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Background:
Systematic Review

Weekly Semaglutide vs. Liraglutide Efficacy Profile: A Network Meta-Analysis

by
Hassan A. Alsugair
1,*,
Ibrahim F. Alshugair
2,
Turki J. Alharbi
1,*,
Abdulaziz M. Bin Rsheed
1,
Ayla M. Tourkmani
1 and
Wedad Al-Madani
3
1
Family Medicine Department, Prince Sultan Military Medical City, Riyadh 12624, Saudi Arabia
2
Orthopedic Surgery Department, King Saud Medical City, Riyadh 12746, Saudi Arabia
3
General Authority of Statistics, Riyadh 11481, Saudi Arabia
*
Authors to whom correspondence should be addressed.
Healthcare 2021, 9(9), 1125; https://doi.org/10.3390/healthcare9091125
Submission received: 25 June 2021 / Revised: 20 August 2021 / Accepted: 22 August 2021 / Published: 30 August 2021
(This article belongs to the Section Chronic Care)
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Abstract

:
Introduction: Glucagon-like peptide 1 receptor agonist (GLP-1 RA) is a class of hypoglycemic medications. Semaglutide once-weekly (QW) and liraglutide once-daily (OD) significantly improved glycemic control compared to placebo. To date, no long-term phase III trials directly comparing semaglutide and liraglutide are available. This network meta-analysis (NMA) aims to compare the long-term efficacy of semaglutide and liraglutide. Methods: PubMed, Embase, and Cochrane Library were searched from inception until June 2019 to identify relevant articles. Nine long-term randomized controlled trials comparing once-weekly semaglutide or liraglutide with placebo or other active comparisons were identified. The outcomes of interest were changes in HbA1c and weight after 52 weeks. A Bayesian framework and NMA were used for data synthesis. This is a sub-study of the protocol registered in PROSPERO (number CRD42018091598). Results: The data showed significant superiority in HbA1c reduction of semaglutide 1 mg QW over liraglutide 1.2 and 1.8 mg with a treatment difference of 0.47% and 0.3%, respectively. Semaglutide 0.5 mg QW was found to be significantly superior to liraglutide 1.2 mg in HbA1c reduction with a treatment difference of 0.17%. Regarding weight reduction analysis, semaglutide 0.5 and 1 mg QW were significantly associated with a greater reduction than liraglutide 0.6 mg with a treatment difference of 2.42 and 3.06 kg, respectively. However, no significant reduction was found in comparison to liraglutide 1.2 and 1.8 mg. Conclusions: Semaglutide improved the control of blood glucose and body weight. The capacity of long-term glycemic control and body weight control of semaglutide appears to be more effective than other GLP-1 RAs, including liraglutide. However, considering the number of included studies and potential limitations, more large-scale, head-to-head, well-designed randomized-controlled trials (RCTs) are needed to confirm these findings.

1. Introduction

Type 2 diabetes mellitus (T2DM) is a progressive and complex metabolic disorder characterized by chronic hyperglycemia due to insulin resistance and pancreatic beta cell dysfunction [1]. Chronic hyperglycemia is associated with multiple complications, including retinopathy, nephropathy, and neuropathy, in addition to various manifestations of atherosclerotic cardiovascular disease (CVD) [1,2]. According to one large randomized controlled trial (RCT) involving 11,140 participants, with every 1% increase in glycosylated hemoglobin (HbA1c), risk was increased up to 40% of all-cause and cardiovascular mortality [3]. Glycemic control becomes progressively difficult with time, and advancements in therapy are needed to maintain glycemic targets [4,5].
Glucagon-like peptide 1 receptor agonist (GLP-1 RA) is a class of hypoglycemic medications that has shown benefit in glucose metabolism, beta-cell function enhancement, and weight loss promotion with a low risk of hypoglycemia [6]. GLP-1 RAs are classified into short- and long-acting preparations based on their mode of action [7,8]. Compared with other hypoglycemic medications, RCTs have reported promising long-term effects, especially with respect to cardiovascular outcomes [6]. The U.S. Food and Drug Administration (FDA) has approved several GLP-1 RAs, including exenatide twice-daily (Bid), lixisenatide once-daily (OD), liraglutide OD, exenatide once-weekly (QW), albiglutide QW, dulaglutide QW, and semaglutide QW [9,10,11,12,13].
The US FDA approved liraglutide in 2010 as a daily subcutaneous injection with therapeutic doses of 1.2 mg and 1.8 mg for T2DM [6,10,14]. In head-to-head RCTs, liraglutide showed a greater reduction in mean HbA1c and fasting plasma glucose (FPG) than exenatide Bid, exenatide QW, albiglutide QW and lixisenatide and was non-inferior to dulaglutide QW [15,16]. Additionally, RCTs reported greater weight reduction from baseline in liraglutide compared to lixisenatide, exenatide QW, dulaglutide QW, and albiglutide QW [16]. RCTs showed similar weight reduction in exenatide Bid compared to liraglutide [16]. The U.S. FDA approved semaglutide in 2017 as a once-weekly subcutaneous injection [9]. A 30-week phase III RCT on semaglutide reported a significant reduction in HbA1c and weight from baseline compared with placebo [17]. In a head-to-head comparison with dulaglutide and exenatide QW, semaglutide was superior in achieving glycemic control and weight reduction [18,19]. A review published by Courtney et al. on GLP-1 medications showed clinically significant glycemic control and weight reduction of liraglutide [20]. In two recent network meta-analyses on GLP-1 RA RCTs, semaglutide was found superior to liraglutide in glycemic control and weight reduction. However, conclusions were drawn from only data gathered at 24 ± 4 weeks [21,22].
To date, no long-term phase III trials directly comparing semaglutide QW and liraglutide OD are available. In the absence of long-term head-to-head RCTs, network meta-analysis is a statistical method that allows the estimation of the comparative effectiveness of multiple treatments [23,24]. This network meta-analysis (NMA) compared the long-term efficacy in HbA1c reduction and weight change between semaglutide QW and liraglutide OD.

