Objective Medication adherence is impacted by regimen complexity. The SIMPLE (Simple basal Insulin titration, Metformin Plus Liraglutide for type 2 diabetes with very Elevated HbA1c) study compared GLP1RA plus basal insulin (GLP1RA+BI) to basal-bolus insulin (BBI) regimen in participants with very uncontrolled type 2 diabetes mellitus (T2DM). This analysis aimed to evaluate medication adherence to GLP1RA+BI compared with BBI, the effect of adherence on clinical and patient-reported outcomes, and baseline predictors of adherence.
Research design and methods This was an analysis of the SIMPLE study based on prespecified outcome. The study took place in pragmatic, real-world setting. A total of 120 adults with T2DM and HgbA1c≥10% were randomized to detemir plus liraglutide, or detemir plus aspart before each meal; 6-month follow-up. The main outcomes evaluated were: adherence, HgbA1c, weight, quality of life, and hypoglycemia. Adherence rate was calculated for each study medication at each follow-up visit; participants were classified as ≥80% or <80% adherent.
Result A higher percentage of participants in the GLP1RA+BI compared with the BBI group had ≥80% adherence to detemir (59.3% vs 35.7%, p=0.02) as well as liraglutide versus aspart (57.4% vs 30.4%, p=0.007). Higher age was predictive of ≥80% adherence (OR per 5-year increment=1.48, 95% CI 1.09 to 2.0, p=0.01). Higher adherence led to greater improvement in HbA1c and weight in both groups. Treatment with GLP1RA+BI compared with BBI led to greater improvement in HbA1c, weight, and quality of life and lower risk of hypoglycemia even after adjusting for the difference in adherence between groups.
Conclusions Adherence was higher with the simplified regimen of GLP1RA+BI compared with BBI. Greater adherence to the simpler regimen amplified the treatment effect on HbA1c, weight, quality of life, and risk of hypoglycemia, yet statistically significant greater benefits were noted even when adjusted for adherence.
Trial registration number NCT01966978
- adherence to medications
- glycemic control
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Significance of this study
What is already known about this subject?
The rate of adherence with glucose-lowering medications is associated with glycemic control.
Adherence to glucose-lowering agents in adults with type 2 diabetes is low.
The complexity of the treatment regimen is an important contributor to medication adherence rate.
What are the new findings?
Medication adherence is greater with glucagon-like peptide-1 receptor agonist (GLP1RA) plus basal insulin compared with basal-bolus insulin.
The GLP1RA plus basal insulin treatment group had improved glycemic control, greater weight loss and lower risk of hypoglycemia compared with the basal-bolus insulin group.
How might these results change the focus of research or clinical practice?
A less complex treatment regimen improves medication adherence.
Treatment with GLP1RA plus basal insulin compared with basal-bolus insulin regimen led to greater improvement in glucose control, as well as better weight profile, less likelihood of hypoglycemia, and improved quality of life.
Diabetes prevalence in the US adult population was estimated at 14% from 2013 to 2016, which includes 9.3% diagnosed diabetes and 4.3% undiagnosed diabetes.1 According to the Centers for Disease Control and Prevention 2011 data, 30.8% of patients diagnosed with diabetes are treated with either insulin alone or insulin plus oral agents.2 Approximately 50% of patients with type 2 diabetes mellitus (T2DM) are not at target glycemic control of HbA1c<7%,3 an outcome that is at least partially due to poor adherence to medication.4 Poor adherence to glucose-lowering agents can result in poor glycemic control and may lead to increased hospitalization, diabetic complications, and healthcare resource use.5
Adherence to chronic therapies is disappointing in many chronic disease states.6 Adherence to glucose-lowering agents has been shown to be low overall. For example, Farr et al reported that in the USA, adherence rates measured as proportion of days covered (PDC) ≥80% were less than 50% across three oral glucose-lowering classes at 1 year after initiation, and even lower at the 2 years after initiation where adherence was approximately 40%.7 Non-adherence to glucose-lowering agents is influenced by multiple factors including tolerability, efficacy, cost of medications, complexity of the treatment regimen (frequency and route of administration, number of additional agents in the treatment regimen), and patient–provider interaction.8 9 Adherence to injectable therapies like insulin is very low, especially if multiple daily injections are prescribed.10 Pfeiffer et al evaluated 398 patients treated with basal-bolus insulin (BBI) regimen and concluded that the complicated nature of basal-bolus therapy contributes to the difficulties that patients with type 2 diabetes (T2D) have with the regimen and low adherence rates.10 Even with the newer classes of injectable glucose-lowering agents, the glucagon-like peptide-1 receptor agonists (GLP1RA), adherence has been low, with retrospective studies showing PDC≥80% of 34%–54.2%.11 12 GLP1RAs are potent glucose-lowering agents, and when used in conjunction with insulin they can further improve glycemic control, lower the dose of insulin, and minimize hypoglycemia.13 Combination therapy with a GLP1RA plus basal insulin (GLP1RA+BI) is effective and more convenient compared with either a BBI or even less intense insulin-based regimens like basal-plus one or premixed insulins.14–18 The GLP1RA+BI can be administered at the same time of the day, irrespective of meals, can be easily self-titrated by the patients, and therefore a more desirable treatment strategy compared with other more complex insulin-based regimens, which could also translate to increased adherence to therapy.19
