Abstract
Introduction
Dipeptidyl peptidase 4 (DPP4) inhibitors are widely used in patients with type 2 diabetes mellitus (T2DM) on maintenance hemodialysis (HD), but the efficacy of the once-weekly DPP4 inhibitor omarigliptin is not known.
Methods
This prospective, randomized, open-label, parallel-group, non-inferiority/superiority, once-daily DPP4 inhibitor linagliptin-controlled, multicenter study examined glycemic control and safety of omarigliptin (UMIN000024284). Sample size was calculated to confirm non-inferiority in terms of changes in glycated hemoglobin (HbA1c). We enrolled 33 patients with T2DM on maintenance HD who had been treated with linagliptin for at least 3 months. The patients were randomized to receive omarigliptin (12.5 mg/week; n = 16) or linagliptin (5 mg/day; n = 17). Primary endpoints were changes in HbA1c and glycoalbumin (GA) over 24 weeks.
Results
Differences in the mean change in primary endpoint values between the omarigliptin and linagliptin groups were − 0.61% [− 1.14, − 0.09] for HbA1c, with a two-tailed upper 95% limit (i.e., one-tailed 97.5% upper limit) of 0.25%, below the non-inferiority limit, and − 1.67% [− 4.23, + 0.88] for GA, with a two-tailed upper 95% limit of 0.75%, above the non-inferiority limit. At 24 weeks, the omarigliptin group showed significantly greater reduction in HbA1c than the linagliptin group (− 0.2% ± 0.6% vs. 0.4% ± 0.8%, two-tailed p = 0.024) and significantly greater reduction in blood glucose after a single HD session (− 18.4 ± 31.4 mg/dL vs. 25.2 ± 59.5 mg/dL, respectively, two-tailed p = 0.019). No subjects in the omarigliptin group developed hypoglycemia.
Conclusions
Our data showed that omarigliptin was non-inferior to linagliptin in glycemic control. Omarigliptin is feasible for glycemic control in patients with T2DM on maintenance HD.
Clinical Trials Registration
UMIN000024284.
Supplementary Information
The online version contains supplementary material available at 10.1007/s13300-020-00991-y.
Keywords: Linagliptin, Hemodialysis, Once-weekly dipeptidase 4 inhibitor, Omarigliptin, Type 2 diabetes mellitus
Key Summary Points
| Why carry out this study? |
| Efficacy of the once-weekly DPP4 inhibitor omarigliptin is unknown in patients with type 2 diabetes mellitus on maintenance hemodialysis. |
| There are no reports of comparisons between once-weekly and once-daily DPP4 inhibitors in glycemic control and treatment satisfaction in patients with type 2 diabetes mellitus on maintenance hemodialysis. |
| What was learned from the study? |
| Once-weekly DPP4 inhibitor omarigliptin was non-inferior to once-daily DPP4 inhibitor linagliptin in its glycemic control. |
| If patients on hemodialysis can take once-weekly drugs, such as omarigliptin, at a hemodialysis center, they might maintain adherence almost perfectly. |
| Once-weekly DPP4 inhibitor omarigliptin is feasible for glycemic control in patients with type 2 diabetes mellitus on maintenance hemodialysis. |
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Introduction
Insulin injection therapy is mainly used for glycemic control in patients on maintenance hemodialysis (HD) with type 2 diabetes mellitus (T2DM). Some problems arise in insulin therapy though, such as hypoglycemia, cumbersomeness, and pain from the injection itself [1]. Patients on maintenance HD endure repeated venipuncture for venous access at each HD session (usually three times a week) and also need daily injections of insulin. It would be ideal to achieve good glycemic control without insulin injection by using only oral hypoglycemic agents (OHAs), but the use of available OHAs is limited in these patients because of the risk of prolonged hypoglycemia.
