Association of thiazolidinediones with liver cancer and colorectal cancer in type 2 diabetes mellitus

被引:155
作者
Chang, Chia-Hsuin [2 ,3 ]
Lin, Jou-Wei [3 ,4 ]
Wu, Li-Chiu [1 ]
Lai, Mei-Shu [1 ]
Chuang, Lee-Ming [2 ,3 ]
Arnold Chan, K. [5 ]
机构
[1] Natl Taiwan Univ, Inst Prevent Med, Coll Publ Hlth, Taipei 10764, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[3] Natl Taiwan Univ, Dept Med, Coll Med, Taipei 10764, Taiwan
[4] Natl Taiwan Univ Hosp, Ctr Cardiovasc, Yun Lin Branch, Dou Liou City, Yun Lin County, Taiwan
[5] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
ACTIVATED RECEPTOR-GAMMA; CELL LUNG-CANCER; PEGYLATED INTERFERON ALPHA-2A; CHRONIC HEPATITIS-C; LONG-TERM SURVIVAL; PPAR-GAMMA; HEPATOCELLULAR-CARCINOMA; COLON-CANCER; MYOCARDIAL-INFARCTION; PHYSICAL-ACTIVITY;
D O I
10.1002/hep.25509
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The objective of this nationwide case-control study was to evaluate the risk of specific malignancy in diabetic patients who received thiazolidinediones (TZDs). A total of 606,583 type 2 diabetic patients, age 30 years and above, without a history of cancer were identified from the Taiwan National Health Insurance claims database during the period between January 1 2000 and December 31 2000. As of December 31 2007, patients with incident cancer of liver, colorectal, lung, and urinary bladder were included as cases and up to four age- and sex-matched controls were selected by risk-set sampling. Logistic regression models were applied to estimate the odds ratio (OR) and 95% confidence interval (CI) between TZDs and cancer incidence. A total of 10,741 liver cancer cases, 7,200 colorectal cancer cases, and 70,559 diabetic controls were included. A significantly lower risk of liver cancer incidence was found for any use of rosiglitazone (OR: 0.73, 95% CI: 0.65-0.81) or pioglitazone (OR: 0.83, 95% CI: 0.72-0.95), respectively. The protective effects were stronger for higher cumulative dosage and longer duration. For colorectal cancer, rosiglitazone, but not pioglitazone, was associated with a significantly reduced risk (OR: 0.86; 95% CI: 0.76-0.96). TZDs were not associated with lung and bladder cancer incidence, although a potential increased risk for bladder cancer with pioglitazone use =3 years could not be excluded (OR: 1.56; 95% CI: 0.51-4.74). Conclusion: The use of pioglitazone and rosiglitazone is associated with a decreased liver cancer incidence in diabetic patients. The effects on occurrence of specific cancer types may be different for pioglitazone and rosiglitazone. (HEPATOLOGY 2012;)
引用
收藏
页码:1462 / 1472
页数:11
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