scholarly journals Treatment and Prevention of Osteoarthritis through Exercise and Sports

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Victor Valderrabano ◽  
Christina Steiger

Osteoarthritis (OA) is a degenerative joint disease with a high prevalence among older people. To date, the pathogenesis of the disease and the link between muscle function and OA is not entirely understood. As there is no known cure for OA, current research focuses on prevention and symptomatic treatment of the disorder. Recent research has indicated that muscle weakness precedes the onset of OA symptoms. Furthermore, several studies show a beneficial effect of land-based aerobic and strengthening exercises on pain relief and joint function. Therefore, current research focuses on the possibility to employ exercise and sports in the prevention and treatment of OA.

2015 ◽  
Vol 4 ◽  
pp. 300-306
Author(s):  
Andrzej Kotela ◽  
Sylwia Sarzyńska ◽  
Maria Woźniak ◽  
Paweł Łęgosz ◽  
Małgorzata Starczyńska ◽  
...  

2019 ◽  
pp. 76-83
Author(s):  
O. A. Shavlovskaya

Osteoarthritis (OA) is a degenerative joint disease. Modern theories consider various structural (cartilage destruction) and biophysical disorders (matrix loss of glycosaminoglycans) as the basis of acute and chronic pain syndrome. The main aim of OA therapy is pain relief and functional improvement. To manage pain syndrome in OA it is reasonable to use complex bioregulatory drugs (CBD) (Traumeel S, Zeel T, Discus compositum) both in monotherapy and in combined treatment. The effectiveness of CBD is comparable to that of NSAIDs and CS.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 919-919
Author(s):  
Saaib Al Shehadat ◽  
Gregory R. Bociek ◽  
William Haire

Abstract Background: Studies suggest that thrombosis may play an important etiologic role in adults with idiopathic osteonecrosis. Thrombotic occlusion in the bone leads to increased intraosseus venous pressure, reduced arterial flow, and ultimately hypoxic bone death. Total joint arthroplasty is the standard treatment for advanced osteonecrosis. The majority of untreated patients with idiopathic osteonecrosis will progress to significant degenerative disease. We report our experience in five consecutive patients who were referred to our institute and were treated with anticoagulant therapy instead of surgical intervention. Methods: Five adult patients (median age 38 years old, range 28–49 years) were evaluated first by an orthopedic surgeon for knee or hip pain. The diagnosis of osteonecrosis was confirmed by Magnetic Resonance Image (MRI) interpreted in all cases by both a radiologist and an orthopedic surgeon. Osteonecrosis was designated as idiopathic after eliminating other known associated factors, mainly drugs (glucocorticoids) or diseases (alcoholism, sickle cell disease). The response to treatment was measured by pain relief, bone imaging stability or improvement, and subsequent need for surgical intervention. Treatment was discontinued if the patient developed severe toxicity or disease progression requiring surgical intervention. Four patients were treated with warfarin with a target international normalized ratio (INR) of 2–3, while one patient was treated with enoxaparin (1 mg/kg twice a day). Patients were followed up every three months by both a hematologist and an orthopedic surgeon, and MRI evaluation was performed at three month intervals for one year or when symptoms worsened. After achieving pain relief and stability of lesions on MRI, patients were given the choice of discontinuing the treatment. Results: Three out of four patients on warfarin and the patient on enoxaparin had pain improvement within three months of initiating therapy. All patients reported a reduction of pain at a median of 7.5 months (6–9 months). MRI revealed disease stability in those patients within three months, and some radiographic signs of improvement at 9 months. Complete resolution of imaging abnormalities was seen in 5 years in one patient. Patients tolerated the therapy well without any major toxicity and decided to continue the anticoagulation therapy. One patient preferred to discontinue therapy after 4.5 years, and continued to be asymptomatic 10 months later. The fifth patient had bilateral distal femoral and proximal tibial osteonecrosis. The patient had severe degenerative joint disease involving the right knee from previous motor vehicle accident. The patient eventually underwent right knee arthroplasty for severe pain, and the microscopic examination of the bone and debridement tissue from the joint replacement procedure showed focal avascular necrosis and features of degenerative joint disease. The patient resumed the warfarin therapy postoperatively with stability of imaging abnormalities on the left side after 3.5 years of continuous therapy. Warfarin was replaced by aspirin with eighteen months of follow up, the patient continued to be asymptomatic with stable imaging abnormalities of the left leg. Conclusion: The findings suggest that anticoagulation therapy may benefit patients with early stage of idiopathic osteonecrosis, and may delay or eliminate the need for surgical intervention. Further studies are warranted in he future to compare different anticoagulants with placebo.


