Osteoporosis is a skeletal disorder characterized by compromised bone strength and increased risk of fracture. It is caused by low bone mineral density and deterioration of bone microarchitecture. The document defines osteoporosis and discusses its classification, risk factors, clinical presentation, diagnosis, screening, and treatment including lifestyle modifications and medications like bisphosphonates, denosumab, calcitonin, and teriparatide. Management of osteoporotic fractures and the condition in men is also covered.
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Osteoporosis: Mohd Fikri Bin Mustapa
Osteoporosis is a skeletal disorder characterized by compromised bone strength and increased risk of fracture. It is caused by low bone mineral density and deterioration of bone microarchitecture. The document defines osteoporosis and discusses its classification, risk factors, clinical presentation, diagnosis, screening, and treatment including lifestyle modifications and medications like bisphosphonates, denosumab, calcitonin, and teriparatide. Management of osteoporotic fractures and the condition in men is also covered.
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OSTEOPOROSIS
Mohd Fikri bin Mustapa
DEFINITIONS Osteoporosis : skeletal disorder characterised by compromised bone strength that increased risk of fracture.
Bone strength : integration of bone density and bone quality.
Bone density (g/cm2) : determined by peak bone mass and amount of bone loss.
Bone quality refers to the architecture, turnover, damage accumulation, and mineralisation of the bone. CLASSIFICATION Primary Osteoporosis Postmenopausal osteoporosis. Age-related osteoporosis. Idiopathic (rare) Secondary Osteoporosis Risk factors Osteoporosis is a silent disease until fractures have occurred.
screening is not cost effective
identification of risk factors will help in case finding Clinical Presentation Most patients are asymptomatic and diagnosis is made only after a fracture.
Common clinical presentations include: Increasing dorsal kyphosis (Dowagers hump) Low trauma fracture Loss of height Back pain The common sites of fracture are the spine, wrist and hip. Diagnosis primary osteoporosis is made after excluding secondary causes.
patient with a low trauma fracture, osteoporosis is a presumptive diagnosis.
BMD measure with dual energy x-ray absorptiometry (DXA) is a the gold standard Fracture Risk Assessment Tool (FRAX) FRAX is used to evaluate the 10-year probability of hip and major osteoporotic fracture risk that integrates clinical risk factors and bone mineral density at the femoral neck If FRAX is not accessible, individuals over 65 years of age with risk factors, can be started on treatment. Screening BMD measurement is recommended for all women above 65 and men above 70 years old.
based on age and weight, Osteoporosis Self-Assessment Tool for Asians (OSTA), was developed for postmenopausal Asian women. Radiological osteopenia is apparent in plain X-rays only after more than 30% of bone loss has occurred. Densitometry
BMD is an accurate reflection of bone mass
T-scores (comparison with the young adult mean)
Z-scores (comparison with the mean of individuals of the same age)
The risk of fracture is increased two fold for each SD reduction of T-score in BMD
Currently available methods in Malaysia for measuring BMD include: a) Dual energy X-ray absorptiometry (DXA) b) Quantitative computed tomography (QCT)
DXA The gold standard measured at the hip and lumbar spine.
Indications for BMD Measurement* Quantitative computed tomography (QCT)
is an alternative technique for measuring bone density in the axial skeleton.
It is able to measure vertebral volumetric bone density.
The main limitations the lack of availability in Malaysia higher radiation dose compared to DXA Quantitative Ultrasound (QUS)
not recommended. Problems diversity of techniques, the lack of standardisation
The criteria for diagnosis not well established.
Women with low QUS results should be referred for BMD measurement. Bone Turnover Markers (BTM) useful to identify patients at high risk of future fractures.
used to evaluate treatment efficacy and compliance to therapy.
not for the diagnosis
Changes in level of BTM can be seen within 3-6 months after initiation of drug therapy Currently available biochemical markers Monitoring of Therapy to assess the response to treatment.
two separate baseline need followed by one repeat 2-3 months after initiating therapy and yearly thereafter
These measurements should be taken at the same time of the day to minimise the effect of diurnal variation PREVENTION OF OSTEOPOROSIS Nutrition
Suggested Daily Calcium Intake When dietary intake is insufficient, calcium supplementation may be needed.
