Title of article :
Circulating Serum Amyloid A, hs-CRP and Vitamin D Levels in Postmenopausal Osteoporosis Running
Author/Authors :
Safari, Anahid Stem Cells Technology Research Center - Shiraz University of Medical Sciences , Borhani-Haghighi, Afshin Clinical Neurology Research Center - Shiraz University of Medical Sciences , Dianatpour, Mehdi Stem Cells Technology Research Center - Shiraz University of Medical Sciences , Heydari, Taghi Health Policy Research Center - Shiraz University of Medical Sciences , Foroughinia, Farzaneh Clinical Neurology Research Center - Shiraz University of Medical Sciences , Ranjbar Omrani, Gholamhossein Endocrinology & Metabolism Research Center - Shiraz University of Medical Sciences
Abstract :
Background: Both vitamin D and inflammation were investigated as important players in the
pathogenesis of postmenopausal osteoporosis. This study compared vitamin D, inflammatory
the biomarkers serum levels and their association with bone mineral density (BMD) in case
and control groups to evaluate the possible immune-regulatory effect of vitamin D in this
population. Materials and Methods: Participants in post-menopausal age, were categorized
to 44 osteoporotic vs. 44 healthy aged-matched women according to WHO criteria. Total
BMD, T- scores, Z-scores as well as fracture risk were measured in both groups, using Hologic
system Dual-energy X-ray absorptiometry (DEXA). Serum 25-OH vitamin D, high sensitive
CRP (hs-CRP) and serum amyloid A (SAA) were compared between groups. The association
between serum biomarkers level and BMD were also investigated. The same evaluations were
performed for vitamin D deficient (<20 ng/mL) and non-deficient (≥20 ng/mL) subgroups.
Results: Vitamin D deficiency was higher in the osteoporotic group (32.6%) in comparison
with the control group (25.6%), but the differences were not significant (P=0.47). There were
no significant differences in serum levels of hs-CRP and SAA (P=0.83 and P=0.39) as well.
No significant association between serum inflammatory biomarkers, vitamin D, and BMD
were detected (P≥0.05). The results were the same for vitamin D deficient and non-deficient
subgroups (P≥0.05). Conclusion: In the current study, the beneficial effects of vitamin D as a
result of its immune-regulatory mechanisms was not reached. Larger scale studies might pave
the way to define vitamin D benefits in postmenopausal osteoporosis.
Keywords :
Osteoporosis , Postmenopausal , Vitamin D C , Reactive Protein , Serum Amyloid A Protein , Bone Density
Journal title :
Galen Medical Journal (GMJ)