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Risk of Fracture with Thiazolidinediones: Disease or Drugs?

The use of thiazolidinediones (TZDs) has been associated with an increased fracture risk. In addition, type 2 diabetes mellitus (T2DM) has been linked with fracture. We evaluated to what extent the association between TZD use and fracture risk is related to the drug or to the underlying disease. We...

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Autores principales: Bazelier, Marloes T., Vestergaard, Peter, Gallagher, Arlene M., van Staa, Tjeerd-Pieter, Cooper, Cyrus, Leufkens, Hubert G. M., de Vries, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349019/
https://www.ncbi.nlm.nih.gov/pubmed/22488176
http://dx.doi.org/10.1007/s00223-012-9591-8
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author Bazelier, Marloes T.
Vestergaard, Peter
Gallagher, Arlene M.
van Staa, Tjeerd-Pieter
Cooper, Cyrus
Leufkens, Hubert G. M.
de Vries, Frank
author_facet Bazelier, Marloes T.
Vestergaard, Peter
Gallagher, Arlene M.
van Staa, Tjeerd-Pieter
Cooper, Cyrus
Leufkens, Hubert G. M.
de Vries, Frank
author_sort Bazelier, Marloes T.
collection PubMed
description The use of thiazolidinediones (TZDs) has been associated with an increased fracture risk. In addition, type 2 diabetes mellitus (T2DM) has been linked with fracture. We evaluated to what extent the association between TZD use and fracture risk is related to the drug or to the underlying disease. We conducted a population-based cohort study using the Danish National Health Registers (1996–2007), which link pharmacy data to the national hospital registry. Oral antidiabetic users (n = 180,049) were matched 1:3 by year of birth and sex to nonusers. Cox proportional hazards models were used to estimate hazard ratios (HRs) of fracture. Time-dependent adjustments were made for age, comorbidity, and drug use. We created a proxy indicator for the severity of disease. The first stage was defined as current use of either a biguanide or a sulfonyluerum, the second stage as current use of a biguanide and a sulfonyluerum at the same time, the third stage as patients using TZDs, and the fourth stage as patients using insulin. The risk of osteoporotic fracture was increased 1.3-fold for stages 3 and 4 compared with controls. Risk with current TZD use (stage 3 HR = 1.27, 95 % CI 1.06–1.52) and risk with current use of insulin (stage 4 HR = 1.25, 95 % CI 1.20–1.31) were similar. In the first (HR = 1.15, 95 % CI 1.13–1.18) and second (HR = 1.00, 95 % CI 0.96–1.04) stages risks were lower. Risk of osteoporotic fracture was similar for TZD users and insulin users. When studying fracture risk with TZDs, the underlying T2DM should be taken into account.
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spelling pubmed-33490192012-05-30 Risk of Fracture with Thiazolidinediones: Disease or Drugs? Bazelier, Marloes T. Vestergaard, Peter Gallagher, Arlene M. van Staa, Tjeerd-Pieter Cooper, Cyrus Leufkens, Hubert G. M. de Vries, Frank Calcif Tissue Int Original Research The use of thiazolidinediones (TZDs) has been associated with an increased fracture risk. In addition, type 2 diabetes mellitus (T2DM) has been linked with fracture. We evaluated to what extent the association between TZD use and fracture risk is related to the drug or to the underlying disease. We conducted a population-based cohort study using the Danish National Health Registers (1996–2007), which link pharmacy data to the national hospital registry. Oral antidiabetic users (n = 180,049) were matched 1:3 by year of birth and sex to nonusers. Cox proportional hazards models were used to estimate hazard ratios (HRs) of fracture. Time-dependent adjustments were made for age, comorbidity, and drug use. We created a proxy indicator for the severity of disease. The first stage was defined as current use of either a biguanide or a sulfonyluerum, the second stage as current use of a biguanide and a sulfonyluerum at the same time, the third stage as patients using TZDs, and the fourth stage as patients using insulin. The risk of osteoporotic fracture was increased 1.3-fold for stages 3 and 4 compared with controls. Risk with current TZD use (stage 3 HR = 1.27, 95 % CI 1.06–1.52) and risk with current use of insulin (stage 4 HR = 1.25, 95 % CI 1.20–1.31) were similar. In the first (HR = 1.15, 95 % CI 1.13–1.18) and second (HR = 1.00, 95 % CI 0.96–1.04) stages risks were lower. Risk of osteoporotic fracture was similar for TZD users and insulin users. When studying fracture risk with TZDs, the underlying T2DM should be taken into account. Springer-Verlag 2012-04-10 2012 /pmc/articles/PMC3349019/ /pubmed/22488176 http://dx.doi.org/10.1007/s00223-012-9591-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Research
Bazelier, Marloes T.
Vestergaard, Peter
Gallagher, Arlene M.
van Staa, Tjeerd-Pieter
Cooper, Cyrus
Leufkens, Hubert G. M.
de Vries, Frank
Risk of Fracture with Thiazolidinediones: Disease or Drugs?
title Risk of Fracture with Thiazolidinediones: Disease or Drugs?
title_full Risk of Fracture with Thiazolidinediones: Disease or Drugs?
title_fullStr Risk of Fracture with Thiazolidinediones: Disease or Drugs?
title_full_unstemmed Risk of Fracture with Thiazolidinediones: Disease or Drugs?
title_short Risk of Fracture with Thiazolidinediones: Disease or Drugs?
title_sort risk of fracture with thiazolidinediones: disease or drugs?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349019/
https://www.ncbi.nlm.nih.gov/pubmed/22488176
http://dx.doi.org/10.1007/s00223-012-9591-8
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