Author(s):  
Kelly J. Shields ◽  
John R. Owen ◽  
Jennifer S. Wayne

Degenerative joint disease, age, and trauma lead to progressive articular cartilage damage due to the tissue’s limited repair capabilities. Numerous clinical repair techniques with varying degrees of success have been developed in order to repair damaged tissue and restore joint function. One approach is the development of articular cartilage repair tissue to implant into the damaged or diseased articular surface. Determining the viability of an articular repair technique or tissue under in vivo stresses and wear is crucial to predict its success.


2014 ◽  
Vol 28 (2) ◽  
pp. 346-350 ◽  
Author(s):  
M.E. Gruen ◽  
E. Griffith ◽  
A. Thomson ◽  
W. Simpson ◽  
B.D.X. Lascelles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Marie-Lisa Hülser ◽  
Yubin Luo ◽  
Klaus Frommer ◽  
Rebecca Hasseli ◽  
Kernt Köhler ◽  
...  

AbstractOsteoarthritis (OA) is a degenerative joint disease characterized by cartilage loss and reduced joint function. OA risk factors are age and obesity. Many adipokines are altered by obesity but also OA although systemic adipokine regulation in OA is not always clear. Therefore, metabolic effects of diet-induced obesity on OA development as well as the influence of obesity and OA progression on systemic vs. local adipokine expression in joints were compared. C57Bl/6-mice fed with HFD (high fat diet) or normal diet prior to destabilization of the medial meniscus (DMM) were sacrificed 4/6/8 weeks after surgery. Sera were evaluated for adiponectin, leptin, visfatin, cytokines. Liver grading and staging for non-alcoholic steatohepatitis (NASH) was performed and crown-like structures (CLS) in adipose tissue measured. OA progression was scored histologically. Adipokine-expressing cells and types were evaluated by immunohistochemistry. Time-dependent changes in DMM-progression were reflected by increased systemic adiponectin levels in DMM especially combined with HFD. While HFD increased serum leptin, DMM reduced systemic leptin significantly. OA scores correlated with bodyweight, leptin and hepatic scoring. Locally, increased numbers of adiponectin- and leptin-producing fibroblasts were observed in damaged menisci but visfatin was not changed. Local adipokine expression was independent from systemic levels, suggesting different mechanisms of action.


Author(s):  
Teng Yao ◽  
Yute Yang ◽  
Ziang Xie ◽  
Yining Xu ◽  
Yizhen Huang ◽  
...  

Osteoarthritis (OA) is a degenerative joint disease. Currently, apart from symptomatic treatment or joint replacement, no other effective treatments for OA exist. The mechanisms underlying OA remain elusive and require further research. Circular RNAs (circRNAs) are known to be involved in many diseases; however, their function in OA is not yet fully understood. Here, we identified a novel circRNA, Circ0083429. The role of Circ0083429 in OA was confirmed via western blot (WB), quantitative real-time PCR (qRT-PCR), and immunofluorescence (IF) through knockdown and overexpression experiments. The binding of Circ0083429 to downstream miR-346 and its target gene SMAD3 was predicted via bioinformatics analysis and verified using a luciferase reporter assay and RNA pulldown experiments. Finally, the function of Circ0083429 was evaluated in mouse OA models. In our study, we found that Circ0083429 regulates the homeostasis of the extracellular matrix (ECM) in human chondrocytes. Mechanistically, Circ0083429 affects OA by regulating the mRNA level of SMAD3 through the sponging of microRNA (miRNA)-346. Injecting adeno-associated virus Circ0083429 into the intra-junction of the mouse knee alleviated OA. In conclusion, Circ0083429 regulates the ECM via the regulation of the downstream miRNA-346/SMAD3 in human chondrocytes, which provides a new therapeutic strategy for OA.