2. Materials and Methods

This is a sub-study of the protocol registered in PROSPERO (number CRD42018091598). This network meta-analysis was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement [25].
Database Search: Electronic database search included the PubMed, Embase, and Cochrane’s Library from inception to June 2019. The key term “Liraglutide OR NN2211 OR Semaglutide OR NN9535” was used for all of the databases. The search was restricted to English, French, and Spanish language publications. The earliest publication found using the above search key-term dated back to 2001. However, early publications did not meet the inclusion criteria for this NMA.
Study Selection: This review included double-blind, single-blind, or open-label RCTs with available data on HbA1c or weight. In which once-weekly semaglutide (0.5 mg or 1.0 mg) and liraglutide (1.2 mg or 1.8 mg) compared with other active intervention or placebo. RCTs with adults aged at least 18 years with T2DM and a duration of ≥52 weeks on intervention were only included. Final end-point data were used for the analysis of RCTs longer than 52 weeks. Nonrandomized, experimental studies, crossover trials, and reviews in addition to studies with less than fifty participants were excluded. The eligibility of included studies was assessed independently by two reviewers (A.H.A. and A.I.F.). Discrepancies were resolved by a third reviewer (A.T.J.).
Data Extraction and Quality Evaluation: Unified extraction forms were used to extract the following data: (1) authors’ information; (2) publication year; (3) demographic data including age, gender, diabetes duration, and background therapy; (4) baseline of outcome measures; (5) sample sizes; (6) interventions of each arm; (7) dosages of each arm; (8) outcomes of interest (see above); and (9) duration. For extension trials, data were extracted from the extension phase. Data that were not reported in the original manuscripts were retrieved from ClinicalTrials.gov (accessed on 22 August 2021). Two investigators (A.H.A. and A.I.F.) extracted data independently. The quality of eligible studies was evaluated according to the Cochrane Collaboration’s risk of bias tool for assessing risk of bias [26].
Data synthesis and analysis: The network meta-analysis was conducted based on the Cochrane institute instructions to compare the efficacy of weekly semaglutide 0.5 mg and 1 mg versus liraglutide 1.2 mg and 1.8 mg for the reduction of HbA1c and weight as a primary intervention [27]. Other medications went on the equation to complete the network of comparisons and they were; oral semaglutide 14 mg, liraglutide 3 mg, sitagliptin 100 mg, glimepiride 4 mg, glimepiride 8 mg, oral anti-diabetic drugs, exenatide 2 mg, and placebo. All continuous outcomes were performed using normal likelihood analysis and random effect was used for a better fit between trials. The NMA model was implemented using GeMTC software [28]. It used the Bayesian evidence network, which all indirect comparisons are taken into account to arrive at a single, integrated, estimate of the effect of all included treatments based on the included studies. The Bayesian analysis also allows assessing the consistency of the results to draw conclusions. Bayesian analysis is a type of analysis that is widely used to improve the estimate of the standard error used in a good old-fashioned t-test. The Bayesian has many advantages over the frequentist analysis; of them, it gives more coherent results that can be analyzed and interpreted in such a complicated review as network meta-analysis. Additionally, Bayesian inference allows for the flexible implementation of relatively complicated statistical techniques, such as those that involve hierarchical nonlinear model [29]. The results of the NMA was presented in mean treatment difference and 95% credible intervals (Crl) for mean treatment effect. The treatment that results in a greater treatment reduction from baseline was favored. Forest plots were generated using DistillerSR [30]. Surface under the cumulative ranking curve (SUCRA) was used for ranking interventions for each outcome [31].

3. Results

The search process yielded 12,315 results. Of these, 11,492 results were manually excluded during initial screening, as we did not augment the search filter to exclude publications by language, animal vs. human design, published protocols, reviews, and so forth. By abstract screening, 629 results were excluded. This was followed by a full-text assessment. Of these, 101 were excluded as they did not meet the inclusion criteria. Furthermore, 85 results were excluded due to duplication or not reporting the outcomes of interest. As a result, nine studies were included in the final review. Flowchart of trial selection is shown in Figure 1.

3.1. Study Characteristics

Interventions included in the analysis once-weekly semaglutide 0.5 mg, once-weekly semaglutide 1 mg, once-daily liraglutide 1.2 mg, once-daily liraglutide 1.8 mg, once-daily oral semaglutide 14 mg, once-daily liraglutide 3 mg, once-weekly exenatide ER 2 mg, once-daily sitagliptin 100 mg, once-daily glimepiride 4 mg, once-daily glimepiride 8 mg, and metformin 1500–2000 mg daily. Overall, nine trials with a total of 9618 patients included to the analysis. The publication year ranged from 2009 to 2018. Trial duration ranged from 52 to 104 weeks. Trials design and baseline characteristics are shown in Table 1 and Table 2, respectively. Overall, the risk of bias was low in the included studies. However, due to limited long-term studies on liraglutide, 60% completion rate was accepted. Additionally, other biases that were due to the interference of the pharmaceutical companies in funding studies were permitted.

