PMID- 21102326 OWN - NLM STAT- MEDLINE DCOM- 20110418 LR - 20211020 IS - 1473-6535 (Electronic) IS - 0957-9672 (Print) IS - 0957-9672 (Linking) VI - 22 IP - 1 DP - 2011 Feb TI - Role of fibrates in cardiovascular disease prevention, the ACCORD-Lipid perspective. PG - 55-61 LID - 10.1097/MOL.0b013e328341a5a8 [doi] AB - PURPOSE OF REVIEW: To examine the results of the Action to Control Cardiovascular Risk in Diabetes (ACCORD)-Lipid trial, particularly the subgroup analyses. It is important, when a study fails to meet its overall primary endpoint, to ensure that interpretation of the results include analyses of subgroups that might benefit from the treatment tested. The goal of this review, therefore, is to provide insight and advice to physicians and healthcare workers treating patients similar to those enrolled in ACCORD. RECENT FINDINGS: The recently published results of ACCORD-Lipid trial will be presented upon the background of previous trials that have tested the ability of fibrates to lower cardiovascular risk. SUMMARY: Although ACCORD-Lipid trial did not provide support for the general addition of fenofibrate to statin-treated patients with type 2 diabetes mellitus (T2DM), it added significantly to the results from fibrate monotherapy trials indicative of benefit from such treatment in subgroups of patients who present with significant dyslipidemia. In particular, ACCORD-Lipid trial, in our view, supports the addition of fenofibrate to statin therapy in patients with T2DM and optimal low-density lipoprotein cholesterol levels but persistent, significant hypertriglyceridemia (>200 mg/dl) and low high-density lipoprotein cholesterol levels (<35-40 mg/dl). FAU - Elam, Marshall AU - Elam M AD - Department of Pharmacology, University of Tennessee Health Sciences Center-Memphis, Memphis, Tennessee, USA. FAU - Lovato, Laura C AU - Lovato LC FAU - Ginsberg, Henry AU - Ginsberg H LA - eng GR - N01HC95184/HL/NHLBI NIH HHS/United States GR - Y01 HC001010/HC/NHLBI NIH HHS/United States GR - N01-HC-95180/HC/NHLBI NIH HHS/United States GR - Y01 HC009035/HC/NHLBI NIH HHS/United States GR - IAAY1-HC-9035/HC/NHLBI NIH HHS/United States GR - R01 DK075504/DK/NIDDK NIH HHS/United States GR - IAAY1-HC-1010/HC/NHLBI NIH HHS/United States GR - N01HC95181/HL/NHLBI NIH HHS/United States GR - N01-HC-95182/HC/NHLBI NIH HHS/United States GR - N01-HC-95178/HC/NHLBI NIH HHS/United States GR - N01HC95182/HL/NHLBI NIH HHS/United States GR - N01-HC-95181/HC/NHLBI NIH HHS/United States GR - N01HC95178/HL/NHLBI NIH HHS/United States GR - N01HC95183/HL/NHLBI NIH HHS/United States GR - N01-HC-95184/HC/NHLBI NIH HHS/United States GR - R01 HL073030/HL/NHLBI NIH HHS/United States GR - N01HC95179/HL/NHLBI NIH HHS/United States GR - N01-HC-95183/HC/NHLBI NIH HHS/United States GR - N01HC95180/HL/NHLBI NIH HHS/United States GR - N01-HC-95179/HC/NHLBI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Review PL - England TA - Curr Opin Lipidol JT - Current opinion in lipidology JID - 9010000 RN - 0 (Hypolipidemic Agents) RN - U202363UOS (Fenofibrate) SB - IM MH - Cardiovascular Diseases/*prevention & control MH - Clinical Trials as Topic MH - Diabetes Mellitus, Type 2/drug therapy MH - Fenofibrate/therapeutic use MH - Humans MH - Hypolipidemic Agents/therapeutic use PMC - PMC6067007 MID - NIHMS742944 EDAT- 2010/11/26 06:00 MHDA- 2011/04/19 06:00 PMCR- 2018/07/31 CRDT- 2010/11/25 06:00 PHST- 2010/11/25 06:00 [entrez] PHST- 2010/11/26 06:00 [pubmed] PHST- 2011/04/19 06:00 [medline] PHST- 2018/07/31 00:00 [pmc-release] AID - 10.1097/MOL.0b013e328341a5a8 [doi] PST - ppublish SO - Curr Opin Lipidol. 2011 Feb;22(1):55-61. doi: 10.1097/MOL.0b013e328341a5a8.