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A Real-World Approach to Insulin Therapy in Primary Care Practice

Type 2 diabetes is a progressive disease characterized by relentless deterioration of pancreatic ß-cell function.¹ With the increasing incidence of type 2 diabetes, especially among younger individuals who will live longer with their disease, more patients will develop severe insulin deficiency and require insulin replacement. Because primary care providers see the vast majority of patients with type 2 diabetes, they may soon find themselves overwhelmed with insulin-requiring patients.

This article provides some practical guidelines for initiating insulin therapy in primary care practice. It is important to remember, however, that these are general guidelines and that management should be individualized for each patient.

WHY INSULIN THERAPY?

Some primary care providers may be apprehensive about using insulin in patients with type 2 diabetes. Wallace and Matthews² have gone so far as to suggest that patients and providers have often "colluded in implicit and unspoken contracts to continue oral agents for as long as possible."

Concerns about hypoglycemia and patient willingness and/or ability to inject insulin are good reasons why many providers may approach insulin therapy with caution. Compounding this reluctance is the perception that insulin therapy is too complex to manage in a busy primary care practice; prescribing information provided by manufacturers has been somewhat vague regarding initial dosing and titration. Because of these factors, providers may delay in making the necessary transition from oral agents to insulin. Indeed, recent evidence suggests that the hemoglobin A_1c (A1C) result that triggers glucose-lowering action is 9%.³ This is unfortunate because numerous studies have shown that excellent glycemic control can be achieved with insulin therapy in patients with type 2 diabetes.^4-7 Moreover, there is an increasing body of evidence showing that early and effective intervention with insulin is more important than had been previously believed.^8-10

Early and Aggressive Intervention Matters
Insulin is considered the most effective treatment for lowering extremely high glucose. This is important because inhibition of glucotoxicity may be beneficial in preserving functional ß-cell mass.¹ Oral agents do not work as quickly or lower glucose enough to effectively address glucotoxicity in many patients. For example, patients treated with sulfonylureas show a decrease in fasting glucose of only 60-70 mg/dl; the A1C value will decrease by 1.5-2.0 percentage points.^11,12

New data from the Epidemiology of Diabetes Interventions and Complications (EDIC) study highlight the importance of early intervention to aggressively lower glucose.⁸ The EDIC study is an ongoing effort that follows the cohort from the Diabetes Control and Complications Trial (DCCT).¹³ In the EDIC study, glycemic levels no longer differed substantially between the two original DCCT treatment groups at 7 years. However, subjects who had been intensively treated during the DCCT showed significant decreases in risk for nephropathy and retinopathy compared with subjects from the conventional treatment arm. In other words, the benefits of 6.5 years of intensive treatment during the DCCT have extended well beyond the time of intensive therapy.

Insulin May Have a Protective Quality
Insulin therapy may actually protect against endothelial damage. Observational and interventional evidence consistently indicates that glycemic control with insulin therapy in the hospital setting can improve clinical outcomes.^14-17 Malmberg et al.¹⁴ demonstrated that the unfavorable long-term prognosis for myocardial infarction could be improved by insulin treatment. In that study, diabetic patients who received insulin infusion immediately within 24 hours of myocardial infarction, followed by multidose subcutaneous insulin treatment for at least 3 months, showed a significantly lower mortality rate (19%) at 1 year compared with subjects who received standard treatment (26%), which generally included sulfonylurea therapy.

