» Articles » PMID: 12843167

Efficacy of Atorvastatin and Gemfibrozil, Alone and in Low Dose Combination, in the Treatment of Diabetic Dyslipidemia

Overview
Specialty Endocrinology
Date 2003 Jul 5
PMID 12843167
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

To compare the effects of atorvastatin, gemfibrozil, and their combination on the components of diabetic dyslipidemia, 44 type 2 diabetic patients with low density lipoprotein cholesterol (LDLc) levels greater than 100 mg/dl and triglyceride levels less than 400 mg/dl were included. Twelve-week treatments with atorvastatin (10-20 mg/d) and gemfibrozil (900-1200 mg/d) were given in random order in an open, cross-over study and then combined (10 mg atorvastatin and 900 mg gemfibrozil) for 12 additional wk. Triglyceride, LDLc, high density lipoprotein cholesterol (HDLc), non-HDLc, apolipoprotein B (apoB), and LDL size were measured at baseline and after each treatment. Atorvastatin was more effective (P < 0.001) in lowering LDLc, non-HDLc, and apoB and in achieving treatment goals, whereas gemfibrozil lowered triglyceride levels more effectively (P < 0.001) and increased LDL size (from 25.59 +/- 0.06 to 25.69 +/- 0.06 nm; P < 0.05). Combined treatment with both drugs reduced LDLc, triglyceride, non-HDLc, and apoB by 26.5%, 24.1%, 30.4%, and 21.8%, respectively; increased HDLc by 4.8% and LDL size by 0.1 nm; and was the most effective treatment in reaching the therapeutic targets, especially in patients with triglyceride levels higher than 150 mg/dl. In conclusion, statins are first choice drugs in diabetic patients with low to moderate risk LDLc, although their combination with fibrates might be the most appropriate treatment, especially when triglyceride levels are above the therapeutic goal.

Citing Articles

Benefits and harms of fibrate therapy in patients with type 2 diabetes: a systematic review and meta-analysis.

Rodriguez-Gutierrez R, Garcia-Leal M, Raygoza-Cortez K, Flores-Rodriguez A, Moreno-Alvarado M, Heredia-Martinez E Endocrine. 2023; 81(2):231-245.

PMID: 37247046 DOI: 10.1007/s12020-023-03401-y.


Metabolic syndrome impairs reactivity and wall mechanics of cerebral resistance arteries in obese Zucker rats.

Brooks S, DeVallance E, dAudiffret A, Frisbee S, Tabone L, Shrader C Am J Physiol Heart Circ Physiol. 2015; 309(11):H1846-59.

PMID: 26475592 PMC: 4698385. DOI: 10.1152/ajpheart.00691.2015.


Studies on two polyherbal formulations (ZPTO and ZTO) for comparison of their antidyslipidemic, antihypertensive and endothelial modulating activities.

Aziz N, Mehmood M, Gilani A BMC Complement Altern Med. 2013; 13:371.

PMID: 24370063 PMC: 4029524. DOI: 10.1186/1472-6882-13-371.


Impact of the LDL subfraction phenotype on Lp-PLA2 distribution, LDL modification and HDL composition in type 2 diabetes.

Sanchez-Quesada J, Vinagre I, de Juan-Franco E, Sanchez-Hernandez J, Bonet-Marques R, Blanco-Vaca F Cardiovasc Diabetol. 2013; 12:112.

PMID: 23915379 PMC: 3750253. DOI: 10.1186/1475-2840-12-112.


Myopathy with statin-fibrate combination therapy: clinical considerations.

Jacobson T Nat Rev Endocrinol. 2009; 5(9):507-18.

PMID: 19636324 DOI: 10.1038/nrendo.2009.151.