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Bone health and aldosterone excess.
L Ceccoli1, V Ronconi, L Giovannini
1Division of Endocrinology, Polytechnic University of Marche, Ospedali Riuniti "Umberto I-G.M. Lancisi-G. Salesi", Ancona, Italy.
Summary
Primary aldosteronism (PA) causes secondary hyperparathyroidism and bone loss due to increased urinary calcium. Treatment significantly reduces parathyroid hormone (PTH) and improves bone mineral density (BMD) in PA patients.
Area of Science:
- Endocrinology
- Metabolic Bone Disease
- Mineral Metabolism
Background:
- Aldosterone excess in primary aldosteronism (PA) increases urinary calcium excretion, leading to hypocalcemia and secondary hyperparathyroidism.
- This condition can result in diminished bone mineral density (BMD).
- Treatment for PA, including surgery or medication, has shown potential to reverse these effects.
Purpose of the Study:
- To investigate calcium and phosphate metabolism in PA patients compared to essential hypertension (EH).
- To assess the impact of treating aldosterone excess on bone health in PA patients.
Main Methods:
- A study involving 226 patients: 116 with PA and 110 with EH.
- Biochemical parameters and bone mass were evaluated in 40 PA patients before and after a mean 24-month follow-up post-treatment.
- Dual-energy X-ray absorptiometry (DXA) was used to assess bone mineral density.
Main Results:
- PA patients exhibited higher parathyroid hormone (PTH) levels and urinary calcium excretion, with lower serum calcium, compared to EH patients.
- Following treatment, PA patients showed significantly reduced PTH levels and improved BMD at the lumbar spine, femoral neck, and total hip.
- These improvements in BMD occurred despite stable vitamin D levels.
Conclusions:
- The findings confirm secondary hyperparathyroidism in PA, which is reversible upon effective treatment.
- Targeted treatment for PA significantly improves bone mineral density at both spinal and hip sites.
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