Osteoarthritis (OA) is a complex joint disorder characterized by sclerosis of subchondral bone. The knee is one of the most commonly affected joints. Given that the genetic mechanisms underlying knee OA remain elusive, our study aims were to first confirm the association of the gene alleles with the risk of knee OA and, second, to evaluate the relationship between peripheral TGFA concentrations and knee OA in an independent Han Chinese population. We performed a case-control study consisting of 392 knee OA patients and 808 unrelated healthy controls. Single-marker-based association analyses and haplotype-based analyses using 3 single nucleotide polymorphisms (SNPs) were performed to confirm the association of gene alleles with the risk of knee OA. Furthermore, we used enzyme-linked immunosorbent assay (ELISA) kits to detect the peripheral blood TGFA concentrations in patients and healthy controls and then evaluated the relationships between the TGFA alleles and genotypes with serum TGFA levels. We replicated the genetic association of the rs2862851 T allele with the risk of knee OA ( = 1.68 × 10, = 1.41). Moreover, we observed that the peripheral TGFA concentrations were higher in knee OA patients than in healthy controls ( = 8.15 × 10). The peripheral TGFA concentrations were significantly different among the various rs2862851 genotypes for both cases ( = 4.16 × 10) and controls ( = 7.24 × 10). The individuals with the TT genotype in both cases and controls, had the highest peripheral TGFA concentrations. Moreover, with the increase in knee OA grade, peripheral TGFA concentration also increased ( = 1.36 × 10). Our study confirmed the association of the gene with the risk of knee OA and identified a positive correlation between peripheral TGFA levels and the severity of knee OA in the Han Chinese population, providing clues for understanding the etiology of knee OA.
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http://dx.doi.org/10.1089/gtmb.2020.0119 | DOI Listing |
Adv Clin Exp Med
February 2024
College of Stomatology, Guangxi Medical University, Nanning, China.
Eur J Med Res
September 2023
Department of Emergency, The First Medical Center, Chinese PLA General Hospital, 28th Fuxing Road, Beijing, China.
Background: High throughput gene expression profiling is a valuable tool in providing insight into the molecular mechanism of human diseases. Hypoxia- and lactate metabolism-related genes (HLMRGs) are fundamentally dysregulated in sepsis and have great predictive potential. Therefore, we attempted to build an HLMRG signature to predict the prognosis of patients with sepsis.
View Article and Find Full Text PDFJ Neuroinflammation
January 2023
Department of Neurology, University of California at Davis, MIND Institute Biosciences Building Room 2417, 2805 50th Street, Sacramento, CA, USA.
Background: This study identified early immune gene responses in peripheral blood associated with 90-day ischemic stroke (IS) outcomes.
Methods: Peripheral blood samples from the CLEAR trial IS patients at ≤ 3 h, 5 h, and 24 h after stroke were compared to vascular risk factor matched controls. Whole-transcriptome analyses identified genes and networks associated with 90-day IS outcome assessed using the modified Rankin Scale (mRS) and the NIH Stroke Scale (NIHSS).
Int J Mol Sci
August 2022
Laboratory of Medical Genetics, Faculty of Biology and Environmental Protection, University of Lodz, 90-236 Lodz, Poland.
The preclinical research conducted so far suggest that depression development may be influenced by the inflammatory pathways both at the periphery and within the central nervous system. Furthermore, inflammation is considered to be strongly connected with antidepressant treatment resistance. Thus, this study explores whether the chronic mild stress (CMS) procedure and agomelatine treatment induce changes in , , , and expression and methylation status in peripheral blood mononuclear cells (PBMCs) and in the brain structures of rats.
View Article and Find Full Text PDFMol Vis
December 2021
Department of Ophthalmology, Xinhua Hospital, Affiliated to Medicine School of Shanghai Jiaotong University, No. 1665, Kongjiang Road, Shanghai, China.
Purpose: To identify a novel mutation in with clinical and functional analysis among 516 familial patients with exudative vitreoretinopathy (FEVR).
Methods: Next-generation sequencing was performed on 516 patients with FEVR between January 2015 and October 2017. Clinical data were collected from patient charts, including sex, age at presentation, visual acuity if available, axial length, stage, and systemic clinical findings.
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