Effectiveness and Safety of Once-Weekly Semaglutide in Japanese Patients with Type 2 Diabetes in Treatment Intensification: A Retrospective Observational Single-Center Study.

INTRODUCTION: Once-weekly (OW) glucagon-like peptide 1 receptor agonist (GLP-1RA) semaglutide has been shown to have a more potent glycated hemoglobin (HbA1c)-lowering effect than other oral hypoglycemic agents and existing GLP-1RAs in global randomized controlled trials. The study aim was to evaluate the safety and effectiveness of OW semaglutide in Japanese patients with type 2 diabetes mellitus (T2DM) in a real-world clinical setting and identify pre- and post-treatment predictors of good response.
METHODS: We investigated the change in HbA1c, percentage of patients achieving < 7% HbA1c, and factors contributing to the effect 6 months after OW semaglutide use in Japanese patients with T2DM. We also examined differences in effectiveness between patients with different backgrounds.
RESULTS: At baseline, the 77 patients had a mean baseline HbA1c of 8.1% ± 1.23%, 74% of the patients were injecting another GLP-1RA, and 42.9% of the patients were being treated with insulin. HbA1c decreased by 0.89% and by 0.66% in the other GLP-1RA users. The rate of achievement of < 7% HbA1c increased from 21% to 43%. There were no differences in effect by age, sex, or body mass index. Higher baseline HbA1c and shorter duration of diabetes were associated with greater HbA1c reduction. OW semaglutide was tolerable for the majority of our study population.
CONCLUSION: This study provided real-world evidence showing that OW semaglutide significantly reduced HbA1c in Japanese patients with T2DM who had inadequate HbA1c control.

Key Summary Points

Introduction

The pathophysiology of type 2 diabetes mellitus (T2DM) involves decreased insulin secretion from pancreatic β-cells and decreased activity in target organs [1]. Insulin secretion capacity and resistance are lower in East Asians, including Japanese people, than in Caucasians [2, 3]. In particular, acute insulin secretion in response to higher glucose levels is decreased and causes postprandial hyperglycemia in early-stage T2DM [4]. Glucagon-like peptide 1 (GLP-1), a gut-derived hormone, maintains glucose homeostasis through glucose-stimulated insulin secretion (GSIS) from pancreatic β-cells (pancreatic action) and other direct or indirect actions on the central nervous system, liver, gut, and adipose tissue (extrapancreatic action) [5, 6]. GLP-1 stimulates GSIS in pancreatic β-cells by activating the ATP-sensitive K+ channel pathway via GLP-1/cyclic adenosine 3′,5′-monophosphate (cAMP)/exchange protein directly activated by the cAMP 2 (EPAC2) pathway or another mechanism [7-9] and improves glucose intolerance. Administration of GLP-1, not incretin enhancers such as dipeptidyl peptidase 4 inhibitors, also reduces appetite and food intake [10]. GLP-1 receptor agonists (GLP-1RAs) are an established glucose-lowering therapeutic option for treatment of T2DM proven in numerous clinical trials [11]. Presently, once-weekly (OW) administered GLP-1RA semaglutide is available (in Japan since June 2020), and patients can choose the most appropriate formulation (oral or injectable) depending on their individual factors [12]. On the other hand, other GLP-1RAs and/or new sodium-glucose transporter 2 (SGLT2) inhibitors have become widely used in Japan, but some patients still have difficulty reducing glycated hemoglobin (HbA1c) [13-15]. OW semaglutide has been reported to have a more potent effect on HbA1c than placebo or existing drugs or another GLP-1 receptor agonist in the Semaglutide Unabated Sustainability in Treatment of Type 2 Diabetes (SUSTAIN) clinical trial program, which includes clinical trials on Japanese patients [16, 17]. The SUSTAIN-6 trial, a cardiovascular outcome trial, showed significant reduction in major adverse cardiovascular events by treatment with semaglutide relative to those in the placebo group [18]. Currently published clinical trials suggest that semaglutide may be useful for therapeutic intensification of diabetes treatment and provide a cardiovascular benefit, but few studies have been conducted in real-world clinical settings in Japanese patients with T2DM. A recent meta-analysis of six GLP-1RA clinical trials, including the SUSTAIN-6 trial, reported that the benefit of GLP-1 on major adverse cardiovascular events was greater in Asians than in White patients [19]. We planned a study of the efficacy and safety of semaglutide in Japanese patients with T2DM. To reinforce the previous randomized clinical trial (RCT) findings, the present study aim was to evaluate the safety and effectiveness of OW semaglutide and identify pre- and post-treatment predictors of good response in Japanese patients with T2DM in a real-world clinical setting.