2020 ◽  
Vol 22 (11) ◽  
pp. 1069-1083
Author(s):  
Nathalie Dowgray ◽  
Eithne Comerford

Practical relevance: An understanding of the process of musculoskeletal ageing – which all senior and geriatric cats will experience – is vital to maintaining the health and welfare of our ageing cat population. Clinical challenges: Assessment of the feline musculoskeletal system is not always straightforward. Diagnosis of impairment relies on input from owners and veterinarians in terms of visual observation, and clinical and orthopaedic examination, in addition to diagnostic imaging Audience: This review is written for the primary care veterinary team. Aims: The goals are to raise awareness and improve clinical diagnosis of musculoskeletal impairment as a result of ageing. The article also reviews therapeutic options and considers the evidence available for the prevention/deceleration of musculoskeletal ageing and impairment. Evidence base: There is good evidence of a high prevalence of osteoarthritis (OA) and degenerative joint disease (DJD) in older cats. There is also good evidence to indicate that functional impairment and chronic pain are sequelae of musculoskeletal disease. However, there is a paucity of information for what is best practice for the management and treatment of musculoskeletal impairment in a clinical situation. There is also a lack of evidence on how prevention of central stimulation of the nervous system caused by musculoskeletal impairment and, in turn the development of chronic pain, can be avoided.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Shan Huang ◽  
Kristina A. Thomsson ◽  
Chunsheng Jin ◽  
Sally Alweddi ◽  
André Struglics ◽  
...  

AbstractLubricin (PRG4) is a mucin type protein that plays an important role in maintaining normal joint function by providing lubrication and chondroprotection. Improper lubricin modification and degradation has been observed in idiopathic osteoarthritis (OA), while the detailed mechanism still remains unknown. We hypothesized that the protease cathepsin G (CG) may participate in degrading lubricin in synovial fluid (SF). The presence of endogenous CG in SF was confirmed in 16 patients with knee OA. Recombinant human lubricin (rhPRG4) and native lubricin purified from the SF of patients were incubated with exogenous CG and lubricin degradation was monitored using western blot, staining by Coomassie or Periodic Acid-Schiff base in gels, and with proteomics. Full length lubricin (∼300 kDa), was efficiently digested with CG generating a 25-kDa protein fragment, originating from the densely glycosylated mucin domain (∼250 kDa). The 25-kDa fragment was present in the SF from OA patients, and the amount was increased after incubation with CG. A CG digest of rhPRG4 revealed 135 peptides and 72 glycopeptides, and confirmed that the protease could cleave in all domains of lubricin, including the mucin domain. Our results suggest that synovial CG may take part in the degradation of lubricin, which could affect the pathological decrease of the lubrication in degenerative joint disease.


2021 ◽  
Vol 14 (4) ◽  
Author(s):  
Juracy Barbosa Santos ◽  
Lanussy Rassi Mangili ◽  
Mylene Rassi Mangili ◽  
Isabela Rassi Mangili ◽  
Durval Ribas Filho

Osteoarthritis (OA) is the most prevalent joint disease, considered the rheumatic condition with the greatest consequences in terms of socioeconomic impacts, especially knee osteoarthritis since it makes walking difficult. To date, there is no cure for OA, so available treatments aim to reduce symptoms such as pain and inflammation, maintain joint mobility, and limit the loss of function. As OA has a known inflammatory component, it is believed that nutrition can play a vital role in the prevention and ongoing management of OA. This article aims to analyze the available evidence in the prevention and treatment of knee OA with a dietary intervention that may play a potential role in the management of the disease. To carry out this literature review, articles were searched in the Scielo, Pubmed, and Bireme databases with the time frame of the last 10 years. The results showed that some nutrients, vitamins, and antioxidants are widely discussed in the literature in the treatment and prevention of the disease. Management of free radicals is necessary and the influence of nutrients and diet on cartilage and OA metabolism may represent a long-term adjuvant alternative in the treatment of patients with knee OA. Effects of dietary modifications on lipid and cholesterol profiles, adequate vitamin levels, and weight reduction in obese patients may influence the course of the disease.


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