osteoporosis

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OSTEOPOROSIS Dr. K K Sawlani Department of Medicine KGMU, Lucknow 30.07.14

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OSTEOPOROSIS. Dr. K K Sawlani Department of Medicine KGMU, Lucknow 30.07.14. OSTEOPOROSIS. A disease characterized by low bone mass - PowerPoint PPT Presentation

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Page 1: OSTEOPOROSIS

OSTEOPOROSIS

Dr. K K SawlaniDepartment of Medicine

KGMU, Lucknow30.07.14

Page 2: OSTEOPOROSIS

OSTEOPOROSIS

• A disease characterized by low bone mass (reduced bone density) and micro-architectural

deterioration of bone tissue, leading to enhanced bone fragility and a consequent increase in fracture risk.

• Most common bone disease

• Affects million of people worldwide

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Development of osteoporotic bone

Rizzoli R ed In Atlas of Postmenopausal Osteoporosis (1st edition) Science Press, 2004

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OSTEOPOROSIS

• Fractures related to osteoporosis affect around 30 % of women and 12 % of men in developed countries.

• Major public health problem

• Osteoporotic fractures can affect any bone

• The most common sites are– Spine (vertebral fracture)– Forearm (Colles fracture)– Hip

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Vertebral Fracture

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Hip Fracture

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Wrist Fracture (Colles fracture)

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OSTEOPOROSIS

• Hip fractures are the most serious

• Immediate mortality is about 12 %

• Continued increase in mortality of about 20 % when compared with age matched controls.

• Account for the majority of health care cost associated with osteoporosis.

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OSTEOPOROSIS

• The prevalence increases with age reflecting that bone density decreases with age especially in women

• Accompanied by increased risk of fractures– Fall in bone density– Increased risk of falling

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Pathopysiology

• Occurs because of defect in attaining peak bone mass and/or because of accelerated bone loss.

• In normal individuals bone mass increases to reach a peak between the age of 20 and 40 years but falls thereafter.

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0 10 20 30 40 50 60

Bone

mas

s

Age (years)

Attainment of peak bone mass Consolidation

Age-related bone loss

Men

Women

Menopause

Fracture threshold

Age-related changes in bone mass

Compston JE. Clin Endocrinol 1990; 33: 653–682.

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Pathopysiology

• Peak bone mass and bone loss are regulated by both genetic and environmental factors.

• Polymorphisms have been identified in several genes that contribute to pathogenesis.

• Many of these are in the RANK and Wnt signaling pathways which play critical role in regulating bone turnover.

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Major risk factors• Non modifiable

– Age – Race– Female gender– Early menopause– Slender build– Positive family history

• Modifiable– Low calcium intake– Low vitamin D intake– Estrogen deficiency– Sedentary lifestyle– Cigarette smoking– Alcohol excess (> 2 drinks/day)– Caffeine excess (> 2 servings / day)

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Post menopausal osteoporosis

• Most common cause

• Accelerated phase of bone loss after menopause due to estrogen deficiency.

• Causes uncoupling of bone resorption and bone formation

• Amount of bone reduced by osteoclasts exceeds the rate of new bone formation by osteoblasts

• Early menopause ( before the age of 45 years ) is important risk factor

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Male osteoporosis• Less common in men

• Secondary cause can be identified in 50% of cases

• The most common causes are– Hypogonadism– Corticosteroid use– Alcoholism

• Testosterone deficiency results in increase in bone turnover and uncoupling of bone resorption and bone formation.

• Genetic factors important in the cases with no identifiable cause.

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Corticosteroid induced osteoporosis

• Risk increases with prednisolone use 5-7.5 mg daily for more than 3 months.

• Reduced bone formation due to– Inhibitory effect on osteoblast function– Osteoblast and osteocyte apoptosis

• Also reduce serum calcium– Inhibit intestinal calcium absorption– Renal leak of calcium

• Secondary hyperparathyroidism with increased bone resorption

• Hypogonadism may also occur with high doses.