3.2. Network Meta-Analysis Results

Two outcomes were analysed and presented in this NMA. A random-effect, meta-regression analysis was conducted on HbA1c and weight for a better model fit. Significant treatment differences were found as shown in the matrix, Table 3 and Table 4. The evidence network for Hba1c and weight analysis shown in Figure 2 and Figure 3, respectively.
HbA1c was reported in all nine studies. The HbA1c reduction from baseline was presented in the SUCRA score for ranking the main medications versus comparators, Table 5. Semaglutide 1 mg scored the highest in HbA1c reduction, 90.5% in SUCRA score, Table 5. As shown in the matrix, Table 3, semaglutide 1 mg QW found to be significantly superior to liraglutide 0.6 mg, 1.2 mg, 1.8 mg with a treatment difference of 0.56%, 0.47% and 0.3%, respectively. Semaglutide 0.5 mg QW was found to be significantly superior to liraglutide 0.6 mg and 1.2 mg with a treatment difference of 0.25% and 0.17%, respectively. The results of the NMA are presented as treatment differences in Figure 4.
Eight out of nine studies reported weight reduction. The weight reduction from baseline was presented in the SUCRA score for ranking the main medications versus comparators, Table 5. Semaglutide 1 mg scored the highest in weight reduction, 84.9% in SUCRA score, Table 5. As shown in the matrix, Table 4, semaglutide 0.5 mg and 1 mg QW were significantly associated with greater weight reduction than liraglutide 0.6 mg with a treatment difference of 2.42 kg and 3.06 kg, respectively. However, no significant reduction was found in comparison to liraglutide 1.2 mg and 1.8 mg. The results of the NMA are presented as treatment differences in Figure 5.

4. Discussion

This network meta-analysis aimed to prove the long-term effects of semaglutide QW versus liraglutide OD on HbA1c and weight change in patients with T2DM. To our knowledge, no other NMA explored the long-term efficacy of semaglutide versus liraglutide. However, several reviews reported the early effects of semaglutide and liraglutide on HbA1c and weight change.
Dose-dependent effect was seen in all the doses of interest, that is, semaglutide (0.5 mg, 1 mg) and liraglutide (1.2 mg, 1.8 mg). While, liraglutide 3 mg was included in a single RCT as part of this NMA, this might have led to the wide credible intervals and no significance.
In an NMA published in 2019 by Mishriky et al., semaglutide QW with other GLP-1 RA and dipeptidyl peptidase-4 inhibitors (DPP-4i) was compared in five trials with a duration of ≥12 weeks, where they found that semaglutide 1 mg was significantly superior in reducing HbA1c, with a change of −0.38% and −1.14%, respectively [40]. Additionally, a meta-analyses (MA) by Shi et al. focused on semaglutide RCTs found that semaglutide was more effective in glycemic control in comparison to exenatide and dulaglutide, with a significant difference of −0.47% [41]. However, they reported high heterogeneity (I2 = 92%) with regard to the study duration and dosage used [41]. Another MA published by Li et al. also compared semaglutide to placebo and other active comparators including exenatide and dulaglutide, where semaglutide showed further reduction of HbA1c with a change of 0.85% [42]. However, as disclosed in the Limitations section, the analysis may be restricted due to the significant heterogeneity (I2 = 94%), as the analysis included trials ranging from 12 weeks up to 104 weeks [42]. Furthermore, both MA used only direct comparison in their model. Thus, liraglutide was not included in the aforementioned MAs [41,42]. Our analysis suggested superiority on the long-term effects of semaglutide 1 mg QW over liraglutide OD, based on studies with a duration of ≥52 weeks, as shown by the SUCRA score in Table 5.
In an NMA published by Witkowski et al., semaglutide 1 mg QW was the most effective compared to other GLP-1 RA in reducing weight in 24 ± 4-week trials [21]. Again, our analysis showed constant superiority of semaglutide 1 mg QW over liraglutide OD even with longer-term use, as shown in the SUCRA score in Table 5. In a phase II trial by Nauck et al., comparing a 12-week weight change of semaglutide versus liraglutide, they reported statistically significant weight reduction with semaglutide versus liraglutide [43]. Both doses of once-weekly semaglutide 0.8 mg and 1.6 mg were greater in weight reduction compared to liraglutide 1.8 mg OD. However, doses of semaglutide used in the trial were experimental non-FDA approved. Additionally, the dose escalation protocol varied between the arms of semaglutide. The reported superiority of semaglutide 0.8 mg QW compared to liraglutide 1.8 mg was found to be consistent with the semaglutide 1 mg QW and semaglutide 0.5 mg QW generated in the SUCRA score of this NMA, Table 5. In the recently published SUSTAIN 10, a phase 3b trial, liraglutide 1.2 mg was compared against subcutaneous semaglutide 1 mg over a duration of 30 weeks. Semaglutide 1 mg showed significant superiority over liraglutide 1.2 mg with a treatment difference of 0.69% in HbA1c reduction. Due to the short duration of the trial, the presumed long-term effect of semaglutide was not reached as mentioned in the limitation section of the study [44]. Nevertheless, treatment differences reported in SUSTAIN 10 was supportive of this NMA results. An NMA by Webb et al. included long-term RCTs reported significant superiority of injectable semaglutide over other GLP-1 RAs including liraglutide. However, this NMA included only Japanese population using the Japanese protocol for liraglutide, a maximum dose of liraglutide 0.9 mg, which is not the recommended therapeutic dose by the manufacturing pharmaceutical company, and the U.S. FDA [14]. Additionally, the number of analyzed trials was considerably low, only four, with only a single trial including the therapeutic dose of semaglutide [45].
The strengths of this NMA includes the quality of the analyzed RCTs. In addition, to ensure all relevant RCTs were included, a through systematic literature review was conducted. Furthermore, the robustness of the results and conclusions were demonstrated across several sensitivity and restricted analyses. Exploratory meta-regression analyses also validated the choice model used for the key analyses, change in HbA1c and weight. Some common limitations were faced during this NMA, affecting the heterogeneity in the overall risk of bias. Analyses included different study designs, open-label, double-blind, and extension trials. In addition, there were variabilities in completion rates among the trials. Additionally, the low number of RCTs included in the NMA, a total of nine trials. Furthermore, some of the included RCTs were funded by the manufacturing pharmaceutical company. Moreover, this NMA included studies with multiple races and ethnicities while, no specific analysis was conducted regarding their distribution.

