2021
DOI: 10.2217/pgs-2020-0171
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Negative Symptoms in Schizophrenia: Correlation with Clinical and Genetic Factors

Abstract: Aim: Explore the possible association between clinical factors and genetic variants of the dopamine pathways and negative symptoms. Materials & methods: Negative symptoms were assessed in 206 patients with schizophrenia using the Arabic version of the self-evaluation of negative symptoms scale and the Positive and Negative Syndrome Scale. Genotyping for COMT, DRD2, MTHFR and OPRM1 genes was performed. Results: Multivariable analysis showed that higher self-evaluation of negative symptoms scale scores were … Show more

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Cited by 4 publications
(5 citation statements)
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“…However, the DDD for typical and atypical anti-psychotics had not shown any statistically significant correlation with either SNS total or subdomain scores. These findings are somehow inconsistent with results obtained in a previous Lebanese study, 32 where the total SNS score was significantly correlated with the total daily dose of chlorpromazine-equivalent and a higher daily dose of chlorpromazine-equivalent for typical anti-psychotics, while it was negatively related to a higher chlorpromazine-equivalent daily dose for atypical anti-psychotics. This contradiction could perhaps be explained by the difference in the mean of the total equivalent dose of chlorpromazine among patients in Hajj, et al 30 (1150.91 ± 973.70 mg), which is mainly composed of typical anti-psychotics (1010.57 ± 973.63 mg), more than the newer atypical group (163.57 ± 305.97 mg).…”
Section: Discussioncontrasting
confidence: 99%
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“…However, the DDD for typical and atypical anti-psychotics had not shown any statistically significant correlation with either SNS total or subdomain scores. These findings are somehow inconsistent with results obtained in a previous Lebanese study, 32 where the total SNS score was significantly correlated with the total daily dose of chlorpromazine-equivalent and a higher daily dose of chlorpromazine-equivalent for typical anti-psychotics, while it was negatively related to a higher chlorpromazine-equivalent daily dose for atypical anti-psychotics. This contradiction could perhaps be explained by the difference in the mean of the total equivalent dose of chlorpromazine among patients in Hajj, et al 30 (1150.91 ± 973.70 mg), which is mainly composed of typical anti-psychotics (1010.57 ± 973.63 mg), more than the newer atypical group (163.57 ± 305.97 mg).…”
Section: Discussioncontrasting
confidence: 99%
“…Consistent with our findings, no serious correlation was found between either gender or age with medication adherence in Alsalem's study. 25 Nevertheless, there are inconsistencies between the current study findings and those of Hajj et al 32 with regard to the analyses of negative symptoms, as older age patients and female gender were considerably connected with higher scores of SNS (p<0.001).…”
Section: Discussioncontrasting
confidence: 99%
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“…In our study, patients with predominantly negative symptoms exhibited cognitive impairment, particularly in the domains of processing speed and attention, which may be related to the neural mechanisms associated with these symptoms. The negative symptoms of psychosis are thought to arise from disruptions in genetic variants of the dopamine pathway 22 and hypodopaminergic activity in the mesocortical pathway and prefrontal cortex, 23 which are responsible for cognitive and emotional processing. The dysfunction of these pathways may lead to slower information processing and lower attention, resulting in deficits in cognitive performance.…”
Section: Discussionmentioning
confidence: 99%
“…A recent pharmacogenomic study on treatment response to risperidone used an SNP microarray-based GWAS and whole-exome sequencing-based GWAS to identify genetic variants underlying antipsychotic responses which may ultimately facilitate precision medicine in schizophrenia (Zhao et al , 2022). Furthermore, research on the genetic underpinnings of positive and negative symptom score domains and cognitive deficit in schizophrenia has discovered shared and distinct gene associations for the symptom domains and cognitive deficit (Xavier and Vorderstrasse, 2017; Hajj et al , 2021; Wu et al , 2021). In addition, polygenetic risk scores were employed to evaluate the relationship between schizophrenia genetic liability and phenotypic features (Mallet et al , 2020; Richards et al , 2020; Legge et al , 2021).…”
Section: Discussionmentioning
confidence: 99%