Article

Treating the Common Dyslipidemia in Patients with Type 2 Diabetes—Insights from FIELD on the Effects of Fenofibrate on CVD Risk

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Current Indications for Statin and Fibrate Therapy

The evidence of cardiovascular protection afforded by statins has recently extended beyond patients with hypercholesterolemia. With the publication of several trials,1-7 bold extrapolations of the power of statin therapy in cardiovascular prevention have been offered:

  1. statins equally reduce risk in subjects with or without hypercholesterolemia;
  2. statins may be the first choice in patients with diabetes; and
  3. the guideline goal for low-density lipoprotein (LDL)-cholesterol may need to be lowered to 70mg/dl.

Thus, it seems that statin therapy may become necessary in high-risk individuals, even in the absence of dyslipidemia and possibly even when LDL-cholesterol levels are <100mg/dl. However, it should be emphasized that the optional goal of LDL-cholesterol levels <70mg/dl applies only to individuals who are very high-risk (i.e. established cardiovascular disease (CVD) plus multiple major risk factors), as there are potential side effects of using high statin doses to reduce LDL-cholesterol to very low levels.8

Similar momentum has been building for fibrates. These agents were originally indicated for patients with severely high triglyceride levels. However, the benefit of fibrates has recently been extended to treat the atherogenic dyslipidemia that afflicts most patients with type 2 diabetes, which is characterized by high levels of triglycerides, LDL particles that are small and dense, and low levels of high-density lipoprotein (HDL)-cholesterol.9-11 The Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study, discussed in detail below, provides important data regarding the potential for fenofibrate to reduce cardiovascular risk in patients with type 2 diabetes both with and without dyslipidemia.

Treatment of Atherogenic Dyslipidemia to Reduce Cardiovascular Risk

The current guidelines of the National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III)10 and the American Diabetes Association (ADA)12 highlight the importance of LDL-cholesterol reduction in high-risk patients, but at the same time encourage physicians to position all patients with type 2 diabetes and insulin resistance in the high cardiovascular risk category. Because patients with type 2 diabetes and insulin resistance are commonly affected by the atherogenic dyslipidemia, characterized by high triglycerides and low HDL-cholesterol, one could argue that the optimal lipid intervention in these patients should be one targeting these abnormalities.

Triglyceride and HDL-cholesterol levels have been shown to predict coronary event rates independently of LDL-cholesterol levels in populations from Europe and the US.13-15 The knowledge that the ratio of total cholesterol to HDL-cholesterol is the most sensitive index of cardiovascular disease progression highlights the important contribution of atherogenic dyslipidemia to cardiovascular risk, given that this ratio is mostly determined by abnormalities of triglyceride metabolism.This is reflected in the current NCEP ATP III guidelines, which suggest a secondary goal of non-HDL-cholesterol to be only 30mg/dl higher than that for LDL-cholesterol.10 A subject whose LDL-cholesterol is already at goal but has an inappropriate level of non-HDL cholesterol is a subject affected by hypertriglyceridemia. Thus, current guidelines support aggressive treatment of triglycerides in the high-risk patient.10 Indeed, normalization of the entire lipid profile is becoming the ultimate goal for optimal risk reduction in the high-risk individual.

Clinical Evidence from Statin Trials

The importance of properly treating atherogenic dyslipidemia can be indirectly inferred by the results of the major statin trials. For example, the most impressive statin effects on coronary heart disease (CHD) risk reduction in a high-risk population were observed in the Scandinavian Simvastatin Survival Study (4S), in which patients had high baseline LDL-cholesterol (188mg/dl) but near-normal baseline triglycerides (133mg/dl) and HDL-cholesterol (46mg/dl).16 However, the Cholesterol and Recurrent Events (CARE) study and the Long Term Intervention With Pravastatin in Ischemic Disease (LIPID) trial, where subjects had lower baseline LDL-cholesterol (139-151mg/dl) but higher baseline triglycerides (up to 168mg/dl) and lower baseline HDL-cholesterol (33-39mg/dl), showed more modest cardiovascular outcomes results with pravastatin.17,18 These data indicate that in a population of patients with mixed dyslipidemia, the exclusive attention to LDL-cholesterol may not be as beneficial as targeting all lipid abnormalities presented. Along these lines, CARE patients with baseline triglycerides above the median value (144mg/dl) did not experience significant cardiovascular risk reduction despite a significant LDL-cholesterol lowering effect.17

