Background
The Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation (ADVANCE) study [
1‐
3] demonstrated that progressive uptitration of a modified release (MR) formulation of gliclazide as part of an intensive treatment regimen provides consistent glycemic control associated with long-term benefits on the combined microvascular and macrovascular endpoint. Despite the availability of newer classes of antihyperglycemic agents, sulfonylureas (in particular gliclazide) still retain an important position in diabetes management because of considerations around familiarity, guideline recommendations, cost and coverage [
4‐
12].
With the overarching goal of improving adherence, the once daily (QD) gliclazide MR 60 mg formulation is available as a scored tablet to allow for convenient titration. The effectiveness and tolerability of this gliclazide tablet were evaluated in the real-world ObsErvationAl Study to analYse titration of Diamicron MR 60 mg in daily clinical practice in a large population with uncontrolled type 2 diabetes (EASYDia) study. Following 6 months of progressive uptitration, individuals in the EASYDia cohort experienced significantly improved glycemic control, mild weight loss and rare events of hypoglycemia [
13]. We describe herein the temporal and dose-associated efficacy of gliclazide MR 60 mg, how efficacy varied with the participants’ baseline features, and the potential clinical implications of these observations.
Methods
Study conduct and population
EASYDia was an international, open-label, nonrandomized, non-comparative observational study (ISRCTN00943368) that was conducted according to the standards and principles of the Declaration of Helsinki. Ethics approval was site specific and written informed consent obtained at or before the baseline visit.
Screening took place from July 2011 to February 2014 at 596 sites in eight countries (Armenia, Georgia, Lebanon, Malaysia, Russia, Slovenia, Switzerland and Turkey). Potential participants were required to fulfill all of the following criteria: ≥ 35 years old with type 2 diabetes, HbA1c ≥ 7.5%, and either treatment-naïve or using non-insulin antihyperglycemic therapies. Individuals who were pregnant or breast feeding, exhibited hypersensitive reactions to sulfonylureas, displayed severe hepatic or renal failure (creatinine clearance < 30 mL/min), were taking miconazole, demonstrated contraindication to gliclazide, presented with uncontrolled and clinically significant disease or known malignancy, had a high probability of non-adherence to the EASYDia study expectations were excluded.
Individuals entered into the study were prescribed 30–120 mg gliclazide MR 60 mg QD by their physicians as first line, add-on or a switch from a previous oral glucose-lowering regimen [
13]. Dosing was capped at 120 mg QD and uptitration, initiated at the discretion of the investigators, was driven by fasting plasma glucose (FPG) levels measured at months 1, 2, and 3. There were provisions to introduce another oral antihyperglycemic agent should glycemic control remain sub-optimal with gliclazide 120 mg QD. HbA1c goals were personalized and the final visit occurred 6 months after study initiation.
Endpoints
We report herein the efficacy and safety outcomes of gliclazide MR therapy according to the participants’ baseline features and background glucose-lowering regimens. The primary efficacy endpoint and secondary efficacy endpoints that included treatment doses (daily average and temporal changes) as well as HbA1c improvements and the percentage of participants achieving an HbA1c of ≤ 7.0 and ≤ 6.5% at study end have been reported [
13].
Data collection
In this post hoc subanalysis, data collected at baseline, month 3 and the end of the study were stratified according to initial HbA1c (> 7.0 to ≤ 8.0%, > 8.0 to ≤ 9.0%, > 9.0 to ≤ 10.0%, and > 10.0%), body mass index (BMI 18.5 to < 25.0, 25.0 to < 30.0 and ≥ 30.0 kg/m2) and prior glucose-lowering regimens. With regards to hypoglycemia, only severe episodes were collected on the case report forms. Severe hypoglycemic incidents were classified as those associated with transient central nervous system dysfunction without other apparent cause, in which the individual was unable to treat him/herself and required assistance from another party.