Dipeptidyl peptidase 4 (DPP4) inhibitors have the benefits of not only providing proper glycemic control but also being associated with a lower incidence of hypoglycemia and good safety, even in patients with chronic kidney disease [2], so they are widely used in patients on maintenance HD [3]. Once-weekly DPP4 inhibitors recently became commercially available, and compared with once-daily DPP4 inhibitors, they are not inferior in terms of glycemic control and their efficacy has been reported [4]. The once-weekly DPP4 inhibitor omarigliptin is reported to be non-inferior to other OHAs and to have improved adherence in patients with T2DM [5]. Omarigliptin is also an option for patients with severe renal dysfunction [6]. Because patients on maintenance HD need to take many oral medications and often have problems with adherence [7, 8], it is likely that omarigliptin could improve their adherence.
However, no reports have compared once-weekly and once-daily DPP4 inhibitors in terms of changes in glycemic control in patients with T2DM on maintenance HD. Therefore, in this study, we investigated the non-inferiority of once-weekly omarigliptin compared with the once-daily DPP4 inhibitor linagliptin in these patients. We also studied the efficacy of omarigliptin in association with changes in plasma glucagon and active glucagon-like peptide 1 (GLP-1) levels and treatment satisfaction.
Methods
Participants
Eligible patients (1) had been on maintenance HD for more than 6 months, (2) were aged at least 20 years with T2DM treated using DPP4 inhibitors for more than 3 months, and (3) had given written informed consent for the use of their clinical data in this study. Exclusion criteria were (1) treatment with GLP-1 receptor agonists, (2) hypersensitivity to DPP4 inhibitors or GLP-1 receptor agonists, (3) severe diabetic ketosis, coma, or pre-coma, (4) severe active infection, severe trauma, or in the perioperative period, (5) severe heart or liver dysfunction, (6) other conditions such as pituitary gland or adrenal gland dysfunction, impaired nutrition, starvation, irregular or insufficient dietary intake, hyposthenia, excessive muscular exercise, or heavy alcohol consumption, (7) pregnant, breastfeeding, or may be pregnant, (8) uncontrolled hyperglycemia (glycated hemoglobin [HbA1c] ≥ 9% or glycoalbumin [GA] ≥ 27%) on current treatment with OHAs, or (9) considered ineligible for this trial by the attending physician for any medical reasons.
Study Design
This was a prospective, randomized, open-label, parallel-group, non-inferiority/superiority, once-daily linagliptin-controlled, multicenter study conducted at Niigata University Medical and Dental Hospital and three affiliated dialysis facilities between April 2017 and March 2018 (UMIN000024284). This study was approved by the Ethics Committee of Niigata University (approval number 2015-1277).
The overall study design is shown in Fig. 1. After providing written informed consent to participate, patients who had been taking linagliptin continued as they were, but those who had been taking other DPP4 inhibitors changed to linagliptin. We provided a pre-observation period of at least 3 months and checked for adverse events or side effects through medical interviews and by investigating standard laboratory parameters. We then randomized the patients into a group that continued linagliptin and a group that switched to omarigliptin after the pre-observation period. Patients in the linagliptin group took one tablet daily after breakfast (5 mg/day), whereas patients in the omarigliptin group took one tablet every first HD day of the week at their HD center (12.5 mg/week). The nurses confirmed that the patients in the omarigliptin group took a tablet at their HD center and instructed the patients in the linagliptin group to take a tablet every day.
Fig. 1.
Study design. DPP4 dipeptidyl peptidase 4, R randomization, q.d. once daily, q.w. once weekly
For randomization, we used the sealed envelope method. The random sequence of envelope allocations was generated using block randomization. The block sequence was determined on the basis of random numbers generated in Excel™. A controller outside the trial administration center performed the randomization process and created the sealed envelopes.
The observation period was 24 weeks. From the start of the observation period, no replacement or addition of OHAs was allowed until 12 weeks. After 12 weeks, if patients had not achieved HbA1c < 10% or GA < 29%, physicians were permitted to add other OHAs such as glinides or alpha-glucosidase inhibitors at their discretion in both treatment groups. However, additional use of insulin was not allowed. We did not restrict the use of therapeutic drugs for other conditions, such as antiplatelet, antihypertensive, or antidyslipidemia drugs.
Study Evaluations
The primary objectives of this study were to assess the efficacy, safety, and effect on quality of life (QOL) of once-weekly omarigliptin compared with once-daily linagliptin over 24 weeks of treatment. The hypothesis was that treatment with omarigliptin would provide a non-inferior reduction in HbA1c and GA compared with linagliptin over the 24 weeks of treatment.
