According to the International Diabetes Federation, more than 285 million people (6.4% of the world population) are currently estimated to suffer from diabetes, a figure which is expected to rise to 438 million (7.8%) by 2030. Moreover, the World Health Organisation calculates that nearly three million deaths worldwide are attributable to diabetes each year; by 2030, this figure is expected to double. Type 2 diabetes mellitus (T2DM) accounts for approximately 90% of the cases of diabetes. These astonishing statistics help to illustrate the epidemic prevalence of T2DM, and the major need for effective diagnostic, intervention and disease management strategies.
Prediabetes is presently defined as moderately elevated fasting blood glucose (FBG), and is estimated to affect 79 million adult Americans, or 35% of the adult population. This altered glucose metabolism state is associated with an increased risk of developing T2DM (Figure 1), although other parameters including excess adiposity, inflammation and dyslipidemia are risk factors associated with the development of insulin resistance, loss of pancreatic function, worsening of hyperglycemia and progression to diabetes1.
Type 2 diabetics, but also prediabetics, are at increased risk for a wide range of debilitating diseases and diabetes is the leading cause of new cases of kidney failure and blindness and of nontraumatic lower limb amputation. Moreover, cardiovascular disease (CVD) is 2-4 times higher in diabetics2. An emerging lesser known, but potentially fatal complication of T2DM is the accumulation of fat in hepatocytes (steatosis), that leads to the chronic liver disorder Non-Alcoholic Fatty Liver Disease (NAFLD) and its more advanced form, Non-Alcoholic Steato-Hepatitis (NASH). NAFLD/NASH can progress to hepatitis, cirrhosis, and even liver cancer, thus illustrating the importance of addressing these serious complications of T2DM.
Despite beneficial effects of current glucose-lowering treatments, disease-related morbidity and mortality remain considerable in T2DM patients, galvanising the search for innovative medications that target the multiple metabolic abnormalities as well as inflammatory processes and other pathways predisposing to diabetes-associated disorders. One of the greatest challenges in T2DM disease management is the prevention of its long-term complications and the treatment of associated disorders, including NAFLD/NASH and CVD.
Prospective studies in T2DM have shown an association between the degree of hyperglycemia and the risk of micro- and macrovascular complications, including fatal CVD events. However, the recent ACCORD and ADVANCE trials in patients with longstanding T2DM have shown that aggressive glucose control in such patients has no clear benefits, or may even increase CVD events3. Therefore, other independent risk factors may exist that contribute significantly to CVD risk in these patients. Alternatively, such findings may simply reflect the limitations of current anti-diabetic therapies, due to off-target effects that counter the potential benefits of glucose lowering.
New therapeutics must therefore address the multi-factorial nature of T2DM, and aim to treat diabetic patients at an earlier stage of the disease, if pharmacological interventions hope to halt the epidemic.
Current and future therapeutic approaches
Current widespread treatments for T2DM include metformin (suppressor of hepatic glucose production), sulfonylureas (insulin secretagogues), and the thiazolidinedione pioglitazone (PPAR agonist). More recent incretin-based treatment strategies include glucagon-like peptide-1 (GLP-1) mimetics and inhibitors of the enzyme that degrades GLP-1, dipeptidyl peptidase-4 (DPP-4). GLP-1 is an intestinally-derived peptide that stimulates insulin secretion in response to food intake, as well as reducing the rate of gastric emptying, thus promoting satiety and weight loss. Despite a certain number of gastrointestinal side-effects, the GLP-1 mimetic exenatide was approved by the FDA in 2005, and its indication was extended in 2009 to standalone therapy for T2DM. A retrospective analysis of almost 40,000 patients treated with exenatide showed a reduced incidence of cardiovascular events4, although these results should be confirmed by prospective studies.
New therapeutic approaches in the T2DM drug discovery pipeline are specifically designed to take into account the multi-factorial nature of T2DM by targeting multiple diabetes-related indications, and not simply focusing on glucose-lowering. Moreover, due to the elevated CVD risk in T2DM patients, current FDA recommendations require that all new anti-diabetic drugs show exemplary cardiovascular safety profiles. Thus, drugs that target molecular pathways potentially implicated in both diabetes and CVD are especially desirable. Such approaches include the targeting of 11- hydroxysteroid dehydrogenase type 1 (11- HSD1), GPR119, TGR5, sirtuin 1 (SIRT1), the sodium-glucose co-transporter 2 (SGLT2), and GPR40, for each of which the rationale is briefly described below (Table 1).
