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(99)Tc-Methylene Diphosphonate Treatment is Safe and Efficacious for Osteoporosis in Postmenopausal Differentiated Thyroid Cancer Patients Undergoing TSH Suppression: A Three-Center Non-Randomized Clinical Study

OBJECTIVE: To investigate the effects of (99)Tc-methylene diphosphonate ((99)Tc-MDP) on osteoporosis (OS) in postmenopausal patients with differentiated thyroid cancer (DTC) under thyroid stimulating hormone (TSH) suppression. PATIENTS AND METHODS: Patients (n = 142) were divided into two groups: (1...

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Detalles Bibliográficos
Autores principales: Xie, Jianhao, Yuan, XueYu, Mao, Weiqing, Cai, Haidong, Gao, Kejia, Lv, Zhongwei, Wang, Hui, Ma, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906701/
https://www.ncbi.nlm.nih.gov/pubmed/35283644
http://dx.doi.org/10.2147/CMAR.S354471
Descripción
Sumario:OBJECTIVE: To investigate the effects of (99)Tc-methylene diphosphonate ((99)Tc-MDP) on osteoporosis (OS) in postmenopausal patients with differentiated thyroid cancer (DTC) under thyroid stimulating hormone (TSH) suppression. PATIENTS AND METHODS: Patients (n = 142) were divided into two groups: (1) (99)Tc-MDP (n = 70) and (2) alendronate (n = 72) treatments (NCT 02304757). Bone mineral density (BMD) in the lumbar spine and hip was evaluated by DXA, along with bone turnover markers, safety, and quality of life (QOL) using SF-36 at three time points: before treatment and at 6 and/or 12 months after treatment. RESULTS: The percentage change of BMD in total lumbar spine or hip showed no significant difference throughout the study (P > 0.025). (99)Tc-MDP and alendronate treatment alone significantly increased BMD in the lumbar spine, but alendronate treatment also significantly increased BMD in total hip at 6 and 12 months, as compared with the baseline. There were no significant differences in the results of the SF-36 scores between the two treatment groups at any time during the whole study period. (99)Tc-MDP significantly increased bone formation markers of osteocalcin at 6 and 12 months (P all < 0.05), PINP at 12 months (P = 0.001), and bone resorption markers of β-CTX at 6 and 12 months (p < 0.05) as compared with the alendronate treated group. No adverse event was observed in the (99)Tc-MDP treatment group compared with alendronate (P = 0.014). CONCLUSION: (99)Tc-MDP was as efficacious as alendronate in the improvement of lumbar BMD for DTC patients with OS under TSH stimulation. (99)Tc-MDP was shown to be safe and improved patients’ QOL.