Primary endpoints were changes from baseline HbA1c and GA in both groups. Secondary endpoints were changes in blood glucose, plasma glucagon, and active GLP-1 before and after a single HD session and treatment satisfaction determined using the Diabetes Therapy-Related QOL (DTR-QOL) questionnaire score. Safety endpoints included incidence of adverse events due to omarigliptin, such as hypoglycemia.
Laboratory Investigations
Body mass index (BMI) was determined by dividing average body weight (kilograms) after a single HD session by height (meters) squared. Pre-HD venous blood samples were obtained at the beginning of the week. Routine biochemical parameters were analyzed in the laboratory at each facility. Samples were obtained for blood glucose, plasma glucagon, and plasma active GLP-1 measurements in the middle of the week. Then, measurements were performed at SRL, Inc. (Tokyo, Japan). Plasma glucagon levels were measured using a commercially available sandwich ELISA kit, which uses monoclonal antibodies against both the C-terminal and N-terminal of glucagon (10-1271-01, Mercodia AB, Uppsala, Sweden). Plasma active GLP-1 levels were measured using a Glucagon-Like Peptide-1 (Active) ELISA Kit (Millipore, Billerica, MA).
Patient satisfaction was assessed using the 29-item, self-administered DTR-QOL questionnaire [9, 10]. The DTR-QOL consists of four primary scales: domain 1, burden on social activities and daily activities (13 items); domain 2, anxiety and dissatisfaction with treatment (8 items); domain 3, hypoglycemia (4 items); and domain 4, satisfaction with treatment (4 items) [9, 10].
Statistical Analysis
The primary hypothesis of this study was that once-weekly omarigliptin was not significantly inferior to once-daily linagliptin in terms of glycemic control for patients with T2DM on maintenance HD. The recommended non-inferiority margin of HbA1c was 0.30–0.40%, but we defined that value as 0.25% to show the non-inferiority more precisely [11]. We also defined the non-inferiority margin of GA as 0.75%, because the GA value was about three times the HbA1c value reported in a previous clinical study [12]. For sample size calculation, we used the non-inferiority margin of HbA1c reduction. It was assumed that the HbA1c reduction would be similar to that in previous clinical trials where omarigliptin resulted in an HbA1c decrease of 0.80% [6], whereas linagliptin resulted in a decrease of 0.87% [13], with a standard deviation (SD) of 0.16% for both treatments. With a non-inferiority margin of 0.25%, one-sided alpha of 0.025, and power of 0.8, the sample size was calculated as 13 for each group. Considering a dropout rate of 10%, the minimum sample size was set to 30 in total.
Efficacy analyses were performed for the full analysis set, which included participants who received an allocated treatment and provided assessable outcome data. Safety data were evaluated for all participants who received the allocated treatment at least once. Numerical variables were expressed as means ± SD, and categorical variables were expressed as n (%). Changes in all assessed numerical data during the 24-week study period were compared between the groups using the two-sample t test, and two-sided p values less than 0.05 were considered significant. For HbA1c and GA, the primary endpoints of this study, baseline-adjusted mean changes were also compared between groups on the basis of linear regression models in post hoc analyses. For the difference in each primary endpoint between the omarigliptin and linagliptin groups, the two-tailed 95% confidence interval (CI) was calculated and the upper limit was used to evaluate the non-inferiority. For HbA1c, Welch’s t test was used for unadjusted comparison and robust 95% confidence intervals were calculated for both unadjusted and baseline-adjusted models because variances of mean changes were statistically different between the groups. All statistical analyses, except for the robust 95% confidence interval for the baseline-adjusted model, were performed using IBM SPSS Statistics for Windows ver. 21.0 (IBM Corp., Armonk, NY). The robust 95% interval was estimated using HAD, an Excel-based free statistical program package that can be downloaded via the internet (https://norimune.net/had, Japanese) [14].