11-HSD1: This enzyme mediates the generation of the glucocorticoid cortisol from its inactive precursor cortisone. Since cortisol increases insulin resistance, gluconeogenesis and glycogenolysis, the development of inhibitors for 11-HSD1 provides a potential therapeutic anti-diabetic approach. Indeed, the treatment of murine T2DM models with such an inhibitor improved insulin sensitivity, hyperglycemia and other glycemic parameters5. Moreover, this same study showed that 11-HSD1 inhibition was associated with decreased weight gain in a mouse obesity model, as well as a decrease in lipid parameters and lesion size in a murine atherosclerosis model. The oral, selective 11-HSD1 inhibitor INCB13739, was tested in a Phase II clinical trial as a 12-week add-on therapy to metformin, and resulted in significant reductions in glycemic parameters, plasma lipid levels, and body weight6. However, a recently-published study with another 11-HSD1 inhibitor, MK-0916, reported only modest beneficial effects of a 12-week treatment in patients with T2DM and metabolic syndrome7. Thus, further clinical studies are required to clarify the therapeutic interest of 11-HSD1 inhibitors to address multiple aspects of the metabolic syndrome and, in particular, T2DM.
GPR119: This G protein-coupled receptor (GPCR) is predominantly expressed in pancreatic -cells and in the gastrointestinal tract. GPR119 activation increases cAMP signalling, resulting in enhanced glucose-dependent insulin secretion and increased levels of GLP-1 and the related incretin GIP (Glucose-dependent Insulinotropic Peptide). Oral administration of small molecule GPR119 agonists has been shown to improve glucose tolerance in rodents8, while molecules such as APD5979 and MBX-2982 are in clinical development. Similar to GLP-1 mimetics, GPR119 agonists are also expected to have beneficial effects on obesity, and were indeed shown to decrease feeding, body weight gain, and adiposity in rats10. Thus, GPR119 represents an attractive potential target for both T2DM and associated obesity, although its cardiovascular effects remain to be determined.
TGR5: This widely expressed bile acid-activated GPCR has recently emerged as an attractive therapeutic target in T2DM, obesity, NASH and the metabolic syndrome in general. Similar to GPR119, TGR5 activation in the intestine results in cAMP accumulation and enhanced GLP-1 secretion11. In addition, TGR5 activation in the skeletal muscle enhances energy expenditure via increased thyroid hormone activity, and may have beneficial effects on obesity and insulin resistance12. Finally, TGR5 activation in liver macrophages has anti-inflammatory effects13 and also enhances hepatic nitric oxide production14, with potential beneficial effects on bile acid homeostasis and diabetes-associated liver injury. Evidence of the therapeutic potential of TGR5 in T2DM and associated pathologies was provided by a report of the beneficial effects of the specific TGR5 agonist INT-777 on body weight, hepatic steatosis, preservation of liver and pancreatic function, and maintenance of glucose homeostasis and insulin sensitivity in mouse models15.
SIRT1: This NAD+-dependent deacetylase has been identified as one of the principal downstream mediators of the beneficial effects of caloric restriction on lifespan and metabolic parameters. Potent small molecule activators of SIRT1 have recently been identified, and were shown to improve insulin sensitivity, lower plasma glucose and increase mitochondrial capacity in murine obesity models, and to improve whole-body glucose homeostasis and insulin sensitivity in the Zucker rat T2DM model16. In addition to their beneficial effects on diabetes parameters, SIRT1 activators are expected to have pleiotropic cardioprotective effects. For example, SIRT1 over-expression has shown protection against atherosclerosis in a murine model, likely via anti-apoptotic effects in endothelial cells17. Furthermore, recent studies have demonstrated protective effects of SIRT1 over-expression on ischemia/reperfusion (I/R) injury in the heart18, and on neointima formation following vascular injury in mice19. It will therefore be of great interest to determine the effect of SIRT1 activators on cardiovascular risk in clinical studies.
SGLT2: Via the transporter SGLT2, the kidney plays a key role in the regulation of glucose homeostasis, by mediating glucose reabsorption into the plasma. The development of SGLT2 inhibitors therefore holds promise for glycemic control in T2DM, since the inhibition of renal glucose reabsorption results in increased glucose excretion in the urine. A number of SGLT2 inhibitors (including dapagliflozin, BI-10773, and LX4211) have been developed, and are in the advanced stages of Phase II/III clinical trials, where they have shown efficacy on glycated haemoglobin (HbA1c) levels, fasting plasma glucose, glucose tolerance, weight loss and blood pressure lowering20,21. Moreover, SGLT inhibition may show additional cardioprotective effects, since a recent study showed that treatment with a SGLT inhibitor led to a reduction in infarct size and edema in a murine stroke model22. Thus, the results of Phase III clinical trials of SGLT2 inhibitors are awaited to determine their effects on CVD.
