Publications by authors named "Jingbiao Huang"

Article Synopsis
  • This study explored the effectiveness of medical chitosan injections for treating knee osteoarthritis (KOA) and examined lipid metabolism in synovial tissue.
  • Sixty KOA patients were divided into two groups: one receiving chitosan injections (CSI group) and one without (OA group), with various functional scoring assessments conducted to gauge outcomes.
  • Results indicated that the CSI group had a longer time before needing knee surgery compared to the OA group, and there were notable differences in lipid profiles, especially lower levels of triacylglycerides in the CSI group.
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This study aims to analyse the pathological features of skeletal muscle injury repair by using rats to model responses to different exercise intensities. Eighty-four rats were randomly divided into five groups for treadmill exercise. The short-term control, low-intensity, medium-intensity and high-intensity groups underwent gastrocnemius muscle sampling after 6, 8 and 12 weeks of exercise.

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Purpose: The purpose of this study was to predict the probability of postoperative pulmonary infection in elderly patients with hip fractures by developing and validating a precise model.

Methods: The clinical data of 1008 elderly hip fracture patients undergoing surgical treatment in Shanghai Tenth Peoples' Hospital were retrospectively selected. A univariate analysis and multivariate regression were used to analyze the independent risk factors for postoperative pulmonary infection in elderly patients with hip fractures.

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Background: Tendinopathy is the leading sports-related injury and will cause severe weakness and tenderness. Effective therapy for tendinopathy remains limited, and extracellular vesicles (EVs) derived from adipose tissue-derived mesenchymal stem cells (ADMSCs) have demonstrated great potential in tendinopathy treatment; however, the influence of aging status on EV treatment has not been previously described.

Results: In this study, it was found that ADMSCs derived from old mice (ADMSC) demonstrated remarkable cellular senescence and impaired NAD+ metabolism compared with ADMSCs derived from young mice (ADMSC).

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