5. Conclusions

To date, no long-term phase III trials directly comparing semaglutide QW and liraglutide OD are available. Thus, the estimates driven from this NMA provide valuable evidence in the decision-making process for patients with T2DM. This NMA illustrated that semaglutide could improve the control of blood glucose and body weight. The capacity of long-term glycemic control and body weight reduction of injectable semaglutide appears to be more effective than other GLP-1 RAs, including liraglutide. However, considering the number of included studies and potential limitations, more large-scale, head-to-head, well-designed RCTs are needed to confirm these findings.

Author Contributions

H.A.A., I.F.A., T.J.A., A.M.B.R. and A.M.T. helped with the design of the study protocol. Data extraction done by H.A.A. and I.F.A. independently. Statistical analysis and NMA model were done by W.A.-M. Manuscript draft was written by H.A.A. and I.F.A. Manuscript revised by A.M.T., T.J.A. and A.M.B.R. H.A.A. and I.F.A. equally contributed in producing the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.

Acknowledgments

We thank Mostafa F. Abbas for his great support in protocol submission, ethical approval process and guidance.

Conflicts of Interest

The authors declare no conflict of interest.

Registration

This is a sub-study of the protocol registered in PROSPERO, number CRD42018091598.

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Figure 1. Flowchart of studies considered for inclusion.
Figure 1. Flowchart of studies considered for inclusion.
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Figure 2. Evidence network of included studies for HbA1c analysis. Semaglutide 1 = Semaglutide 1 mg once-weekly (QW), Semaglutide 0.5 = Semaglutide 0.5 mg QW, Semaglutide 14 = oral semaglutide 14 mg, Glimpiride 4 = Glimepiride 4 mg, Glimpiride 8 = Glimepiride 8 mg, Liraglutide 0.6 = Liraglutide 0.6 mg once-daily (OD), Liraglutide 1.2 = Liraglutide 1.2 mg OD, Liraglutide 1.8 = Liraglutide 1.8 mg OD, Liraglutide 3 = Liraglutide 3 mg OD, OAD = Oral anti-diabetic drugs, Exenatide = Exenatide 2 mg, Sitagliptin = Sitagliptin 100 mg, HbA1c = glycated hemoglobin, Green: Low risk of bias, Yellow: Unclear risk of bias, Red: High risk of bias.
Figure 2. Evidence network of included studies for HbA1c analysis. Semaglutide 1 = Semaglutide 1 mg once-weekly (QW), Semaglutide 0.5 = Semaglutide 0.5 mg QW, Semaglutide 14 = oral semaglutide 14 mg, Glimpiride 4 = Glimepiride 4 mg, Glimpiride 8 = Glimepiride 8 mg, Liraglutide 0.6 = Liraglutide 0.6 mg once-daily (OD), Liraglutide 1.2 = Liraglutide 1.2 mg OD, Liraglutide 1.8 = Liraglutide 1.8 mg OD, Liraglutide 3 = Liraglutide 3 mg OD, OAD = Oral anti-diabetic drugs, Exenatide = Exenatide 2 mg, Sitagliptin = Sitagliptin 100 mg, HbA1c = glycated hemoglobin, Green: Low risk of bias, Yellow: Unclear risk of bias, Red: High risk of bias.
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Figure 3. Evidence network of included studies for weight analysis. Semaglutide 1 = Semaglutide 1 mg once-weekly (QW), Semaglutide 0.5 = Semaglutide 0.5 mg QW, Glimpiride 4 = Glimepiride 4 mg, Glimpiride 8 = Glimepiride 8 mg, Liraglutide 0.6 = Liraglutide 0.6 mg once-daily (OD), Liraglutide 1.2 = Liraglutide 1.2 mg OD, Liraglutide 1.8 = Liraglutide 1.8 mg OD, Liraglutide 3 = Liraglutide 3 mg OD, OAD = Oral anti-diabetic drugs, Exenatide = Exenatide 2 mg, Sitagliptin = Sitagliptin 100 mg, Green: Low risk of bias, Yellow: Unclear risk of bias, Red: High risk of bias.