GPR40: Similar to GPR119, this free fatty acid (FFA)-activated GPCR is expressed in both pancreatic -cells and in the endocrine cells of the gastrointestinal tract, where it mediates FFAinduced incretin secretion23. GPR40 overexpression in pancreatic -cells has been shown to increase glucose-stimulated insulin secretion and improve glucose tolerance in normal and diabetic mice24, and small-molecule GPR40 agonists improved glucose tolerance in mice with high-fat diet-induced obesity25. However, a recent study showed that the treatment of Zucker diabetic rats with a small-molecule GPR40 antagonist improved insulin tolerance, while having no effect on glucose tolerance26. Thus, the specific role of GPR40 in T2DM remains open to debate, and should be thoroughly addressed before proceeding with the clinical development of GPR40 modulators.
In addition to the new generation of potential anti-diabetic drug targets described above, opinion is evolving concerning the targeting of members of the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptor transcription factors.
The PPAR agonist pioglitazone has shown beneficial effects on several clinical outcomes in prediabetic and diabetic patients, including reducing the overall risk of cardiovascular events (ProActive Study27), renal complications28, and NASH/ NAFLD29. Moreover, Roche is developing aleglitazar, a balanced mixed PPAR/ agonist, for secondary cardiovascular prevention after myocardial infarction, with the promise of greater preventive effects due to reduction of multiple risk factors, as compared to current glitazone medications30. A Phase III clinical trial with aleglitazar is currently ongoing in patients with T2DM who have recently experienced a cardiac event. Interestingly, the primary endpoint of this study is not glycemic control, but cardiovascular events. Thus, future progress is likely to be focused on the development of PPAR agonists with specific profiles that enable them to address not only T2DM, but also its associated pathologies.
An emerging target in T2DM management is PPAR, due to the positive effects of this PPAR sub-type on multiple features of the metabolic syndrome. Indeed, in pre-clinical studies, PPAR activation increased lipid catabolism in multiple tissues and improved the serum lipid profile, glucose homeostasis, and insulin sensitivity, while reducing inflammation and weight gain31. Finally, the FIELD32 and ACCORD33 studies showed that the PPAR agonist fenofibrate could lower the risk of retinopathy and diabetic nephropathy, as well as reducing CVD events in dyslipidemic patients, thus illustrating the interest of developing mixed PPAR/ or mixed PPAR/ agonists.
GFT505, a potent agonist of the PPAR and PPAR receptors, shows a unique therapeutic profile, notably due to its activity on PPAR. It thus targets multiple micro- and macrovascular risk factors including hyperglycemia and insulin resistance, atherogenic dyslipidemia, the proinflammatory state, and liver dysfunction. GFT505 is currently being developed for T2DM (HbA1c reduction), with a potential to address NAFLD/NASH, cardiovascular prevention in diabetics, and the microvascular complications of diabetes.
GFT505 has undergone Phase IIa clinical trials in pre-diabetic patients and in patients with atherogenic dyslipidemia (high triglycerides, low HDLcholesterol) 34. The data from pre-diabetic patients demonstrate that GFT505 treatment for 28 days results in a significant decrease in fasting plasma glucose, fasting plasma insulin and improvement of the insulin resistance index (HOMA). Furthermore, patients showed a significant reduction in LDL-cholesterol, in parallel with a reduction in triglycerides and an increase in HDL-cholesterol. Importantly, a study conducted in healthy volunteers demonstrated that GFT505 significantly lowered the fasting free fatty acid (FFA) plasma concentration, and potentiated the effect of a meal test on plasma FFA, which is indicative of increased insulin sensitivity35.
GFT505 also shows significant beneficial effects on various abnormalities associated with NAFLD/NASH. Notably, GFT505 treatment reduced liver enzymes (alanine aminotransferase ALAT, gamma-glutamyltransferase GT), and had anti-inflammatory effects34. Moreover, all trials have confirmed the excellent tolerability of GFT505, and the absence of PPAR-related sideeffects34,35. GFT505 is currently in advanced Phase II clinical trials.
