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10.1097/MD.0000000000005429

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C5120943!5120943 !27861386
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suck abstract from ncbi


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pmid27861386
      Medicine+(Baltimore) 2016 ; 95 (46 ): e5429
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  • Statins and risk for new-onset diabetes mellitus: A real-world cohort study using a clinical research database #MMPMID27861386
  • Yoon D ; Sheen SS ; Lee S ; Choi YJ ; Park RW ; Lim HS
  • Medicine (Baltimore) 2016[Nov]; 95 (46 ): e5429 PMID27861386 show ga
  • Although concern regarding the increased risk for new-onset diabetes mellitus (NODM) after statin treatment has been raised, there has been a lack of evidence in real-world clinical practice, particularly in East Asians. We investigated whether statin use is associated with risk for NODM in Koreans. We conducted a retrospective cohort study using the clinical research database from electronic health records. The study cohort consisted of 8265 statin-exposed and 33,060 matched nonexposed patients between January 1996 and August 2013. Matching at a 1:4 ratio was performed using a propensity score based on age, gender, baseline glucose levels (mg/dL), and hypertension. The comparative risks for NODM with various statins (atorvastatin, fluvastatin, pitavastatin, pravastatin, rosuvastatin, and simvastatin) were estimated by both statin exposure versus matched nonexposed and within-class comparisons. The incidence of NODM among the statin-exposed group (6.000 per 1000 patient-years [PY]) was higher than that of the nonexposed group (3.244 per 1000 PY). The hazard ratio (HR) of NODM after statin exposure was 1.872 (95% confidence interval [CI], 1.432-2.445). Male gender (HR, 1.944; 95% CI, 1.497-2.523), baseline glucose per mg/dL (HR, 1.014; 95% CI, 1.013-1.016), hypertension (HR, 2.232; 95% CI, 1.515-3.288), and thiazide use (HR, 1.337; 95% CI, 1.081-1.655) showed an increased risk for NODM, while angiotensin-converting enzyme inhibitor or angiotensin II receptor blocker showed a decreased risk (HR, 0.774; 95% CI, 0.668-0.897). Atorvastatin-exposed patients showed a higher risk for NODM than their matched nonexposed counterparts (HR, 1.939; 95% CI, 1.278-2.943). However, the risk for NODM was not significantly different among statins in within-class comparisons. In conclusion, an increased risk for NODM was observed among statin users in a practical healthcare setting in Korea.
  • |*Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage/adverse effects/classification [MESH]
  • |*Hypertension/drug therapy/epidemiology [MESH]
  • |Adult [MESH]
  • |Age Factors [MESH]
  • |Aged [MESH]
  • |Blood Glucose/analysis [MESH]
  • |Diabetes Mellitus/*epidemiology [MESH]
  • |Dyslipidemias/drug therapy [MESH]
  • |Electronic Health Records/statistics & numerical data [MESH]
  • |Female [MESH]
  • |Humans [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |Republic of Korea/epidemiology [MESH]
  • |Research Design [MESH]
  • |Retrospective Studies [MESH]


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