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      Comparative efficacy and safety profile of once-weekly Semaglutide versus once-daily Sitagliptin as an add-on to metformin in patients with type 2 diabetes: a systematic review and meta-analysis

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          Abstract

          Background

          The emergence of genetically-modified human proteins and glucagon-like peptide-1 (GLP-1) receptor agonists have presented a promising strategy for effectively managing diabetes. Due to the scarcity of clinical trials focusing on the safety and efficacy of semaglutide as an adjunctive treatment for patients with type 2 diabetes who had inadequate glycemic control with metformin, we conducted a systematic review and meta-analysis. This was necessary to fill the gap and provide a comprehensive assessment of semaglutide compared to sitagliptin, a commonly prescribed DPP-4 inhibitor, in this patient population.

          Methods

          A comprehensive and systematic search was carried out on reputable databases including PubMed, the Cochrane Library, and Elsevier’s ScienceDirect to identify relevant studies that compared the efficacy of once-weekly Semaglutide with once-daily Sitagliptin in individuals diagnosed with type 2 diabetes mellitus. The analysis of the gathered data was performed utilizing the random-effects model, which considers both within-study and between-study variations.

          Results

          The meta-analysis incorporated three randomized controlled trials (RCTs), encompassing 2401 participants, with a balanced distribution across the treatment groups. The primary focus of the study revolved around evaluating changes in HbA1C, blood pressure, pulse rate, body weight, waist circumference, and BMI. The findings revealed that once-weekly Semaglutide showed substantially improved HbA1C (WMD: −0.98; 95% CI: −1.28, −0.69, p-value: < 0.0001; I2: 100%), systolic (WMD: −3.73; 95% CI: −5.42, −2.04, p-value: <0.0001; I2: 100%) and diastolic blood pressures (WMD: −0.66; 95% CI: −1.02, −0.29, p-value: 0.0005; I2: 100%), and body weight (WMD: −3.17; 95% CI: −3.84, −2.49, p-value: <0.00001; I2: 100%) compared to once-daily Sitagliptin. However, there was an observed increase in pulse rate (WMD: 3.33; 95% CI: 1.61, 5.06, p-value: <0.00001; I2: 100%) associated with Semaglutide treatment. Regarding secondary outcomes, there was an elevated risk of total adverse events and premature treatment discontinuation with Semaglutide. The risk of serious, severe, moderate, and mild adverse events did not significantly differ between the two treatments.

          Conclusions

          In conclusion, the administration of once-weekly Semaglutide exhibited a substantial reduction in HbA1c, average systolic blood pressure (SBP), mean diastolic blood pressure (DBP), body weight, waist circumference, body mass index (BMI), and a rise in pulse rate, as opposed to the once-daily administration of Sitagliptin.

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          Most cited references28

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          The PRISMA 2020 statement: an updated guideline for reporting systematic reviews

          The Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement, published in 2009, was designed to help systematic reviewers transparently report why the review was done, what the authors did, and what they found. Over the past decade, advances in systematic review methodology and terminology have necessitated an update to the guideline. The PRISMA 2020 statement replaces the 2009 statement and includes new reporting guidance that reflects advances in methods to identify, select, appraise, and synthesise studies. The structure and presentation of the items have been modified to facilitate implementation. In this article, we present the PRISMA 2020 27-item checklist, an expanded checklist that details reporting recommendations for each item, the PRISMA 2020 abstract checklist, and the revised flow diagrams for original and updated reviews.
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            Measuring inconsistency in meta-analyses.

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              The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials

              Flaws in the design, conduct, analysis, and reporting of randomised trials can cause the effect of an intervention to be underestimated or overestimated. The Cochrane Collaboration’s tool for assessing risk of bias aims to make the process clearer and more accurate
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                Author and article information

                Journal
                Ann Med
                Ann Med
                Annals of Medicine
                Taylor & Francis
                0785-3890
                1365-2060
                27 July 2023
                2023
                27 July 2023
                : 55
                : 2
                : 2239830
                Affiliations
                [a ]Medicine, American University of Antigua , Antigua and Barbuda
                [b ]Medicine, Ghulam Muhammad Mahar Medical College, Sukkur , Pakistan
                [c ]Medicine, Quaid-e-Azam Medical College Bahawalpur, Pakistan , Pakistan
                [d ]Medicine, United Medical and Dental College, Karachi , Pakistan
                [e ]Medicine, Chanda Medical College, Larkana , Pakistan
                [f ]Medicine, American University of the Carribean , United States of America
                [g ]Medicine, University of Medicine and health sciences, St. Kitts, Carribean , United States of America
                [h ]Medicine, Bacha Khan Medical College, Mardan , Pakistan
                [i ]Anesthesiology, Paolo Procacci Foundation, Rome , Italy
                [j ]Medicine, Dow University of Health Sciences, Karachi , Pakistan
                [k ]Medicine, Shaheed Mohtarma Benazir Bhutto Medical College, Karachi , Pakistan
                Author notes

                Supplemental data for this article can be accessed online at https://doi.org/10.1080/07853890.2023.2239830.

                CONTACT Tirath Patel Tirathp611@ 123456gmail.com American University of Antigua, Medicine Antigua and Barbuda
                Author information
                https://orcid.org/0000-0003-0217-8331
                https://orcid.org/0000-0001-7975-6297
                Article
                2239830
                10.1080/07853890.2023.2239830
                10375936
                37498865
                4a013474-4e17-42ae-a09b-bbc929f4d4fa
                © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

                History
                Page count
                Figures: 9, Tables: 3, Pages: 14, Words: 7241
                Categories
                Research Article
                Endocrinology

                Medicine
                semaglutide,sitagliptin,once-weekly,once daily,type 2 diabetes mellitus,meta-analysis
                Medicine
                semaglutide, sitagliptin, once-weekly, once daily, type 2 diabetes mellitus, meta-analysis

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