Double-blinded Randomized Controlled Trial Investigating the Effectiveness of Vitamin D Supplementation in Patients With End-stage Knee Osteoarthritis
Overview
- Phase
- Not Applicable
- Intervention
- Vitamin D
- Conditions
- Vitamin D Deficiency
- Sponsor
- Chinese University of Hong Kong
- Enrollment
- 56
- Locations
- 1
- Primary Endpoint
- Quadriceps and hamstring muscle strength assessment
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
Osteoarthritis (OA) knee is one of the commonest chronic degenerative conditions. It causes disability in elderlies due to pain and stiffness. The prevalence of radiologic knee osteoarthritis increases in proportion to age, reaching an astounding 64.1% for patients who are over 60 years of age. In 2021, there were over 26,000 patients on the Hospital Authority (HA) waiting list for knee total knee replacement (TKR) and with only 4300 TKRs performed, the nominal waiting time for TKR was almost 89 months.
Low vitamin D can adversely affect cartilage thickness and study suggested that low serum vitamin D is associated with increased radiographic knee OA progression. A systematic review concluded that vitamin D supplements can improve pain and function in patients with knee OA.
Vitamin D has long been recognized for its effect on musculoskeletal health and increasing attention has been focused for its effect on muscle function. Vitamin D have a direct effect on muscle hypertrophy by acting on specific vitamin D receptors (VDRs) on myocytes, and sufficient levels of vitamin D in patients have been found to correlate with an increase in the size, number, and strength of muscle fibres. Vitamin D also seems to exert beneficial effects by its interplay with myokines such as myostatin and irisin.
One study also showed that muscle nuclear VDR was increased by 30% and augmented muscle fibre size by 10% in elderly females (mean age of 78 years) taking vitamin D orally at a rate of 100 µg/day (4000 IU/day) for 4 months.
This will be a double-blinded RCT investigating the effect of vitamin D supplements or knee muscle strength, physical function, pain symptoms and, sarcopenia status. The study will be a follow-up study with assessment at baseline, 3- ,6-and 12-months post vitamin D intervention.
Detailed Description
Osteoarthritis (OA) knee is one of the common chronic degenerative conditions. It causes disability in elders, leading to pain and stiffness. The prevalence of radiologic knee osteoarthritis and symptomatic knee OA were 37.4% and 12.1% among adults over 60 years of age. Often, patients with end-stage knee OA often adopt a sedentary lifestyle to avoid joint pain and stiffness. This can have an adverse effect on muscle function both locally around the knees as well as on generalized muscle health. Ageing and inactivity leads to a progressive loss of muscle mass and strength until an abnormally low level, termed "sarcopenia". Sarcopenic elderlies are more likely to develop deterioration of functional outcomes and higher mortality resulting in socioeconomic and healthcare burdens. In contrast, our previous study investigating the prevalence of sarcopenia in end-stage OA showed that 32.8% of severe knee OA patients also suffered sarcopenia, and these patients showed a slower recovery after undergoing TKR. Vitamin D has long been recognized for its effect on musculoskeletal health, and increasing attention has been focused on its effect on muscle function. Vitamin D directly affects muscle hypertrophy by acting on specific vitamin D receptors (VDRs) in myocytes, and sufficient vitamin D levels in patients have been found to correlate with an increase in the size, number, and strength of muscle fibers. In the Chinese population aged over 65, 30.6% of the population studied presented with vitamin D deficiency (25(OH)D \<20 ng/mL). A systematic review concluded that vitamin D supplements can improve pain and function in patients with knee OA. Moreover, patients with end stage OA knees will have more pain, leading to decreased mobility, a higher risk of sarcopenia, and vitamin D insufficiency that would warrant attention. 56 patients with end-stage knee OA scheduled for TKR will be recruited from the Li Ka Shing Orthopaedic Specialist clinic at the Prince of Wales Hospital (PWH) Hong Kong. Oral and written consents will be obtained from individuals who agree to participate in the study. The recruitment period will last for 12 months and the whole project period is 2 years in total. Basic demographics, sarcopenia assessment and Outcome Measurement Questionnaires will be carried out. The patients will be advised to avoid taking supplements and keep a record of medication intake throughout the study period. We will use 4000 IU/day, for 6 months adapted from previous study. All study tablets including the placebo will be manufactured according to Good Manufacturing Practice (GMP) guidelines for quality assurance. Assessments including quadriceps and hamstring muscle strength, handgrip strength, 6-meter timed walking gait test, chair stand test, muscle mass using Dual Energy X-ray Absorptiometry and questionnaires will be conducted.
Investigators
Prof. Tim-Yun Michael ONG
Clinical Assistant Professor
Chinese University of Hong Kong
Eligibility Criteria
Inclusion Criteria
- •Male and female patients aged over 50 with end-stage knee OA
- •Patient are on the waiting list for TKR at Prince of Wales Hospital
- •Walk unaided for 6 meters
- •Able to comply with the assessments and has given oral and written consent
- •Patients with vitamin D insufficiency and deficiency at the baseline measurement (25(OH)D \<30 ng/mL)
Exclusion Criteria
- •Patients with connective tissue disorders or myositis condition
- •History of any Hip \& Knee surgery
- •Patients with malnutrition were assessed by Mini-Nutritional assessment.
- •Patients with acute immobility (i.e., post-hip fracture or post-acute hospital admission)
- •Patient scheduled for TKR within six months
- •Patients already taking vitamin D supplements
- •Patients with a known contraindication to vitamin D treatment (such as allergy)
- •Patients who have renal impairment with glomerular filtration rate (eGFR) \< 30 ml/minute
Arms & Interventions
Intervention group
The intervention group will receive vitamin D supplement for 6 months
Intervention: Vitamin D
Control group
The control group will receive placebo for 6 months
Intervention: Placebo
Outcomes
Primary Outcomes
Quadriceps and hamstring muscle strength assessment
Time Frame: Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement
Hand-held dynamometer microFET2 (Hoggan Scientific, Salt Lake City UT, USA) will be used to assess lower limb strength and power. Assessment of isometric muscle strength and power will be performed with the participants in a seated position to assess knee extensors and knee flexors. All tests will involve maximal voluntary isometric contractions. Both limbs will be assessed to record side-to-side difference. Two trials were recorded for each muscle group.
Secondary Outcomes
- Knee Injury and Osteoarthritis Outcome Score (KOOS)(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Short-Form 36 (SF-36)(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- The 6-meter timed walking test(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- 5-time Chair stand test(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Dual Energy X-ray Absorptiometry (DXA)(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- International Physical Activity Questionnaire (IPAQ)(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Nutritional intake questionnaire(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Sunlight exposure questionnaire(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Handgrip strength(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Serum myokine evaluation(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)
- Serum vitamin D assays(Baseline, 3 months, 6 months, 12 months after the the commencement of vitamin D supplement)