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Osteoporosis: The silent killer
Michele T. Glasgow, MD Midwest Orthopaedic Institute Bone Health Center 2111 Midlands Court Sycamore, Illinois
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What is osteoporosis? Means “porous bone.”
Skeletal disorder characterized by compromised bone strength predisposing to an increased risk of fracture
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Osteoporosis is Common
9 million Americans have osteoporosis (~80% women) 200 million people worldwide 1 in 2 women and 1 in 4 men >50yo will have an osteoporosis fracture in their lifetime By 2020, it is projected that there will be ~14 million Americans with osteoporosis.
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Osteoporosis is Costly
Responsible for 2 million fractures annually $19 billion in related costs per year By 2025, experts estimate osteoporosis will be responsible for ~3 million fractures and $25.3 billion in costs each year
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Osteoporosis is Serious
20% of hip fractures die within one year REGARDLESS OF REPAIR from complications related to surgery or other co-morbidities ~50% of hip fracture survivors require long term nursing home care and have some degree of permanent disability
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Osteoporosis is “Silent”
Bone loss occurs without symptoms Often it is not detected until a fracture occurs Compression fractures of the spine often occur without trauma and may present with back pain, kyphosis, or simple height loss
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Osteoporosis = TICKING TIME BOMB!!
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Bone Composition Bone Matrix 90% collagen and 10% other proteins
Bone mineral Hydroxyapatite (calcium and phosphorus) Bone cells Osteoclasts, osteoblasts, osteocytes
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Bone Basics Cancellous Bone Cortical Bone
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Bone science Bone is constantly remodeling in a coordinated sequence of resorption (osteoclasts) and formation (osteoblasts). Peak bone mass occurs between ages Bone loss occurs when resorption > formation. Age related bone loss occurs at a rate of ~ % per year. Bone loss accelerates with menopause (early and surgically induced) at an estimated rate of 1-2% per year. Women can lose up to 20% of bone mass in 5-7 years after menopause.
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Fracture Rates Displayed by Age and Gender
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Who needs to be screened?
ASK YOUR DOCTOR!!
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Osteoporosis Risk Factors
Female Thin, petite frame Post menopausal Age (>50 for women, >70 for men) Race (Caucasian or Asian) Family history Hx of fracture or height loss Poor calcium and vitamin D diet Smoking Excessive alcohol Inactive lifestyle Excessive caffeine intake
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Diseases that cause bone loss
Autoimmune Disorders - RA, MS, Lupus Digestive and GI Disorders - IBD, Celiac Disease, Wt loss surgery Endocrine/Hormonal Disorders –DM, Hyperparathyroidism, Hyperthyroid, Low estrogen or testosterone Hematologic/ Oncology - Cancer, Leukemia, Lymphoma, MM, Sickle Cell Disease Neurological Disorders - PD, Stroke, MS Mental Illness - Eating Disorders, Depression Other - AIDS/HIV, Kidney/Liver Disease, COPD
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Medications that cause bone loss
Medroxyprogesterone acetate (Depo provera) Methotrexate PPIs (Nexium, Prevacid, Prilosec) SSRIs (Lexapro, Prozac, Zoloft) Steroids (glucocorticosteroids IE prednisone) Tamoxifen (pre-menopausal use) Thiazolidinediones (Actos, Avandia) Anticonvulsants (Dilantin, Phenobarbital) Aromatase inhibitors (Arimidex, Aromasin, Femara) Chemotherapy/XRT Cyclosporine/Tacrolimus GnRH (Lupron, Zoladex) Heparin Lithium Thyroid Hormones (In excess)
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Fractures Most typical osteoporosis sites: Hip, Spine and Wrist
Disease is systemic – occurs throughout the body Fall from a standing height or low trauma resulting in a fracture IS by definition an osteoporotic fracture (aka fragility fracture)
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Prevention Balanced diet of calcium and vitamin D
Regular weight bearing and muscle strengthening exercise Healthy lifestyle, avoid excess alcohol, caffeine, soda Bone density testing and medication when appropriate Fall prevention
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Detection DXA or bone density scan can:
Detect osteoporosis before a fracture occurs Predict your chances of fracturing in the future Determine your rate of bone loss and/or monitor the effects of treatment if the test is conducted at intervals of a year or more Paid for by Medicare every two years
