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Supplements Pathways to Success: Utilizing Managed Care Models to Improve Clinical and Economic Outcomes in Diab

Current State of Type 2 Diabetes Management

Mark E. Molitch, MD
Type 2 diabetes mellitus (T2DM) and its associated comorbidities are a major public health issue in the United States. Although a sizable pharmacotherapeutic armamentarium exists to combat this disease and several sources have published evidence-based management guidelines, the management of patients with T2DM remains complex and suboptimal. Currently available medications target various organs in an attempt to normalize hyperglycemia; however, newer agents targeting additional organ systems are in development. Among these, a class of medications that inhibit the sodium glucose cotransporter 2 (SGLT2) in the kidney show promise in their ability to decrease glucose reabsorption and increase glucose excretion. In particular, one of these compounds, canagliflozin, recently was approved by the US Food and Drug Administration. Despite such advances, the natural course of T2DM often eventually leads to the initiation of insulin therapy. A working knowledge of management guidelines, particularly concerning when and how to initiate monotherapies, combination therapies, and complex insulin regimens, is essential for optimal patient management. Insulin therapies should mimic normal physiologic levels of insulin through the use of both basal and bolus insulin analogues. Recognition of the various factors influencing therapeutic choices is also critical for improved patient management.

(Am J Manag Care. 2013;19:S136-S142)
Type 2 diabetes mellitus (T2DM), which accounts for approximately 90% to 95% of those with diabetes mellitus (DM), is primarily due to insulin resistance and relative insulin deficiency.1,2 According to data collected by the Centers for Disease Control and Prevention (CDC) in 2010, a total of 25.8 million people, or 8.3% of the US population, are estimated to have DM.3 This figure reflects both diagnosed (18.8 million) and undiagnosed (7.0 million) cases.3 Furthermore, 79 million adults over age 20 years were found to have “prediabetes,” a condition marked by levels of blood glucose or glycated hemoglobin (A1C) that are above normal ranges, but not high enough to be classified as T2DM.3 Additional CDC statistics indicate that DM is associated with significant morbidity and mortality. For example, the risk for death among people with T2DM is about twice that of people of similar age without T2DM, and T2DM is the seventh-leading cause of death in the United States.3 Furthermore, T2DM is the leading cause of kidney failure, nontraumatic lower-limb amputations, and new cases of blindness among adults in the United States, and is a major cause of heart disease and stroke.3

Evidence That T2DM Is Treated Suboptimally

The American Diabetes Association (ADA) has published recommendations for glycemic, blood pressure (BP), and lipid control for adults with T2DM in its annual Standards of Medical Care publication.4 The ADA recommends that A1C should be less than 7%, although more or less stringent glycemic goals may be appropriate for individual patients. In addition, goals should be individualized based on the duration of DM, patient age and life expectancy, comorbid conditions, known cardiovascular disease (CVD) or advanced microvascular complications, hypoglycemia unawareness, and individual patient considerations. BP should be less than 140/80 mm Hg; however, higher or lower systolic blood pressure targets may be appropriate based on patient characteristics and response to therapy. Regarding lipids, low-density lipoprotein cholesterol (LDL-C) should be less than 100 mg/ dL (<2.6 mmol/L) and a lower goal of less than 70 mg/dL (<1.8 mmol/L) is recommended for individuals with overt CVD, with the use of a high dose of statin as an option.4 Data collected from the National Health and Nutrition Examination Survey (NHANES) from 2003 to 2006 demonstrated a clear lack of adherence to these recommendations, with 57.1% of participants reaching the recommended A1C goal, 45.5% reaching the recommended blood pressure goal, 46.5% reaching the recommended LDL-C goal, and only 12.2% meeting all 3 goals.5 Additionally, a CDC analysis of NHANES data from 2007 to 2010 showed that 16% of those with diagnosed DM were not receiving any pharmacotherapy for the disease.3 An additional analysis of NHANES data from 2007 to 2010 reported the proportion of diabetic patients with A1C values over 9% as a function of source of care and insurance status.6 Study results regarding source of care revealed that patients receiving care outside of a hospital, clinic, or physician’s office had the highest adjusted prevalence, slightly above 20%, and insurance data indicated that the uninsured had the highest adjusted prevalence, slightly below 30%, compared with those on Medicare, or with public or private insurance.6 It should be noted that most of the source of care and insurance status categories showed adjusted prevalences of approximately 10% or greater; however, among the privately insured, 7.2% had an A1C over 9%.6 Based on these data, it seems clear that T2DM is treated suboptimally; however, the question remains as to why this is the case. Several barriers to effective DM control have been postulated, including clinical inertia, financial issues, cultural issues, adverse effects associated with oral agents, the reality that targets of treatment require careful adjustment in each individual patient, and issues pertaining to the use of insulin such as fear of injections, fear of hypoglycemia, and the complexity of management.

