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Circulating IL-17A Levels in Postmenopausal Women with Primary Hyperparathyroidism.
E Dozio1, E Passeri2, E Vianello1
1Department of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Mediators of Inflammation
|April 8, 2020
Summary
Interleukin-17A (IL-17A) levels in postmenopausal women with primary hyperparathyroidism (PHPT) were similar to controls, suggesting a potential osteogenic effect of IL-17A in PHPT, despite a disrupted relationship with bone metabolism markers.
Area of Science:
- Endocrinology
- Immunology
- Bone Biology
Background:
- Primary hyperparathyroidism (PHPT) is a common cause of secondary osteoporosis in postmenopausal women.
- Th17 lymphocytes and their cytokine IL-17A are implicated in bone metabolism and can be activated by parathyroid hormone (PTH).
- Elevated IL-17A mRNA has been observed in peripheral blood T cells of PHPT patients.
Purpose of the Study:
- To investigate circulating IL-17A levels and the RANKL/OPG ratio as markers of osteoclastogenesis.
- To compare these markers in postmenopausal women with PHPT versus those with non-PHPT osteoporosis.
Main Methods:
- Assessed circulating IL-17A levels and the soluble RANKL/OPG ratio in 50 postmenopausal PHPT women and 20 postmenopausal non-PHPT osteoporotic women.
- Correlated IL-17A levels with PTH, ionized calcium, urine calcium, and bone mineral density (femur neck and total hip T-scores).
Main Results:
- Circulating IL-17A levels were comparable between PHPT and non-PHPT osteoporotic postmenopausal women.
- IL-17A levels did not correlate with PTH but showed negative correlations with ionized calcium and urine calcium.
- IL-17A levels positively correlated with femur neck and total hip T-scores in PHPT women.
- No significant correlation was found between IL-17A and sRANKL, OPG, or the sRANKL/OPG ratio in PHPT women.
Conclusions:
- Circulating IL-17A levels are similar in postmenopausal PHPT and non-PHPT osteoporotic women.
- The relationship between PTH, IL-17A, and bone demineralization is disrupted in postmenopausal PHPT.
- Findings suggest a potential osteogenic role for IL-17A in postmenopausal PHPT.
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