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Diagnosis Central dual-energy DXA (GOLD STANDARD)
In the absence of a fracture, T-score > -2.5 in the spine, femoral neck or total hip. Fracture of the hip or spine AACE American Association of Clinical Endocrinologists) Guidelines for Diagnosis and Treatment of Osteoporosis 2010
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Limitations of World Health Organization Definition
Established in post-menopausal osteoporosis Does not recognize fragility fractures and therefore may have a “normal result” in patients with osteoporotic fractures Only for central DXA and forearm REMEMBER: This is a SCREENING TOOL!! It is in conjunction with clinical information and judgement
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Alternative Tools: Peripheral DXA
Should NOT be used for monitoring patient’s response to therapy Ease and availability Often used as a screening tool
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Central DXA Capable of measuring the spine and hip “Gold Standard”
Used in most epidemiologic studies and clinical trials Diagnosis is based on the lowest site
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Contraindications for central DXA
Pregnancy Recent contrast study or nuclear medicine scan (wait 72 hours) Calcium supplements taken day of the study Extensive orthopaedic instrumentation Severe obesity
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Lumbar Bone Mineral Density
Use L1-L4 Often falsely elevated due to osteoarthritis May need to exclude arthritic segments, or, the entire study if necessary
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Femoral (Hip) Bone Mineral Density
Use total hip or femoral neck, whichever is the lowest. Do NOT use Ward’s area for diagnosis Mean hip BMD can be used for monitoring (Total hip is preferred as ROI)
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Medical Evaluation: Osteoporosis Labs
Intact PTH Ionized calcium SPEP/UPEP Testosterone 24 hour creatine clearance Bone turnover markers CBC CMP TSH Magnesium Vitamin D 25-OH
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Bone Turnover Markers Product of bone remodeling
Noninvasive, easily repeated Cannot be used to diagnose 733.0 Can be used to monitor response to treatment Expensive $$$$ Bone resorption markers NTX CTX Alkaline phosphatase Bone formation marker Procollagen 1-N terminal S
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FRAX Developed by WHO in 2008
Prediction tool to assess an individual’s fracture risk Risk factors + BMD (femoral neck only) = probability of osteoporosis fx in 10 yrs in untreated patients ages Indication for treatment: Use clinical judgement!! Low bone mass and a 10 year probability of a hip fx >3% or a 10 year probability of a major osteoporosis-related fx >20% (US-adapted WHO algorithm).
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DXA, labs, FRAX, clinical judgement
Osteoporosis Tools: DXA, labs, FRAX, clinical judgement
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AACE Guidelines for treatment 2010
Patients with a history of spine or hip fracture Patients without a history of fractures but with a T-score of less than -2.5 Patients with a T-score between -1.0 and -2.5 if FRAX suggests a 10 year probability for major osteoporotic fracture is >20% or hip fracture > 3%.
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“The skinny” on Calcium
Food is the best source! Read the label. Food labels list calcium as a % of the DV (or 1000mg) i.e. 30% DV of calcium equals 300mg Supplement ONLY if needed. Calcium is absorbed best when taken in amounts of mg or less. Calcium carbonate is best absorbed with food Calcium citrate is absorbed +/- food
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The Sunshine Vitamin: Vitamin D
3 Sources: Sunlight, Food, Supplements Promotes calcium absorption Maintains serum Ca and PO4 (bone mineralization) Needed for bone growth and remodeling
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National Osteoporosis Foundation Calcium/Vit D recommendations
VITAMIN D Women and Men <50 = IU >50 = IU CALCIUM Women <50 = 1000mg >50 = 1200mg Men <70 = 1000mg >70 = 1200mg
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Supplements Caltrate 600 + D: one tablet BID dosing w/ food
Citracal + D: 2 tablets BID dosing Citracal Slow Release 1200: once daily Citracal Petites
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AACE 2010 Medication Recommendations
Use alendronate, risedronate, zoledronic acid or denosumab as first line therapy. Use ibandronate as a second line agent. Use raloxifene as a second or third line agent. Use calcitonin as the last line of therapy. Use teriparatide for patients with very high fracture risk or in patients who have failed bisphosphonate therapy. Combination therapy is not advised.