Diabetes Management

There are several classes of therapeutic agents available to treat T2DM (Table)7-10 and each agent acts on different pathways to control hyperglycemia.11,12 For example, sulfonylureas act in the pancreas, stimulating insulin release by binding to the sulfonylurea receptors on β-cell membranes.11 Meglitinides, another class of short-acting insulin secretagogues, are used to control postprandial hyperglycemia and also act in the pancreas, stimulating insulin release by binding to several sites on β cells.11 Thiazolidinediones (TZDs) are selective peroxisome proliferator-activated receptor gamma agonists that work in muscle and can also exert effects in the liver and adipose tissue and act by reducing insulin resistance and decreasing hepatic glucose output.11,12 Alpha-glucosidase inhibitors lower postprandial blood glucose concentrations by inhibiting disaccharidase enzymes in the gut, thereby delaying carbohydrate absorption and retarding glucose entry into the systemic circulation.11 Biguanides (metformin) act predominantly by reducing hepatic glucose production.7 Metformin also enhances insulin sensitivity in muscle and decreases intestinal absorption of glucose.7,11,13,14 Based on their different mechanisms of action, these drugs may be used in combination. The dipeptidyl peptidase-4 (DPP-4) inhibitors prevent the enzyme DPP-4 from degrading and inactivating glucagon-like peptide-1 (gLP-1) and gastric inhibitory polypeptide, incretin hormones that are produced in the gut and help regulate insulin production and secretion.15 This glucose-dependent mechanism targets 2 key defects: insulin release and hepatic glucose production (via reduced glucagon production). Although some concern has been expressed regarding the use of DPP-4 inhibitors and the development of pancreatitis, a retrospective cohort study of a large medical and pharmacy claims database that analyzed data from 786,656 patients using Cox proportional hazard models demonstrated an increased incidence of acute pancreatitis in diabetic versus nondiabetic patients; however no association was found between the use of the DPP-4 inhibitors, exenatide or sitagliptin, and acute pancreatitis.16 exenatide and liraglutide are injectable gLP-1 receptor agonists that exert their antihyperglycemic effects through increasing insulin secretion, inhibiting glucagon secretion, and reducing appetite.17

Emerging Novel Therapeutic Class of Antidiabetic Drugs: Sodium Glucose Cotransporter 2 (SGLT2) Inhibitors

In a review, published in 2012, of novel pharmacologic approaches to the treatment of T2DM, Verspohl reviewed the reasons why new agents are being actively pursued and explained that nearly 1000 compounds have been described, approximately 180 of which are already in clinical studies in the united States.18 Some of these compounds in development would exert an antidiabetic effect by inhibiting the sodium glucose cotransporter 2 (SgLT2) in the kidney, which plays a critical role in the reabsorption of glucose (Figure 1). each day, 180 g of plasma glucose are filtered by the kidney and virtually all is reabsorbed into plasma in the proximal tubules.19-21 In healthy individuals, virtually all the glucose filtered is reabsorbed and glucose does not appear in the urine. However, glucose starts appearing in urine once levels exceed the maximum capacity (Tm) of the carrier protein, usually corresponding to a plasma glucose level of approximately 200 mg/dL.21 Hyperglycemia results in hyperfiltration of glucose in the kidney in patients with DM, which in turn leads to increased luminal glucose that exceeds the maximum reabsorption rate, resulting in glucosuria (Figure 2). SgLT2 inhibitors can act in the kidney to decrease reabsorption and increase excretion of glucose (Figure 2).21,22 One of these SgLT2 inhibitors, canagliflozin, has recently been approved by the US Food and Drug Administration. In a 26-week, randomized, double-blind, placebo-controlled, phase 3 trial, 584 adult subjects with T2DM who were inadequately controlled with diet and exercise received canagliflozin 100 or 300 mg or placebo once daily.23 At week 26, canagliflozin 100 and 300 mg (compared with placebo) significantly reduced A1C from baseline (–0.77, –1.03, and 0.14%, respectively; P <.001 for both). Additionally, both canagliflozin doses significantly decreased body weight (P <.001 for both). Regarding safety results, the overall incidences of adverse events (AEs) were modestly higher with canagliflozin versus placebo. Low and similar rates of serious AEs and AE-related discontinuations were reported across groups. In addition, the incidences of genital mycotic infections, urinary tract infections, and osmotic diuresis–related AEs were higher with canagliflozin, although these led to few discontinuations. Lastly, the incidence of hypoglycemia was low across groups. The study authors concluded that treatment with canagliflozin improved glycemic control, reduced body weight, and was generally well tolerated in subjects with T2DM inadequately controlled with diet and exercise.23 Canagliflozin, as a monotherapy, has A1C-lowering abilities of 0.77 to 1.03 percentage points depending on dose.23

Natural History of T2DM

Before the manifestation of the metabolic defects that lead to T2DM, fasting and postprandial insulin levels are similar and constant. In the majority of patients in whom T2DM develops, increasing insulin resistance leads to compensatory increases in circulating insulin which prevent an increase in glucose levels. As time progresses, the insulin resistance reaches a peak and stabilizes, while the compensatory increase in insulin continues to prevent fasting glucose levels from becoming abnormal. However, at some point, either because of early β-cell dysfunction or because of a natural limit of β-cell capacity, challenge of this delicate balance with a glucose load may demonstrate that, although fasting glucose levels remain normal, postprandial glucose levels become abnormal as a limitation in insulin response is reached. Following the onset of β-cell dysfunction, insulin levels can no longer keep up in overcoming the insulin resistance, and fasting and postprandial glucose levels increase progressively over time.24 Based on this pattern, there may be a need to add additional drugs or change to insulin to achieve adequate glycemic control with longer duration of T2DM.

Treatment Guidelines

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