The SIMPLE (Simple basal Insulin titration, Metformin Plus Liraglutide for type 2 diabetes with very Elevated HbA1c) study was a randomized trial which compared two treatment strategies (GLP1RA+BI vs BBI) in participants with T2DM and very elevated HbA1c (≥10%). A total of 120 participants were randomized with an average age of 47.4±9.5, diabetes duration of 10.5±7.2 years, and HbA1c 12.1%±1.4%. Treatment with GLP1RA+BI improved HgbA1c more than treatment with BBI regimen (estimated treatment difference (ETD) of −1.1%, 95% CI −2.0% to −0.1%, p=0.03), while this group also had better weight outcomes (ETD −3.7 kg, 95% CI −5.8 to −1.5, p=0.001), lower risk of hypoglycemia (35.2% vs 66.1%, respectively) and greater improvement in several quality of life (QoL) domains.18
The objective of this analysis is to compare adherence between the two treatment strategies, assess if any baseline characteristics predict adherence to treatment, and evaluate the impact of adherence on relevant clinical outcomes (HbA1c, weight, and hypoglycemia) and patient-reported outcomes (QoL).
Materials and methods
This is an analysis of the SIMPLE study, which was a prospective, randomized, open-label, parallel group trial comparing two treatment strategies (GLP1RA+BI vs BBI), both in addition to metformin in individuals with very uncontrolled (HbA1c≥10%) T2D. The intention-to-treat data set of the SIMPLE trial included n=110 with 54 patients in GLP1RA+BI group and 56 patients in the BBI group.18
In the SIMPLE study, participants were recruited from the outpatient clinics at Parkland Health and Hospital System if they were ≥18 years of age and had T2DM with a confirmed HgbA1c≥10%. Participants were excluded if they had type 1 diabetes, were using prandial insulin (or had used it within the past 30 days), DDP-4 inhibitors or GLP1RA, had a history of pancreatitis or pancreatic disease, a baseline lipase level more than three times the upper limit of normal, creatinine clearance <30 mL/min, or decompensated comorbidities.
Intervention and medication titration
All participants initiated basal insulin detemir at randomization and self-titrated the dose daily according to a prespecified protocol targeting a fasting blood glucose of 71–100 mg/dL.
Participants randomized to the GLP1RA+BI treatment group were initiated on liraglutide and titrated according to the label to the final dose of 1.8 mg/day, or highest tolerated dose. Participants randomized to the BBI initiated insulin aspart subcutaneously before each main meal and self-titrated the dose according to a prespecified protocol.
Metformin was continued or initiated and titrated after randomization if not contraindicated. The dose was titrated to maximum tolerated dose or to 1000 mg twice daily. A full description of the study design, interventions, and outcomes can be found in the primary manuscript.18
Liraglutide, insulin detemir and insulin aspart were all dispensed in prefilled pen devices and provided at no cost to participants throughout the study. Participants were required to return all study medications (used or unused) at each clinic visit. Follow-up clinic visits occurred at 1, 3, and 6 months after randomization. An adherence rate was calculated for each study medication at each visit by dividing the amount of each product used by the expected amount of product to be used over the number of days between the respective visits. Adherence to metformin, which was not provided by the study, was based on pharmacy product fill rate. All participants recorded their daily insulin dose in a study-specific logbook which was reviewed at each visit and used to calculate the expected amount of product to be used.
For analysis purpose, participants were considered ‘adherent’ if they had at least two (out of three) visits where adherence could be assessed (product was returned) and the calculated time-adjusted average adherence rate for the entire duration of the study was ≥80%. Participants who did not meet these criteria were considered <80% adherent.
Age, gender, and race were self-reported by participants. Weight was measured on the same scale at each visit in accordance with usual clinic procedures (no shoes or outerwear, empty pockets). HgbA1c was measured in the local laboratory at baseline, 3 and 6 months’ follow-up. QoL was assessed via a modified Diabetes Quality of Life Clinical Trial Questionnaire at the time of randomization and at the 6-month clinic visit, and reported as individual domain scores.
Hypoglycemia was defined as a blood glucose level of <70 mg/dL regardless of symptoms, or if a participant needed assistance from a third party to treat symptoms suggestive of hypoglycemia regardless of whether a blood glucose measurement was performed.
