What are the treatment options for patients with abnormal Dual-Energy X-ray Absorptiometry (DXA) scan results?

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Last updated: October 16, 2025View editorial policy

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Treatment Options for Abnormal DXA Scan Results

The primary treatment for patients with abnormal DXA scan results should include bisphosphonates as first-line therapy, along with calcium and vitamin D supplementation, lifestyle modifications, and regular follow-up monitoring. 1

Diagnosis and Classification

  • DXA (Dual-Energy X-ray Absorptiometry) is the gold standard for diagnosing osteoporosis and is recommended for all women 65 years and older, as well as postmenopausal women younger than 65 with risk factors 1
  • Osteoporosis is defined as a T-score of -2.5 or less, while osteopenia (low bone mass) is defined as a T-score between -1.0 and -2.5 1
  • Risk factors for osteoporotic fracture include increasing age, female sex, postmenopausal status, low body weight, history of parental hip fracture, previous fracture, rheumatoid arthritis, smoking, alcohol intake, and long-term use of certain medications (especially glucocorticoids) 1

Treatment Recommendations Based on DXA Results

For Patients with Osteoporosis (T-score ≤ -2.5):

  • Bisphosphonates are strongly recommended as first-line therapy for adults with high or very high fracture risk 1
  • Oral bisphosphonates are preferred due to their proven efficacy in reducing total and vertebral fractures and increasing hip and lumbar spine BMD 1
  • For patients at very high fracture risk, parathyroid hormone/parathyroid hormone-related protein (PTH/PTHrP) analogs may be considered over anti-resorptives (bisphosphonates or denosumab) 1
  • Denosumab is an option for patients with high fracture risk who cannot tolerate bisphosphonates 1
  • Teriparatide should be reserved for patients with severe osteoporosis or those who have had fractures 1

For Patients with Osteopenia (T-score between -1.0 and -2.5):

  • Treatment decisions should be based on fracture risk assessment using FRAX (Fracture Risk Assessment Tool) 1
  • Pharmacologic treatment should be considered in women with a 10-year risk of major osteoporotic fracture of at least 20% or a risk of hip fracture of at least 3% 1
  • Treatment should also be considered in patients who have had a low-trauma fracture, even if DXA does not indicate osteoporosis 1

Calcium and Vitamin D Supplementation

  • All patients should receive calcium and vitamin D supplementation based on age 1:
    • Ages 19-50: 1,000 mg calcium, 600 IU vitamin D daily
    • Ages 51-70: 1,200 mg calcium, 600 IU vitamin D daily
    • Ages 71+: 1,200 mg calcium, 800 IU vitamin D daily
  • Serum vitamin D levels should be maintained at ≥20 ng/mL (50 nmol/L) for good bone health 1
  • For patients on glucocorticoid therapy, vitamin D levels should be maintained at ≥30-50 ng/mL 1

Monitoring Treatment Response

  • The American College of Physicians recommends against bone density monitoring during the 5-year pharmacological treatment period for osteoporosis in women due to low-quality evidence 1
  • However, more recent guidelines suggest follow-up BMD testing to monitor response to therapy 1
  • Follow-up BMD testing should be performed if a fracture has occurred or new risk factors have developed 1
  • Shorter intervals between BMD testing may be indicated for patients on medications associated with rapid bone loss (glucocorticoids, aromatase inhibitors, androgen deprivation therapy) 1

Special Considerations

For Patients on Glucocorticoid Therapy:

  • Patients on glucocorticoids ≥2.5 mg/day for >3 months should receive osteoporosis therapy if at high or very high fracture risk 1
  • Yearly clinical fracture risk assessment is recommended for these patients 1
  • BMD testing should be performed every 1-2 years, with more frequent monitoring for very high-risk patients 1

For Patients Receiving Denosumab:

  • Serum calcium should be measured before starting denosumab, as hypocalcemia is a common side effect 2
  • Vitamin D levels should be evaluated before starting therapy 2
  • Regular monitoring of serum calcium is necessary, especially after the first few doses 2
  • A baseline dental assessment is mandatory before initiating denosumab to reduce the risk of osteonecrosis of the jaw 2

Lifestyle Modifications

  • Weight-bearing and resistance exercises are recommended to optimize bone density 1
  • Smoking cessation and limiting alcohol to ≤2 servings per day 1
  • Maintaining weight in the recommended range 1
  • Fall prevention strategies should be implemented, particularly in elderly patients 1

Common Pitfalls to Avoid in DXA Interpretation

  • Artifacts in the lumbar spine (such as osteoarthritis, aortic calcifications) can cause spurious increases in BMD values 1
  • Incorrect positioning of the patient can lead to inaccurate measurements 1
  • Vertebral fractures may show increased BMD due to trabecular impaction and condensation 1
  • Hip prostheses or osteosynthesis hardware make the site unsuitable for diagnostic purposes 1
  • Failure to exclude vertebrae affected by significant structural changes or differing by more than a T-score of 1.0 from adjacent vertebrae 1

By following these evidence-based recommendations, clinicians can effectively manage patients with abnormal DXA scan results to reduce fracture risk and improve bone health.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Laboratory Tests and Monitoring for Denosumab Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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