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Evaluation of Serum and Urine Biomarker Panels for Developmental Dysplasia of the Hip Prior to Onset of Secondary Osteoarthritis. | LitMetric

AI Article Synopsis

  • - The study aimed to evaluate serum and urine biomarker panels to distinguish between healthy hip individuals and those with developmental dysplasia of the hip (DDH) to help predict secondary hip osteoarthritis (OA) in young adults.
  • - Researchers collected and analyzed samples from individuals with DDH and healthy controls, finding that specific biomarker panels could effectively differentiate between the two groups, with the best-performing panel showing a high Area Under Curve (AUC) score of 0.959.
  • - The findings suggest that these biomarker panels could be clinically useful for early diagnosis and monitoring of DDH, providing a cost-effective screening method for at-risk populations.

Article Abstract

Objective: Evaluate serum and urine biomarker panels for their capabilities in discriminating between individuals (13- to 34-years-olds) with healthy hips versus those with developmental dysplasia of the hip (DDH) prior to diagnosis of secondary hip osteoarthritis (OA).

Design: Urine and serum were collected from individuals (15-33 years old) with DDH, prior to and following diagnosis of hip OA, and from age-matched healthy-hip controls. Samples were analyzed for panels of protein biomarkers with potential for differentiation of hip status using receiver operator characteristic curve (area under curve [AUC]) assessments.

Results: Multiple urine and serum biomarker panels effectively differentiated individuals with DDH from healthy-hip controls in a population at risk for developing secondary hip OA with the best performing panel demonstrating an AUC of 0.959. The panel comprised of two serum and two urinary biomarkers provided the highest combined values for sensitivity, 0.85, and specificity, 1.00, while a panel of four serum biomarkers provided the highest sensitivity, 0.93, while maintaining adequate specificity, 0.71.

Conclusion: Results of this study indicate that panels of protein biomarkers measured in urine and serum may be able to differentiate young adults with DDH from young adults with healthy hips. These data suggest the potential for clinical application of a routine diagnostic method for cost-effective and timely screening for DDH in at-risk populations. Further development and validation of these biomarker panels may result in highly sensitive and specific tools for early diagnosis, staging, and prognostication of DDH, as well as treatment decision making and monitoring capabilities.

Level Of Evidence: III.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11368892PMC
http://dx.doi.org/10.1177/19476035231163032DOI Listing

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