MARKERS OF BONE TURNOVER IN HYPERTHYROIDISM AND THE EFFECTS OF TREATMENT

Citation
P. Garnero et al., MARKERS OF BONE TURNOVER IN HYPERTHYROIDISM AND THE EFFECTS OF TREATMENT, The Journal of clinical endocrinology and metabolism, 78(4), 1994, pp. 955-959
Citations number
31
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
0021972X
Volume
78
Issue
4
Year of publication
1994
Pages
955 - 959
Database
ISI
SICI code
0021-972X(1994)78:4<955:MOBTIH>2.0.ZU;2-M
Abstract
Serum osteocalcin (OC) and bone-specific alkaline phosphatase (B-ALP), reflecting bone formation, and urinary pyridinoline cross-link (Pyr) excretion, reflecting bone resorption, have been measured in 27 patien ts with hyperthyroidism and 30 age-matched controls using direct and n ovel immunoassays. Hyperthyroid patients had higher (P < 0.001) levels of all 3 markers compared with control values: Pyr, 246 +/- 181 nmol/ mmol creatinine us. 40 +/- 12 (+515%); OC, 55 +/- 23 vs. 23 +/- 7.4 mu g/L (+139%); and B-ALP, 22 +/- 17 vs. 10.0 +/- 5.0 mu g/L (+120%). OC and Pyr levels were elevated above the normal range in most patients and were significantly correlated with serum free T-3 concentrations ( r = 0.53; P < 0.01 and r = 0.76; P < 0.001; for OC and Pyr, respective ly). B-ALP levels were elevated in 11 of the 27 patients and did not c orrelate with serum thyroid hormone concentrations. After therapy for hyperthyroidism, Pyr and OC levels returned to normal within 1 month, whereas B-ALP transiently increased after 1 month before falling to ba seline levels. The relapse of hyperthyroidism observed in 1 patient wa s associated with a steep increase in bone markers. These results indi cate that Pyr, measured using a new and convenient immunoassay, is a h ighly sensitive marker for altered bone metabolism in hyperthyroidism. The increases in OC and B-ALP were less impressive, suggesting an imb alance between resorption and formation with subsequent rapid bone los s in untreated hyperthyroidism. OC and B-ALP also appear to reflect di fferent aspects of osteoblast metabolism during the treatment of hyper thyroid patients.