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Secondary causes of osteoporosis• Endocrine disease

– Hypogonadism– Hyperthyroidism– Hyperparathyroidism– Cushing,s disease

• Inflammatory disease– Inflammotory bowel disease– Ankylosing spondylitis– RA

• Gastrointestinal– Malabsorption– Chronic liver disease

• Lung disease– COPD– Cystic fibrosis

• Drugs• Miscellaneous

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Secondary causes of osteoporosis

• Drugs– Corticosteroids– Thyroxine over-replacement– Anticonvulsants– GnRH agonists– Thiazolidinediones- pioglitazone– Alcohol intake – Heparin

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Secondary causes of osteoporosis

• Miscellaneous– Myeloma– HIV infection– Systemic masotcytosis– Renal failure– BMI < 18– Anorexia nervosa– Heavy smokers

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Clinical Features

• Asymptomatic until a fracture occurs

• Incidental osteopenia on X-ray performed for other reasons.

• Spine fracture– Acute back pain ( 1/3 cases)– gradual loss of height , kyphosis and chronic pain

• Peripheral fracture– Local pain, tenderness and deformity– Often with an episode of minimal trauma

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Investigations

• Measurement of bone mineral density (BMD) by dual energy X-ray absorptiometry (DEXA).

• BMD can also be measured by computed tomography (CT) and ultrasound.

• Central (spine and hip) are best predictors of fracture risk.

• Peripheral( radius, heel and hands) are less expensive and widely available.

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Investigations

• T-Score: The number of SDs the patient value is below or above the mean value for young normal subjects.– Good predictor of fracture risk

• Z-score: The number of SDs the patient value is below or above the mean value for age matched normal controls.– Whether or not the BMD is appropriate for age.

• Absolute BMD: expressed in g/cm2

– Used to calculate changes in BMD during follow up.

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Diagnosis

• Any patient who sustains a fragility fracture.

• On the basis of BMD T-score

≥ -1 = normal

Between -1 and -2.5 = Osteopenia

≤ -2.5 = Osteoporisis

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Changes in BMD with age (T-score values)

Souce- Davidsons textbook of Medicine 22nd edition

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Diagnosis

• History: early menopause, smoking, excessive alcohol intake, corticosteroid therapy

• Examination: Signs of endocrine disease, neoplasia, and inflammatory diseases

• A history of fall should be taken

• Unstable gait and unsteadiness

Page 27: OSTEOPOROSIS

Diagnosis - Investigations• Renal function• Alkaline phosphatase• Serum calcium, Vit D 25 (OH)• Parathyroid (PTH)• Thyroid function tests• Immunoglobulins and ESR• Celiac disease antibody testing• Testosterone (men)• 24 hour urine calcium, sodium and creatinine.

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Management

• The aim of treatment is to reduce the risk of fractures

– Non-pharmacological– Pharmacological

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Non Pharmacological Treatment

• Smoking cessation• Moderation of alcohol intake• Adequate dietary calcium intake• Exercise• Vitamin D• Fall prevention• Good nutrition

Page 30: OSTEOPOROSIS

Pharmacological Treatment

• Several drugs have been shown to reduce the risk of osteoporotic fractures.

• Effect on vertebral and non-vertebral fracture is variable.

• Considered with – BMD T-score < 2.5– BMD T-score < 1.5 in corticosteroid induced – Vertebral Fractures ,unless resulted from significant trauma

Page 31: OSTEOPOROSIS

DXA Results

T Score Classification Action

> minus 1.0 Normal Lifestyle measures.

< minus 1.0 > minus 2.5 Osteopenia

Lifestyle measures. Consider specific treatment

where there is ongoing risk, e.g. steroids, and in those who have had a minimal trauma fracture.

< minus 2.5 Osteoporosis Lifestyle measures.Prevent falls.Treatment may be

indicated.

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CURRENT THERAPIES

• Anti-resorptive

• Anabolic

• Calcium, Vitamin D, lifestyle modification– Adjunct to other treatments– 1000-1200 mg/day of calcium– 800-1200 U/day of vitamin D

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Treatment Options in OsteoporosisAntiresorptive drugs

• BisphosphonatesEtidronateAlendronateRisedronateIbandronateZoledronate

• Denosumab (monoclonal antibody against RANK-L)• SERMs

Raloxifene• Calcitonin• HRT (estrogen)

Anabolic drugsTeriparatide(PTH 1-34)

Dual Action Bone Agents (DABAs)Strontium ranelate

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Bisphosphonates

• Inhibit bone resorption by binding to hydroxyapatite crystals on bone surface

• Osteoclasts reabsorb bone-drug released within cell-inhibt key signaling pathways.

• Increase in Spine BMD of 5-8% and Hip BMD 2-4%.