Compliance with Ethics Guidelines
The study was approved by the institutional review boards of Niigata University and Shinrakuen Hospital. All procedures were performed in accordance with the Helsinki Declaration of 1964, and its later amendments, and conformed with national regulations. The study was a prospective randomized controlled trial, and all patients provided written informed consent for participation in this study and publication of their clinical data for research purposes.
Results
The patient disposition is shown in Fig. 2. A total of 57 patients were screened and 24 were excluded (screening failure or rejection). A total of 33 patients were randomized, 17 to omarigliptin and 16 to linagliptin. Thirty patients received the study treatment. Three patients dropped out before starting treatment because of unexpected worsening of glycemic control, withdrawal of consent, or transfer to another hospital. None of patients in the omarigliptin group experienced hypoglycemia over the 24 weeks; one patient in the linagliptin group dropped out at week 21 because of hypoglycemia (about 50–60 mg/dL) during HD. This patient was not administered insulin or another antihyperglycemic agent. Two patients in the omarigliptin group dropped out because of long-term hospitalization due to cerebral infarction or lumbar compression fracture. Their attending physicians deemed that there was no relationship between omarigliptin and these diseases. The full analysis set comprised 14 patients in the omarigliptin group and 16 patients in the linagliptin group, making a total of 30 patients (Fig. 2). The baseline clinical characteristics are shown in Table 1. Mean age was 67.6 years, approximately 80% were male, mean BMI was 23.5 kg/m2, mean HbA1c was 6.3%, mean GA was 20.4%, mean duration of maintenance HD was 6.1 years, and mean duration of T2DM was 18.8 years (20.8 ± 11.3 in the linagliptin group; 16.0 ± 8.7 years in the omarigliptin group). Most of the patients were started on maintenance HD treatment because of diabetic nephropathy. For concomitant drugs, the mean number of tablets per week was 124.3. There were no changes in insulin doses and prescribed OHAs in either group during the study period.
Fig. 2.
Patient disposition. *Included in the full analysis set
Table 1.
Baseline clinical characteristics
| Omarigliptin group | Linagliptin group | |
|---|---|---|
| n | 14 | 16 |
| Age, years | 67.7 ± 8.9 | 67.5 ± 9.0 |
| Male, n (%) | 12 (85.7) | 12 (75.0) |
| Duration of diabetes (years) | 16.0 ± 8.7 | 20.8 ± 11.3 |
| Duration of HD (years) | 5.6 ± 4.9 | 6.3 ± 4.4 |
| BMI (kg/m2) | 23.5 ± 2.7 | 23.5 ± 3.8 |
| HbA1c (%) | 6.2 ± 0.9 | 6.5 ± 1.0 |
| GA (%) | 18.8 ± 4.3 | 21.9 ± 3.8 |
| Hemoglobin (g/dL) | 10.5 ± 1.2 | 10.3 ± 1.1 |
| Hematocrit (%) | 31.9 ± 3.9 | 31.7 ± 3.2 |
| Insulin use, n (%) | 1 (7.1) | 3 (18.5) |
| Glinide use, n (%) | 0 (0) | 3 (18.5) |
| α-GI use, n (%) | 0 (0) | 3 (18.5) |
| Other concomitant drugs (tablets/week) | 121.1 ± 81.2 | 127.2 ± 82.1 |
| Primary disease for ESRD | ||
| Diabetic nephropathy, n (%) | 12 (85.7) | 11 (68.8) |
| Nephrosclerosis, n (%) | 1 (7.1) | 1 (6.3) |
| Other diseases, n (%) | 2 (14.3) | 3 (18.5) |
Data are presented as mean ± standard deviation, or n (%)
BMI body mass index, HbA1c glycated hemoglobin, GA glycoalbumin, ESA erythropoiesis-stimulating agents, HD hemodialysis, α-GI α-glucosidase inhibitors, ESRD end-stage renal disease
The between-group differences in the changes in HbA1c and GA at 24 weeks are shown in Table 2 and Figs. 3 and 4. In the full analysis set (n = 30), the differences in the mean change in primary endpoint values between the omarigliptin and linagliptin groups were − 0.61% [− 1.14, − 0.09] for HbA1c, with a two-tailed upper 95% limit of 0.25%, below the non-inferiority limit, and − 1.67% [− 4.23, + 0.88] for GA, with a two-tailed upper 95% limit of 0.75%, above the non-inferiority limit. In post hoc analyses adjusted for baseline values, the differences in the mean change between the omarigliptin and linagliptin groups were − 0.62% [− 1.20, − 0.04] for HbA1c, with a two-tailed upper 95% limit of 0.25%, below the non-inferiority limit, and − 2.49% [− 5.15, + 0.18] for GA, with a two-tailed upper 95% limit of 0.75%, below the non-inferiority limit (Fig. S1 in the supplementary material). Also, HbA1c reduction was significantly greater in the omarigliptin group (− 0.2% ± 0.6%) than in the linagliptin group (0.4% ± 0.8%, p = 0.024). GA tended to be reduced in the omarigliptin group (− 0.3% ± 3.4%) compared with the linagliptin group (1.4% ± 3.4%; P = 0.190).
