Evidence map›Paper›PMID 41691684›Full record

ArticleCurrent diabetes reviews2026

Comparative Clinical and Metabolic Outcomes of GLP-1 Receptor Agonists

Ayman Al Hayek, Asirvatham Alwin Robert, Abdullah Khalid Al Burayk, Abdulrhman Nasser Alwadai, Asma Mutni Almutairi, Abdullah Ali Shabani, Mohamed Abdulaziz Al Dawish

Abstract readComparative Study
In one paragraph

Article in Current diabetes reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ayman Al HayekDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Asirvatham Alwin RobertDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Abdullah Khalid Al BuraykDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Abdulrhman Nasser AlwadaiDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Asma Mutni AlmutairiDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Abdullah Ali ShabaniDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Mohamed Abdulaziz Al DawishDepartment of Endocrinology and Diabetes, Diabetes Treatment Center, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis research is designed to compare the clinical characteristics, metabolic outcomes, and safety profiles of patients with Type 1 Diabetes (T1D) treated with Glucagon-Like Peptide-1 Receptor Agonists (GLP-1 RAs) against Sodium-Glucose co-transporter 2 (SGLT2) inhibitors in a real-world clinical setting over 12 months.

methodsData from 112 adult T1D patients on intensive insulin therapy at Prince Sultan Military Medical City in Riyadh were examined for this retrospective cohort study. Among the 112 T1D, 96 were treated with GLP-1 receptor agonists and 16 were treated with SGLT2 inhibitors. Baseline demographics, the presence of comorbidities, diabetes complications, glycemic control (HbA1c), weight, insulin dosage, renal function, and lipid profiles were assessed at initiation and after 12 months of treatment.

resultsPatients getting GLP-1 receptor agonists were younger (p = 0.006), had shorter diabetes duration (p = 0.030), and were more likely to use insulin pumps (p = 0.040). The SGLT2 group showed significantly higher albumin-to-creatinine ratios (p = 0.047) and higher statin use (p = 0.038). GLP-1 therapy led to significant HbA1c (p < 0.05) and weight reduction, while SGLT2 treatment improved renal markers and reduced insulin dose. LDL cholesterol decreased significantly in the GLP-1 group (p = 0.014),while the SGLT2 group showed more favorable changes in HDL and total cholesterol. Comorbidities and diabetes related complications were similar between groups. DISCUSSION: GLP-1 RAs produced notable reductions in HbA1c levels and weight reduction, while SGLT2 inhibitors offered renal protection and decreased insulin needs. These real-world findings emphasize the value of tailoring adjunct therapies to each patient's profile. Personalized treatment strategies are crucial for optimizing metabolic outcomes in T1D.

conclusionBoth GLP-1 RAs and SGLT2 inhibitors effectively improve glycemic control and cardiovascular risk markers in T1D, with distinct advantages in weight loss and renal function, respectively. These findings highlight the value of personalized adjunct therapy choices to optimize patient outcomes. Larger prospective studies are needed to confirm long-term benefits and safety.

Indexed as

Diabetes Mellitus, Type 1Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsAdultBlood GlucoseFemaleGlycated HemoglobinGlycemic ControlHumansMaleMiddle AgedRetrospective StudiesSaudi ArabiaTreatment OutcomeBlood GlucoseGlucagon-Like Peptide-1 Receptor AgonistsGlycated Hemoglobinhemoglobin A1c protein, humanHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsGLP-1 receptorglycemic controlischemic heart diseaseSGLT2 inhibitorssodium-glucose cotransporter-2Type 1 diabetes mellitus

Identifiers

PMID41691684
PMCPMC13725149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.