It has been proposed that immune abnormalities may be implicated with pathophysiology of schizophrenia. The nod-like receptor pyrin domain-contraining protein 3 (NLRP3) can trigger immune-inflammatory cascade reactions. In this study, we intended to identify the role of gene encoding NLRP3 () in susceptibility to schizophrenia and its clinical features. For the mRNA expression analysis, 53 drug-naïve patients with first-episode schizophrenia and 56 healthy controls were enrolled. For the genetic study, a total of 823 schizophrenia patients and 859 controls were recruited. Among them, 239 drug-naïve patients with first-episode schizophrenia were enrolled for clinical evaluation. There is no significant difference in mRNA levels between patients with schizophrenia and healthy controls ( = 0.07). We did not observe any significant differences in allele and genotype frequencies of rs10754558 polymorphism between the schizophrenia and control groups. We noticed significant differences in the scores of RBANS attention and total scores between the patients with different genotypes of rs10754558 polymorphism ( = 0.001 and < 0.01, respectively). Further eQTL analysis presented a significant association between the rs10754558 polymorphism and in frontal cortex ( = 0.0028, = 0.028 after Bonferroni correction). Although our findings did not support confer susceptibility to schizophrenia, may be a risk factor for cognitive impairment, especially attention deficit in this disorder.
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http://dx.doi.org/10.3389/fgene.2021.781625 | DOI Listing |
Behav Brain Res
December 2024
Center of Health Sciences, Catholic University of Pelotas, Pelotas, Rio Grande do Sul, Brazil. Electronic address:
Clin Rheumatol
January 2025
Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, 62 Qarib St., Keshavarz Blvd., Tehran, 14194, Iran.
Background: Although juvenile idiopathic arthritis (JIA) is one of the most common pediatric rheumatologic diseases, the exact etiology of JIA remains unclear. Genetic factors, including variations in the NLRP3 gene, have been implicated in the pathogenesis of autoimmune diseases. Therefore, we aimed to investigate the association between NLRP3 polymorphisms and JIA.
View Article and Find Full Text PDFBMC Cardiovasc Disord
November 2024
School of Public Health, Bengbu Medical University, Bengbu, Anhui, 233030, China.
Hum Immunol
November 2024
Departamento de Genética, Universidade Federal de Pernambuco, Recife, PE, Brazil.
Turner syndrome (TS) is associated with an increased susceptibility to inflammatory and autoimmune diseases. This study investigates the association between genetic polymorphisms in the IL1B and NLRP3 genes, as well as the expression profiles of IL1B, NLRP3, and NLRP1, and the risk of inflammatory and autoimmune conditions in TS patients compared to healthy controls. The genetic association analysis included 92 TS patients (case) and 146 healthy controls (HC), evaluating IL1B rs16944, NLRP3 rs10754558 and rs4925659 using TaqMan genotyping assays.
View Article and Find Full Text PDFMol Biol Rep
October 2024
Department of Zoology, Government College University, Lahore, 54000, Pakistan.
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