Osteopenia Treatment: A Risk-Stratified Approach
For patients with osteopenia, treatment decisions must be driven by absolute fracture risk calculated using the FRAX tool, not by the T-score alone—pharmacological therapy is indicated only when 10-year hip fracture risk reaches ≥3% or major osteoporotic fracture risk reaches ≥20%, while all patients regardless of risk require calcium, vitamin D, and lifestyle modifications. 1, 2
Risk Stratification: The Critical First Step
Calculate fracture risk using FRAX (www.sheffield.ac.uk/FRAX), which integrates BMD with clinical risk factors including age, prior fracture, parental hip fracture, smoking, glucocorticoid use, and other factors. 1, 2 This calculation determines whether you observe or treat pharmacologically.
Key thresholds for pharmacological intervention: 1, 2
- 10-year hip fracture risk ≥3%, OR
- 10-year major osteoporotic fracture risk ≥20%
Special adjustment for glucocorticoid users (≥7.5 mg/day prednisone): Multiply major osteoporotic fracture risk by 1.15 and hip fracture risk by 1.2 before applying treatment thresholds. 1, 2
Universal Non-Pharmacological Management (All Patients)
Every patient with osteopenia requires these foundational interventions regardless of fracture risk: 1, 2
Calcium supplementation:
- Ages 19-50: 1,000 mg daily 1, 2
- Ages ≥51: 1,200 mg daily 1, 2
- Calcium citrate formulations taken between meals optimize absorption and minimize gastrointestinal side effects 3
Vitamin D supplementation:
- Ages 19-70: 600 IU daily 1, 2
- Ages ≥71: 800 IU daily 1, 2
- Target serum 25-hydroxyvitamin D level ≥20 ng/mL (some guidelines recommend ≥30 ng/mL) 1
- Doses of 800 IU/day combined with adequate calcium reduce non-vertebral fractures by 15-20% 4
Exercise prescription:
- Weight-bearing exercises (walking, jogging, stair climbing) 1, 2
- Muscle-strengthening/resistance training 1, 2
- Balance training (tai chi, physical therapy, dancing) to reduce fall risk 1, 2
- Minimum 30 minutes of moderate physical activity daily 2
Lifestyle modifications:
- Smoking cessation (mandatory) 1, 2
- Limit alcohol to 1-2 drinks per day maximum 1, 2
- Maintain weight in recommended range (low BMI is an independent risk factor) 1, 2
Fall prevention strategies:
- Vision and hearing assessment 1, 2
- Medication review (sedatives, antihypertensives causing orthostasis) 1, 2
- Home safety evaluation (remove tripping hazards, improve lighting, install grab bars) 1, 2
Pharmacological Treatment (High-Risk Patients Only)
First-line therapy: Oral bisphosphonates 1, 2
- Alendronate 10 mg daily or 70 mg weekly 1
- Risedronate 5 mg daily, 35 mg weekly, or 150 mg monthly 1
- Preferred due to proven efficacy in reducing vertebral, non-vertebral, and hip fractures, favorable safety profile, low cost (generics available), and extensive clinical experience 4, 1
Second-line alternatives when oral bisphosphonates are inappropriate (due to esophageal disorders, inability to remain upright ≥30 minutes post-dose, malabsorption, non-compliance, or patient preference): 1
IV zoledronic acid 5 mg once yearly 1
Denosumab 60 mg subcutaneously every 6 months 1
Teriparatide (anabolic agent) 1
Raloxifene 60 mg daily (postmenopausal women only) 1
Critical Pre-Treatment Evaluation
Before initiating any pharmacological therapy, you must identify and correct secondary causes of low bone density: 1, 2
- Vitamin D deficiency (measure serum 25-hydroxyvitamin D) 1
- Hypogonadism 1, 2
- Excessive alcohol use 1, 2
- Glucocorticoid exposure 1, 2
- Hyperparathyroidism 1
- Thyroid disease 1
Excluding osteomalacia is mandatory before prescribing bisphosphonates—treating osteomalacia (commonly from vitamin D deficiency) with anti-resorptive agents increases bone fragility and fracture risk. 1
Special Populations Requiring Modified Approach
Cancer survivors (especially on aromatase inhibitors or causing hypogonadism): 4, 1, 2
- Obtain baseline DEXA and repeat every 2 years 4
- Bisphosphonates or denosumab are preferred agents for high fracture risk 4, 1, 2
- Perform dental screening before initiating bone-modifying agents to reduce osteonecrosis of jaw risk 2
Glucocorticoid users (≥2.5 mg/day prednisone for ≥3 months): 4, 1
- Fracture risk assessment within 6 months of starting therapy 1
- Apply FRAX dose adjustment (multiply risks by 1.15 and 1.2 as noted above) 1, 2
- Annual clinical fracture risk reassessment mandatory 1, 2
- More aggressive treatment thresholds apply 4
Liver transplant recipients: 1, 2
- Calcium and vitamin D supplementation plus weight-bearing exercise 1, 2
- Initiate bisphosphonates for established osteoporosis or recurrent fractures 1
Women of childbearing potential: 4
- If not planning pregnancy and using effective contraception: oral bisphosphonates preferred 4
- If oral bisphosphonates unsuitable: teriparatide second-line 4
- Denosumab and IV bisphosphonates only after discussion of potential fetal harm in unplanned pregnancy 4
Monitoring Strategy
For patients NOT on pharmacological therapy (low fracture risk): 1, 2
For patients ON pharmacological therapy: 1, 2
- Repeat DEXA every 2 years to evaluate treatment response 1, 2
- Do not perform BMD assessment more frequently than annually 4, 1
- Monitor adherence systematically—poor adherence is extremely common 4, 1
- Consider discontinuation of bone-modifying agent when T-scores improve, followed by periodic DEXA surveillance 2
Common Pitfalls to Avoid
Over-treating low-risk patients: Osteopenia is not a disease—it encompasses a wide range of fracture risks. 5 The T-score alone does not justify pharmacological treatment; absolute fracture risk calculated by FRAX determines intervention. 1, 2, 5
Under-treating high-risk patients: Only 5-62% of patients who meet treatment criteria actually receive appropriate therapy. 1, 2 Systematic identification and treatment of high-risk patients is essential.
Failing to address secondary causes: Treating with bisphosphonates without correcting vitamin D deficiency, hypogonadism, or other reversible contributors renders therapy ineffective or harmful. 1
Ignoring adherence: Long-term adherence to osteoporosis medications is notoriously poor. 4 Structured follow-up, patient education, risk communication, and shared decision-making substantially improve adherence (up to 90% in fracture liaison services). 4
Stopping denosumab without transition therapy: This causes rapid bone loss and vertebral fracture risk elevation—always plan sequential therapy. 1