Methods

Study Design and Participants

This was a retrospective cohort study conducted at a single center. We enrolled patients with T2DM who had been treated with OW semaglutide (Ozempic® subcutaneous injection SD) in the Jichi Medical University Saitama Medical Center between June 2021 and December 2021. Semaglutide was used for better glycemic control at the discretion of the attending physician according to the Japanese package insert, with a starting dose of 0.25 mg. We evaluated clinical parameters 6 months after OW semaglutide initiation. The inclusion criteria were as follows: Japanese patients with T2DM who initiated OW semaglutide in an outpatient setting. The exclusion criteria were patients with acute metabolic disorders, such as diabetic ketoacidosis and hyperosmolar hyperglycemic syndrome; who were taking steroids, had acute infectious disease, or had any newly diagnosed cancer; who required hospitalization, self-discontinued, or had poor adherence to injections; who exhibited a change in an oral antidiabetic drug (OAD) or new insulin induction during the observation period; and whose adverse events led to discontinuation within 6 months.

Figure 1 shows the flowchart of patient enrollment. After application of the inclusion and exclusion criteria, we analyzed the data from 77 patients. No patient discontinued the treatment because of side effects. The primary outcome was the change in HbA1c at 6 months after initiation of OW semaglutide. The secondary outcome was the proportion of participants achieving HbA1c < 7.0%. Additionally, we investigated clinical factors that potentially caused a change in HbA1c, and the information in the medical records on adverse events. We obtained baseline demographic data of the patients, such as age, sex, body mass index (BMI), duration of diabetes, presence of macroangiopathy and cardiovascular disease, concomitant medications, adverse events, and OW semaglutide dose at 6 months, from the medical records. Additionally, we collected the following clinical laboratory data: HbA1c, total cholesterol, high-density lipoprotein cholesterol, triglyceride, and estimated glomerular filtration rate (eGFR). This study was conducted in accordance with the Declaration of Helsinki of 1964, as revised in 2013, and was approved by the Ethics Committee at Jichi Medical University Saitama Medical Center (No. S19-005). This study used non-identifiable data obtained by the treating physicians and therefore, on the basis of the decision from our local Ethics Committee of Jichi Medical University Saitama Medical Center (No. S19-005), informed consent was not required. Patients had the opportunity to object to the use of their data for retrospective scientific research; however, none of the patients objected.

Fig. 1

Flowchart of patient enrollment

Statistical Analysis

We expressed continuous variable data as means (± standard deviations) and categorical variable data as numbers and percentages. We compared each parameter before and after initiating OW semaglutide by using paired t tests or the t test. One-way analysis of variance (ANOVA) or the Kruskal–Wallis test was used to compare the clinical characteristics among three or more groups. Categorical variables were compared by performing Fisher’s exact test. We defined patients who showed a change in HbA1c greater than the median (≥ 0.7%) as the good-response group and those who showed a change in HbA1c less than the median (< 0.7%) as the poor-response group.

To explore the effects of various clinical factors on the deterioration of OW semaglutide in the good-response group, we performed logistic regression analysis. We divided the patients into the younger and elderly groups (age < 65, ≥ 65 years), non-obese and obese groups (BMI < 25, ≥ 25 kg/m2), and the chronic kidney disease (CKD) and non-CKD groups (eGFR < 60, ≥ 60 mL/min/1.73 m2). We defined baseline HbA1c < 8.1% or ≥ 8.1% and duration of diabetes as < 14 or ≥ 14 years according to these medians. We performed all statistical analyses using EZR (Jichi Medical University, Saitama Medical Center), a graphical user interface for R (The R Foundation for Statistical Computing), and a modified version of R commander designed to add statistical functions frequently used in biostatistics. We accepted all P values less than 0.05 as indicating statistical significance.

