Observation and Analysis of the Postoperative Analgesic Effect of Subanaesthetic Dose of Ketamine in Kashin-BeckDisease Patients after Total Knee Arthroplasty. With the transformation of modern medical models, the medical needs of patients have changed from treatment to safe, comfortable, and painless treatment. Therefore, it is clinically important to find an ideal analgesia model to reduce
Polymorphism of MMP-3 gene and imbalance expression of MMP-3 / TIMP-1 in articular cartilage are associated with an endemic osteochondropathy, Kashin- Beckdisease. The etiology of Kashin-Beckdisease (KBD), an endemic osteochondropathy, is largely unknown. Matrix metalloproteinase-3 (MMP-3) plays a central role in the initiation and progression of cartilage destruction, however, no study has
Association of oxidative stress and Kashin-Beckdisease integrated Meta and Bioinformatics analysis. To explore the association between oxidative stress (OS) and Kashin-Beckdisease (KBD). Terms associated with "KBD" and "OS" were searched in the six different databases up to October 2021. Stata 14.0 was used to pool the means and standard deviations using random-effect or fixed-effect model
Magnetic resonance imaging at 7.0 T for evaluation of early lesions of epiphyseal plate and epiphyseal end in a rat model of Kashin-Beckdisease. Kashin-Beckdisease (KBD) is a disabling osteoarticular disease involving growth and joint cartilage. Early diagnosis can effectively prevent the progress of the disease. However, the early diagnosis of it is still very difficult. Our aim was to study
Comparison of the responsiveness of the WOMAC and the 12-item WHODAS 2.0 in patients with Kashin-Beckdisease. Several questionnaires have been used to assess the health status of patients with Kashin-Beckdisease (KBD) in clinical trials, but the evidence regarding the responsiveness of these instruments in KBD patients is limited. Therefore, the aim of this study was to evaluate and compare
Pathway-based network analyses and candidate genes associated with Kashin-Beckdisease. To perform a comprehensive analysis focusing on the biological functions and interactions of Kashin-Beckdisease (KBD)-related genes to provide information towards understanding the pathogenesis of KBD.A retrospective, integrated bioinformatics analysis was designed and conducted. First, by reviewing
Conservative tibiotalocalcaneal fusion for partial talar avascular necrosis in conjunction with ankle and subtalar joint osteoarthritis in Kashin-Beckdisease: A case report. Kashin-Beckdisease (KBD) is known for some typical characters like finger joint enlargement, shortened fingers, and dwarfism. However, Avascular necrosis (AVN) of the talus in KBD has rarely been reported in the literature
Endemic Kashin-Beckdisease: A food-sourced osteoarthropathy. Kashin-Beckdisease (KBD) is an endemic osteoarthropathy, which causes disability and heavy socioeconomic burdens. The preventive measures have been taken in the past few decades. However, recent KBD-epidemiological trend and comprehensive effect of its preventive measures need to be evaluated. By employing typical survey, cross
The study on polymorphisms of Sep15 and TrxR2 and the expression of AP-1 signaling pathway in Kashin-Beckdisease. The aim of the study was to investigate the association between rs5859 in Sep15, rs1139793 in TrxR2 polymorphisms with the risks of KBD and to detect the expression of AP-1 pathway in KBD subjects and in vitro. 208 KBD and 206 control subjects were included. PCR-Restriction Fragment
The study of GPX3 methylation in patients with Kashin-BeckDisease and its mechanism in chondrocyte apoptosis. Selenium deficiency is a risk factor for Kashin-BeckDisease (KBD), an endemic osteoarthropathy. Although promoter hypermethylation of glutathione peroxidase 3 (GPX3) (a selenoprotein) has been identified in several cancers, little is known about promoter methylation and expression
Comparative Analysis of Gene Expression Profiles of Human Dental Fluorosis and Kashin-BeckDisease To explore the pathologies of Kashin-Beckdisease (KBD) and KBD accompanied with dental fluorosis (DF), we conducted a comparative analysis of gene expression profiles. 12 subjects were recruited, including 4 KBD patients, 4 patients with KBD and DF and 4 healthy subjects. Genome-wide expression
Serum levels of PIICP, PIIANP, and PIIBNP are decreased in patients with an endemic osteochondropathy, Kashin-BeckdiseaseKashin-Beckdisease (KBD) is an endemic, chronic, degenerative osteoarthropathy. KBD is usually diagnosed by using X-ray image and clinical symptoms, lacking of serological biomarkers. The serum level of PIICP, PIIANP, and PIIBNP can specifically reflect the damage
Integrating genome-wide DNA methylation and mRNA expression profiles identified different molecular features between Kashin-Beckdisease and primary osteoarthritis Kashin-Beckdisease (KBD) is an endemic osteochondropathy of unknown etiology. Osteoarthritis (OA) is a form of degenerative joint disease sharing similar clinical manifestations and pathological changes to articular cartilage ). This study identified different molecular features between Kashin-Beckdisease and primary osteoarthritis and provided novel clues for clarifying the pathogenetic differences between KBD and OA.
Dietary exosome-miR-23b may be a novel therapeutic measure for preventing Kashin-Beckdisease Previous studies have identified a close association between diet and the prevalence of Kashin-Beckdisease (KBD); however, the mechanisms via which the diet protects against KBD-associated cartilage injury has remained elusive. Recent international research studies have revealed a therapeutic role
[The heat-reinforcing needling for Kashin-Beckdisease with cold-dampness blocking collaterals syndrome]. To compare the efficacy differences between heat-reinforcing needling and conventional treatment of western medicine on Kashin-Beckdisease (KBD) with cold-dampness blocking collaterals syndrome. Sixty KBD patients of cold-dampness blocking collaterals syndrome were randomly assigned
Long-term efficacy of repeated sodium hyaluronate injections in adult patients with Kashin-Beckdisease of the knee. To prospectively evaluate the long-term efficacy and safety of repeated sodium hyaluronate injections for the treatment of knee pain due to Kashin-Beckdisease (KBD). A total of 85 patients with KBD-based knee pain were treated with two cycles of a 5-week course of sodium
Altered expression of chondroitin sulfate structure modifying sulfotransferases in the articular cartilage from adult osteoarthritis and Kashin-Beckdisease. To investigate the expression of enzymes involved in chondroitin sulfate (CS) sulfation in the articular cartilage isolated from adult patients with osteoarthritis (OA) and Kashin-Beckdisease (KBD), using normal adults as controls
Association study of candidate genes for susceptibility to Kashin-Beckdisease in a Tibetan population. Many osteoarthritis (OA) susceptibility genes have been identified in recent years. Given the overlap in the phenotype of joint inflammation between OA and Kashin-Beckdisease (KBD), the aim of this study is to explore whether the reported OA susceptibility genes and two genes that may link
Genome-wide DNA methylation profiling of articular cartilage reveals significant epigenetic alterations in Kashin-Beckdisease and osteoarthritis. To determine genome-wide DNA methylation profiles of knee cartilage from patients with Kashin-Beckdisease (KBD) and osteoarthritis (OA). Knee cartilage was collected from 14 grade III KBD patients, 5 primary OA patients and 13 healthy subjects
Long noncoding RNA expression profile reveals lncRNAs signature associated with extracellular matrix degradation in kashin-beckdiseaseKashin-Beckdisease (KBD) is a deformative, endemic osteochondropathy involving degeneration and necrosis of growth plates and articular cartilage. The pathogenesis of KBD is related to gene expression and regulation mechanisms, but long noncoding RNAs (lncRNAs