Statistical analyses
Demographic data and other baseline characteristics are reported for the included set. FPG and HbA1c information were derived from the full analysis set [FAS; participants who had taken at least one dose of the study treatment that they had been prescribed and had at least one baseline value and one post-baseline value of FPG (or HbA1c) on file]. Weight results were calculated from the safety set. Unless otherwise stated, data are presented as mean (standard deviation, SD). Changes from the corresponding baseline values were assessed with a Wilcoxon signed rank test and two-sided 95% confidence interval. Statistical significance was set at an unadjusted P value of < 0.05. Statistical analyses were conducted with SAS version 9.1.
Discussion
We report herein that incremental dosing of gliclazide MR 60 mg QD over 6 months was well tolerated and led to significant and clinically meaningful HbA1c reductions, as early as 3 months, in individuals with type 2 diabetes, not treated with insulin and with a broad range of baseline HbA1c. Additionally, HbA1c improvements of approximately 1.80% were documented in individuals regardless of whether they had a healthy BMI or if their BMI was 25.0 kg/m2 and above. Of note, baseline BMI values of 25.0 kg/m2 and higher were associated with significant weight losses. As seen with many antihyperglycemic agents, participants with the highest baseline HbA1c levels and BMI experienced the greatest HbA1c and weight improvements while the converse was true for those in the lowest baseline HbA1c and BMI strata.
The last 5 years have seen a steady stream of publications focused on the cardiovascular and renal safety as well as efficacy signals of novel diabetes medicines in large type 2 diabetes cohorts, the majority of whom had known cardiovascular disease [
14‐
23]. While the results of these megatrials have generated much excitement albeit alongside some concerns about the newer classes of antihyperglycemic agents, sulfonylureas, in particular gliclazide, remain an important treatment option for many physicians and patients when glucose levels remain elevated despite the maximum tolerable dose of metformin [
4‐
12].
Aside from metformin, the only other oral antihyperglycemic agent cited in the 2017 version of the World Health Organization Model List of Essential Medicines is gliclazide [
9]. Along the same vein, several national guidelines [
6,
10,
11] currently position gliclazide as a second-line choice, one recommends early initiation of gliclazide MR or glimepiride [
12] while another [
4] suggests adding a sulfonylurea, a DPP-4i, pioglitazone or a dual combination of the three when maximally tolerated metformin monotherapy does not achieve the desired glycemic outcome. Of note, gliclazide MR is recommended and widely used for the management of diabetes during Ramadan [
24‐
26], a period during which prolonged fasting can render glycemic management challenging. The recommendations of these professional groups clearly support the continual role of gliclazide MR in contemporary diabetes management.
Inasmuch as progressive uptitration of gliclazide MR over 6 months produced clinically meaningful improvements in glycemic control regardless of baseline HbA1c suggests that individuals with suboptimally controlled type 2 diabetes along much of the diabetes continuum could benefit from the gliclazide MR regimen described in this report. Of further interest are the additional HbA1c reductions noted in EASYDia participants who had been switched from either another sulfonylurea or a DPP-4i to gliclazide MR. It is often believed that sulfonylureas as a class are typically associated with weight gain while DPP-4i are generally considered to be weight neutral. The unwanted weight effects of the former and the relatively more desirable weight profile of the latter frequently drive prescription decisions since weight gain is not only a common comorbidity and concern of individuals with type 2 diabetes but may also contribute to diminished adherence and hence propagate deranged glycemic control. The EASYDia subgroup with baseline BMI values of 25.0 kg/m
2 to less than 30.0 kg/m
2 lost a mean of 0.88 kg over 6 months while that with a BMI 30.0 kg/m
2 and greater experienced a mean weight loss of 2.2 kg over the same time span. These observations might be considered unexpected since, as mentioned earlier, sulfonylureas have on average been linked with weight gain. That said, individuals who were newly diagnosed with type 2 diabetes made up almost one-fifth of the EASYDia cohort and given the early stages of their disease, these participants may have been more motivated to make lifestyle changes. Accordingly, we cannot discount the possibility that at least some of the weight benefits observed in the EASYDia program was in fact resultant of behavioural modifications. Regardless, the gliclazide MR regimen described herein may be a doubly favourable option for those with uncontrolled type 2 diabetes and a BMI that is above the healthy range. In support of this school of thought, the ADVANCE trial showed an overall no increase in weight over a median of 5 years in the gliclazide-based intensive therapy arm despite the improved glycemic control [
1]. Additionally, the STudy Evaluating vildAgliptin compareD to gliclazide in patients with type 2 diabetes FASTing during Ramadan (STEADFAST) trial reported improvements in glycemic efficacy alongside small weight losses (mean − 1.1 ± 0.2 kg) with gliclazide therapy [
27]. Accordingly, the current findings extend those of previous reports by demonstrating that progressive uptitration optimizes the impact gliclazide MR has on glycemic control with potential modest weight benefits in those with elevated BMI values.