Figure 3. Evidence network of included studies for weight analysis. Semaglutide 1 = Semaglutide 1 mg once-weekly (QW), Semaglutide 0.5 = Semaglutide 0.5 mg QW, Glimpiride 4 = Glimepiride 4 mg, Glimpiride 8 = Glimepiride 8 mg, Liraglutide 0.6 = Liraglutide 0.6 mg once-daily (OD), Liraglutide 1.2 = Liraglutide 1.2 mg OD, Liraglutide 1.8 = Liraglutide 1.8 mg OD, Liraglutide 3 = Liraglutide 3 mg OD, OAD = Oral anti-diabetic drugs, Exenatide = Exenatide 2 mg, Sitagliptin = Sitagliptin 100 mg, Green: Low risk of bias, Yellow: Unclear risk of bias, Red: High risk of bias.
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Figure 4. Forest plots of the NMA results: HbA1c outcomes for the primary comparators. The NMA results are presented as forest plots for a change from baseline in HbA1c. OR = treatment difference, LCL and UCL = lower and upper credible intervals (95% Crl) for mean treatment effect. Treatment differences are considered significant when the 95% CrI excludes 0. HbA1c = glycated hemoglobin, NMA = network meta-analysis.
Figure 4. Forest plots of the NMA results: HbA1c outcomes for the primary comparators. The NMA results are presented as forest plots for a change from baseline in HbA1c. OR = treatment difference, LCL and UCL = lower and upper credible intervals (95% Crl) for mean treatment effect. Treatment differences are considered significant when the 95% CrI excludes 0. HbA1c = glycated hemoglobin, NMA = network meta-analysis.
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Figure 5. Forest plots of the NMA results: weight outcomes for primary comparators. The NMA results are presented as forest plots for a change from baseline in weight. OR = treatment difference, LCL and UCL = lower and upper credible intervals (95% Crl) for mean treatment effect. Treatment differences are considered significant when the 95% CrI excludes 0. NMA = network meta-analysis.
Figure 5. Forest plots of the NMA results: weight outcomes for primary comparators. The NMA results are presented as forest plots for a change from baseline in weight. OR = treatment difference, LCL and UCL = lower and upper credible intervals (95% Crl) for mean treatment effect. Treatment differences are considered significant when the 95% CrI excludes 0. NMA = network meta-analysis.
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Table
Table 1. Design of phase III RCT in type 2 diabetes included in the NMA.
Table 1. Design of phase III RCT in type 2 diabetes included in the NMA.
Study (Duration in Weeks)DesignTreatment ArmsInclusion CriteriaPrimary EndpointKey Secondary Endpoints
LEAD-2 extension (104) [32]Multinational, randomized, parallel assignment, open-label, active-comparator trialLira 0.6 mg, Lira 1.2 mg, Lira 1.8 mg, Glim 4 mg, PLA18–80 years, diagnosed with T2DM, on OAD for >3 months, HbA1c 7–11%, BMI ≤ 40Change in HbA1cChange in weight
LEAD-3
(52) [33]		Multicenter, randomized, parallel assignment, double-blind, double-dummy, active-control trialLira 1.2 mg, Lira 1.8 mg, Glim 8 mg18–80 years, diagnosed with T2DM, treated with diet/exercise or with not more than half maximal dose of OAD for >2 months, HbA1c 7–11%, BMI ≤ 45Change in HbA1cChange in weight
SUSTAIN-2 (56) [34]Multinational, randomized, parallel assignment, double-blind, active-comparator trialSema QW 0.5 mg, Sema QW 1 mg, Sita 100 mg≥18 years, diagnosed with T2DM, stable treatment OAD for >3 months (OAD: MET, PIO, ROSI, or combination), HbA1c 7–10.5%Change in HbA1cChange in weight
SUSTAIN-3 (56) [19]Multinational, randomized, parallel assignment, open-label, active-comparator trialSema QW 1 mg, Exe 2 mg≥18 years, diagnosed with T2DM, 1–2 OAD for >3 months (OAD: MET, TZD, or SU), HbA1c 7–10.5%Change in HbA1cChange in weight
