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KMID : 1141520210360040895
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Endocrinology and Metabolism
2021 Volume.36 No. 4 p.895 ~ p.903
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Comparison of the Effects of Various Antidiabetic Medication on Bone Mineral Density in Patients with Type 2 Diabetes Mellitus
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Ha Jeong-Hoon
Lim Ye-Jee
Kim Mee-Kyoung
Kwon Hyuk-Sang
Song Ki-Ho
Ko Seung-Hyun
Kang Moo-Il
Moon Sung-Dae
Baek Ki-Hyun
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Abstract
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Background: Prospective comparative studies on the effects of various antidiabetic agents on bone metabolism are limited. This study aimed to assess changes in bone mass and biochemical bone markers in postmenopausal patients with type 2 diabetes mellitus (T2DM).
Methods: This prospective, multicenter, open-label, comparative trial included 264 patients with T2DM. Patients who had received a metformin, or sulfonylurea/metformin combination (Group 1); a thiazolidinedione combination (Group 2); a dipeptidyl peptidase-4 inhibitor (gemigliptin) combination (Group 3); or an sodium-glucose cotransporter 2 inhibitor (empagliflozin) combination (Group 4) were prospectively treated for 12 months; bone mineral density (BMD) and bone turnover marker (BTM) changes were evaluated.
Results: The femoral neck BMD percentage changes were ?0.79%±2.86% (Group 1), ?2.50%±3.08% (Group 2), ?1.05%±2.74% (Group 3), and ?1.24%±2.91% (Group 4) (P<0.05). The total hip BMD percentage changes were ?0.57%±1.79% (Group 1), ?1.74%±1.48% (Group 2), ?0.75%±1.87% (Group 3), and ?1.27%±1.72% (Group 4) (P<0.05). Mean serum BTM (C-terminal type 1 collagen telopeptide and procollagen type 1 amino-terminal propeptide) levels measured during the study period did not change over time or differ between groups.
Conclusion: Significant bone loss in the femoral neck and total hip was associated with thiazolidinedione combination regimens. However, bone loss was not significantly associated with combination regimens including gemigliptin or empagliflozin. Caution should be exercised during treatment with antidiabetic medications that adversely affect the bone in patients with diabetes at a high risk of bone loss.
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KEYWORD
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Osteoporosis, Diabetes mellitus, Bone density, Thiazolidinediones, Sodium-glucose transporter 2 inhibitors
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