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Division of Nephrology and Internal Medicine (J.T.M.), the Section of Clinical Chemistry (G.G.K., P.C.K.) Rochester, Minnesota 55905
The Division of Endocrinology, Metabolism, and Internal Medicine (S.F.H), Mayo Clinic and Mayo Foundation Rochester, Minnesota 55905
Address requests for reprints to: Dr. J. T. McCarthy, Division of Nephrology and Internal Medicine, Mayo Clinic, 200 First Street SW, Rochester, Minnesota 55905.
In 41 hemodialysis patients with bone disease (histological diagnosis with histomorphometric confirmation of PTH activity) results from a serum immunoreactive PTH (iPTH) assay correlated with results from a new serum bioactive PTH (bio-PTH) assay (r = 0.84; P < 0.001). The serum bio-PTH values correlated well with osteoclast numbers (r = 0.70; P < 0.001), resorption surfaces (r = 0.55; P < 0.001), and presence of marrow fibrosis (P < 0.02). The serum iPTH values also correlated with osteoclast numbers (r = 0.61; P < 0.001), resorption surfaces (r = 0.47; P < 0.003), and presence of marrow fibrosis (P < 0.02). Serum bio-PTH and iPTH values were higher in patients with severe hyperparathyroidism than in other patients. The assays were equally useful in identifying dialysis patients with severe hyperparathyroidism. Patients with osteomalacia or low turnover bone disease had low serum bio-PTH and/or iPTH values. Low bio-PTH values (
3.6 pmol/L) had a sensitivity and a specificity of 93% for osteomalacia or low turnover bone disease. Low bio-PTH values also were useful in identifying those patients with positive aluminum staining in bone. The serum bio-PTH assay was useful in identifying patients with osteomalacia, low turnover bone disease, or aluminum accumulation.
* Copyright 1988 The Endocrine Society.
Received February 4, 1988.
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