Taken together, these clinical results provide compelling arguments for PPAR agonists as a potential treatment for T2DM and associated disorders. Moreover, the beneficial effect of the PPAR/ agonist GFT505 on liver enzymes in Phase IIa indicates that PPAR agonism may show a unique potential for the treatment of NAFLD/NASH, for which no approved treatment exists.
A novel approach to new target identification
Beyond the present potential T2DM therapeutic targets being addressed, there is a need to identify other innovative non-glucosecentric approaches. Access to appropriate patient cohorts and clinical samples is important for novel target identification studies. A public/private research consortium (IT-Diab) has recently been established that focuses on recruiting rare patient cohorts for the purpose of identifying and validating new therapeutic targets in T2DM. One such cohort involves the recruitment of 500 prediabetic patients who will be followed longitudinally for up to five years, or until the onset of T2DM. Blood and tissue samples collected from these patients at regular time-points, followed by transcriptomics and proteomics studies, will provide valuable insight into the mechanisms and players involved in the progression from prediabetes to diabetes.
Another potential source of samples for the identification of novel targets is patients undergoing bariatric surgery, a common therapeutic solution to morbid obesity. Interestingly, a meta-analysis of 136 studies involving patients undergoing bariatric surgery showed that T2DM was completely resolved (defined as the ability to discontinue all diabetes-related medicines and to maintain blood glucose at normal levels) in an impressive 77% of affected patients36.
The mechanism of diabetes resolution after bariatric surgery remains unclear, but is apparently independent of weight loss, since diabetes remission generally occurs in the days and weeks following surgery, prior to significant weight loss. It is believed that surgical manipulation of the gastrointestinal tract plays a direct role in T2DM regression due to effects on metabolic pathways resulting in enhanced insulin sensitivity and/or improved -cell function. Two major hypotheses have been proposed to explain the dramatic effects of bariatric surgery on glycemic control. The ‘lower intestinal hypothesis’37 suggests that the rapid delivery of nutrients to the lower intestine enhances the stimulation of intestinal L cells that produce GLP-1, leading to improved insulin sensitivity. The ‘upper intestinal hypothesis’38 suggests that the exclusion of a short segment of upper small intestine from contact with ingested nutrients may result in reduced production of anti-incretins such as ghrelin, with subsequent improvement of glucose tolerance. It is, of course, highly plausible that both these mechanisms contribute to the anti-diabetic effects of bariatric surgery39.
Whatever the ultimate mechanisms implicated in diabetes regression after bariatric surgery, this dramatic effect, as well as the growing prevalence of bariatric surgery interventions, provides a pool of patients that can be studied with the aim of identifying novel factors that may be implicated in T2DM development. The IT-Diab consortium is therefore recruiting a cohort of more than 600 obese diabetic and non-diabetic patients undergoing gastric banding or bypass surgery. Blood and tissue samples will be harvested from these patients at the time of surgery and during longitudinal follow- up over a period of up to five years. The profiling of gene and protein expression in these samples will provide valuable insight into novel therapeutic targets for T2DM.
Taken together, these two cohorts recruited by the IT-Diab consortium provide innovative and complementary clinical tools for the cross-validation of newly identified therapeutic targets in T2DM. In conjunction with cutting-edge translational technology, these approaches may thus provide new areas of research for the discovery and development of novel T2DM therapies.
The past 30 years have witnessed a revolution in diabetes management, with a move away from simple insulin treatment for glycemic control to improved understanding of the underlying mechanisms of the pathology, and the development of an impressive number of potential therapeutic approaches. Unfortunately, at the same time, sedentary lifestyles and the explosion of unbalanced dietary habits have led to the current obesity pandemic, with the worldwide obese population now estimated at 300 million. Due to the high association between obesity and T2DM, there is thus an ever-growing need to improve prediabetes and diabetes diagnosis and management. While treatment strategies have undeniably progressed, the International Diabetes Federation considers that many, if not the majority, of diabetic patients still have unmet medical needs.
Indeed, the benefit of aggressive HbA1c-lowering therapy has been questioned by major clinical trials such as ACCORD, ADVANCE and VADT, in which the intensive control of HbA1c levels had beneficial effects on microvascular diabetic complications, but did not reduce macrovascular disease or overall mortality3. It is thus now recognised that future anti-diabetic strategies should be designed to address multiple clinical endpoints related to the multifactorial nature of T2DM.