SUSTAIN-6 (104) [35]Multinational, randomized, parallel assignment, double-blind, placebo-controlled trialSema QW 0.5 mg, Sema QW 1 mg, 2 volume matched PLA≥50 years, diagnosed with T2DM, antidiabetic drug naïve or on 1–2 OAD or insulin (NPH, long acting analogue, or premixed insulin), both types of insulin alone or with combination 1–2 OAD, HbA1c ≥ 7%First occurrence of MACE *Change in HbA1c, change in weight
SCALE (56) [36]Multinational, randomized, parallel assignment, double-blind, placebo-controlled trialLira 3 mg, Lira 1.8 mg, PLA≥18 years, diagnosed with T2DM, treated with diet/exercise or OAD (OAD: MET, TZD, or SU) or combination, HbA1c 7–10%, BMI ≥ 27Change in weightchange in HbA1c
PIONEER-4 (52) [37]Multinational, randomized, parallel assignment, double-blind, double-dummy, active-controlled and placebo-controlled trialSema OD 14 mg, Lira 1.8 mg, PLA≥18 years, diagnosed with T2DM, treated with MET alone or in combination with SGLT-2 inhibitor >3 months, HbA1c 7–9.5%Change in HbA1cChange in weight
Pratley et al.; (52) [38]Multinational, randomized, parallel group, open-label, active-comparator trialLira 1.2 mg, Lira 1.8 mg, Sita 100 mg≥18 years, diagnosed with T2DM, treated with MET for >3 months, HbA1c 7.5–10%Change in HbA1c-
Kaku et al.; (56) [39]Multicenter, single-country randomized, parallel group,
open-label, active-controlled trial		Sema QW 0.5 mg, Sema QW 1 mg, OAD (one additional OAD + Pre-trial treatment)≥20 years, diagnosed with T2DM, treated with diet/exercise for >1 month or OAD monotherapy (SU, Glinide, a-GI, TZD) for >2 months, HbA1c 7–10.5%Emergent adverse eventsChange in HbA1c, change in weight
Lira = Liraglutide, Sema QW = Semaglutide once weekly, Sema OD = Semaglutide once daily, Glim = Glimepiride, Sita = Sitagliptin, Exe = exenatide, OAD = Oral anti-diabetic drugs, PLA = Placebo, T2DM = Type 2 diabetes mellitus, HbA1C = Glycosylated hemoglobin, MET = Metformin, PIO = Pioglitazone, ROSI = Rosiglitazone, TZD = Thiazolidinedione, SU = Sulfonylurea, NPH = Neutral protamine Hagedorn, SGLT-2 = Sodium-glucose transport protein 2, a-GI = Alpha- glucosidase inhibitor, Glinide = Meglitinides, MACE = Major adverse cardiovascular events, N/R = Not reported.* MACE defined as cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke.
Table
Table 2. Baseline characteristics of included studies.
Table 2. Baseline characteristics of included studies.
Study (Duration; Weeks)YearArmsSample SizeAge in Years Means (SD)Male
%		DOD Means
(SD)		HbA1c Means
(SD)		Weight Means
(SD)		BMI
Means
(SD)
LEAD-2 extension (104)2013Lira 0.6 mg88056 (10.5)62.47 (5)8.4 (0.9)88 (17)N/R
Lira 1.2 mg57.2 (9.2)53.87 (5)8.3 (0.9)88 (19)N/R
Lira 1.8 mg56.8 (9.4)58.78 (5)8.3 (0.9)88 (16)N/R
Glim 4 mg57.3 (8.8)57.48 (5)8.4 (0.9)89 (17)N/R
PLA56 (9.4)608 (6)8.4 (1)91 (17)N/R
LEAD-3 (52)2009Lira 1.2 mg74653.7 (11)46.65.2 (5.5)8.3 (1)92.5 (19.2)33.2 (5.6)
Lira 1.8 mg52 (10.8)495.3 (5.1)8.3 (1.1)92.8 (20.7)32.8 (6.3)
Glim 8 mg53.4 (10.9)53.65.6 (5.1)8.4 (1.2)93.4 (19.2)33.2 (5.6)
SUSTAIN-2 (56)2017Sema QW 0.5 mg122554.8 (10.2)516.44 (4.7)8 (0.92)89.93 (20.39)32.43 (6.2)
Sema QW 1 mg56 (9.4)506.7 (5.6)8 (0.93)89.21 (20.74)32.5 (6.6)
Sita 100 mg54.6 (10.4)516.6 (5.9)8.17 (0.92)89.29 (19.67)32.45 (5.8)
SUSTAIN-3 (56)2018Sema QW 1 mg80956.4 (10.3)54.29 (6)8.36 (0.95)96.21 (22.5)33.97 (7.2)
Exe 2 mg56.7 (11.1)56.39.4 (6.7)8.33 (0.96)95.37 (20.46)33.57 (6.2)
SUSTAIN-6 (104)2016Sema QW0.5 mg329764.6 (7.3)59.914.3 (8.2)8.7 (1.39)91.8 (20.25)32.7 (6.29)
Sema QW 1 mg64.7 (7.1)6314.1 (8.2)8.7 (1.51)92.9 (20.05)32.9 (6.18)
PLA 164.8 (7.6)58.514 (8.5)8.7 (1.49)91.8 (20.35)32.9 (6.35)
