Ann Surg Treat Res.  2014 Feb;86(2):55-60. 10.4174/astr.2014.86.2.55.

Bone mineral density and bone turnover markers in patients on long-term suppressive levothyroxine therapy for differentiated thyroid cancer

Affiliations
  • 1Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
  • 2Department of Surgery, Yonsei University Wonju College of Medicine, Wonju, Korea. mdkang@yonsei.ac.kr
  • 3Institute of Life-Long Health, Yonsei University Wonju College of Medicine, Wonju, Korea.

Abstract

PURPOSE
Current management for patients with differentiated thyroid cancer includes near total thyroidectomy and radioactive iodine therapy followed by administration of supraphysiological doses of levothyroxine (L-T4). Although hyperthyroidism is a well known risk factor for osteoporosis, the effects of L-T4 treatment on bone mineral density (BMD) in patients with thyroid cancer do not appear to be as significant as with endogenous hyperthyroidism. In this study, we evaluated the impact of long-term suppressive therapy with L-T4 on BMD and bone turn over markers in Korean female patients receiving L-T4 suppressive therapy.
METHODS
We enrolled 94 female subjects (mean age, 50.84 +/- 11.43 years) receiving L-T4 after total or near total thyroidectomy and radioactive iodine therapy for thyroid cancer (mean follow-up period, 12.17 +/- 4.27 years). The subjects were divided into three groups by thyroid stimulating hormone (TSH) level (group 1 with TSH level < or =0.001 microIU/mL, group 2 with TSH level between 0.001 and 0.17 microIU/mL, group 3 with TSH level >0.17 microIU/mL) and four groups by quartile of free T4 level. L-T4 dosage, BMD (examined by dual-energy x-ray absorptiometry), and bone turnover markers were evaluated according to TSH and free T4 levels.
RESULTS
No significant decrease was detected in BMD or bone turnover markers according to TSH level or free T4 level. Also, the prevalence of osteoporosis and osteopenia was not different among groups.
CONCLUSION
Long-term L-T4 suppressive therapy after thyroid cancer management did not affect bone density or increase the prevalence of osteoporosis even though TSH levels were supraphysiologically suppressed.

Keyword

Thyroid neplasms; Levothyroxine; Bone mineral density; Osteoporosis; Osteopenia

MeSH Terms

Bone Density*
Bone Diseases, Metabolic
Female
Follow-Up Studies
Humans
Hyperthyroidism
Iodine
Osteoporosis
Prevalence
Risk Factors
Thyroid Gland*
Thyroid Neoplasms*
Thyroidectomy
Thyrotropin
Thyroxine*
Iodine
Thyrotropin
Thyroxine

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Change of Bone Mineral Density and Biochemical Markers of Bone Turnover in Patients on Suppressive Levothyroxine Therapy for Differentiated Thyroid Carcinoma
Chei Won Kim, Seokbo Hong, Se Hwan Oh, Jung Jin Lee, Joo Young Han, Seongbin Hong, So Hun Kim, Moonsuk Nam, Yong Seong Kim
J Bone Metab. 2015;22(3):135-141.    doi: 10.11005/jbm.2015.22.3.135.

Effects of Thyrotropin Suppression on Bone Health in Menopausal Women with Total Thyroidectomy
Eun Heui Kim, Yun Kyung Jeon, Kyoungjune Pak, In-Joo Kim, Seong-Jang Kim, Seunghyeon Shin, Bo Hyun Kim, Sang Soo Kim, Byung-Joo Lee, Jeong-Gyu Lee, Tae Sik Goh, Keunyoung Kim
J Bone Metab. 2019;26(1):31-38.    doi: 10.11005/jbm.2019.26.1.31.

TSH Suppression after Differentiated Thyroid Cancer Surgery and Osteoporosis
Kyoung Sik Park
Korean J Endocr Surg. 2016;16(1):1-5.    doi: 10.16956/kjes.2016.16.1.1.

Bone Mineral Density in Thyroid Cancer Patients: Data from the Korea National Health and Nutrition Examination Survey
Myung-Chul Chang
J Endocr Surg. 2017;17(4):153-159.    doi: 10.16956/jes.2017.17.4.153.

Evaluation and Management of Bone Health in Patients with Thyroid Diseases: a Position Statement from the Korean Thyroid Association
A Ram Hong, Hwa Young Ahn, Bu Kyung Kim, Seong Hee Ahn, So Young Park, Min-Hee Kim, Jeongmin Lee, Sun Wook Cho, Ho-Cheol Kang
Int J Thyroidol. 2022;15(1):1-16.    doi: 10.11106/ijt.2022.15.1.1.

Evaluation and Management of Bone Health in Patients with Thyroid Diseases: A Position Statement of the Korean Thyroid Association
A Ram Hong, Ho-Cheol Kang
Endocrinol Metab. 2023;38(2):175-189.    doi: 10.3803/EnM.2023.1701.


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