Results

Baseline Characteristics

The baseline characteristics of the 77 patients (aged 64.6 ± 11.6 years, 50 men) are shown in Table 1. The average baseline HbA1c and BMI were 8.1% ± 1.23% and 27.3 ± 5.03 kg/m2, respectively. The elderly group (age ≥ 65 years) comprised 41 patients, and the obese group (BMI ≥ 25 kg/m2) comprised 49 patients. The most used OADs were the SGLT2 inhibitor (66.2%) and biguanides (52%). The percentage of patients treated only by an OAD was 14.3%. We found that 74% of the patients were injecting GLP-1RAs and 42.9% of the patients were being treated with insulin. All patients were initially administered semaglutide 0.25 mg, and at the time of data evaluation, the semaglutide dosages were 0.25 mg in 13 patients, 0.5 mg in 59 patients, and 1.0 mg in 5 patients.

Table 1

Clinical baseline characteristics of the patients

Variables
Number of patients, n	77
Men/women, n	50/27
Age, years	64.6 (11.6)
BMI, kg/m2	27.3 (5.03)
BW, kg	70.4 [65–82]
Duration of diabetes, years	14 [9–22]
HbA1c, %	8.1 (1.23)
eGFR, mL/min/1.73 m2	65.5 (26.9)
TC, mg/dL	178 (37.3)
TG, mg/dL	146 [103–205]
HDL-C, mg/dL	49 [20–56]
Dyslipidemia, yes, n (%)	51 (66.2)
Hypertension, yes, n (%)	48 (62.3)
Ischemic heart disease, yes, n (%)	17 (22.1)
Diabetic retinopathy yes, n (%)	11 (14.3)
Diabetic nephropathy yes, n (%)	27 (35.1)
Medications
Sulfonylurea, n (%)	14 (18.2)
Biguanide, n (%)	40 (52)
Glinide, n (%)	23 (29.8)
α-Glucosidase inhibitor, n (%)	21 (27.3)
Thiazolidinedione, n (%)	7 (9.1)
SGLT2 inhibitor, n (%)	51 (66.2)
DPP4 inhibitor n (%)	14 (18.2)
OAD only, n (%)	11 (14.3)
Insulin therapy, n (%)	33 (42.9)
Basal insulin only, n (%)	21 (27.3)
Bolus insulin only, n (%)	0 (0)
Basal–bolus therapy, n (%)	12 (15.6)
GLP-1 receptor agonist, n (%)	57 (74)
Liraglutide, n (%)	10 (13)
Lixisenatide, n (%)	10 (13)
Dulaglutide, n (%)	37 (48.1)

Data are presented as n (%) for categorical variables and as the mean (standard deviation) or median [interquartile range] for continuous variables

BMI body mass index, BW body weight, HbA1c glycated hemoglobin, eGFR estimated glomerular filtration rate, TC total cholesterol, HDL-C high-density lipoprotein cholesterol, TG triglyceride, SGLT2 sodium-glucose cotransporter 2, DPP4 dipeptidyl peptidase 4, OAD oral antidiabetic drug, GLP-1 glucagon-like peptide 1

Change in HbA1c and Response Predictors

Overall, reduction of HbA1c was − 0.89% from baseline HbA1c at 6 months. The percentage of patients who achieved HbA1c < 7% was significantly changed from 21% at baseline to 43% (Fig. 2). The changes in HbA1c in the two groups were significantly improved from their baseline HbA1c values (Fig. 2). The degree of change in HbA1c between the two groups did not differ by age, sex, BMI, and duration (Fig. 3a–d), but significant changes were observed between previous GLP-1RA users and OAD-only users (Fig. 3e, f). Among the following four categories, patients who were < 65 years with BMI < 25 kg/m2, < 65 years with BMI ≥ 25 kg/m2, ≥ 65 years with BMI < 25 kg/m2, and ≥ 65 years with BMI ≥ 25 kg/m2, the changes in HbA1c decreased relative to their respective baseline HbA1c values. However, the degree of change in HbA1c by category was not significant (Fig. 4). Weight data were available for 64 patients. The overall change in body weight was a decrease of 1.25 kg, with a decrease of 4.2 kg for semaglutide 0.25 mg (n = 4), 0.63 kg for 0.5 mg (n = 55), and 5.7 kg for 1.0 mg (n = 5), and significant differences in weight changes were observed. (p = 0.016). Significant reductions from baseline weight were also observed overall and in the group using OW semaglutide 0.5 mg (Supplementary Material 1).

