Cardiologia para todos

jueves, marzo 29, 2012

Thiazolidinediones can prevent new onset atrial fibrillation in patients with non-insulin dependent diabetes

International Journal of Cardiology
Volume 156, Issue 2 , Pages 199-202, 19 April 2012
Thiazolidinediones can prevent new onset atrial fibrillation in patients with non-insulin dependent diabetes
Tze-Fan Chao, Hsin-Bang Leu, Chin-Chou Huang, Jaw-Wen Chen, Wan-Leong Chan, Shing-Jong Lin, Shih-Ann Chen
Abstract
Background
Accumulative evidence suggested that oxidative stress and inflammation were involved in the pathogenesis of atrial fibrillation (AF). Thiazolidinediones (TZDs), agonists of peroxisome proliferator-activated receptor gamma (PPAR-γ), have been proven to have anti-inflammatory and anti-oxidant effects in addition to their anti-diabetic activity. The goal of this nationwide, population based cohort study was to evaluate whether the use of TZDs will protect diabetic patients from AF.

Methods
The study population was comprised of 12,065 non-insulin dependent diabetic patients identified from the “National Health Insurance Research Database” released by the Taiwan National Health Research Institutes. Among the study patients, a total of 4137 patients with TZD use were recognized as the study cohort and 7928 patients without TZD use were included as the comparison cohort. The study endpoint was defined as AF occurrence during the follow up period.

Results
During the follow up of 63±25months, 194 patients (1.6% of the study population) developed AF: 49 from the study cohort (1.2% of the TZD group) and 145 from the comparison cohort (1.8% of the non-TZD group). After an adjustment for the baseline characteristics and medications, the TZDs independently protected diabetic patients from new-onset AF with a hazard ratio of 0.69 (95% confidence interval=0.49–0.91, p value=0.028).

Conclusion
In this cohort study, we demonstrated that TZDs had obvious protective effects on the development of AF in diabetic patients. Drugs acting as ligands to the PPAR-γ may be potential up-stream therapies for AF prevention.