[Fragility fracture in the Chronic Kidney Disease (CKD)]

Maria Fusaro1,2, Andrea Aghi3, Maria Cristina Mereu4

  • 1Consiglio Nazionale delle Ricerche (CNR) - Istituto di Fisiologia Clinica (IFC), Pisa e Dipartimento di Medicina, Università di Padova.

Insights

Fragility fractures are a significant concern in chronic kidney disease (CKD) patients. Advanced diagnostic tools and bone biomarkers can help identify high-risk individuals for better fracture prevention.

Area of Science:

  • Nephrology
  • Orthopedics
  • Bone Metabolism

Background:

  • Fragility fractures (FF) are prevalent in chronic kidney disease (CKD) patients, occurring more frequently and at younger ages than in the general population.
  • These fractures contribute to substantial morbidity, mortality, and healthcare expenses.
  • The exact mechanisms linking CKD and FF, beyond CKD-Mineral Bone Disorder (CKD-MBD), remain unclear, though uremic toxicity affecting bone quality (uremic osteoporosis) is implicated.

Purpose of the Study:

  • To review current understanding and diagnostic approaches for fragility fractures in CKD patients.
  • To highlight limitations of existing fracture risk prediction algorithms (FRAX, DeFRA) in CKD populations.
  • To discuss the utility of various imaging and biochemical markers for assessing fracture risk in CKD.

Main Methods:

  • Review of existing literature and guidelines (e.g., KDIGO) on CKD-MBD and fracture risk.
  • Discussion of diagnostic techniques including Quantitative Vertebral Morphometry (QVM), Dual-energy X-ray Absorptiometry (DXA) for Bone Mineral Density (BMD), Trabecular Bone Score (TBS), and Quantitative Computerized Tomography (QCT).
  • Evaluation of specific bone biomarkers such as parathyroid hormone (PTH) and bone alkaline phosphatase (BAP).

Main Results:

  • DXA measurement of BMD is recognized by KDIGO for fracture risk assessment in stages G3a-G5D CKD.
  • TBS provides valuable assessment of bone quality and fracture risk prediction.
  • QCT, particularly HR-pQCT, and bone biomarkers (PTH, BAP) are useful adjuncts for risk stratification in CKD-MBD patients.

Conclusions:

  • Multiple tools, including advanced imaging and biomarkers, are available for identifying CKD patients at high risk of fragility fractures.
  • Accurate interpretation by experienced clinicians is crucial for effective implementation of these diagnostic approaches.
  • Further research into pathogenic mechanisms and prospective studies are needed to refine risk prediction in this population.

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