New Insulin Analogs More Closely Match Normal Physiology
New insulin analogs (rapid and long acting) closely match normal physiology.^18-20 Rapid-acting insulin analogs, such as insulin aspart and insulin lispro, produce higher serum insulin levels earlier and have a shorter duration of action than regular human insulin. This results in lower postprandial glucose excursions and shorter durations of postprandial hyperglycemia, with significantly reduced incidence of severe hypoglycemia in patients with type 2 diabetes.^18,19 Additionally, studies that have looked at the effects of rapid-acting insulin analogs combined with intermediate-acting insulins (free-mixed and premixed preparations) in patients with type 2 diabetes have shown improved postprandial glucose control with reduced hypoglycemia.^21-23

New Evidence Links Glucose Excursions to Cardiovascular Risk
Reducing postprandial glucose excursions is particularly important in light of new data that show a relationship between postprandial hyperglycemia and atherosclerotic risk. A recent study from Esposito et al.¹⁰ demonstrated that reduction of postprandial hyperglycemia in patients with type 2 diabetes is associated with carotid intima-media thickness (CIMT) regression; CIMT is a clinical marker for atherosclerosis. Recent data from Ceriello et al.⁹ showed that postprandial hyperglycemia is accompanied by endothelial dysfunction in patients with type 2 diabetes and that rapid-acting insulin at mealtime improved endothelial function. Earlier reports from Ceriello et al.²⁴ suggest that postprandial hyperglycemia and hypertriglyceridemia induce endothelial dysfunction through oxidative stress. Other studies support the link between postprandial glucose excursions and atherosclerotic risk.^25-28

Chiasson et al.²⁹ showed that addressing postprandial hyperglycemia using an -glucosidase inhibitor actually delayed progression from impaired glucose tolerance to type 2 diabetes and was associated with a significant reduction in combined cardiovascular events. This is not a recommendation to initiate nonapproved pharmacological therapy in patients with impaired glucose tolerance. However, a significant body of evidence strongly supports the rationale for initiating therapy to achieve glycemic control in patients with type 2 diabetes much earlier and much more aggressively.

Patients Will Eventually Need Insulin Therapy
As stated earlier, type 2 diabetes is a progressive disease in which ß-cell function deteriorates. Findings from the U.K. Prospective Diabetes Study (UKPDS) showed that deterioration in ß-cell function occurred in the diet-only treatment group as well as in patients treated with sulfonylureas or metformin, suggesting that neither of these agents slowed the rate of decline.³⁰ The UKPDS also showed that even basal insulin (ultralente) did not slow ß-cell deterioration.³⁰ Another study found that 30% of patients initially treated with a sulfonylurea drug have a poor response; the remaining 70% experience a failure rate of 4-5% per year.³¹ It is, therefore, reasonable to conclude that most patients with type 2 diabetes will eventually need exogenous insulin.

Unfortunately, insulin therapy too often is used as a "punishment" for above-target hyperglycemia. A better approach would be to explain to patients early in the course of their disease, instead of at the end, the natural history of insulin deficiency in type 2 diabetes.²

WHO SHOULD BE STARTED ON INSULIN?

Initiating therapy with oral agents is a reasonable approach to take with most patients, the exception being patients with extreme hyperglycemia (fasting plasma glucose > 250 mg/dl).³² These patients require insulin, even basal-bolus insulin therapy, to lower glucose levels. Otherwise, starting with oral therapy can be very effective, especially in patients with a short duration of diabetes and, thus, relatively adequate ß-cell function. However, clinicians often wait too long to move patients from oral therapy to insulin.^33,34 In the UKPDS, only 33% of patients treated with metformin and sulfonylurea had an A1C < 7% after 3 years of treatment.³⁵

When determining whether a patient should be put on insulin therapy, it is helpful to look to the guidelines for glycemic control. The American Diabetes Association (ADA)³⁶ and American College of Endocrinology (ACE)³⁷ publish goals for A1C, postprandial glucose, and fasting/preprandial glucose (Table 1). Most patients who are unable to achieve these goals using oral agents are candidates for insulin therapy. Table 2 lists the more commonly used insulins, along with information about their peak activity.

