What are the recommendations for diagnosing and treating osteoporosis in patients with Turner's syndrome?

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Last updated: June 23, 2025View editorial policy

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From the Research

Patients with Turner's syndrome should undergo regular screening for osteoporosis with dual-energy X-ray absorptiometry (DXA) scans starting in adolescence and continuing throughout adulthood, with initial screening recommended at age 12-14 years and follow-up scans every 3-5 years depending on results, as supported by the most recent study 1.

Importance of Early Screening and Treatment

The importance of early screening and treatment for osteoporosis in patients with Turner's syndrome cannot be overstated, given their inherently increased risk due to estrogen deficiency, abnormal bone architecture, and often shorter stature with lower bone mass.

  • Regular monitoring of bone mineral density (BMD) is crucial, as it allows for early intervention and can significantly reduce fracture risk and improve long-term skeletal health in this population.
  • Estrogen replacement therapy (ERT) should be initiated at the appropriate age for puberty, typically around 12 years, and continued through adulthood to maintain bone health, as evidenced by studies showing the positive effects of ERT on BMD and trabecular bone score (TBS) 1.
  • Calcium supplementation (1000-1500 mg daily) and vitamin D (800-1000 IU daily) are essential components of management, alongside weight-bearing exercise, which should be encouraged as part of the comprehensive treatment plan.

Pharmacological Treatment

For patients with established osteoporosis or significant fracture risk, bisphosphonates are the first-line pharmacological treatment, with alendronate (70 mg weekly) or risedronate (35 mg weekly) being common choices.

  • Teriparatide may be considered for severe cases with multiple fractures, highlighting the need for a tailored approach to treatment based on individual patient risk factors and response to initial therapies.
  • The use of TBS as an additional tool for fracture risk prediction, as suggested by recent research 1, may further refine treatment strategies and improve outcomes for patients with Turner's syndrome.

Conclusion is not allowed, so the answer will continue without one.

Given the complexities of managing osteoporosis in Turner's syndrome, a multidisciplinary approach is necessary, incorporating endocrinologists, orthopedic specialists, and other healthcare professionals to ensure comprehensive care.

  • The role of growth hormone therapy in optimizing peak bone mass, as discussed in earlier studies 2, 3, underscores the importance of considering the broader context of bone health in Turner's syndrome, beyond just osteoporosis prevention.
  • As research continues to evolve, particularly with the introduction of novel imaging modalities like TBS, guidelines and recommendations for the management of osteoporosis in Turner's syndrome will likely be refined, emphasizing the need for ongoing education and updates in clinical practice.

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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