For optimal absorption, calcium should not exceed 500 to 600 mg per dose Vitamin D Vitamin D supplementation at 800 IU/day in combination with calcium
Activated Vitamin D calcitriol 0.25 g bd, alfacalcidol 1 g od avoid taking more than 800 mg of calcium supplements to reduce the risk of hypercalcemia and renal stone disease. Serum and urinary calcium monitored 6 weeks after initiation of therapy and at 3 to 6 monthly intervals thereafter Body Weight Low body weight associated with low bone mineral status and increased fracture risk.
BMI of not less than 19 kg/m2 is recommended for prevention of osteoporosis Caffeine intake should less than 1 to 2 servings (240 to 360 ml in each serving) per day.
leads to slight decrease in intestinal calcium absorption and an increase in urinary calcium excretion Smoking Cigarette smoking increases osteoporotic fracture risk and thus should be avoided.
Alcohol intake Excessive intake of alcohol should be avoided because alcohol has detrimental effects on fracture risk. Exercise Regularly, in particular weight-bearing exercise to maximise peak bone mass, decrease age- related bone loss, maintain muscle strength and balance
Prevention of falls Most osteoporosis-related fractures, especially in the elderly, are a consequence of decreased BMD and falls
Recommendations for Hormonal Therapy
not be used solely for the prevention of osteoporosis
recommended in women with premature menopause
not recommended in women with breast cancer, coronary heart disease or stroke
used for the shortest duration (< 5years), in the lowest possible dose Bisphosphonates They inhibit the cells that break down bone (osteoclasts) and allow the cells that rebuild bone (osteoblasts) to work more effectively. Alendronate Risedronate Ibandronate
Two adverse effects have been noted in bisphosphonate therapy: 1. Atypical femoral shaft fractures 2. Osteonecrosis of the jaw (ONJ) Atypical Femoral Shaft Fractures The risk of atypical femoral shaft fracture increased duration of bisphosphonate use.
Although this is a useful process to prevent bone loss and fractures, there are concerns that over a prolonged period of time, this may result in bones becoming older and more brittle. Osteonecrosis necrosis of the jaw (ONJ) some of the cells die in the affected bone in the jaw and delayed healing
mostly very high doses of bisphosphonate given intravenously zoledronate for cancer treatment
Fosamax is very unlikely affecting between 1 in 10,000 people per year taking the treatment for osteoporosis. Use of bisphosphonates in Chronic Kidney Disease (CKD)
CKD Stages 1-3 Bisphosphonates can be used safely Patients should be well hydrate nephrotoxic drugs (NSAIDs), should be avoided
CKD Stages 4-5 not recommended for patients with an estimated GFR < 30 ml/min MANAGEMENT OF OSTEOPOROTIC FRACTURES The goals are early mobilisation and a return to normal activities.
Conservative management of hip fractures is discouraged because patient at risk of respiratory problems, thromboembolic disease, pressure ulcers further bone loss.
The majority of osteoporotic vertebral fractures are stable. Operative intervention is indicated for those fractures complicated by spinal cord or nerve root compression. OSTEOPOROSIS IN MEN
Osteoporosis is increasingly recognised in older men.
Men account for up to 30% of hip fractures and 42% of clinical vertebral fractures.
Fifty to sixty percent of cases are due to secondary causes
For every one SD reduction in age-matched mean BMD (Z score), fracture risk increases two-fold Strontium Ranelate
reduces bone resorption while promoting bone formation Available as Protelos Dose 2g sachet of tasteless powder to be mixed in a glass of water Denosumab
human monoclonal antibody (IgG2) that inhibits the formation,function and survival of osteoclasts by preventing RANK (receptor activator of nuclear factor kappa- B) thus reducing bone resorption.
denosumab 60mg given 6 monthly subcutaneously, Calcitonin Daily intranasal dose of 200 IU calcitonin,
Calcitonin has also been shown to have an analgesic effect for acute pain in osteoporosis related vertebral fractures.
Side effects of calcitonin include nausea, flushing, vomiting and nasal irritation. Teriparatide (r-PTH)
effective in the treatment of osteoporosis in men.
Recombinant human PTH 1-34 (r-PTH), teriparatide, is a potent anabolic agent.
indicated for severe osteoporosis or osteoporosis not responsive to other therapy.
Subcutaneously administered r-PTH at 20 micrograms daily for 21 months
Current recommendation is up to 24 months thank you...