The key to making this determination is timely (preferably weekly) titration of dosages until either glucose targets are met or maximum effective dosages fail to achieve target levels. For example, weekly titration of sulfonylurea dosages, in combination with daily fasting glucose data (provided by the patient), will show whether monotherapy with sulfonylurea can provide adequate glycemic control. If not, the addition and timely titration of a second agent (metformin or a thiazolidinedione) over the next 2 months, along with continued blood glucose monitoring, will show whether combination oral therapy can provide adequate glycemic control. If not, insulin therapy is clearly warranted and should be promptly initiated (Figure 1).

View larger version (36K): [in this window] [in a new window]   Figure 1. Algorithm for initiating insulin therapy.

Although it may be tempting to add a third oral agent, clinicians must consider the added cost and potential side effects associated with triple oral therapy. A recent study by Schwartz et al.³⁸ showed that a regimen of premixed insulin in combination with metformin was as effective as but much less expensive than triple oral therapy; a high percentage of subjects (16.3%) from the triple oral agent treatment group did not complete the regimen because of a lack of efficacy or side effects.

HOW TO START PATIENTS ON INSULIN

Starting patients on insulin does not have to be difficult. This section presents an approach that takes the uncertainty and complexity out of initiating insulin therapy in patients with type 2 diabetes. Figure 1 provides an algorithm for transition from oral therapy to insulin.

Match the Regimen to the Patient
A basal-bolus regimen—glargine with rapid-acting insulin analogs at each meal—is the ideal regimen in terms of physiological action and overall glycemic control. However, many patients are reluctant to start with a basal-bolus insulin regimen. Furthermore, basal-bolus insulin management requires not only motivation of both patient and provider, but also comprehensive training in carbohydrate counting (or some method of food/insulin matching) and insulin adjustment. Therefore, it is important to match the insulin regimen to the individual needs, concerns, and capabilities of each patient.

Patients who are reluctant to do basal-bolus management initially often make the transition to multiple daily injection (MDI) regimens after gaining confidence in their ability to safely and effectively use insulin through less intensive regimens. Table 3 presents common insulin regimens based on patient clinical status and lifestyle characteristics.

Although regimens for once-daily glargine and once-daily and twice-daily premixed insulin are listed, it is important to note that recent studies comparing once-daily regimens to twice-daily regimens have demonstrated significant differences between the two approaches.^39-41

One study showed that twice-daily premixed insulin (25% lispro/75% NPL) provided lower A1C levels compared with once-daily glargine when patients were randomized to one or the other insulin regimen in addition to existing metformin therapy³⁹ Results also showed a smaller rise in postprandial glucose levels and a higher proportion of patients achieving an A1C of 7.0% on twice-daily premixed therapy. In one study, there was a slight increase in overall hypoglycemia with no increase in nocturnal hypoglycemia,³⁹ whereas another study showed no difference in overall hypoglycemia with less nocturnal hypoglycemia in the premix group.⁴⁰ A third study showed similar findings regarding overall hypoglycemia.⁴¹ In short, no definitive differences in hypoglycemia were consistently seen in these studies.

When postprandial glucose is not adequately controlled by combination therapy using basal insulin and oral agents, a twice-daily regimen using a premixed insulin preparation (prebreakfast, presupper) is preferred. Clinicians can start patients on once-daily injections at the evening meal and add the second injection as needed. Rapid-acting analog premixed insulin is an option if the patient eats small lunches or misses lunch regularly. Although no definitive studies have looked at this issue, the authors agree that for individuals eating large lunches (e.g., > 40% of their total daily calories), a better premix insulin would be 70% NPH/30% regular insulin. The problem with this regimen, however, is that the lunchtime meal needs to be consumed at about the same time each day to avoid hypoglycemia.

Basal-bolus insulin therapy may be required for patients with glucose toxicity (fasting plasma glucose > 250 mg/dl).⁴² Basal-bolus insulin therapy can be continued or modified after glucose returns to near-normal levels. Additionally, basal-bolus insulin management should be presented as the next option if patients are unable to achieve targets with a premixed insulin regimen. This will be the rule for patients with more severe insulin deficiency.