Table 2.
Primary endpoints
| Omarigliptin group | Linagliptin group | p value | |||||||
|---|---|---|---|---|---|---|---|---|---|
| n | Week 0 | Week 24 | Δ24 weeks | n | Week 0 | Week 24 | Δ24 weeks | ||
| HbA1c (%) | 14 | 6.2 ± 0.9 | 6.0 ± 0.6 | − 0.2 ± 0.6 | 16 | 6.5 ± 1.0 | 6.9 ± 1.5 | 0.4 ± 0.8 | 0.024 |
| GA (%) | 14 | 18.8 ± 4.3 | 18.5 ± 4.0 | − 0.3 ± 3.4 | 16 | 21.9 ± 3.8 | 23.3 ± 4.7 | 1.4 ± 3.4 | 0.190 |
Date are presented as mean ± standard deviation. Δ24 weeks indicates changes from baseline to 24 weeks
HbA1c glycated hemoglobin, GA glycoalbumin
Fig. 3.
Between-group differences in 24-week changes in glycated hemoglobin (HbA1c) and glycoalbumin (GA). The vertical dotted line at 0.25% represents the margin of non-inferiority for the HbA1c change and 0.75% for the GA change. Two-headed horizontal arrow bars represent one-sided 95% confidence intervals
Fig. 4.
Changes from baseline in glycated hemoglobin (HbA1c) and glycoalbumin (GA) after 24 weeks in the full analysis set. Changes in a HbA1c levels and b GA levels between the two groups. Between-group differences were compared using the t test. p values less than 0.05 were considered statistically significant. Data are shown as the mean ± standard error
The secondary endpoints are shown in Table 3 and Table S1. Blood glucose reduction after a single HD session was significantly greater in the omarigliptin group (− 18.4 ± 31.4 mg/dL) than in the linagliptin group (25.2 ± 59.5 mg/dL, p = 0.019). Plasma glucagon levels before a single HD session tended to be reduced in the omarigliptin group compared with the linagliptin group (− 9.9 ± 30.3 pg/mL and 6.1 ± 31.6 pg/mL, p = 0.176). Plasma glucagon levels after a single HD session also tended to be reduced in the omarigliptin group compared with the linagliptin group (− 6.8 ± 14.1 pg/mL and 2.6 ± 16.6 pg/mL, p = 0.109). Plasma active GLP-1 levels before a single HD session tended to be increased in the omarigliptin group compared with the linagliptin group (7.6 ± 12.5 pmol/L and 2.1 ± 7.1 pmol/L, p = 0.168). The mean change in the total DTR-QOL score was − 1.5 ± 18.3 in the omarigliptin group and − 3.0 ± 10.2 in the linagliptin group (p = 0.799). There were no significant differences in any subscale score of the DTR-QOL between the two groups.
Table 3.