Risk of hypoglycemia remains an important treatment consideration and is a major barrier for medication adherence, thereby hindering achievement of glycemic targets. Severe hypoglycemic episodes were uncommon, even amongst participants with only modest elevations in glycemia, with only five incidents reported by four EASYDia participants (0.06%). On further evaluation, however, it was noted that only three of these individuals experienced a total of four events that were suspected to be gliclazide-related (0.04%). The uncommon occurrences of severe hypoglycemia echo the low risk for hypoglycemia (relative to other sulfonylureas) reported with gliclazide MR in recent retrospective cohort studies (
P < 0.001 vs. glyburide) [
28] and an earlier five-country observational study that monitored gliclazide- and other sulfonylurea-treated individuals undergoing Ramadan fasting [
26]. Although a small meta-analysis of three randomized trials calculated comparable occurrences of hypoglycemia in individuals using gliclazide and DPP-4i while fasting during Ramadan [
29], small observational studies have documented greater, comparable or lower risk of hypoglycemia for gliclazide relative to sitagliptin and vildagliptin [
27,
30,
31].
The EASYDia study has several strengths and limitations. First, the large multinational real-world dataset was obtained from clinically diverse individuals who were positioned along the entire diabetes continuum thus capturing a close representation of the global diabetes population. Second, the non-regimented design and setting allowed for a more realistic documentation of the benefits and harms associated with intensive gliclazide MR uptitration. At the same time, the non-randomized nature of this observational study, lack of formal comparator, and relatively short duration of follow-up, should be noted. Furthermore, given the fact that many of the EASYDia participants had newly diagnosed diabetes, it is possible that they may have been more motivated to initiate and sustain recommendations for lifestyle recommendations. Of specific consideration in this sub-analysis, there were imbalances in the sample sizes of the sub-cohorts examined and these likely contributed to the larger outcome variability observed in the smaller groups and tighter ranges measured in those with more participants.
In conclusion, the large, contemporary, real-world EASYDia study has shown that progressive uptitration of gliclazide MR over 6 months is well tolerated in individuals with type 2 diabetes not treated with insulin and is associated with clinically meaningful HbA1c reductions across a broad range of HbA1c and clinical scenarios. Individuals with BMI 25.0 kg/m2 and higher also experienced significant weight loss. Importantly, the rarity of severe hypoglycemia events observed with the gliclazide treatment, diminishes an important concern routinely surrounding the sulfonylurea class. Overall, these data highlight that the described gliclazide MR regimen is an effective option for a wide variety of non-insulin treated individuals with diabetes and inadequate glycemic control.
Authors’ contributions
LAL contributed to the development of the study concept and design, interpreted the results, wrote, reviewed and critically revised the manuscript for important scientific and intellectual content. MVS was the national coordinator for Russia, reviewed and critically revised the manuscript for important intellectual content. IS was the national coordinator for Turkey, interpreted the results, reviewed and critically revised the manuscript for important scientific and intellectual content. All authors read and approved the final manuscript.