Evidence mapPaperPMID 39723311Full record

ReviewCureus2024

Comparing the Efficacy and Long-Term Outcomes of Sodium-Glucose Cotransporter-2 (SGLT2) Inhibitors, Dipeptidyl Peptidase-4 (DPP-4) Inhibitors, Metformin, and Insulin in the Management of Type 2 Diabetes Mellitus.

Farhan Khan, Tanjil Hussain, Taha Zahid Chaudhry, Fnu Payal, Abdullah Shehryar, Abdur Rehman, Afif Ramadhan, Muhammad Tassaduq Hayat, Muath M Dabas, Mustafa Khan

Registry-linked trialAbstract readReview
In one paragraph

Review in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07452913 (Comparative Efficacy and Safety of Metformin-Empagliflozin-Sitagliptin vs. Metformin-Empagliflozin-Linagliptin as Initial Triple Therapy in Type 2 Diabetes Mellitus), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07452913 phase4enrolling by invitationstarted 2026, after this paper: background citation

Comparative Efficacy and Safety of Metformin-Empagliflozin-Sitagliptin vs. Metformin-Empagliflozin-Linagliptin as Initial Triple Therapy in Type 2 Diabetes Mellitus

Ran2026Enrolled110Registered outcomes5Posted comparisons0ConditionsType 2 Diabetes MellitusArmsMetformin + Empagliflozin + Linagliptin, Metformin+ Empagliflozin + Sitagliptin
Open the trial in the graph
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Farhan KhanInternal Medicine, Rehman Medical Institute, Peshawar, PAK.
Tanjil HussainInternal Medicine, London North West Hospitals NHS Trust, London, GBR.
Taha Zahid ChaudhryInternal Medicine, Holy Family Hospital, Rawalpindi, PAK.
Fnu PayalInternal Medicine, Ghulam Muhammad Mahar Medical College, Karachi, PAK.
Abdullah ShehryarInternal Medicine, Allama Iqbal Medical College, Lahore, PAK.
Abdur RehmanSurgery, Mayo Hospital, Lahore, PAK.
Afif RamadhanInternal Medicine, Gadjah Mada University, Yogyakarta, IDN.
Muhammad Tassaduq HayatInternal Medicine, Chandka Medical College, Larkana, PAK.
Muath M DabasSurgery, The University of Jordan, Amman, JOR.
Mustafa KhanGeneral Surgery, Nishtar Medical University, Multan, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder characterized by hyperglycemia, insulin resistance, and decreased insulin secretion. With its rising global prevalence, effective management strategies are critical to reducing morbidity and mortality. This systematic review compares the efficacy, safety, and long-term outcomes of four major pharmacological treatments for T2DM: sodium-glucose cotransporter-2 (SGLT2) inhibitors, dipeptidyl peptidase-4 (DPP-4) inhibitors, metformin, and insulin. We focused on randomized controlled trials (RCTs) published within the last five years (2019-2024) to provide an up-to-date assessment of glycemic control, cardiovascular and renal benefits, weight effects, and the risk of hypoglycemia. The review highlights that while all four medication classes effectively reduce HbA1c levels, SGLT2 inhibitors stand out for their additional cardiovascular and renal benefits, including significant reductions in major adverse cardiovascular events and chronic kidney disease progression. Metformin remains a cornerstone first-line therapy due to its safety, efficacy, and affordability. DPP-4 inhibitors are a weight-neutral, well-tolerated option, although their efficacy may diminish over time. Insulin, while the most potent glucose-lowering agent, carries a higher risk of hypoglycemia and weight gain. Our findings emphasize the importance of personalized, patient-centered approaches that account for the distinct therapeutic profiles of these treatments. Future research should prioritize head-to-head comparisons and optimal therapy sequencing to refine treatment guidelines for diverse patient populations.

Indexed as

cardiovascular outcomesdpp-4 inhibitorsglycemic controlhypoglycemia riskinsulinmetforminrenal protectionsglt2 inhibitorstype 2 diabetes mellitusweight changes

Identifiers

PMID39723311
PMCPMC11669386

What Socratic holds

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Registered trials

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 Socratic graph.