A wide range of different therapeutic approaches are being applied to tackle the multifactorial nature of T2DM, as discussed here, and the ClinicalTrials.gov website currently lists almost 1,000 active Type 2 diabetes trials worldwide. The inclusion of cardiovascular parameters in the study endpoints of these trials, together with the growing awareness of the importance of tackling cardiometabolic disease, including associated liver diseases, as a whole, means that the coming years hold great promise for the identification of novel therapeutic strategies for T2DM and its associated diseases.
Dr Lesley Millatt completed post-doctoral training at the University of Virginia, and in 2000 joined Genfit, a biopharmaceutical company focused on the early diagnosis and treatment of diabetes and related disorders (from risk factors to complications).
Dr Rémy Hanf is in charge of Drug Development & Translational Research at Genfit. Before joining Genfit in 2003, he held various R&D management positions in pharmaceutical companies involved in cardiovascular and metabolic disorders.
Dr Dean W Hum joined Genfit in 2000 and is presently responsible for Scientific Affairs. Before joining Genfit he was Associate Professor at Laval University, where he worked on functional genomics and the regulation of gene transcription in Endocrinology.
1 Grundy, SM. Drug therapy of the metabolic syndrome: minimizing the emerging crisis in polypharmacy. Nat Rev Drug Discov, 2006. 5(4): p. 295-309.
2 Haffner, SM et al., Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction. N Engl J Med, 1998. 339(4): p. 229-34.
3 Meier, M and Hummel, M. Cardiovascular disease and intensive glucose control in type 2 diabetes mellitus: moving practice toward evidence-based strategies. Vasc Health Risk Manag, 2009. 5: p. 859-71.
4 Best, JH et al. Risk of cardiovascular disease events in patients with type 2 diabetes prescribed the glucagon-like peptide 1 (GLP- 1) receptor agonist exenatide twice daily or other glucoselowering therapies: a retrospective analysis of the LifeLink database. Diabetes Care, 2011. 34(1): p. 90-5.
5 Hermanowski-Vosatka, A et al. 11beta-HSD1 inhibition ameliorates metabolic syndrome and prevents progression of atherosclerosis in mice. J Exp Med, 2005. 202(4): p. 517-27.
6 Rosenstock, J et al. The 11- beta-hydroxysteroid dehydrogenase type 1 inhibitor INCB13739 improves hyperglycemia in patients with type 2 diabetes inadequately controlled by metformin monotherapy. Diabetes Care, 2010. 33(7): p. 1516-22.
7 Feig, PU et al. Effects of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor, MK-0916, in patients with type 2 diabetes mellitus and metabolic syndrome. Diabetes Obes Metab, 2011. 13(6): p. 498-504.
8 Chu, ZL et al. A role for beta-cell-expressed G proteincoupled receptor 119 in glycemic control by enhancing glucose-dependent insulin release. Endocrinology, 2007. 148(6): p. 2601-9.
9 Semple, G et al. Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control. Bioorg Med Chem Lett, 2011. 21(10): p. 3134-41.
10 Overton, HA et al. Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of smallmolecule hypophagic agents. Cell Metab, 2006. 3(3): p. 167- 75.
11 Katsuma, S, Hirasawa, A and Tsujimoto, G. Bile acids promote glucagon-like peptide- 1 secretion through TGR5 in a murine enteroendocrine cell line STC-1. Biochem Biophys Res Commun, 2005. 329(1): p. 386-90.
12 Watanabe, M et al. Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation. Nature, 2006. 439(7075): p. 484-9.
13 Keitel, V et al. Expression and function of the bile acid receptor TGR5 in Kupffer cells. Biochem Biophys Res Commun, 2008. 372(1): p. 78- 84.
14 Keitel, V et al. The Gprotein coupled bile salt receptor TGR5 is expressed in liver sinusoidal endothelial cells. Hepatology, 2007. 45(3): p. 695-704.
15 Thomas, C et al. TGR5- mediated bile acid sensing controls glucose homeostasis. Cell Metab, 2009. 10(3): p. 167- 77.
16 Milne, JC et al. Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes. Nature, 2007. 450(7170): p. 712-6.
17 Zhang, QJ et al. Endothelium-specific overexpression of class III deacetylase SIRT1 decreases atherosclerosis in apolipoprotein E-deficient mice. Cardiovasc Res, 2008. 80(2): p. 191-9.
