define a role of this system in schizophrenia.


OBJETIVO: A esquizofrenia é um transtorno psiquiátrico cujos mecanismos permanecem apenas parcialmente elucidados. As atuais propostas relativas à base biológica, tais como a hipótese dopaminérgica, não explicam por completo a diversidade de seus sintomas, o que indica que outros processos podem estar envolvidos. Este artigo tem como objetivo revisar indícios que sustentem o envolvimento do sistema endocanabinoide (SECB), um grupo de neurotransmissoresalvo dos compostos da Cannabis sativa, nesse transtorno. MÉTODOS: Revisão sistemática dos artigos originais, publicados em inglês e indexados no PubMed até abril de 2012. RESULTADOS: A maioria dos estudos empregou métodos neuroquímicos ou de neuroimagem genéticos e histológicos - tanto in vivo quanto post-mortem - para investigar se os componentes do SECB estão comprometidos nos pacientes. De modo geral, os dados mostram mudanças nos receptores canabinoides em determinadas regiões cerebrais, bem como a alteração dos níveis de endocanabinoides no líquido cefalorraquidiano e/ou no sangue. CONCLUSÕES: Ainda que a disfunção do SECB tenha sido descrita, os resultados dos estudos não são totalmente consistentes. São necessários mais dados para definir melhor o papel desse sistema na esquizofrenia.


Subject(s)
Humans , Endocannabinoids/physiology , Receptor, Cannabinoid, CB1/physiology , Schizophrenia/physiopathology , Antipsychotic Agents/therapeutic use , Endocannabinoids/analysis , Endocannabinoids/genetics , Polymorphism, Genetic , Receptor, Cannabinoid, CB1/analysis , Receptor, Cannabinoid, CB1/genetics , Schizophrenia/drug therapy , Schizophrenia/genetics
9.
Braz J Psychiatry ; 34 Suppl 2: S163-77, 2012 Oct.
Article in English, Portuguese | MEDLINE | ID: mdl-23429846

ABSTRACT

OBJECTIVE: Schizophrenia is a psychiatric disorder whose mechanisms have remained only partially elucidated. The current proposals regarding its biological basis, such as the dopaminergic hypothesis, do not fully explain the diversity of its symptoms, indicating that other processes may be involved. This paper aims to review evidence supporting the involvement of the endocannabinoid system (ECS), a neurotransmitter group that is the target of Cannabis sativa compounds, in this disorder. METHODS: A systematic review of original papers, published in English, indexed in PubMed up to April, 2012. RESULTS: Most studies employed genetics and histological, neuroimaging or neurochemical methods - either in vivo or post-mortem - to investigate whether components of the ECS are compromised in patients. Overall, the data show changes in cannabinoid receptors in certain brain regions as well as altered levels in endocannabinoid levels in cerebrospinal fluid and/or blood. CONCLUSIONS: Although a dysfunction of the ECS has been described, results are not entirely consistent across studies. Further data are warrant to better define a role of this system in schizophrenia.


Subject(s)
Endocannabinoids/physiology , Receptor, Cannabinoid, CB1/physiology , Schizophrenia/physiopathology , Antipsychotic Agents/therapeutic use , Endocannabinoids/analysis , Endocannabinoids/genetics , Humans , Polymorphism, Genetic , Receptor, Cannabinoid, CB1/analysis , Receptor, Cannabinoid, CB1/genetics , Schizophrenia/drug therapy , Schizophrenia/genetics
SELECTION OF CITATIONS
SEARCH DETAIL
...