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Estrogen Replacement Class: Hormone
MOA: anticatabolic (antiresorptive) FDA approved for prevention of PMO **NIH Recommendations 2002** **Women should consult their doctor and weigh the benefits of HT against the risks for stroke, heart attack, blood clots, breast and colon cancer (WHI).
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Calcitonin Nasal Spray
Class: Biologic agent MOA: anticatabolic (antiresoprtive) Administration: Nasal spray (Miacalcin) FDA: Approved for women with 5+ yrs PMO Side effects: Nasal irritation, possible analgesic effect, no known drug interactions. Minimal increase spine BMD. No increase hip BMD. Calcitonin Nasal Spray
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Bisphosphonates MOA: anticatabolic (antiresorptive)
Administration: Oral, IV (Boniva and Reclast) Side effects: Avoid in renal patients (GFR <30ml/min) Osteonecrosis of the jaw (rare) 15 min IV infusion may have an acute phase reaction (30-40% have fever, myalgias)
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Bisphosphonates Fosamax (Alendronate) Actonel (Risedronate)
Boniva (Ibandronate) Reclast (Zolendronic Acid) Fosamax (Alendronate) Actonel (Risedronate) Boniva (Ibandronate) Reclast (Zolendronic Acid) FDA approved for prevention and tx of PMO, GIO and osteoporosis in men FDA approved for prevention and tx in PMO FDA approved for tx of PMO and men with osteoporosis Reduces spine, hip and non vertebral fractures Reduces spine fractures **Effect on hip and non vertebral fractures is unknown** Increases BMD in spine and hip
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AACE Stance on Bisphosphonates 2010
Consider a drug holiday after 4-5 years of stability on bisphosphonate therapy. Follow BMD and bone turnover markers during a drug holiday. Reinitiate therapy if bone declines sustantially, bone turnover markers increase or fracture occurs.
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Evista (Raloxifene) Class: SERM (selective estrogen receptor modulator) MOA: anticatabolic (antiresorptive) FDA approved for prevention and tx of PMO FDA approved as an agent to reduce breast cancer Reduces spine fractures **hip and non vertebral fractures not proven** (2nd or 3rd line agent) Side effects: Increased risk of DVT, does not alleviate hot flashes
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PROLIA (denosumab) Class: anticatabolic (antiresorptive)
MOA: RANK ligand inhibitor Administration: 60mg SQ every 6 months FDA approved for prevention and tx of osteoporosis in PMO and osteoporosis tx in men. Good option in pts who have failed or are intolerant to other available osteoporosis therapy Side effects: hypocalcemia, infection, dermatologic rxn, ONJ
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Forteo (teriparatide)
Class: Biologic agent MOA: anabolic Administration: 20mcg injection SQ daily for max 2 years FDA: approved for PMO women with osteoporosis at high risk of fracture and men with primary or hypogonadal osteoporosis at high risk of fracture BLACK BOX WARNING: Osteosarcoma DO NOT USE in pts with Paget’s, unexplained increase in alk phosphatase, kids, or prior skeletal XRT
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Forteo Mechanism of Action
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How is treatment monitored?
Baseline DXA with repeat DXA every 1-2 years until findings are stable. Then repeat every 2 years. Monitor changes in BMD of spine or total hip. F/U patients should repeat DXA same facility, same machine. Bone turnover markers
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Defining successful treatment
BMD is stable or increasing and no fractures are present. For patients on antiresorptive agents, bone turnover markers at or below the median value. One fracture is NOT a sign of failure!! Consider alternate therapy, compliance, and reassess. Defining successful treatment
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+Men >70
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When to see the Bone Expert
Patient with normal BMD sustains a fracture without trauma. Patients with recurrent fractures or continued bone loss despite therapy. Severe osteoporosis. When a patient has a condition that complicates management (ie. renal failure, hyperparathyroidism, malabsorption).
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Midwest Orthopaedic Institute
Thank you! Midwest Orthopaedic Institute Bone Health Center Michele T. Glasgow, MD Marie Rivers, PA-C
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