Inadequate response to treatment reveals persistent osteoclast bone resorption in osteoporotic patients

Bastien Léger1, Patrice Fardellone2, Catherine Cormier3

  • 1Université de Paris, Bioscar INSERM U1132, Hôpital Lariboisière (APHP), Paris, France.

Bone
|September 7, 2021
PubMed

Insights

Inadequate response to osteoporosis drugs is linked to higher bone resorption and poorer bone microarchitecture. This suggests treatments may not sufficiently inhibit bone breakdown, leading to fractures despite therapy.

Area of Science:

  • Bone Biology and Histology
  • Osteoporosis Research
  • Pharmacological Response

Background:

  • Osteoporosis treatments aim to reduce fracture risk, but some patients experience fractures despite adherence.
  • Inadequate response to therapy is potentially linked to elevated bone turnover markers.
  • Understanding the bone microarchitecture and cellular profiles of these inadequate responders is crucial.

Purpose of the Study:

  • To analyze and compare the bone microarchitecture and cellular profiles of inadequate responders (IRs) to osteoporosis treatment.
  • To compare IRs with patients suffering from untreated osteoporosis (U-OP) and healthy controls (Ctrl).

Main Methods:

  • Retrospective analysis of bone biopsies from IRs (n=31), U-OP patients (n=31), and Controls (n=16).
  • Histomorphometry and micro-computed tomography (micro-CT) for bone microarchitecture assessment.
  • Evaluation of clinical data, bone turnover markers, and bone mineral density (BMD).

Main Results:

  • IRs were older and had lower hip BMD and T-scores compared to U-OP patients.
  • Reduced bone volume/total volume (BV/TV) and trabecular thickness were observed in IRs versus U-OP and Controls.
  • Higher osteoclast numbers and an imbalance favoring bone resorption (lower osteoblast surface) were found in IRs.

Conclusions:

  • Inadequate responders exhibit an imbalance in bone remodeling, with bone resorption dominating over formation.
  • This persistent high bone resorption may indicate insufficient inhibition by anti-osteoporotic drugs, explaining treatment failure.
  • Strategies to enhance bone resorption inhibition should be considered to improve treatment efficacy and prevent fractures.

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