• Should be taken on an empty stomach with plain water.

• No food should be eaten 30-45 minutes after administration

Page 36: OSTEOPOROSIS

Adverse effects of biphosphonates

• Common

– Upper GI intolerance (oral)– Acute phase response(intravenous)

• Less Common

– Atrial fibrillation (IV zoledronic acid)– Renal impairment (IV zoledronic acid)– Atypical subtrochanteric fractures

• Rare

– Uveitis– Osteonecrosis of the jaw

Page 37: OSTEOPOROSIS

INDICATIONS FOR ANABOLISM

• Pre-existing osteoporotic fractures• Very low BMD• Very high fracture risk• Unsatisfactory response to antiresorptive

therapy• Intolerant to anti-resorptive therapy

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TERIPARATIDE

• Daily SC injection 20 mcg

• Maximum 18-24 months

• May be followed by anti-resorptive therapy

• PTH is expensive and is reserved for severe osteoporosis, who fail to response to other therapies.

• No advantage of combined anabolic and anti-resorptive therapy

Page 39: OSTEOPOROSIS

Selective estrogen receptor modulator (SERM)

Raloxifene

• 60 mg daily orally

• Partial agonist of estrogen receptor in bone & liver

• Antagonist in breast & endometrium

• SE: muscle cramps, hot flushes, increased risk of VTE.

• Bazedoxifene is a related SREM

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HRT

• Cyclical HRT wirh estrogen and progestogen

• Prevents post menopausal bone loss and reduces risk of fractures in post menopausal women

• Primarily indicated for prevention of osteoporosis in women with early menopause

• Women in early fifties with troublesome menopausal symptoms.

• Increased risk of breast cancer and cardiovascular disease

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Duration of therapy

• Oral biphosphonates long term (5 YRS)

• HRT, raloxifene continuously

• Denosumab continuously

• Strontium ranelate not established

• Teriparatide 2 yrs fb antiresorptive Tt

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Response to drug treatment

• Repeat BMD measurements after 2-3 yrs.

• Spine BMD best for monitoring

• Biochemical markers ( N-telopeptide) respond more quickly; can be used to assess adherence.

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Surgery

• Reduce and stabilize osteoporotic fractures

Painful vertebral compression fractures• Vertebroplasty ( Injection of MMA)• Kyphoplasty ( balloon inflation – MMA)

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Response to Drugs

Fracture risk reduction• 30-40% # risk reduction with antiresorptives• 60% # risk reduction with teriparatide

BMD • 2-3% BMD increase with anti-resorptives• 4-6% BMD increase with teriparatide

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Osteoporosis MCQ

1. Most common cause of osteoporosis

a. Hypogonadismb. Malabsorptionc. Post menopausald. Hyperparathyroidism

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Osteoporosis MCQ

2. Most common bone disease is

a. Osteomalaciab. Osteoporosisc. Secondaries boned. Osteopetrosis

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Osteoporosis MCQ

3. Which of the following drug is most common cause of drug induced osteoporosis

a. Thyroxine over-relacementb. Corticosteroidsc. Pioglitazoned. Anticonvulsants

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Osteoporosis MCQ

4. Osteopenia is defined as T- Score of

a. < -1b. < -1 to < -2.5c. < -2.5

d. None of the above

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Osteoporosis MCQ

5. Risk of fracture in osteoporosis is best predicted by

a. T-scoreb. Z-scorec. Absolute BMDd. Serum calcium levels

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Osteoporosis MCQ

6. Risk factors for osteoporosis are all except

a. BMI > 30b. Smokingc. Low calcium intake

d. Immobilization

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Osteoporosis MCQ

7. Following are all anti-resroptive drugs except

a. Biphophonatesb. Raloxifenec. Estrogend. Teriparatide (PTH analogue)

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Osteoporosis MCQ

8. Which of the following is drug of choice for severe osteoporosis (T-score 0f < -3.5 )

a. Teriparatideb. Biphosphonatesc. Calcitonind. Strontium

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Osteoporosis MCQ

9. Osteonecrosis of the jaw is seen with the use of

a. Calcitoninb. PTH analoguesc. Biphosphonatesd. Raloxifene

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Osteoporosis MCQ

10. The response to drug therapy is assessed by repeating BMD measurements after

a. 3 monthsb. 6monthsc. 1 yeard. 2 year