PLA 264.4 (7.5)61.513.2 (7.4)8.7 (1.45)91.9 (20.75)32.7 (5.97)
SCALE (56)2015Lira 3 mg84655 (10.8)527.54 (5.65)7.9 (0.8)105.7 (21.9)37.1 (6.5)
Lira 1.8 mg54.9 (10.7)51.27.43 (5.16)8 (0.8)105.8 (21)37 (6.9)
PLA54.7 (9.8)45.86.71 (5.07)7.9 (0.8)106.5 (21.3)37.4 (7.1)
PIONEER-4 (52)2019Sema OD 14 mg71156 (10)527.8 (5.7)8 (0.7)92.9 (20.6)32.5 (5.9)
Lira 1.8 mg56 (10)527.3 (5.3)8 (0.7)95.5 (21.9)33.4 (6.7)
PLA57 (10)527.8 (5.5)7.9 (0.7)93.2 (20)32.9 (6.1)
Pratley et al. (52)2011Lira 1.2 mg49755.9 (9.6)51.66 (4.5)8.4 (0.8)N/R32.6 (5.2)
Lira 1.8 mg55 (9.1)52.56.4 (5.4)8.4 (0.7)N/R33.1 (5.1)
Sita 100 mg55 (9)54.86.3 (5.4)8.5 (0.7)N/R32.6 (5.4)
Kaku et al. (56)2018Sema QW 0.5 mg60158 (10.6)69.58.1 (6)8 (0.9)71 (15.4)26.2 (4.8)
Sema QW 1 mg58.7 (10.2)72.29.4 (6.5)8.1 (1)71.7 (15.9)26.4 (4.7)
OAD59.2 (10.1)74.29.3 (7)8.1 (0.9)72.2 (14.9)26.7 (4.6)
Lira = Liraglutide, Sema QW = Semaglutide once weekly, Sema OD = Semaglutide once daily, Glim = Glimepiride, Sita = Sitagliptin, Exe = exenatide, OAD = Oral anti-diabetic drugs, PLA = Placebo, HbA1C = Glycosylated hemoglobin, N/R = Not reported, DOD = duration of diabetes, BMI = body mass index, SD = standard deviation.
Table
Table 3. NMA matrix for HbA1c change from baseline: treatment difference.
Table 3. NMA matrix for HbA1c change from baseline: treatment difference.
Exe 2 mgGlim 4 mgGlim 8 mgLira 0.6 mgLira 1.2 mgLira 1.8 mgLira 3 mgOADPLASema QW 0.5 mgSema QW 1 mgSema OD 14 mg
Exe 2 mg
Glim 4 mg−0.203 (0.428, 0.023)
Glim 8 mg0.250 (0.015, 0.484)0.452 (0.272, 0.632)
Lira 0.6 mg−0.063 (−0.288, 0.163)0.140 (−0.009, 0.289)−0.312 (−0.492, −0.132)
Lira 1.2 mg−0.146 (−0.348, 0.057)0.057 (−0.077, 0.191)−0.395 (−0.531, −0.260)−0.083 (−0.217, 0.051)
Lira 1.8 mg−0.315 (−0.512, −0.117)−0.112 (−0.242, 0.018)−0.565 (−0.700, −0.429)−0.252 (−0.382, −0.122)−0.169 (−0.253, −0.086)
Lira 3 mg−0.528 (−0.788, −0.269)−0.326 (−0.544, −0.107)−0.778 (−1.005, −0.551)−0.466 (−0.684, −0.247)−0.383 (−0.581, −0.185)−0.214 (−0.398, −0.029)
OAD0.682 (0.480, 0.883)0.884 (0.676, 1.093)0.432 (0.213, 0.650)0.744 (0.536, 0.953)0.827 (0.643, 1.011)0.997 (0.818, 1.175)1.210 (0.965, 1.456)
PLA0.460 (0.270, 0.649)0.662 (0.527, 0.797)0.210 (0.055, 0.365)0.522 (0.387, 0.657)0.605 (0.502, 0.709)0.775 (0.687, 0.862)0.988 (0.804, 1.172)−0.222 (−0.391, −0.053)
Sema 0.5 mg−0.317 (−0.488, −0.145)−0.114 (−0.283, 0.055)−0.566 (−0.748, −0.385)−0.254 (−0.423, −0.085)−0.171 (−0.309, −0.033)−0.002 (−0.132, 0.128)0.212 (−0.001, 0.425)−0.998 (−1.135, −0.862)−0.776 (−0.893, −0.659)
Sema 1 mg−0.620 (−0.769, −0.471)−0.417 (−0.587, −0.248)−0.870 (−1.051, −0.688)−0.557 (−0.727, −0.388)−0.474 (−0.612, −0.337)−0.305 (−0.435, −0.175)−0.092 (−0.304, 0.121)−1.302 (−1.438, −1.165)−1.080 (−1.197, −0.963)−0.303 (−0.389, −0.218)
Sema 14 mg−0.578 (−0.806, −0.349)−0.375 (−0.555, −0.195)−0.828 (−1.017, −0.638)−0.515 (−0.695, −0.335)−0.432 (−0.586, −0.279)−0.263 (−0.399, −0.127)−0.049 (−0.270, 0.171)−1.259 (−1.471, −1.048)−1.037 (−1.174, −0.901)−0.261 (−0.434, −0.088)0.042 (−0.131, 0.216)
Sita 100 mg−0.369 (−0.764, 0.033)0.571 (0.901, 0.242)0.119 (−0.050, 0.288)−0.431 (−0.780, 0.090)−0.516 (−0.771, −0.263)−0.684 (−0.931, 0.448)−0.894 (−1.270, −0.517)0.313 (−0.042, 0.684)0.091 (−0.151, 0.349)−0.684 (− 0.8, −0.57)0.989 (0.871, 1.106)−0.946 (−0.777, 1.115)
Lira = Liraglutide, Sema QW = Semaglutide once weekly, Sema OD = Semaglutide once daily, Glim = Glimepiride, Sita = Sitagliptin, Exe = exenatide, OAD = Oral anti-diabetic drugs, PLA = Placebo, HbA1C = Glycosylated hemoglobin, Not significant if crosses zero.
Table
Table 4. NMA matrix for weight change from baseline: treatment difference.
Table 4. NMA matrix for weight change from baseline: treatment difference.