Secondary endpoints
| Omarigliptin group | Linagliptin group | p value | |||
|---|---|---|---|---|---|
| n | Δ24 weeks | n | Δ24 weeks | ||
| Glucose before HD (mg/dL) | 13 | 1.2 ± 56.8 | 16 | 45.1 ± 91.8 | 0.127 |
| Glucose after HD (mg/dL) | 13 | − 18.4 ± 31.4 | 16 | 25.2 ± 59.5 | 0.019 |
| Glucagon before HD (pg/mL) | 13 | − 9.9 ± 30.3 | 16 | 6.1 ± 31.6 | 0.176 |
| Glucagon after HD (pg/mL) | 13 | − 6.8 ± 14.1 | 16 | 2.6 ± 16.6 | 0.109 |
| Active GLP-1 before HD (pmol/L) | 13 | 7.6 ± 12.5 | 16 | 2.1 ± 7.1 | 0.168 |
| Active GLP-1 after HD (pmol/L) | 13 | − 3.0 ± 13.0 | 16 | − 0.7 ± 10.5 | 0.610 |
| DTR-QOL | |||||
| Total score | 13 | − 1.5 ± 18.3 | 16 | − 3.0 ± 10.2 | 0.799 |
| Subscale score | |||||
| Domain 1 | 13 | − 2.6 ± 23.5 | 16 | − 2.9 ± 14.6 | 0.966 |
| Domain 2 | 13 | 1.1 ± 15.5 | 16 | − 3.7 ± 12.1 | 0.374 |
| Domain 3 | 13 | − 3.8 ± 17.5 | 16 | − 5.8 ± 26.0 | 0.809 |
| Domain 4 | 13 | − 0.5 ± 31.1 | 16 | − 0.5 ± 17.6 | 0.997 |
Data are presented as mean ± standard deviation. Δ24 weeks indicates changes from baseline to 24 weeks
HD hemodialysis, GLP-1 glucagon-like peptide-1, GIP gastric inhibitory polypeptide, DTR-QOL Diabetes Therapy-Related Quality of Life
There were no significant differences in changes of hemoglobin or hematocrit levels (Table S2). We also examined the doses of erythropoiesis-stimulating agents (ESAs) during the study period (Table S3). From the start to end of the observation period, the dose of ESAs increased in six patients, did not change in eight, and decreased in none in the omarigliptin group, whereas the dose increased in two patients, did not change in 11, and decreased in three in the linagliptin group.
There was also no change in the rate of insulin use or in the dialysis fluid glucose concentration between the two groups during the study period (data not shown).
Discussion
This prospective, randomized, open-label, parallel-group, non-inferiority/superiority, multicenter study examined the efficacy of once-weekly DPP4 inhibitor omarigliptin compared with once-daily DPP4 inhibitor linagliptin in patients with T2DM undergoing maintenance HD. We confirmed the non-inferiority of omarigliptin compared with linagliptin in terms of changes in HbA1c. Moreover, we confirmed greater reduction in HbA1c and blood glucose after a single HD session in the omarigliptin group. None of the patients in the omarigliptin group developed hypoglycemia during the observation period.
Diabetic nephropathy is the leading cause of end-stage renal disease (ESRD) worldwide. Good glycemic control is reported to improve prognosis even in patients with T2DM on maintenance HD [2], but few OHAs can be used in such patients, so insulin injection therapy is the standard. However, adherence to insulin injection therapy is usually lower than adherence to OHAs because of hypoglycemia. DPP4 inhibitors are widely used in patients with T2DM on maintenance HD and have a good safety profile. For example, vildagliptin, a once-daily DPP4 inhibitor, also reduces plasma glucagon levels and might contribute to reduction of blood glucose in patients on maintenance HD [15]. Moreover, it was reported that patients with ESRD including those on peritoneal dialysis with T2DM showed no significant difference in glycemic control among three types of once-daily DPP4 inhibitors [16]. Once-weekly DPP4 inhibitor omarigliptin showed non-inferiority to other OHAs in improving glycemic control and might thus improve adherence and patient satisfaction [17]. In a meta-analysis, omarigliptin showed obviously better efficacy and safety and lower risk of hypoglycemia than placebo [5]. Also, omarigliptin can be used at low doses in patients with ESRD and is favorably comparable with placebo or glipizide in terms of efficacy and safety [18]. In our study, we found that patients in the once-weekly omarigliptin group had greater reduction in HbA1c and blood glucose after a single HD session compared with patients in the