Abington-Jefferson Health, Abington, Pa (Drs. Skolnik and Jaffa); Johns Hopkins University School of Medicine, Baltimore, Md (Dr. Kalyani); Altru Diabetes Center, Grand Forks, ND (Dr. Johnson); Touro University College of Osteopathic Medicine, Vallejo, Calif (Dr. Shubrook) nskolnik@comcast.net
This article was developed as part of the ADA Primary Care Advisory Group’s initiative to disseminate diabetes information to primary care physicians nationwide.
Drs. Jaffa and Kalyani reported no potential conflict of interest relevant to this article. Dr. Skolnik serves on the AstraZeneca Speakers’ Bureau and has served on advisory panels for AstraZeneca, Boehringer Ingleheim, Eli Lilly, Novartis, Sanofi, and Teva. Dr. Johnson serves on the Novo Nordisk and Medtronic Speakers’ Bureaus and on advisory panels for Novo Nordisk and Sanofi. Dr. Shubrook has received research support from Sanofi, Eli Lilly, AstraZeneca, and Takeda, and has served as a consultant for Novo Nordisk and Eli Lilly.
For patients with diabetes who are <40 years with additional ASCVD risk factors, few clinical trial data exist; nevertheless, consider a moderate- or high-intensity statin and lifestyle therapy. Similarly, for patients >75 years who have diabetes and no additional ASCVD risk factors, consider a moderate-intensity statin and lifestyle modifications. For older adults with additional ASCVD risk factors, consider high-intensity statin therapy.35-37
Statins and cognition. It should be noted that published data have not demonstrated an adverse effect of statins on cognition.38 Statins, however, have been linked to an increased risk of developing diabetes,39,40 although the absolute increase in risk is small, and much smaller than the benefit derived from preventing the development of coronary disease.
Should total cholesterol and LDL levels be used as targets with statin treatment?
No.Statin doses have primarily been tested against placebo in clinical trials, rather than testing to specific target LDL levels, suggesting that the initiation and intensification of statin therapy be based on a patient’s risk profile.35 When maximally tolerated doses of statins do not lower LDL cholesterol by more than 30% from the patient’s baseline, there is currently no good evidence that combination therapy would be helpful, so regular monitoring of lipid levels has limited value. A lipid profile that includes levels of total cholesterol, LDL cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides should be obtained at initial medical evaluation, at diagnosis of diabetes, and every 5 years thereafter or before the initiation of statin therapy. Ongoing testing may be appropriate in individual circumstances and to monitor for adherence to, or efficacy of, therapy.
What should I do for my patients who can’t tolerate statins?
Try a lower dose or a different statin before eliminating the class. Research has shown that even small doses (eg, rosuvastatin 5 mg) have some benefit.41
How do combination treatments figure into the current treatment of lipids in patients with diabetes?
It dependson the agent and the patient’s profile.
Fenofibrate.The ADA does not recommend automatically adding fenofibrate to statin therapy because the combination is associated with increased risks for abnormal transaminase levels, myositis, and rhabdomyolysis. In the ACCORD trial, the combination of fenofibrate and simvastatin did not reduce the rate of fatal CV events, nonfatal MIs, or nonfatal strokes compared with simvastatin alone.42
Recommend statin therapy to all patients with diabetes over age 40; use a moderate- or high-intensity agent depending upon the degree of cardiac risk.
That said, a subgroup analysis suggested a benefit for men with both a triglyceride level ≥204 mg/dL (2.3 mmol/L) and an HDL cholesterol level ≤34 mg/dL (0.9 mmol/L).42 For this reason, the combination of a statin and fenofibrate may be considered for men who meet these laboratory parameters. In addition, consider medical therapy for triglyceride levels ≥500 mg/dL to reduce the risk of pancreatitis.
Ezetimibe. Recommendations regarding ezetimibe are based on the IMPROVE-IT (Improved Reduction of Outcomes: Vytorin Efficacy International Trial), a 2015 RCT including over 18,000 patients that compared treatment with ezetimibe and simvastatin to simvastatin alone.43 Individuals in the trial were ≥50 years of age and had experienced an ACS within the preceding 10 days. In those with diabetes, the combination of moderate-intensity simvastatin (40 mg) and ezetimibe (10 mg) significantly reduced major adverse CV events with an absolute risk reduction of 5% (40% vs 45%) and an RR reduction of 14% over moderate-intensity simvastatin (40 mg) alone.
Based on these results, patients with diabetes and a recent ACS should be considered for combination therapy with ezetimibe and a moderate-intensity statin. The combination should also be considered in patients with diabetes and a history of ASCVD who cannot tolerate high-intensity statins.43
Recommend daily aspirin therapy to patients ages ≥50 years who have diabetes and at least one additional cardiovascular risk factor, but no bleeding risk.
Niacin.The ADA currently does not recommend niacin in combination with a statin because of lack of efficacy on major ASCVD outcomes, possible increased risk of ischemic stroke, and adverse effects.44
What are the recommendations for the use of PCSK-9 inhibitors?
Proprotein convertase subtilisin/kexin type 9 (PCSK-9) inhibitors (ie, evolucumab and alirocumab) may be considered as adjunctive therapy to statins for patients with diabetes at high risk for ASCVD events who require additional lowering of LDL cholesterol. They may also be considered for those in whom high-intensity statin therapy is indicated, but not tolerated.
Antiplatelet agents
Who should take aspirin for primary prevention of CVD?
Both women and men ages ≥50 years who have diabetes and at least one additional CV risk factor (family history of premature ASCVD, hypertension, tobacco use, dyslipidemia, or albuminuria) should consider taking daily aspirin therapy (75-162 mg/d) if they do not have an excessive bleeding risk.45,46The most common dose in the United States is 81 mg. This recommendation is supported by a 2010 consensus statement of the American Diabetes Association, American Heart Association, and the American College of Cardiology.47