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Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women

OBJECTIVES: To evaluate the association between fracture risk and levothyroxine use in elderly women with hypothyroidism, according to previous osteoporosis history. METHODS: We conducted a cohort study from the Korean Health Insurance Review and Assessment Service claims database from January 2005...

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Autores principales: Ko, Young-Jin, Kim, Ji Young, Lee, Joongyub, Song, Hong-Ji, Kim, Ju-Young, Choi, Nam-Kyong, Park, Byung-Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Preventive Medicine 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930806/
https://www.ncbi.nlm.nih.gov/pubmed/24570805
http://dx.doi.org/10.3961/jpmph.2014.47.1.36
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author Ko, Young-Jin
Kim, Ji Young
Lee, Joongyub
Song, Hong-Ji
Kim, Ju-Young
Choi, Nam-Kyong
Park, Byung-Joo
author_facet Ko, Young-Jin
Kim, Ji Young
Lee, Joongyub
Song, Hong-Ji
Kim, Ju-Young
Choi, Nam-Kyong
Park, Byung-Joo
author_sort Ko, Young-Jin
collection PubMed
description OBJECTIVES: To evaluate the association between fracture risk and levothyroxine use in elderly women with hypothyroidism, according to previous osteoporosis history. METHODS: We conducted a cohort study from the Korean Health Insurance Review and Assessment Service claims database from January 2005 to June 2006. The study population comprised women aged ≥65 years who had been diagnosed with hypothyroidism and prescribed levothyroxine monotherapy. We excluded patients who met any of the following criteria: previous fracture history, hyperthyroidism, thyroid cancer, or pituitary disorder; low levothyroxine adherence; or a follow-up period <90 days. We categorized the daily levothyroxine doses into 4 groups: ≤50 µg/d, 51 to 100 µg/d, 101 to 150 µg/d, and >150 µg/d. The hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated with the Cox proportional hazard model, and subgroup analyses were performed according to the osteoporosis history and osteoporosis-specific drug prescription status. RESULTS: Among 11 155 cohort participants, 35.6% had previous histories of osteoporosis. The adjusted HR of fracture for the >150 µg/d group, compared with the 51 to 100 µg/d group, was 1.56 (95% CI, 1.03 to 2.37) in osteoporosis subgroup. In the highly probable osteoporosis subgroup, restricted to patients who were concurrently prescribed osteoporosis-specific drugs, the adjusted HR of fracture for the >150 µg/d group, compared with the 51 to 100 µg/d group, was 1.93 (95% CI, 1.14 to 3.26). CONCLUSIONS: While further studies are needed, physicians should be concerned about potential levothyroxine overtreatment in elderly osteoporosis patients.
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spelling pubmed-39308062014-02-25 Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women Ko, Young-Jin Kim, Ji Young Lee, Joongyub Song, Hong-Ji Kim, Ju-Young Choi, Nam-Kyong Park, Byung-Joo J Prev Med Public Health Original Article OBJECTIVES: To evaluate the association between fracture risk and levothyroxine use in elderly women with hypothyroidism, according to previous osteoporosis history. METHODS: We conducted a cohort study from the Korean Health Insurance Review and Assessment Service claims database from January 2005 to June 2006. The study population comprised women aged ≥65 years who had been diagnosed with hypothyroidism and prescribed levothyroxine monotherapy. We excluded patients who met any of the following criteria: previous fracture history, hyperthyroidism, thyroid cancer, or pituitary disorder; low levothyroxine adherence; or a follow-up period <90 days. We categorized the daily levothyroxine doses into 4 groups: ≤50 µg/d, 51 to 100 µg/d, 101 to 150 µg/d, and >150 µg/d. The hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated with the Cox proportional hazard model, and subgroup analyses were performed according to the osteoporosis history and osteoporosis-specific drug prescription status. RESULTS: Among 11 155 cohort participants, 35.6% had previous histories of osteoporosis. The adjusted HR of fracture for the >150 µg/d group, compared with the 51 to 100 µg/d group, was 1.56 (95% CI, 1.03 to 2.37) in osteoporosis subgroup. In the highly probable osteoporosis subgroup, restricted to patients who were concurrently prescribed osteoporosis-specific drugs, the adjusted HR of fracture for the >150 µg/d group, compared with the 51 to 100 µg/d group, was 1.93 (95% CI, 1.14 to 3.26). CONCLUSIONS: While further studies are needed, physicians should be concerned about potential levothyroxine overtreatment in elderly osteoporosis patients. The Korean Society for Preventive Medicine 2014-01 2014-01-29 /pmc/articles/PMC3930806/ /pubmed/24570805 http://dx.doi.org/10.3961/jpmph.2014.47.1.36 Text en Copyright © 2014 The Korean Society for Preventive Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ko, Young-Jin
Kim, Ji Young
Lee, Joongyub
Song, Hong-Ji
Kim, Ju-Young
Choi, Nam-Kyong
Park, Byung-Joo
Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women
title Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women
title_full Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women
title_fullStr Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women
title_full_unstemmed Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women
title_short Levothyroxine Dose and Fracture Risk According to the Osteoporosis Status in Elderly Women
title_sort levothyroxine dose and fracture risk according to the osteoporosis status in elderly women
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930806/
https://www.ncbi.nlm.nih.gov/pubmed/24570805
http://dx.doi.org/10.3961/jpmph.2014.47.1.36
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