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Borderline-low serum thyrotropin level is correlated with increased fasting urinary hydroxyproline excretion
1Bone and Mineral Division, Henry Ford Hospital, Detroit, Mich. 48202-2689.
Archives of Internal Medicine
|February 1, 1992
Summary
Even slightly elevated thyroid hormones can increase bone turnover and accelerate bone loss. Fasting urinary total hydroxyproline-creatinine excretion (THP/Cr) can detect these changes, indicating potential bone density issues.
Area of Science:
- Endocrinology
- Bone Metabolism
- Biochemistry
Background:
- Thyroid hormones significantly influence bone metabolism.
- Hyperthyroidism accelerates bone loss primarily through increased bone resorption.
- Subtle alterations in thyroid hormone status may impact bone turnover.
Purpose of the Study:
- To investigate the relationship between thyroid hormone status and bone turnover.
- To assess if fasting urinary total hydroxyproline-creatinine excretion (THP/Cr) can serve as a noninvasive marker for detecting changes in bone turnover related to thyroid status.
Main Methods:
- Retrospective analysis of ambulatory patients with thyroid function tests and THP/Cr measurements.
- Patients were categorized based on serum thyrotropin (TSH) levels.
- Correlation analysis between TSH levels, THP/Cr, and serum alkaline phosphatase.
Main Results:
- No correlation between TSH and THP/Cr was observed in patients with TSH > 1.0 mU/L.
- Patients with suppressed TSH (< 0.1 mU/L) showed elevated THP/Cr, consistent with hyperthyroidism.
- A significant negative correlation between TSH and THP/Cr was found in patients with TSH levels between 0.1 and 1.0 mU/L.
- THP/Cr positively correlated with serum alkaline phosphatase, indicating increased bone turnover.
Conclusions:
- Minimal excess of thyroid hormones, even within the low-normal or borderline range, is associated with increased bone turnover.
- These findings support the hypothesis that subtle thyroid hormone imbalances contribute to accelerated bone loss.
- Urinary THP/Cr is a sensitive marker for detecting thyroid hormone-induced changes in bone resorption.