Fig. 2

Change in HbA1c from baseline overall and in the semaglutide dose subgroup (a) and proportion of patients achieving HbA1c < 7% (b). *P < 0.05 in the paired t test (vs. BL). BL baseline, HbA1c glycated hemoglobin

Fig. 3

Change in HbA1c by subgroup a age, b sex, c BMI, d duration of diabetes, e previous GLP-1RA user or not, and f OAD user or not. *P < 0.05 in paired t test (vs. BL HbA1c). BL baseline, HbA1c glycated hemoglobin, BMI body mass index, GLP-1RA glucagon-like peptide 1 receptor agonist, OAD oral antidiabetic drug

Fig. 4

Change in baseline HbA1c by age and BMI. *P < 0.05 in the paired t test (vs. BL HbA1c). BL baseline, HbA1c glycated hemoglobin, BMI body mass index

Multivariate analysis of the potential predictors of a good response to OW semaglutide (> 0.7% HbA1c improvement as defined in the “Methods” section) revealed that shorter duration of diabetes and higher baseline HbA1c level were more likely than the other predictors to achieve a good response (Table 2).

Table 2

Independent clinical factors associated with good response

Parameters	OR	95% CI	P value
Age ≥ 65 years	1.29	0.376–4.44	0.685
Sex, women	0.948	0.282–3.18	0.931
BMI ≥ 25 kg/m2	0.680	0.211–2.20	0.520
Duration of diabetes ≥ 14 years	0.312	0.101–0.962	0.043
eGFR ≥ 60 mL/min/1.73 m2	0.367	0.103–1.30	0.121
Baseline HbA1c ≥ 8.1%	8.87	2.83–27.8	< 0.001

BMI body mass index, eGFR estimated glomerular filtration rate, HbA1c glycated hemoglobin, OR odds ratio, CI confidence interval

Safety

In this study, no patients were discontinued because of side effects. Nausea occurred in eight (10.4%) patients, out of which six whose previous therapy was not GLP-1RA and two who had switched from GLP-1RA. By OW semaglutide dose, seven patients received 0.5 mg, and one patient received 1.0 mg. Seven (9.1%) patients complained of injection pain, but all were able to continue treatment. No hypoglycemic episodes were reported.

Discussion

We showed that the addition of semaglutide or switching from other GLP-1RAs was effective in Japanese patients with T2DM and inadequate HbA1c control using existing therapy. OW semaglutide was particularly effective in patients with high baseline HbA1c, but less effective in those with longer disease duration of diabetes.

In the safety and effectiveness of monotherapy with OW semaglutide versus one additional OAD in Japanese people with T2DM (SUSTAIN OAD combination trial in Japan), OW semaglutide 0.5 mg and 1 mg reduced HbA1c by 1.7% and 2.0% from baseline HbA1c (8.1%, overall), respectively, compared with 0.7% for additional OAD [16]. In the present study, treatment with OW semaglutide reduced HbA1c by 0.89%; however, in previously untreated GLP-1 or treated by OAD-only patients, the addition of OW semaglutide reduced HbA1c by 1.5% to 2.1%, which was similar to the results for the SUSTAIN Japan OAD combination [16]. Otherwise, people who switched from another GLP-1RA to OW semaglutide showed reduction of 0.66% (baseline HbA1c 7.9%) of HbA1c in the present study. In a retrospective study conducted in Canada, switching to OW semaglutide from liraglutide or dulaglutide decreased HbA1c by 0.65% (baseline HbA1c, 7.9%) in 164 patients after 6 months (REALISE-DM study) [20]. Most prior GLP-1RA usage (liraglutide and dulaglutide) was of high doses [20]. In our study, there were few previous users of high-dose GLP-1RAs. Additionally, the final dose of OW semaglutide was 1.0 mg in the REALISE-DM study [20], whereas the average dose in our study was 0.49 mg, and only five (6.5%) patients received 1.0 mg. A prospective, observational study conducted in Switzerland (SURE Switzerland) showed a 0.8% reduction in HbA1c (baseline HbA1c 7.8%) with the introduction of OW semaglutide (mean dose 0.78 mg) at approximately 30 weeks [21]. Patients treated with insulin or other GLP-1RAs were included in SURE Switzerland, and, similar to the results of our study, semaglutide may contribute to HbA1c improvement regardless of prior therapy and without using up to 1.0 mg.

