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Osteoporosis After a Spinal Cord Injury
Birgitte Hansen Clinic of Spinal Cord Injury Hornbæk - Denmark
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Osteoporosis results from reduced bone mass
disruption of the micro-architecture of bone, decreased bone strength increased risk of fracture.
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A Spinal Cord Injury Has
Increase in bone resorption Hormonal alternations Modification of body composition Wide-ranging physiological and pathological effects
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1% - 46% incidence of lower extremity fractures in people who sustain an SCI
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Risk Factors For Osteoporosis in SCI Individuals
Completeness Low BMI (< 25 kg/m2) Age Gender (female) Age at injury ( < 18 years) Duration of injury
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Bone Evaluation - DXA
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What can we do?
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Non pharmacological treatment
Pharmacologic Therapy
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Non pharmacological treatment
MES (muscular electrical stimulation) FES cycle ergometry (functional electrical stimulation) Standing Walking Teach safe transferring skills
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Passive standing do not maintain or improve BMD in the hip or knee region
Kunkel et al (Arch Phys Med Rehabil) 1993 Needham-Shropshire et al. (Arch Phys Med Rehabil) 1997
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FES cycle ergometry Conflicting results for bone parameters for six studies
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MES –FES assisted training
Belanger et al (Arch Phys Med Rehabil 2000) 14 men and women with SCI and 14 controls 5 days/week, 24 weeks Results BMD regained almost 30 % of lost bone mass compared to controls
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Pharmacologic Therapy
Calcium – just supplement Vitamin D – just supplement Calcitonin – optimal dosage and long-term effectiveness unclear Vitamin D analog (Etalpha®) – Increase in lower-limb BMD Bisphosphonates - reduction in bone loss
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Vitamin D Analog Treatment
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19 subjects had 1-α-D2 4 μg/day for 24 months (21 placebo)
Leg BMD increased significantly from baseline in the treatment group at 12, 18 and 24 months. Both groups received calcium (1.3 g/d) and vitamin D (800 IU/d) Smoking prevents bone effect with 1-α-D2 - reason unclear
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Conclusion – Vitamin D Analog
Treatment of 1-α-D2 increased lower-limb BMD Current smokers had not this effect Long-term effect of continued 1-α-D2 therapy in persons with chronic SCI requires further investigation Bisphosphonates + 1-α-D2 or 1-α-D2 followed by bisphosphonates should be investigated 1-α-D2 + physical intervention may be considered
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Bisphosphonates treatment
First-generation Etidronate, clodronate Second-generation Pamidronate Third-generation Alendronate, ibandronate, risedronate, tiludronate and zolendronic acid
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Treatment With Bisphosphonates
Oral bisphosphonates must be Ingested on an empty stomach With ml water Followed by sitting up for 1 hour prior to taking any other food or medication Side effects Joint pain Stomach upset/gastric ulcer
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Treatment With Bisphosphonates II
Intravenous bisphosphonates Available in daily, monthly, quarterly and yearly preparations Assured compliance Reduced relative risk of gastric ulcer Side effects Fever and muscle pain (flu-like symptoms) Low serum calcium
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Clodronate P. Minaire et al. (J. Clin. Invest. 1981) Results
14 had clodronate (2 different doses), 7 placebo (17 males, 4 females) Started 17.6 days after injury. 3.5 months of treatment – total 6 months study Results No decrease in hip and knee region on bone mineral content in the treated groups Etidronate and Tiludronate have positive results for treatment within the 1 year of injury
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Alendronate Y. Zehnder et al. (JBMR, 2004) Results
33 men had Aln + Ca, 32 men had Ca in 2 years 9.8 years since SCI Results BMD in distal and proximal tibia, and total hip remained stable in the Aln – Ca group and decreased in the Ca group
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Future Prospects Large prospective longitudinal studies
DXA methods to target areas Reducing the risk of falls Osteoprotegerin/RANKL system
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Questions to be answered
Who When How – and how long to treat?
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Osteoporosis Research Centre, Hvidovre Hospital
Ulla Pedersen Anne-Mette Rasmussen Solveig Petersen Jenni Teilmann Ole Helmer Sørensen Jens-Erik Bech Jensen Clinic For Spinal Cord Injury, Rigshospitalet Lisbeth Nielsen Fin Biering-Sørensen
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Thank you for your attention
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