Start Low and Titrate Steadily
A common starting dose for insulin therapy in patients with type 2 diabetes is 0.15 units/kg body wt/day;⁴² however, because > 90% of patients with type 2 diabetes are insulin resistant,⁴³ significantly higher doses are often required to achieve glycemic targets.^39-41,44

The Treat-to-Target study⁴⁴ used a starting dose of 10 units/day with glargine or human NPH at bedtime; mean daily dosages at end point adjusted for body weight were 0.48 units/kg for glargine and 0.42 units/kg for NPH in those patients who were maintained on one or two oral agents throughout the study. This is equivalent to 40 units/day in an average 200-lb patient. A study of premixed insulin in patients on oral agents initiated insulin therapy with a dose of 6 units/day; however, the average dosage at 28 weeks was > 75 units/day (0.85 units/kg/day), with no major hypoglycemic episodes reported.⁴¹

The differences in average dosages at end point reported in these studies resulted from differences in baseline A1C levels, durations of diabetes, and overall levels of insulin resistance in the study subjects. Nevertheless, these studies show 10 units/injection to be a safe starting dose for once-daily and twice-daily insulin regimens (Table 4).

It is important to note that although glargine can be taken at any time during the day, it should be injected at the same time every day. Patients should document all results from self-monitoring of blood glucose (SMBG) and insulin doses in their logbooks when starting or adjusting insulin. Glucose meter downloading is another excellent tool for review of SMBG data.⁴⁵

Monitor and Adjust Therapy Until Targets are Achieved
Although insulin is the most effective treatment for lowering glucose, a recent national study showed that only half of patients with type 2 diabetes who are treated with insulin achieve an A1C < 7%.⁴⁶ To be successful, insulin therapy requires timely and appropriate titration of dosages. Table 5 presents a titration schedule that can be used with once-daily and twice-daily regimens to make safe and timely insulin adjustments.

Working with this schedule, patients measure blood glucose once or twice daily (prebreakfast, presupper) depending on their regimen. Based on these blood glucose data reported by the patient, the clinician can then make step-wise adjustments in response to the average glucose values. Prebreakfast dosage adjustments are based on presupper glucose results, whereas presupper dosage adjustments are based on prebreakfast glucose values.

For example, in a patient on 10 units of premixed insulin twice daily who reports prebreakfast glucose values ranging from 148 to 175 mg/dl over the past 3-7 days, the appropriate adjustment would be an additional 4 units of insulin before supper.

Another key aspect of insulin titration is timely adjustment. As with oral therapy, clinicians often wait too long to make adjustments in insulin dosages, allowing excessive glycemic exposure to persist for months (or years, in some cases). A major obstacle to timely insulin adjustment is primarily the logistics of communicating with the patient. Table 6 presents some options for patient follow-up that may expedite achieving glycemic targets on timely basis. Diabetes education is a crucial aspect of patient care and is recommended for all patients, particularly those who are self-adjusting their insulin dosages.

If patients are not at goal after 3-6 months of therapy or if recurrent hypoglycemia limits titration, consider changing the regimen. Table 7 presents strategies for making this transition.

When assessing the need to change regimens, it is important to understand and consider the impact of fasting glucose and postprandial glucose on overall glycemic control. Monnier et al.⁴⁷ recently published findings that showed a variable relationship between fasting and glucose based on current A1C levels. As shown in Figure 2, the report revealed that the relative contribution of fasting glucose to overall glycemia is 70% in patients with an A1C of > 10.2%; the contribution of fasting glucose decreases as A1C levels decrease.