The Heart Protection Study investigated the cardiovascular risk reduction potential afforded by simvastatin in a population of 20,536 patients who were classified as high-risk (65% had prior CHD and 19% had diabetes), even though the mean baseline LDL-cholesterol was 131mg/dl.1 Although the subset of HPS patients with low baseline HDL-cholesterol (<35mg/dl) experienced benefits as large as those in patients with high baseline LDL-cholesterol (≤135mg/dl), the residual risk in patients with low baseline HDL-cholesterol was higher than that in any other lipid subcategory after treatment with simvastatin, except in those patients with triglyceride levels ≤354mg/dl. These data suggest that more aggressive control of HDL-cholesterol and triglyceride levels in these patients may optimize risk reduction. Similarly, the CARDS study3 revealed that patients with type 2 diabetes who were treated with atorvastatin were protected against atherosclerotic complications; however, a lower baseline HDL-cholesterol (<54mg/dl) predicted higher risk in these patients. These data are consistent with the idea that a high residual risk remains after treatment with a statin, especially for those patients with low HDL-cholesterol and/or high triglycerides. Thus, targeting components of the lipid profile beyond LDL-cholesterol may be beneficial in further reducing cardiovascular risk in patients with atherogenic dyslipidemia.

Clinical Evidence From Fibrate Trials

In the Helsinki Heart Study, 4,081 men with no prior history of CVD received gemfibrozil or placebo for five years. Gemfibrozil reduced triglycerides by 35% and LDL-cholesterol by 8% and raised HDL-cholesterol by 9%, resulting in a significant 34% reduction in CHD events (p<0.02) in the overall population. Interestingly, intervention with gemfibrozil provided a 71% CHD risk reduction in a subset of patients with high triglycerides (>204mg/dl) and low HDL-cholesterol (LDL-cholesterol/ HDL-cholesterol ratio >5).19 Furthermore, patients with type 2 diabetes benefited more than the normoglycemic individuals from treatment with gemfibrozil (68% CHD risk reduction).20 These data support the idea that the patient type most amenable to cardiovascular risk reduction by fibrate therapy is a patient with type 2 diabetes and/or atherogenic dyslipidemia.

The Veterans Affairs High-Density Lipoprotein Intervention Trial (VA-HIT) evaluated the effect of gemfibrozil in 2531 men with CHD and low HDL-cholesterol.21 Mean baseline LDL-cholesterol was 111mg/dl, mean baseline HDL-cholesterol was 32mg/dl, and mean baseline triglyceride level was 160mg/dl. Gemfibrozil treatment increased HDL-cholesterol by 6% and reduced triglycerides by 31%.

Although there was no significant alteration of LDL-cholesterol with gemfibrozil treatment, there was a significant 22% reduction in the primary end-point of CHD events (p=0.006) and a significant 29% reduction in the incidence of investigator-designated strokes (p=0.04). Gemfibrozil intervention produced a number-needed-to-treat of 23 for coronary events, which compares favorably with the results of the statin trials. In addition, the effect of gemfibrozil therapy on CHD event rates among the 769 diabetic subjects enrolled in VA-HIT was particularly large and apparently superior to the effects of statins in the same patient type.22 Specifically, patients with type 2 diabetes treated with gemfibrozil experienced a 41% reduction in CHD death (p=0.02) and a 40% reduction in stroke (p=0.046).These data support the value of fibrate therapy in patients with type 2 diabetes, a prior history of CHD, and atherogenic dyslipidemia. However, the notion that fibrate therapy may represent the intervention of choice for vascular protection in type 2 diabetes requires further investigation in large-scale clinical outcomes trials of patients with type 2 diabetes.

The FIELD Study

The recently published FIELD trial represents a landmark study, as this was the largest cardiovascular outcomes trial conducted with a lipid-lowering medication in patients with type 2 diabetes (n=9,795).23 The primary clinical outcome of the study was CHD events, the combined incidence of non-fatal myocardial infarction (MI) and CHD death.23 Secondary clinical outcomes included total CVD events, which was a composite of CHD events, stroke, CVD death, and coronary and carotid revascularizations.Tertiary clinical outcomes included vascular amputations, the progression of renal disease, and laser treatment for diabetic retinopathy.