Exe 2 mgGlim 4 mgGlim 8 mgLira 0.6 mgLira 1.2 mgLira 1.8 mgLira 3 mgOADPLASema QW 0.5 mgSema QW 1 mg
Glim 4 mg0.90 (−6.80, 8.72)
Glim 8 mg−1.85 (−10.17, 6.37)−0.86 (−7.26, 5.32)
Lira 0.6 mg−1.74 (−4.64, 3.98)0.81 (−2.35, 0.93)0.86 (−0.37, 1.14)
Lira 1.2 mg−1.02 (−3.99, 1.95)−1.08 (−2.77, 0.56)−0.80 (−1.74, 0.51)−1.31 (−5.85, 3.36)
Lira 1.8 mg−1.36 (−2.35, 1.47)−2.45 (−4.03, 0.13)−1.54 (−1.93, 1.11)−1.63 (−6.23, 2.85)−0.34 (−3.32, 2.58)
Lira 3 mg−1.66 (−14.68, 1.65)−2.66 (−4.89, 0.78)−2.73 (−4.55, 1.90)−2.85 (−6.26, 3.37)−1.56 (−7.13, 3.78)−1.22 (−6.08, 3.57)
OAD0.89 (−1.04, 4.20)1.93 (−5.20, 9.16)1.09 (−6.44, 8.48)−0.83 (−8.14, 6.41)−2.09 (−8.55, 4.28)2.45 (−3.76, 8.67)−3.65 (−3.56, 11.11)
PLA0.31 (−4.30, 4.93)1.32 (−3.32, 6.06)0.48 (−5.06, 5.95)1.45 (−3.20, 6.08)2.72 (−1.09, 6.43)3.09 (−0.20, 6.32)4.30 (−0.57, 9.20)0.64 (−6.42, 5.30)
Sema 0.5 mg−2.13 (−4.15, −1.89)−4.19 (−8.16, −2.62)1.97 (−4.34, 8.22)−2.42 (−6.22, −1.44)−0.89 (−3.60, 3.97)−0.27 (−4.59, 4.29)−0.48 (−3.51, 3.73)−4.25 (−3.53, −6.13)−3.84 (−2.09, −5.94)
Sema 1 mg−3.80 (−4.60, −2.96)−4.03 (−4.97, −3.07)−2.68 (−3.58, −1.77)−3.06 (−6.02, −0.82,)−1.23 (−4.07, 3.68)−1.58 (−4.16, 2.94)−0.82 (−3.36, 3.00)−4.85 (−5.62, −3.88,)−4.04 (−5.61, −2.47)−0.35 (−3.59, 3.29)
Sita 100 mg1.06 (−1.58, 1.50)1.09 (−1.47, 1.85)0.19 (−2.55, 2.16)1.32 (−4.24, 7.01)0.01 (−4.13, 4.33)0.31 (−3.61, 4.35)1.51 (−4.39, 7.61)−2.16 (−7.98, 3.86)−2.77 (−6.98, 1.60)0.25 (−2.38, 2.85)0.90 (−3.19, 5.01)
Lira = Liraglutide, Sema QW = Semaglutide once weekly, Sema OD = Semaglutide once daily, Glim = Glimepiride, Sita = Sitagliptin, Exe = exenatide, OAD = Oral anti-diabetic drugs, PLA = Placebo, Not significant if crosses zero.
Table
Table 5. Surface under the cumulative ranking curve (SUCRA) values for each intervention.
Table 5. Surface under the cumulative ranking curve (SUCRA) values for each intervention.
TreatmentHbA1cWeight
Semaglutide 1 mg QW0.90550.8486
Semaglutide 0.5 mg QW0.74230.7308
Semaglutide 14 mg OD0.7377
Liraglutide 1.8 mg OD0.74310.7193
Liraglutide 1.2 mg OD0.70290.7165
Liraglutide 3 mg OD0.51370.5340
Sitagliptin 100 mg0.50390.4344
Liraglutide 0.6 mg OD0.45140.4122
Glimepiride 4 mg0.40830.4019
Glimepiride 8 mg0.32370.3426
OAD0.21980.3161
Exenatide 2 mg0.21570.2085
Placebo0.10850.0975
QW = once weekly, OD = once daily, OAD = Oral anti-diabetic drugs, HbA1C = Glycosylated hemoglobin. Green indicate highest score, blue is the second highest, and grey is not included.
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Alsugair, H.A.; Alshugair, I.F.; Alharbi, T.J.; Bin Rsheed, A.M.; Tourkmani, A.M.; Al-Madani, W. Weekly Semaglutide vs. Liraglutide Efficacy Profile: A Network Meta-Analysis. Healthcare 2021, 9, 1125. https://doi.org/10.3390/healthcare9091125

AMA Style

Alsugair HA, Alshugair IF, Alharbi TJ, Bin Rsheed AM, Tourkmani AM, Al-Madani W. Weekly Semaglutide vs. Liraglutide Efficacy Profile: A Network Meta-Analysis. Healthcare. 2021; 9(9):1125. https://doi.org/10.3390/healthcare9091125

Chicago/Turabian Style

Alsugair, Hassan A., Ibrahim F. Alshugair, Turki J. Alharbi, Abdulaziz M. Bin Rsheed, Ayla M. Tourkmani, and Wedad Al-Madani. 2021. "Weekly Semaglutide vs. Liraglutide Efficacy Profile: A Network Meta-Analysis" Healthcare 9, no. 9: 1125. https://doi.org/10.3390/healthcare9091125

APA Style

Alsugair, H. A., Alshugair, I. F., Alharbi, T. J., Bin Rsheed, A. M., Tourkmani, A. M., & Al-Madani, W. (2021). Weekly Semaglutide vs. Liraglutide Efficacy Profile: A Network Meta-Analysis. Healthcare, 9(9), 1125. https://doi.org/10.3390/healthcare9091125

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