View larger version (24K): [in this window] [in a new window]   Figure 2. Relative contribution of fasting and postprandial glucose to A1C. Adapted from Monnier et al.47

Knowing the relative contribution of fasting and postprandial glucose to A1C allows clinicians to make more informed decisions about therapy. For example, if a patient's A1C is at 7.5%, adjustment should focus on lowering postprandial glucose; adding basal insulin will not directly address postprandial hyperglycemia. Although the addition of basal insulin will improve the overall A1C, as shown in the Treat-to-Target study,⁴⁴ it will not lower the degree of postprandial excursions. Only meal plan modification or prandial insulin will address this issue. Figure 3A illustrates how addressing fasting glucose can initially lower fasting levels and even improve postprandial excursions by reducing glucotoxicity and thus improving ß-cell function. However, once fasting glucose levels are normalized, increasing the basal dosage will not adequately address the remaining postprandial hyperglycemia (Figure 3B). Therefore, a regimen that addresses both fasting and postprandial hyperglycemia is needed (Figure 3C).

View larger version (16K): [in this window] [in a new window]   Figure 3(A) . Elevated fasting glucose with large postprandial glucose excursion.

View larger version (15K): [in this window] [in a new window]   (B) . Use of basal insulin normalizes fasting glucose and reduces postprandial glucose excursions by reducing glucotoxicity

View larger version (15K): [in this window] [in a new window]   (C) . Use of basal and mealtime insulin addresses fasting and postprandial hyperglycemia.

CONCLUSION

Insulin therapy in the treatment of type 2 diabetes offers significant advantages in efficacy and outcomes. However, unfounded fear of hypoglycemia and uncertainties regarding initial dosage and titration have been key obstacles for many providers when making the decision to initiate insulin treatment in their patients with type 2 diabetes.

Given the progressive nature and increasing incidence of type 2 diabetes, more patients will be faced with severe insulin deficiencies in their lifetimes. It is hoped that the information and recommendations provided in this article will help primary care providers become more effective in their management of patients with type 2 diabetes.

Acknowledgments

The authors gratefully acknowledge support from Eli Lilly in funding the expenses related to developing this article.

Footnotes

Irl B. Hirsch, MD, is a professor of medicine in the Division of Metabolism, Endocrinology, and Nutrition at the University of Washington Medical Center in Seattle. Richard M. Bergenstal, MD, is executive director of the International Diabetes Center and a clinical professor at the University of Minnesota, both in Minneapolis. Christopher G. Parkin, MS, is a medical writer and consultant to professional medical organizations and healthcare companies and president of CGParkin Communications in Carmel, Ind., Eugene E. Wright, Jr., MD, is medical director of Primary Care and Specialty Practices of Cape Fear Valley Health System in Fayetteville, N.C. John B. Buse, MD, PhD, is an associate professor at the University of North Carolina School of Medicine in Chapel Hill, where he is the division chief of General Medicine and director of the Diabetes Care Center. He is also an associate editor of Clinical Diabetes.

Notes of disclosure: Dr. Hirsch has received consulting fees or honoraria for speaking engagements from Eli Lilly, Novo Nordisk, and Sanofi-Aventis Pharmaceuticals. He also receives research support from Mannkind Corporation.

Dr. Bergenstal has served on advisory panels for, received consulting fees or honoraria from, and received research support from Eli Lilly, Novo Nordisk, and Sanofi-Aventis Pharmaceuticals.

Mr. Parkin has received consulting fees from Abbott Diabetes Care, Bayer Diagnostics, Eli Lilly, EMD Pharmaceuticals, Roche Diagnostics, and Sanofi-Aventis Pharmaceuticals.

Dr. Wright has served on advisory panels and received consulting fees or honoraria from Eli Lilly and Amylin Pharmaceuticals.

The University of North Carolina has received honoraria related to Dr. Buse's speaking engagements for Abbott, Pfizer, and Eli Lilly; grant support related to his research activities from Bristol-Myers Squibb, Novartis Pharmaceuticals, and Pfizer; and consulting fees related to his formal advisory activities from Amylin Pharmaceuticals, BD Research Laboratories, Eli Lilly, Merck, and Bristol-Myers Squibb.

All of these companies manufacture pharmaceutical products for the treatment of diabetes.

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