FIELD—Study Population

The FIELD trial tested the hypothesis of fibrate-induced cardiovascular protection in patients with type 2 diabetes who would not have been typically considered eligible for fibrate therapy according to 'best practice' standards. Entry criteria included total cholesterol of 116-251mg/dl, triglycerides of 89-443mg/dl, and total cholesterol to HDL-cholesterol ratio 4. The vast majority of subjects enrolled had a fairly normal lipid profile (mean LDL-cholesterol 119mg/dl; HDL-cholesterol 43mg/dl; and tri-glycerides, 154mg/dl), and only 38% of subjects met the prespecified definition of dyslipidemia (triglycerides >150mg/dl and HDL-cholesterol <40mg/dl for men or <50mg/dl for women) at baseline.24

The fact that lipid-lowering therapy at baseline was an exclusion criterion also indicates that the patients' own doctors did not feel compelled to treat these patients' minor dyslipidemia. However, once enrolled, subjects were free to seek medical advice and to initiate non-study lipid-lowering agents without being disqualified from the study. Thus, the results of the FIELD trial are partly confounded by the significant drop-in rates of nonstudy lipid-lowering therapies. At the end of the study, 36% of placebo-assigned patients and 19% of fenofibrate-assigned subjects started non-study lipid-lowering therapy.24 Importantly, 93% of these non-study lipid-lowering agents prescribed were statins.24

FIELD—Lipid Effects

In the overall population, fenofibrate lowered LDL-cholesterol by 6% and triglycerides by 22%, and increased HDL-cholesterol by 1.2% compared with the placebo cohort.24 In patients who did not start nonstudy lipid-lowering therapy, fenofibrate provided more significant lipid effects (15% decrease in LDL-cholesterol, 27% decrease in triglyceride levels, and 2.1% increase in HDL-cholesterol). However, in those patients who did start nonstudy lipid-lowering therapy (944 fenofibrate patients and 1776 placebo patients), there were no differences between groups except for a small reduction in triglycerides (11%).Of the 944 patients in the fenofibrate group who started nonstudy lipid-lowering therapy, only 581 patients remained on fenofibrate. These lipid data have important implications:

  1. the LDL lowering effect of fenofibrate reduced the statin drop-in rate in the treatment group; and
  2. discontinuation of fenofibrate by 38% of patients who added non-study lipid-lowering therapy (statin) prevented the evaluation of CVD protection by combination therapy in this subset of patients.
FIELD—Outcome Results

Overall, the FIELD study revealed a positive effect of fenofibrate, with a trend in benefit for the primary outcome of CHD events (11% risk reduction; p=0.16) and significant risk reductions for the secondary outcomes of total CVD events (11% risk reduction; p=0.035) and coronary revascularizations (21% risk reduction; p=0.003).24 The primary outcome was a composite of a significant 24% reduction in non-fatal MI (p=0.01), countered by a nonsignificant increase in CHD mortality (p=0.22).24

Importantly, these cardiovascular outcomes were obtained within the challenging parameters of a study population predominantly without the dyslipidemia targeted by a fibrate (62% of patients did not meet the definition of dyslipidemia at baseline) and with substantial drop-in rates of non-study statin therapy. The protective effect of fenofibrate was more evident in patients with low baseline HDL-cholesterol (<40mg/dl for men and <50mg/dl for women), high baseline triglycerides (151mg/dl), and low LDL-cholesterol (<116mg/dl), patients who were likely to carry the atherogenic dyslipidemia. There was also a significant cardiovascular risk reduction in the 60% of subjects who were younger than 65 years of age (21% risk reduction; p<0.001), and in the 78% of subjects without prior history of CVD (25% reduction; p=0.014).24

In the primary prevention cohort (diabetics without CVD), the absolute risk reduction was 1.9%, with a need to treat 53 patients for five years in order to prevent one CVD event. On the other hand, in patients with pre-existing CVD, fenofibrate did not reduce CHD or total CVD events. The fact that the drop-in rate of non-study lipid-lowering therapy in the secondary prevention placebo group was almost twice the rate in the primary prevention placebo group may help explain why fenofibrate did not appear to have a beneficial effect on cardiovascular outcomes in this cohort.Another way to look at these data is that the higher statin use in the placebo group did not produce the expected benefits of this proven therapy, indirectly providing support to the notion that the protective power of fenofibrate may be in the range of that of statins. Nevertheless, the positive results observed in the patients with type 2 diabetes but without previous CVD indicate that fenofibrate therapy is useful for patients with type 2 diabetes irrespective of baseline lipid values. This is a significant advance in our understanding of fibrate effects on the vessel wall and confirms previous experimental work on vascular protection induced by fenofibrate through non-lipid mechanisms.

Beyond the macrovascular beneficial effects of fenofibrate described above, fenofibrate was also associated with significantly positive effects on the microvasculature. There was significantly less albuminuria progression (14%) and significantly more albuminuria regression (p=0.002) in patients treated with fenofibrate compared with those treated with placebo.24 Furthermore, there was a highly significant 30% reduction in the need for laser treatment for diabetic retinopathy (p=0.0003) in the fenofibrate group.24 These data provide additional evidence that fenofibrate therapy has a relevant place in the comprehensive approach to diabetes management.