18 Hsu, CP et al. Silent information regulator 1 protects the heart from ischemia/reperfusion. Circulation, 2010. 122(21): p. 2170-82.
19 Li, L et al. SIRT1 Acts as a Modulator of Neointima Formation Following Vascular Injury in Mice. Circ Res, 2011. 108(10): p. 1180-9.
20 Komoroski, B et al. Dapagliflozin, a novel, selective SGLT2 inhibitor, improved glycemic control over 2 weeks in patients with type 2 diabetes mellitus. Clin Pharmacol Ther, 2009. 85(5): p. 513-9.
21 Aires, I and Calado, J. BI- 10773, a sodium-glucose cotransporter 2 inhibitor for the potential oral treatment of type 2 diabetes mellitus. Curr Opin Investig Drugs, 2010. 11(10): p. 1182-90.
22 Vemula, S et al. A functional role for sodium-dependent glucose transport across the blood-brain barrier during oxygen glucose deprivation. J Pharmacol Exp Ther, 2009. 328(2): p. 487-95.
23 Edfalk, S, Steneberg, P and Edlund, H. Gpr40 is expressed in enteroendocrine cells and mediates free fatty acid stimulation of incretin secretion. Diabetes, 2008. 57(9): p. 2280-7.
24 Nagasumi, K et al. Overexpression of GPR40 in pancreatic beta-cells augments glucose-stimulated insulin secretion and improves glucose tolerance in normal and diabetic mice. Diabetes, 2009. 58(5): p. 1067-76.
25 Tan, CP et al. Selective smallmolecule agonists of G proteincoupled receptor 40 promote glucose-dependent insulin secretion and reduce blood glucose in mice. Diabetes, 2008. 57(8): p. 2211-9.
26 Zhang, X et al. DC260126, a small-molecule antagonist of GPR40, improves insulin tolerance but not glucose tolerance in obese Zucker rats. Biomed Pharmacother, 2010. 64(9): p. 647-51.
27 Dormandy, JA et al. Secondary prevention of macrovascular events in patients with type 2 diabetes in the PROactive Study (PROspective pioglitAzone Clinical Trial In macroVascular Events): a randomised controlled trial. Lancet, 2005. 366(9493): p. 1279-89.
28 Sarafidis, PA and Bakris, GL. Protection of the kidney by thiazolidinediones: an assessment from bench to bedside. Kidney Int, 2006. 70(7): p. 1223-33.
29 Sanyal, AJ et al. Pioglitazone, vitamin E, or placebo for nonalcoholic steatohepatitis. N Engl J Med, 2010. 362(18): p. 1675-85.
30 Lecka-Czernik, B. Aleglitazar, a dual PPARalpha and PPARgamma agonist for the potential oral treatment of type 2 diabetes mellitus. IDrugs, 2010. 13(11): p. 793- 801.
31 Coll, T et al. Peroxisome proliferator-activated receptor (PPAR) beta/delta: a new potential therapeutic target for the treatment of metabolic syndrome. Curr Mol Pharmacol, 2009. 2(1): p. 46-55.
32 Keech, A 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(9500): p. 1849-61.
33 Chew, EY et al. Effects of medical therapies on retinopathy progression in type 2 diabetes. N Engl J Med, 2010. 363(3): p. 233-44.
34 Cariou, B, Zaïr, Y, Staels, B, Bruckert, E. Effects of the new dual PPAR/ agonist GFT505 on lipid and glucose homeostasis in abdominally obese patients with combined dyslipidemia or impaired glucose metabolism. Diabetes Care, 2011(in press).
35 Hanf, R, Hum, DW, Staels, B. GFT505 Efficacy and Safety in Healthy Volunteers and Patients Suffering from Atherogenic Dyslipidemia. American Diabetes Association, 70th Scientific Session, 2010.
36 Buchwald, H et al. Bariatric surgery: a systematic review and meta-analysis. JAMA, 2004. 292(14): p. 1724-37.
37 Cummings, DE et al. Role of the bypassed proximal intestine in the anti-diabetic effects of bariatric surgery. Surg Obes Relat Dis, 2007. 3(2): p. 109-15.
38 Rubino, F et al. The mechanism of diabetes control after gastrointestinal bypass surgery reveals a role of the proximal small intestine in the pathophysiology of type 2 diabetes. Ann Surg, 2006. 244(5): p. 741-9.
39 Caiazzo, R et al. Gastric bypass and glucose metabolism. Diabetes Metab, 2009. 35(6 Pt 2): p. 528-31.