Diagnostic utility of serum TRACP5b for secondary osteoporosis in ankylosing spondylitis: a comparative cross-sectional study with primary osteoporosis and healthy controls - Report - MDSpire
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Diagnostic utility of serum TRACP5b for secondary osteoporosis in ankylosing spondylitis: a comparative cross-sectional study with primary osteoporosis and healthy controls
Serum TRACP5b as a Diagnostic Marker for Secondary Osteoporosis in Ankylosing Spondylitis
Overview
This cross-sectional study evaluated serum TRACP5b levels in patients with ankylosing spondylitis (AS)-associated secondary osteoporosis compared to primary osteoporosis and healthy controls. Findings demonstrated that TRACP5b is elevated in AS patients with osteoporosis and correlates with disease activity and bone mineral density, supporting its potential as a diagnostic biomarker.
Background
Osteoporosis is characterized by reduced bone mineral density (BMD) and increased fracture risk, classified as primary or secondary based on etiology. Ankylosing spondylitis (AS) is an inflammatory rheumatic disease causing both new bone formation and bone loss, leading to secondary osteoporosis. Dual-energy X-ray absorptiometry (DXA) is the standard for BMD assessment but does not capture dynamic bone turnover changes. Tartrate-resistant acid phosphatase 5b (TRACP5b), a marker of osteoclast activity, may provide complementary information on bone resorption in AS.
Data Highlights
Group
Participants (n)
Median TRACP5b (units)
BMD Sites Assessed
AS Disease Activity (BASDAI)
Ankylosing Spondylitis (AS)
23
Elevated vs controls
Lumbar spine, femoral neck, wrist
Reported (median values)
Primary Osteoporosis
24
Elevated vs controls
Lumbar spine, femoral neck, wrist
Not applicable
Healthy Controls
20
Lowest levels
Lumbar spine, femoral neck, wrist
Not applicable
Key Findings
Serum TRACP5b levels were significantly higher in AS patients with secondary osteoporosis compared to healthy controls.
TRACP5b levels correlated positively with disease activity measured by BASDAI in AS patients.
TRACP5b showed diagnostic utility in distinguishing secondary osteoporosis in AS from primary osteoporosis and healthy states, with favorable sensitivity and specificity.
BMD was reduced in AS patients, consistent with secondary osteoporosis, despite the presence of new bone formation in AS pathology.
TRACP5b measurement provides dynamic insight into osteoclast-mediated bone resorption not captured by DXA alone.
Clinical Implications
Serum TRACP5b may serve as a valuable biomarker to complement DXA in diagnosing and monitoring secondary osteoporosis in AS patients. Its correlation with disease activity suggests it could aid in assessing bone metabolic changes related to inflammation. Incorporating TRACP5b testing could improve fracture risk stratification and guide therapeutic decisions in this population.
Conclusion
Serum TRACP5b is a promising diagnostic marker reflecting osteoclast activity and bone resorption in ankylosing spondylitis-associated secondary osteoporosis. It enhances understanding of bone metabolism beyond static BMD measurements and may improve clinical management of osteoporosis in AS.