We summarized the percent of participants with ≥80% and<80% adherence in each treatment group and by each glucose-lowering medication separately (metformin, insulin detemir, insulin aspart, liraglutide). Detemir insulin was provided by the study to participants in both randomized groups, therefore we used adherence to detemir (the common denominator for both treatment groups) for all further analyses. Predictors of detemir adherence were evaluated with univariable and multivariable logistic regression models. Covariates assessed were age, race, gender, baseline HbA1c, insulin total daily dose (TDD)/kg, weight, QoL, and median income. Treatment group comparisons controlling for adherence and change from baseline contrasts by adherence stratum were made with mixed effects models for the outcomes of HbA1c, weight, and QoL. Binomial frequencies were compared between groups with the Fisher’s exact test. Hypoglycemia was analyzed with Cochran Mantel-Haenszel tests, stratifying by adherence status. A two-sided alpha=0.05 was used for hypothesis testing. Analysis was conducted with SAS V.9.4 (SAS Institute).
We randomized 120 participants with an average age of 47 years, 71% female, and a high minority representation (40% Hispanic, 42% African-American), with a 10-year average duration since diagnosis of diabetes and mean baseline HbA1c of 12.1%. The majority of patients (76%) were already treated with insulin prior to enrollment.
Adherence between groups
The percentage of participants with ≥80% adherence to detemir insulin was higher in the GLP1RA+BI group (n=32, 59.3%) versus the BBI group (n=20, 35.7%) (p=0.021 between groups). The percentage of participants with ≥80% adherence to liraglutide was 57.4% compared with aspart insulin 30.4% (p=0.007 between groups). The percentage of participants with ≥80% adherence with metformin was similar between groups (66.7% in the GLP1RA+BI group and 60.7% in the BBI group, p=0.556 between groups).
Baseline characteristics as predictors of adherence
Age was the only significant predictor of future adherence with detemir insulin, when adjusted for treatment group. ORs for univariable predictors of detemir adherence for all participants combined are shown in figure 1. Higher age was predictive of ≥80% adherence to detemir (OR per 5-year increment=1.48, 95% CI 1.09 to 2.00, p=0.01). Gender, race, income, baseline HbA1c, weight, insulin TDD, and diabetes-related QoL were not associated with adherence in univariable nor multivariable models.
Effect of adherence on clinical and patient-reported outcomes
HbA1c and weight
To explore whether the difference in adherence between the two treatment arms was responsible for the reported clinical benefits, we compared the change in HbA1c and weight between groups adjusting for the adherence rates. The reduction in HbA1c was greater in the GLP1RA+BI group compared with the BBI group after adjustment for adherence (ETD −0.91, 95% CI −1.86 to 0.03, p=0.058). In both treatment groups, participants with ≥80% adherence had numerically greater reduction in HgbA1c than participants with <80% adherence, and a numerically greater reduction in HgbA1c was noted in the GLP1RA versus BBI group in both ≥80% adherence and <80% adherence groups (table 1).
A significant difference between groups in terms of weight change was observed after controlling for the adherence rates (ETD −3.8 kg, 95% CI −6.0 to −1.6, p<0.001). Participants with ≥80% adherence treated with GLP1RA+BI observed weight loss (−1.2 kg; 95% CI −3.1 to 0.6), while those treated with BBI had weight gain (+4.5 kg; 95% CI 2.2 to 6.9). Participants with <80% adherence had no significant change in weight regardless of treatment group (table 1).
Quality of life
A lower QoL score indicates better QoL, that is, a decreased score corresponds with improved QoL. General health perception was improved in participants treated with GLP1RA+BI versus BBI even after adjustment for adherence (ETD −0.53, 95% CI −0.92 to −0.15, p=0.007). Treatment satisfaction and fear of hypoglycemia improved more in the GLP1RA+BI group compared with BBI group even when adjusting for adherence (ETD −0.36, 95% CI −0.67 to −0.06, p=0.02; ETD −0.47, 95% CI −0.79 to −0.15, p=0.005, respectively), while changes in current health perception and diabetes-related worry were similar after adjustment for adherence.
Regardless of adherence rate, the group treated with GLP1RA+BI had a significant improvement in both general health perception as well as treatment satisfaction (table 1). Fear of hypoglycemia numerically improved, regardless of adherence, in the GLP1RA+BI group and numerically increased in the BBI groups (table 1).
Participants in the BBI treatment group were twice as likely to have at least one hypoglycemic event compared with the GLP1RA+BI in both the ≥80% adherent (80.0% vs 40.6%; p=0.009) and <80% adherent subgroups (58.3% vs 27.3%; p=0.03).