FIELD—Safety

Overall, the use of fenofibrate was well tolerated in patients with type 2 diabetes irrespective of concomitant therapy. Although adverse events were rare, there was a greater risk for pancreatitis (0.5% for placebo and 0.8% for fenofibrate) and pulmonary embolism (0.7% for placebo and 1.1% for fenofibrate) in the fenofibrate group.24 Out of 9,795 patients, only three experienced myositis (two patients were on fenofibrate and one was on placebo), and only four patients experienced rhabdomyolysis (three patients were on fenofibrate and one was on placebo). None of the patients with rhabdomyolysis were on combination therapy with a statin.24 The ADA recently issued recommendations that give preference to fenofibrate over gemfibrozil in combination with statins12 as a consequence of previous studies that revealed fenofibrate used in combination with a statin posed less risk for myopathy or rhabdomyolysis than combination therapy with gemfibrozil.25,26 Additional evidence for this ADA recommendation is provided by the FIELD study, which suggests that combination therapy with fenofibrate and a statin appears to be well tolerated and safe.

FIELD—Conclusions

In summary, the FIELD trial supports the use of fenofibrate in patients with type 2 diabetes who have no prior history of CVD, regardless of the presence of diabetic dyslipidemia.These data also support the use of combination statin and fibrate therapy to accomplish optimal normalization of the lipid profile and achieve synergistic effects on the vascular wall. Based on beneficial effects of fenofibrate on macrovascular and microvascular disease, the FIELD study challenges the notion that statin therapy is the mandatory first choice in diabetic patients without hypercholesterolemia. This guideline-supported approach, generated as a result of studies showing that lowering LDL-cholesterol will reduce CVD risk in all patients with diabetes and normal lipids, does not consider the likely possibility that triglyceride and HDL-cholesterol level management with fibrates would produce superior benefits in reducing CVD risk in patients with type 2 diabetes and atherogenic dyslipidemia.

Final Thoughts

Optimal cardiovascular risk reduction will most likely be obtained by carefully matching the diagnosis of a specific lipid abnormality with the therapeutic agent most likely to correct it.The FIELD trial supports this line of reasoning by providing evidence that fenofibrate was most beneficial in reducing CVD risk in patients with type 2 diabetes who had low HDL-cholesterol levels, high triglyceride levels, and low LDL-cholesterol levels—patients who were most likely carriers of the atherogenic dyslipidemia. The current guidelines encourage aggressive lipid lowering in patients with the type 2 diabetes, but one should keep in mind that these patients present with different forms and degrees of dyslipidemia.At a time when guidelines are moving toward endorsement of lower LDL-cholesterol goals, the danger lies in underestimating the risk contributed by atherogenic dyslipidemia and improperly treating this condition in patients with type 2 diabetes. Fibrates, particularly fenofibrate, are safe and effective for the long-term management of patients with high CVD risk, particularly when this increased CVD risk is due to the presence of atherogenic dyslipidemia or type 2 diabetes.

