Bone Health Management in Women Over 50
Screening and Risk Assessment
All postmenopausal women aged 65 and older should undergo bone density testing, while women aged 50-64 require screening only if they have specific risk factors for osteoporosis. 1
For women aged 50-64, screen if any of the following are present:
- History of fragility fracture 2
- Family history of hip fracture in a parent 2
- Body weight less than 127 pounds (58 kg) 2
- Current smoking 2
- Medications causing bone loss (especially glucocorticoids) 2
Treatment Thresholds Based on Risk Stratification
Initiate pharmacologic therapy immediately for any woman over 50 with a history of fragility fracture, regardless of bone density, as this represents high fracture risk that warrants treatment independent of other calculations. 2
For women without prior fracture:
- Calculate 10-year fracture risk using the WHO FRAX tool 2
- Treat if FRAX shows ≥20% risk of major osteoporotic fracture OR ≥3% risk of hip fracture 2, 3
- Treat if T-score is approaching -2.5 or severe osteopenia (T-score <-2.0) 2
First-Line Pharmacologic Treatment
Oral bisphosphonates are the mandatory first-line therapy, reducing hip fractures by 50% and vertebral fractures by 47-56% over 3 years, with the most favorable balance of efficacy, safety, and cost. 2, 3, 4
Specific bisphosphonate regimens:
- Alendronate 70 mg once weekly (oral) 2, 4
- Risedronate 35 mg once weekly (oral) 2, 4
- Zoledronic acid 5 mg IV annually for patients unable to tolerate oral formulations 2, 4
Essential Supplementation (Non-Negotiable)
All women over 50 receiving osteoporosis treatment must take calcium 1,200 mg daily and vitamin D 800 IU daily, as pharmacologic therapy is significantly less effective without adequate supplementation. 2, 3, 4
- Target serum vitamin D level ≥20 ng/mL 2
- These supplements are required even for women not on pharmacologic therapy if they have osteopenia or osteoporosis 3
Treatment Duration and Monitoring Strategy
Treat with bisphosphonates for an initial 5-year period without monitoring bone density during treatment, as monitoring provides no clinical benefit. 2, 3, 4
After 5 years:
- Reassess fracture risk to determine if continued therapy is warranted 2, 3, 4
- Consider drug discontinuation only in patients at low risk for fracture 3, 4
Mandatory Lifestyle Modifications
All women over 50 with bone health concerns require:
- Weight-bearing exercise and resistance training 2, 3, 4
- Smoking cessation 2, 3
- Limit alcohol intake 2, 3
- Fall prevention strategies 2, 3
- Maintain healthy body weight 2
Secondary Causes Evaluation
All women diagnosed with osteopenia or osteoporosis require workup for secondary causes of bone loss, including vitamin D deficiency, hypogonadism, glucocorticoid exposure, malabsorption disorders, hyperparathyroidism, hyperthyroidism, and alcohol abuse. 2
Second-Line Treatment Option
For women who cannot tolerate bisphosphonates or have contraindications, denosumab 60 mg subcutaneously every 6 months is the recommended alternative. 2, 3, 4, 5
Critical warning: Never discontinue denosumab abruptly without transitioning to bisphosphonate therapy, as abrupt discontinuation is associated with multiple vertebral fractures. 2, 3
Agents to Avoid
Strongly avoid menopausal estrogen therapy, estrogen plus progestogen therapy, or raloxifene for osteoporosis treatment due to unfavorable benefit-harm balance. 2, 4
- Teriparatide and romosozumab are reserved for very high-risk osteoporosis only, not as first-line therapy 2, 6
- Teriparatide use should not exceed 2 years during a patient's lifetime due to osteosarcoma risk observed in animal studies 6
Safety Profile
High-certainty evidence shows bisphosphonates cause no difference in serious adverse events compared to placebo at 3+ years. 2, 3, 4
Common mild adverse effects include:
Rare serious adverse effects (risk increases with prolonged use):
Cost Considerations
Prescribe generic bisphosphonates whenever possible rather than expensive brand-name medications or newer agents, as they are significantly more cost-effective while maintaining equivalent efficacy. 3, 4