Introduction of OW semaglutide significantly reduced HbA1c levels from the baseline level; however, there were no significant differences among subgroups divided by age and BMI (Fig. 4). The degree of improvement in HbA1c was greater in the higher HbA1c group (Supplementary Material 2). A post hoc analysis of two SUSTAIN Japan trials also showed that OW semaglutide was effective regardless of age and BMI subgroups (age < 65 and ≥ 65 years and/or BMI < 25 and ≥ 25 kg/m2) [22]. A large US database used to examine the effect of switching other GLP-1RAs to OW semaglutide showed that semaglutide was effective regardless of prior GLP-1RAs, age, or gender [23]. Our real-world evidence (RWE) is consistent with the US RWE, and semaglutide may be effective for further improvement of HbA1c in poorly controlled T2DM regardless of patient background, as well as in Japanese patients.

In the present study, nausea occurred in eight (10.4%) patients, and compared with the SUSTAIN Japan post hoc analysis [22], no new adverse effect concerns were identified. Injection site pain was thought to be due to the use of the SD pen. We concluded that OW semaglutide was tolerable for the majority of our study population.

The current study data showed that baseline HbA1c and disease duration of diabetes were predictors of effectiveness. The results of several real-world studies have shown that higher baseline HbA1c was associated with a greater effect of OW semaglutide [20, 24, 25], consistent with our results (Table 2, Supplemental Fig. 1). Marzullo et al. reported that the shorter duration of diabetes was a significant predictor of a good response after 6 months OW semaglutide induction [25]. Since the retention of GSIS capacity in patients with T2DM is inversely correlated with the duration of diabetes [26], it is speculated that longer duration is responsible for the attenuated effect of insulin secretagogues. Ohbatake et al. reported that the best predictor of GLP-1RA efficacy was residual β-cell function as assessed by the glucagon stimulation test [27]. Consequently, it would be useful to examine the relationship between β-cell function and semaglutide efficacy in the future.

A study showed that weekly dulaglutide was superior to liraglutide with respect to treatment satisfaction in Japanese patients with T2DM [28]. OW semaglutide may also affect treatment satisfaction, but treatment quality of life (QOL) could not be assessed in this study. Future studies on treatment QOL are also needed.

This study had several limitations. First, this was a single-center retrospective observational study without a control group; therefore, there may have been confounding factors that were not eliminated, and the results may not be applicable to the general Japanese diabetes population. Side effects, such as nausea or hypoglycemic episodes, were not documented in the medical records and may have been underestimated. Second, OW semaglutide usage was uneven, with most patients using 0.5 mg (76.6%), and the follow-up period was short (6 months), which may have resulted in inadequate semaglutide dose titration. Third, there was variability in the drug and dose of pre-treatment GLP-1RAs. There was no statistical power to analyze each drug subgroup; consequently, analysis of a large number of cases is desired in the future.

Conclusion

Our study results showed that the introduction of semaglutide in Japanese patients with T2DM who had not achieved the target reduction in HbA1c level with existing therapy, including another GLP-1RA, was useful for lowering HbA1c levels. In addition, patients with shorter disease duration and higher baseline HbA1c were found to be more likely to benefit from treatment. Semaglutide was useful for earlier treatment intensification.

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 168 KB)

Why carry out this study?

Once-weekly (OW) semaglutide has been reported to lower glycated hemoglobin (HbA1c) more potently than other glucagon-like peptide 1 receptor agonists (GLP-1RAs) and dipeptidyl peptidase 4 inhibitors in global randomized controlled trials that included Japanese people.

Few studies have been conducted using real-world evidence (RWE) in Japanese patients with type 2 diabetes mellitus (T2DM).

This retrospective study provides RWE for enhanced treatment using OW semaglutide in Japanese patients with T2DM.

What was learned from this study?

Add-on or switching from another GLP-1RA to OW semaglutide significantly reduced HbA1c at 6 months relative to those supported by RCT. The rate of achievement of HbA1c < 7% also increased.

Patients with higher baseline HbA1c and shorter duration of diabetes were associated with greater reduction of HbA1c.