References

  1. Heart Protection Study Collaborative G, MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20,536 high-risk individuals: a randomised placebo-controlled trial[comment] , Lancet (2002); 360: pp. 7-22
    PubMed
  2. Sever PS, Dahlof B, Poulter NR, et al., Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian Cardiac Outcomes TrialÔÇöLipid Lowering Arm (ASCOT-LLA): a multicentre randomised controlled trial , Lancet (2003); 361: pp. 1149-58.
    Crossref | PubMed
  3. Colhoun HM, Betteridge DJ, Durrington PN, et al., Primary prevention of cardiovascular disease with atorvastatin in type 2 diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled trial , Lancet (2004); 364: 685-96.
    Crossref | PubMed
  4. Rader DJ, Davidson MH, Caplan RJ, Pears JS, Lipid and apolipoprotein ratios: association with coronary artery disease and effects of rosuvastatin compared with atorvastatin, pravastatin, and simvastatin , Am J Cardiol (2003); 91: pp. 20C-23C, discussion pp. 23C-24C.
    Crossref | PubMed
  5. LaRosa JC, Grundy SM,Waters DD, et al., Intensive lipid lowering with atorvastatin in patients with stable coronary disease , N Engl J Med (2005); 352: pp. 1425-35.
    Crossref | PubMed
  6. Pedersen TR, Faergeman O, Kastelein JJ, et al., High-dose atorvastatin vs usual-dose simvastatin for secondary prevention after myocardial infarction: the IDEAL study: a randomized controlled trial , JAMA (2005); 294: pp. 2437-45.
    Crossref | PubMed
  7. de Lemos JA, Blazing MA,Wiviott SD, et al., Early intensive vs a delayed conservative simvastatin strategy in patients with acute coronary syndromes: phase Z of the A to Z trial , JAMA (2004); 292: pp. 1307-16.
    Crossref | PubMed
  8. Grundy SM, Cleeman JI, Merz CN, et al., Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel III guidelines , Circulation (2004); 110: pp. 227-39.
    Crossref | PubMed
  9. Haffner SM, Management of dyslipidemia in adults with diabetes , Diabetes Care (2003); 26 (Suppl. 1): pp. S83-S86.
    Crossref | PubMed
  10. Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report , Circulation (2002); 106: pp. 3143-3421.
    PubMed
  11. Fazio S, Linton MF, The role of fibrates in managing hyperlipidemia: mechanisms of action and clinical efficacy , Current Atherosclerosis Reports (2004); 6: 148-57.
    Crossref | PubMed
  12. American Diabetes Association Standards of medical care in diabetesÔÇö2006 , Diabetes Care (2006); 29 (Suppl. 1): pp. S4-S42.
    PubMed
  13. Austin MA, Hokanson JE, Edwards KL, Hypertriglyceridemia as a cardiovascular risk factor , Am J Cardiol (1998); 81: pp. 7B-12B.
    Crossref | PubMed
  14. Castelli WP, Cholesterol and lipids in the risk of coronary artery diseaseÔÇöthe Framingham Heart Study , Can J Cardiol (1988); 4 (Suppl. A): pp. 5A-10A.
    PubMed
  15. Gordon T, Castelli WP, Hjortland MC, et al., High density lipoprotein as a protective factor against coronary heart disease.The Framingham Study , Am J Med (1977); 62: pp. 707-14.
    Crossref | PubMed
  16. Scandinavian Simvastatin Survival Study Group, Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the scandinavian simvastatin survival study (4S) , Lancet (1994); 344: pp. 1383-9.
    PubMed
  17. Sacks FM, Pfeffer MA, Moye LA, et al., The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators , N Engl J Med (1996); 335: pp. 1001-1009.
    Crossref | PubMed
  18. Keech A, Colquhoun D, Best J, et al., Secondary prevention of cardiovascular events with long-term pravastatin in patients with diabetes or impaired fasting glucose: results from the LIPID trial , Diabetes Care (2003); 26: pp. 2713-21.
    Crossref | PubMed
  19. Manninen V, Tenkanen L, Koskinen P, et al., Joint effects of serum triglyceride and LDL cholesterol and HDL cholesterol concentrations on coronary heart disease risk in the Helsinki Heart Study. Implications for treatment , Circulation (1992); 85: pp. 37-45.
    Crossref | PubMed
  20. Koskinen P, Manttari M, Manninen V, et al., Coronary heart disease incidence in NIDDM patients in the Helsinki Heart Study , Diabetes Care (1992); 15: pp. 820-25.
    Crossref | PubMed
  21. Rubins HB, Robins SJ, Collins D, et al., Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group , N Engl J Med (1999); 341: pp. 410-18.
    Crossref | PubMed
  22. Rubins HB, Robins SJ, Collins D, et al., Diabetes, plasma insulin, and cardiovascular disease: subgroup analysis from the Department of Veterans Affairs high-density lipoprotein intervention trial (VA-HIT) , Arch Intern Med (2002); 162: pp. 2597-2604.
    Crossref | PubMed
  23. Field Study Investigators, The need for a large-scale trial of fibrate therapy in diabetes: the rationale and design of the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study [ISRCTN64783481] , Cardiovasc Diabetol (2004); 3: p. 9.
  24. Keech A, Simes RJ, Barter P, et al., Effects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trial , Lancet (2005); 366: pp. 1849-61.
    Crossref | PubMed
  25. Jones PH, Davidson MH, Reporting rate of rhabdomyolysis with fenofibrate + statin versus gemfibrozil + any statin , Am J Cardiol (2005); 95: 120-22.
    Crossref | PubMed
  26. Davidson MH, Statin/fibrate combination in patients with metabolic syndrome or diabetes: evaluating the risks of pharmacokinetic drug interactions , Expert Opin Drug Saf (2006); 5: 145-56.
    Crossref | PubMed