Osteoarthritis, Knee
Conditions
Keywords
hypertonic dextrose prolotherapy, osteoarthritis
Brief summary
Hypertonic dextrose prolotherapy has been used in knee osteoarthritis (OA) clinically for a long time. However the study about the mechanism is scant. The question of biomarkers of knee OA cartilage response to hypertonic dextrose prolotherapy remains currently unresolved. On this basis, the aim of this study was to characterize the secreted protein factors behind the inflammatory potential involving the hypertonic dextrose prolotherapy of knee OA. 10\ 12 older than 65 years old knee OA patients will be recruited for clinical Western Ontario McMaster University Osteoarthritis (WOMAC) index, knee X ray evaluation and knee joint synovial fluid analysis before and after hypertonic dextrose prolotherapy. The expressions of inflammatory factors will be measured by a novel cytokine antibody array methodology. The study will evaluate inflammation-related cytokines in patients of knee joint synovial fluid. Human Cytokine Antibody Array that allows profiling synovial fluid production of anti and pro-inflammatory cytokines simultaneously. Altered levels of cytokine from the array membranes incubated with tissue lysates will quantitatively depict as a histogram for relative cytokine induction or reduction in the synovial fluid. The cytokines messenger ribonucleic acid levels will be quantified by quantitative reverse-transcription polymerase chain reaction and proteins expression was analyzed by Enzyme-Linked ImmunoSorbent Assay. The WOMAC Index, minimum joint space width, and Human Cytokine Antibody Array between before and after interventions will be compared. Differences between groups will be determined by the Mann-Whitney U test. For the synovial angiogenesis is accompanied with inflammatory feature in knee OA, associations between endothelial growth factor (VEGF) expression and VEGF isoforms pattern will be determined with the Spearman correlation.
Interventions
DRUGhypertonic dextrose prolotherapy
five intra-articular injection at 2-weeks intervals in weeks 0, 2, 4, 6, 8.
Sponsors
National Yang Ming Chiao Tung University Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* at least 6 months of symptomatic knee OA * clinical criteria of moderate or moderate to severe knee OA ( the American Rheumatological Association grade II or III)
Exclusion criteria
* severe knee OA (grade IV) * rheumatoid or other inflammatory arthritis * received physiotherapy, oral NSAIDs, corticosteroids or anticoagulant, during previous 2 weeks prior the treatment * received any knee intra-articular injections during previous one month prior the treatment * poorly controlled diabetes mellitus with fasting blood sugar greater than 200 mg/dL- * history of knee surgery * dementia or psychological disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Western Ontario McMaster University Osteoarthritis Index | change from baseline at week 10 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| standing knee X ray posterior-anterior view | change from baseline at week 10 | the minimum joint space width (mJSW) of the medial and lateral compartment respectively of the tibio-femoral joint |
| protein array method for inflammatory factors | change from baseline at week 10 | Human Angiogenesis Antibody Array |
Countries
Taiwan
Outcome results
None listed