We evaluated a patient population with uncontrolled T2D with HgbA1c≥10.0% and compared adherence between the standard treatment group (BBI) and a less complex treatment regimen (GLP1RA+BI). We found that participants randomized to the simpler regimen consisting of GLP1RA+BI were more likely to have ≥80% adherence with detemir insulin and liraglutide compared with those randomized to BBI and treated with detemir insulin and aspart. Higher age was the only predictor of ≥80% adherence within each treatment group. Treatment with GLP1RA+BI, compared with BBI, led to improvement in HbA1c and weight, lower risk of hypoglycemia, and improved general health perception, treatment satisfaction, and fear of hypoglycemia even after adjustment for difference in adherence between treatment groups. Those with ≥80% adherence, compared with those who had lower adherence, had numerically greater effects on HbA1c and weight, but were more likely to experience hypoglycemia.
Adherence with both oral and injectable glucose-lowering agents is very low and this significantly contributes to inadequate glycemic control in patients with T2DM.20–24 Complexity of a treatment regimen is one of the main reasons for limited adherence to medications.10 25 Prior studies have shown that a less complex regimen with GLP1RA+BI compared with BBI provides similar glycemic control, with greater weight loss and lower hypoglycemic risk,26–28 but none of these studies enrolled patients with elevated HbA1c. This population was exclusively targeted in our study, thus adding to the body of evidence supporting the efficacy and safety of this simpler regimen in this particular population which traditionally has proven to be the more challenging to treat and disproportionately affected by poor adherence. Higher adherence (≥80%) to either insulin or GLP1RA is associated with better clinical outcomes,4 11 23 however adherence with GLP1RA+BI versus BBI has not been previously studied. This is the first report evaluating adherence to GLP1RA+BI and BBI in a population of patients with very elevated HgbA1c (≥10%) and the associated clinical outcomes. These data emphasize and support the findings in the literature promoting less complex treatment regimens for greater adherence with the goal of achieving greater improvements in glycemic control, weight management and reduced risk of hypoglycemic events. In fact, adherence to all components of the treatment regimen was affected by the complexity of the regime as we found that adherence to detemir was similar to that of liraglutide in the GLP1RA+BI group, while adherence to detemir was lower and similar to aspart in the BBI group.
This study was conducted in a county health system, and had a pragmatic design fully embedded in the usual clinical setting. This included the frequency of follow-ups which were in accordance with our clinical practice (and less frequent compared with a usual clinical trial), requirement for self-titration of all medications, and unscheduled contacts limited to those initiated by the participants. As such, these findings are readily translatable to real-world usual clinical practice. Additionally, we directly assessed adherence with each individual agent at each encounter, therefore the estimate of adherence in our study is more precise than reports using pharmacy fill rates as a measure of adherence.
Several limitations are noteworthy. First, calculation of adherence was predicated on participants returning their study medication. If adherence could not be calculated, the participant was included in the <80% adherence group. While this is a conservative approach, it could have underestimated the true adherence rate. Second, after dividing each treatment group by adherence, the number of participants in each subgroup was small and inadequately powered for meaningful comparisons between these subgroups. As such, only numerical comparisons were performed across these subgroups (table 1). Third, adherence was a secondary outcome and even though it was a prespecified outcome results should be hypothesis generating and interpreted in the context of other findings from similar trials. Lastly, insulin detemir, aspart, and liraglutide were provided free of charge to participants. Adherence in such setting could be overestimated compared with the real-world setting where cost of acquiring a medication plays a significant role in adherence.
In conclusion, our results suggest that a less complex treatment regimen consisting of GLP1RA+BI, compared with BBI therapy, is associated with greater adherence as well as improved clinical outcomes (HbA1c, weight, hypoglycemia) and improved QoL (general health perception, treatment satisfaction and hypoglycemia fear). GLP1RA+BI is a safe and effective treatment option for patients with very uncontrolled T2DM.
Contributors SP, MA, BAH and IL contributed to the conception and design of the study, the acquisition, analysis and interpretation of data. AT and XL contributed to the analysis and interpretation of data. SP, MA, BAH, IL, and AT drafted the work and revised it critically for important intellectual content. All authors approved the final version to be published; agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Funding This work was supported by an Investigator-Initiated Study Grant from Novo Nordisk to IL.
Competing interests IL received honoraria for consulting/advising boards from Novo Nordisk, Eli Lilly, Sanofi, Intarcia Therapeutics, AstraZeneca, Valeritas, MannKind, TARGET Pharma, Boehringer Ingelheim and research grants from Novo Nordisk, Merck, GI Dynamics, Pfizer, Novartis, and Mylan. BAH has consulted for Valeritas outside the submitted work. MA has consulted for Novo Nordisk outside the submitted work.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available upon reasonable request. All data relevant to the study are included in the article or uploaded as supplementary information.
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