once-daily DPP4 inhibitor linagliptin group. Although this was not a significant difference, we also found that the omarigliptin group had reduced plasma glucagon and active GLP-1 levels either before or after a single HD session compared with the linagliptin group. There are two possible reasons for the better glycemic control in the omarigliptin group. First, omarigliptin is a long-acting OHA, so this drug can maintain higher DPP4 inhibition over the period of a week [19]. Plasma glucagon levels also tended to be reduced in the omarigliptin group in our study. Furthermore, it has been reported that omarigliptin might decrease DPP4 secretion and ameliorate insulin resistance compared with linagliptin [20]. Accordingly, treatment with omarigliptin might have more strongly suppressed plasma glucagon and increased active GLP-1 than treatment with linagliptin over the period of a week, although more detailed studies are needed. Second, once-weekly drugs, such as omarigliptin, might improve adherence by reducing the medication burden of patients. Some once-weekly DPP4 inhibitors are currently available for use. Inagaki et al. reported that the once-weekly DPP4 inhibitor trelagliptin, which is contraindicated in patients with ESRD, provides well-tolerated long-term safety and efficacy; therefore, once-weekly drugs are considered a good therapeutic alternative in patients with T2DM for improving adherence [21, 22]. The same as in our study, if patients undergoing HD can take once-weekly drugs at the HD center, almost perfect adherence might be possible. It also might be easy for patients to take once-weekly DPP4 inhibitors at the HD center because they are usually also administered other once-weekly drugs such as ESAs.
Some studies have reported improved treatment satisfaction when patients with T2DM switched from once-daily to once-weekly drugs, based on the Diabetes Treatment Satisfaction Questionnaire [23]. The DTR-QOL instrument that we used is an exact reflection of the patient’s satisfaction with treatment, especially in relatively younger patients under the age of 65 years [24], those receiving at most two concomitant drugs for treatment of comorbidities, and those who were treatment naïve before the start of the study [25]. As such, we expected some improvement in patient satisfaction with treatment, but there was no significant improvement in DTR-QOL score in the omarigliptin group. In our study, the participants were relatively old (mean age 67.6 years). They were also not treatment naïve and received many concomitant drugs. The mean number of concomitant drug types was 8.0 per day (17.9 tablets per day, 124.3 tablets per week). In general, patients on maintenance HD require many drugs, including antihypertensives or phosphorus binders. These factors might explain the lack of significant improvement in DTR-QOL score in our study. Among those patients who received hundreds of tablets per week, treatment satisfaction did not improve even when the number of tablets decreased by six tablets per week.
In Japan, rising medical costs for patients with T2DM on HD are a major challenge. Monthly medical expenses for maintenance HD are estimated at about 400,000 JPY per patient. Kanozawa et al. reported that switching from other DPP4 inhibitors to lower-dose sitagliptin on the basis of the patient’s renal function status reduced daily drug costs by 88.1 JPY per patient [26]. Omarigliptin (12.5 mg), as used in this study, costs about 492.9 JPY weekly, and linagliptin (5 mg) costs 1005.2 JPY weekly. Switching linagliptin to omarigliptin reduces drug costs per patient by 512.3 JPY weekly and about 30,000 JPY yearly. Notably, the daily DPP4 inhibitor sitagliptin (12.5 mg dose in patients on hemodialysis), which is widely used worldwide, costs about 400 JPY weekly, which is comparable to the cost of omarigliptin. Omarigliptin can therefore be a good therapeutic option in terms of reducing national medical costs.
