Key result
Post-polio patients with osteoporosis exhibited a significantly smaller reduction in osteocalcin (mean difference 9.01 ng/ml) following at least six months of bisphosphonate treatment compared to non-polio controls.
Why the study?
Levels of bone biomarkers and the response of bone turnover markers to bisphosphonates were unknown in post-polio patients with osteoporosis.
Does bisphosphonate treatment reduce bone turnover markers in post-polio patients with osteoporosis compared to non-polio controls?
Observational (n=56)
No
Does bisphosphonate treatment reduce bone turnover markers in post-polio patients with osteoporosis compared to non-polio controls?
Bisphosphonate treatment significantly reduces bone turnover markers in post-polio patients with osteoporosis, though to a lesser extent than in non-polio controls, indicating these markers are useful for monitoring treatment response.
Bone biomarker profiles in post-polio osteoporosis remain incompletely defined; leaves open whether bisphosphonate responses differ from other populations.
Introduction: Osteoporosis is common in post-polio clinic patients, and is reported in 30%to 50% of middle-aged individuals with previous polio. The levels of bone biomarkers (calcium regulating hormones, bone metabolism markers, and bone turnover markers), and the response of bone turnover markers to bisphosphonates is unknown in post-polio patients with osteoporosis. Objectives: 1) To describe serum levels of bone biomarkers in post-polio clinic patients with osteoporosis and compare these levels to those in controls with osteoporosis without neurological disease. 2) To examine the change in serum levels of bone biomarkers in post-polio patients following at least six months of treatment with bisphosphonates and compare these changes to controls. Methods: We conducted a retrospective chart review of Post-Polio and Bone Metabolism Clinic charts of our center. Patients without osteoporosis, and incomplete lab data were excluded. For the second objective, patients untreated with bisphosphonates were excluded. Results: Mean age and proportion of females were similar in post-polio patients (n=25) and controls (n=31) (66.3 ± 8.1 vs 66.2 ± 10.9 years, 52% vs 61%). Mean baseline serum levels of calcium, calcium regulating hormones [parathyroid hormone (PTH), 25-hydroxy Vitamin D), and serum bone turnover makers (sBTM's; osteocalcin, C-telopeptide, non-specific alkaline phosphatase (ALP)] were normal. PTH (4.4 ± 1.7 vs 5.5 ± 2.3 pmol/L, p=0.05), ALP (63.9 ± 15.8 vs 76.2 ± 26.7 U/L, p=0.04), osteocalcin (18.3 ± 8.8 vs 26.9 ± 8.4 ng/ml, p<0.01), and C-telopeptide (0.35 ± 0.2 vs 0.55 ± 0.21 microgram/L, p=0.01) were significantly lower in post-polio patients. After ≥ six months of treatment with bisphosphonates, sBTM's declined significantly in both groups, with a significantly greater reduction in controls for osteocalcin (p<0.01) and C-telopeptide (p=0.02). Conclusions: While mean levels of all evaluated bone biomarkers were normal, PTH and sBTMs were significantly lower in post-polio patients with osteoporosis compared to controls, indicating reduced bone turnover. With bisphosphonate treatment, osteocalcin and C-telopeptide declined significantly in both groups, but significantly more in controls than in post-polio patients. These results indicate that BTM's could be useful for monitoring treatment response in post-polio patients.
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Madani et al. (2025) conducted an observational in Osteoporosis in post-polio patients (n=56). Post-polio syndrome (with bisphosphonate treatment) vs. Non-polio controls (with bisphosphonate treatment) was evaluated on Change in osteocalcin levels after ≥6 months of bisphosphonate treatment (MD 9.01 ng/ml, 95% CI 4.22-13.81, p=<0.01). Post-polio patients with osteoporosis exhibited a significantly smaller reduction in osteocalcin (mean difference 9.01 ng/ml) following at least six months of bisphosphonate treatment compared to non-polio controls.
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