# GLIMSI: A real-world, multicenter study assessing the effectiveness and safety of Sitagliptin + Glimepiride + Metformin FDC in Indian patients with Type 2 diabetes

**Authors:** Kunal Zaveri, Girish Kulkarni, Rathish Nair, Govarthanan Shanmugan, Shubhada Amol Dharmadhikari, R. P. S. Makkar, Rahul Jalgaonkar, B. D. Chatterjee, Krishnaprasad Korukonda

PMC · DOI: 10.1371/journal.pone.0337107 · PLOS One · 2026-02-06

## TL;DR

This study shows that a combination of three diabetes drugs effectively lowers blood sugar and helps with weight loss in Indian patients.

## Contribution

The study evaluates the real-world effectiveness and safety of a triple-drug combination for managing Type 2 diabetes in India.

## Key findings

- HbA1c, fasting blood glucose, and postprandial glucose levels significantly decreased over 12 weeks.
- Patients experienced a significant reduction in body weight during the treatment period.
- No significant safety concerns were identified with the triple-drug therapy.

## Abstract

Type-2-diabetes-mellitus (T2DM), often linked to obesity, raises risk of microvascular and macrovascular complications. International guidelines recommend triple-therapy to reach haemoglobin A1c (HbA1c) targets when dual therapy fails to adequately control blood glucose levels. Sitagliptin, enhances glycaemic control by prolonging incretin action, boosting insulin secretion, and lowering glucagon levels. When combined with glimepiride and metformin this triple-therapy targets multiple mechanisms. This study evaluated the effectiveness and safety of this combination for improved T2DM management in Indian patients.

This real-world, multicentre, observational chart review evaluated the efficacy and safety of a triple fixed-dose combination therapy in 1235 adult patients with T2DM across 194 clinical sites in India. Data were retrospectively extracted from patient records over a 12-week period. Descriptive and analytical statistics was applied for the study endpoints using SPSS ver. 29.0.1.0(171) and Microsoft Excel 2019.

The study population had a mean age of 56.89 ± 10.29 years, with 64.70% reporting a family history of type 2 diabetes mellitus (T2DM). Smoking was identified as a prominent risk factor, affecting 38.65% of participants. Significant improvements were observed in glycemic parameters over 12 weeks: HbA1c levels decreased from 8.20 ± 0.60% to 7.08 ± 0.77% (p < 0.0001), fasting blood glucose (FBG) from 188.54 ± 47.59 mg/dL to 146.01 ± 41.53 mg/dL (p < 0.0001), and 2-hour postprandial plasma glucose (PPG) from 234.74 ± 50.40 mg/dL to 179.40 ± 42.51 mg/dL (p < 0.0001). Additionally, body weight significantly reduced from 75.99 ± 8.67 kg to 74.76 ± 9.07 kg (p < 0.0001). No significant safety concerns identified during the treatment period.

The triple-combination therapy (sitagliptin, glimepiride, and metformin) demonstrated superior efficacy in achieving glycemic control, as evidenced by significant reductions in HbA1c, fasting blood glucose (FBG), and postprandial plasma glucose (PPG). Furthermore, the therapy facilitated meaningful weight reduction, highlighting its clinical utility as a comprehensive therapeutic option for managing glycemic parameters in both T2DM with overweight and normal-weight patients.

## Linked entities

- **Chemicals:** Sitagliptin (PubChem CID 4369359), Glimepiride (PubChem CID 3476), Metformin (PubChem CID 4091)
- **Diseases:** Type 2 diabetes mellitus (MONDO:0005148), T2DM (MONDO:0005148)

## Full-text entities

- **Genes:** DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** Diabetes (MESH:D003920), Insulin resistance (MESH:D007333), chronic (MESH:D002908), glucose (MESH:D018149), Type 1 diabetes (MESH:D003922), atherosclerosis (MESH:D050197), cardiovascular (MESH:D002318), complications (MESH:D008107), congestive heart failure (MESH:D006333), overweight (MESH:D050177), weight (MESH:D015431), dysregulation (MESH:D021081), CAD (MESH:D003324), ischemic heart disease (MESH:D017202), hypersensitivity (MESH:D004342), albuminuria (MESH:D000419), unstable angina (MESH:D000789), myocardial infarction (MESH:D009203), CKD (MESH:D051436), dyslipidemia (MESH:D050171), peripheral vascular disease (MESH:D016491), kidney disease (MESH:D007674), weight gain (MESH:D015430), inflammation (MESH:D007249), acute coronary syndrome (MESH:D054058), renal function (MESH:D058186), obese (MESH:D009765), stroke (MESH:D020521), cerebrovascular disease (MESH:D002561), retinopathy (MESH:D058437), hypertension (MESH:D006973), nasopharyngitis (MESH:D009304), T2DM (MESH:D003924), proteinuria (MESH:D011507), neuropathy (MESH:D009422), hypoglycemia (MESH:D007003), Symptom (MESH:D012816), OADs (MESH:D000092582)
- **Chemicals:** Glimepiride (MESH:C057619), biguanides (MESH:D001645), Telmisartan (MESH:D000077333), aldosterone (MESH:D000450), blood glucose (MESH:D001786), rosuvastatin (MESH:D000068718), SU (MESH:D013453), lipid (MESH:D008055), glucose (MESH:D005947), atorvastatin (MESH:D000069059), Sitagliptin (MESH:D000068900), Creatinine (MESH:D003404), acarbose (MESH:D020909), Metformin (MESH:D008687), FBG (-), canagliflozin (MESH:D000068896)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** A1C

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12880711/full.md

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Source: https://tomesphere.com/paper/PMC12880711