This study has several limitations. First, although we confirmed that the omarigliptin group had a greater reduction in HbA1c, this result might have been affected by changes in the doses of ESAs in the two groups. Second, we could not confirm non-inferiority of omarigliptin compared with linagliptin in reduction of GA levels in unadjusted data. We calculated the sample size of participants based on the non-inferiority margin in HbA1c. As a result, the sample size may have been too small to identify a significant difference in the reduction of GA levels between the two groups. Setting a larger sample size might help to confirm non-inferiority in terms of not only reduction in GA but also reduction in plasma glucagon and elevation in plasma active GLP-1 levels, so we will consider using a crossover protocol in a future study. Third, most of our participants already had good glycemic control when this study started. For ethical reasons, we excluded the patients with poor glycemic control (HbA1c ≥ 9% or GA ≥ 27%) on current treatment because they had the potential for further exacerbation of glycemic control because of drug changes. Investigating the efficacy of omarigliptin in patients with poor glycemic control remains a topic for future research. Fourth, because of ethical considerations, our protocol permitted patients to change or add OHAs if they had not achieved HbA1c < 10% or GA < 29% after 12 weeks. However, no patients changed or added antidiabetic drugs during the study period, so this point did not appear to affect our results. Fifth, mean duration of diabetes was longer in the linagliptin group than in the omarigliptin group. This difference might have affected our results, but the sample size in this study was too small to perform multivariable analysis. This point would need to be adjusted for in a further study. Sixth, we could not measure morning fasting plasma glucagon or active GLP-1 because some of our patients underwent HD at night. Seventh, the study period was only 24 weeks, so the efficacy, safety, and treatment satisfaction of omarigliptin over longer periods remain unclear. Eighth, we compared only linagliptin and omarigliptin, and therefore the effects of omarigliptin in comparison with other OHAs are not known.
Conclusion
Our data showed that the once-weekly DPP4 inhibitor omarigliptin was non-inferior to once-daily DPP4 inhibitor linagliptin in glycemic control. Use of once-weekly omarigliptin is also practicable for achieving glycemic control in patients with T2DM on maintenance HD. Further research is needed to verify the effectiveness of omarigliptin in longer-term and larger-scale studies.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
Funding
No funding or sponsorship was received for this study. The journal’s Rapid Service Fee was paid by Niigata University.
Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship of this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Authorship Contributions
Y. Yoshizawa, M. Hosojima, and H. Kabasawa were responsible for the conception and design of the study. Y. Yoshizawa was the chief investigator and also responsible for data analysis. M. Hosojima, H. Kabasawa, and N. Tanabe were responsible for data analysis. Y. Yoshizawa, M. Hosojima, and H. Kabasawa were responsible for data acquisition. Y. Yoshizawa, M. Hosojima, H. Kabasawa, N. Tanabe, D. Ugamura, Y. Koda, H. Shimada, T. Takasawa, T. Ito, T. Kitamura, M. Kobayashi, Y. Suzuki, A. Saito, and I. Narita were responsible for data interpretation. Y. Yoshizawa and M. Hosojima were responsible for drafting the manuscript. All authors contributed to writing the final manuscript.
Medical Writing and Editorial Assistance
The authors thank Dr. Hitoshi Ishii (Department of Diabetology, Nara Medical University) for advice on the DTR-QOL. The authors also thank Ms. Maiko Daisaka at Niigata University for providing technical assistance and ThinkSCIENCE Inc. (Tokyo, Japan) for providing language editing services. This assistance was paid for by Niigata University.
Prior Presentation
Data included in this manuscript were presented, in part, at the American Diabetes Association 79th Scientific Sessions 2019 in San Francisco, California.
Disclosures
Michihiro Hosojima, Hideyuki Kabasawa, Tadahiro Kitamura, Akihiko Saito, and Ichiei Narita have received lecture fees from Eli Lilly Japan K.K., MSD K.K., and Nippon Boehringer Ingelheim Co., Ltd.; Yutaka Koda has received lecture fees from MSD K.K.; Michihiro Hosojima has received research support from Eli Lilly Japan K.K. and MSD K.K.; Akihiko Saito and Ichiei Narita have received research support from Eli Lilly Japan K.K., MSD K.K., and Nippon Boehringer Ingelheim Co., Ltd. Yuta Yoshizawa, Naohito Tanabe, Daisuke Ugamura, Hisaki Shimada, Tetsuya Takasawa, Takahito Ito, Masaki Kobayashi and Yoshiki Suzuki have nothing to disclose.
Compliance with Ethics Guidelines
The study was approved by the institutional review boards of Niigata University and Shinrakuen Hospital. All procedures were performed in accordance with the Helsinki Declaration of 1964, and its later amendments, and conformed with national regulations. The study was a prospective randomized controlled trial, and all patients provided written informed consent for participation in this study and publication of their clinical data for research purposes.
Data Availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.