Risk of Fracture with Thiazolidinediones: Disease or Drugs?

被引:19
作者
Bazelier, Marloes T.
Vestergaard, Peter [2 ]
Gallagher, Arlene M. [3 ]
van Staa, Tjeerd-Pieter [3 ,4 ]
Cooper, Cyrus [4 ,5 ]
Leufkens, Hubert G. M.
de Vries, Frank [1 ,4 ,6 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Pharmacoepidemiol & Clin Pharmacol, NL-3584 CG Utrecht, Netherlands
[2] Aarhus Univ Hosp, Osteoporosis Clin, DK-8000 Aarhus, Denmark
[3] Med & Healthcare Prod Regulatory Agcy, Gen Practice Res Database, London, England
[4] Univ Southampton, MRC Lifecourse Epidemiol Unit, Southampton, Hants, England
[5] Univ Oxford, Inst Musculoskeletal Sci, Oxford, England
[6] Maastricht Univ, Med Ctr, Dept Clin Pharm & Toxicol, Maastricht, Netherlands
基金
英国医学研究理事会;
关键词
Thiazolidinedione; Type 2 diabetes mellitus; Fracture risk; Osteoporosis; BONE-MINERAL DENSITY; DIABETES-MELLITUS; OSTEOBLAST; TYPE-1; PIOGLITAZONE; INSULIN; WOMEN;
D O I
10.1007/s00223-012-9591-8
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
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 ( = 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 similar to CI 1.13-1.18) and second (HR = 1.00, 95 similar to 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.
引用
收藏
页码:450 / 457
页数:8
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