A. Siddiqi et al., A LONGITUDINAL-STUDY OF MARKERS OF BONE TURNOVER IN GRAVES-DISEASE AND THEIR VALUE IN PREDICTING BONE-MINERAL DENSITY, The Journal of clinical endocrinology and metabolism, 82(3), 1997, pp. 753-759
Whether biochemical markers can predict improvement in reduced bone mi
neral density (BMD) associated with thyrotoxicosis is unclear. We inve
stigated the relationship between serum osteocalcin (OC), bone-specifi
c alkaline phosphatase (b-ALP), serum deoxypyridinoline (Sdpd) and pyr
idinoline (Spyr), 24-hour urinary deoxypyridinoline (Udpd), and BMD in
17 thyrotoxic patients during 1 yr of treatment. Coinciding with euth
yroidism at 4-8 weeks, there was a peak in b-ALP and OC and a prompt f
all into the normal range in Udpd and Sdpd, but not Spyr, levels. Mean
b-ALP continued to be raised at week 52 when it was inversely correla
ted with BMD. Mean BMD rose approximately 6%, P < 0.01, over 1 yr. Cou
pling indices were calculated as a measure of bone balance and, at dia
gnosis, was [minus4.26 in favor of bone resorption and rose viith trea
tment in favor of bone formation: weeks 2: -0.23; 4: +4.01; 8: +4.37;
12: +4.44; 24: +2.32; and 52: +1.56.Bone turnover is balanced within 2
weeks of starting treatment for thyrotoxicosis. Udpd accurately indic
ates thyrotoxic bone resorption. Serum b-ALP indicates continuing bone
formation and, at 1 yr, may provide a marker for low BMD. OC, Sdpd, a
nd Spyr are less sensitive in documenting bone remodeling during treat
ment of thyrotoxicosis.