# Preliminary Real-World Experience with Semaglutide in Obese Patients with Type 2 Diabetes on Chronic Hemodialysis: A Multicenter Pilot Study

**Authors:** Alejandra Yugueros, Luis D’Marco, Alejandro Valero, Elena Vivó, Amparo Martínez-Mas, Manuel Calvé, Juan Carlos Alonso, Belén Vizcaíno, Mercedes González-Moya, Ana Checa-Ros, Asunción Sancho, Pablo Molina

PMC · DOI: 10.3390/medicina62020386 · Medicina · 2026-02-16

## TL;DR

A small study found that semaglutide, a diabetes drug, helped reduce weight and fat in obese dialysis patients with type 2 diabetes, with few side effects.

## Contribution

This is the first real-world pilot study exploring semaglutide's effects on weight and body composition in obese hemodialysis patients with type 2 diabetes.

## Key findings

- Semaglutide reduced BMI and fat mass in hemodialysis patients with type 2 diabetes.
- The drug was generally well tolerated, with only transient nausea reported in a few patients.
- Lean tissue mass and serum albumin levels remained stable during treatment.

## Abstract

Background and Objectives: Semaglutide is a glucagon-like peptide-1 receptor agonist (GLP-1RA) that has demonstrated metabolic and weight benefits in diabetic and obese patients with chronic kidney disease (CKD) who are not on dialysis; however, evidence in the hemodialysis (HD) population is scarce. Weight control and body composition optimization are particularly challenging in HD because of fluid shifts and the risk of protein-energy wasting. Materials and Methods: This prospective, multicenter, real-world, uncontrolled observational pilot study explored the short-term safety and changes in anthropometric and body-composition parameters after semaglutide initiation in obese adults with type 2 diabetes mellitus (T2DM) undergoing chronic HD. Patients were assessed at baseline and at 3 and 6 months. The primary endpoint was the change in body mass index (BMI), dry weight, and fat mass assessed by bioimpedance spectroscopy (BIS). Results: Thirteen patients were included (10 male, 77%), with a median age of 61.9 years (IQR 55–69). Semaglutide was started at 0.25 mg/week and titrated up to 1 mg/week according to tolerance. Three patients (23.1%) experienced transient nausea that was resolved over time or after dose adjustment, without discontinuation. From baseline to month +6, BMI decreased by a median of 1.5 kg/m2 and dry weight by 5.0 kg, mainly driven by a median reduction in fat mass of 9 kg; lean tissue mass and serum albumin did not change significantly. Conclusions: In this small, uncontrolled exploratory study, semaglutide was generally well tolerated and was associated with short-term reductions in body weight and fat mass in obese patients with T2DM on HD. These findings are hypothesis-generating and require confirmation in larger controlled prospective studies to define safety and clinical benefit in this population.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331)
- **Diseases:** type 2 diabetes (MONDO:0005148), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}
- **Diseases:** vasculopathy (MESH:D000090122), cancer (MESH:D009369), Diabetes (MESH:D003920), pancreatitis (MESH:D010195), CKD (MESH:D051436), inflammation (MESH:D007249), sarcopenia (MESH:D055948), injury to (MESH:D014947), metabolic disturbances (MESH:D024821), peripheral vascular disease (MESH:D016491), dyslipidemia (MESH:D050171), metabolic dysfunction (MESH:D008659), composition (MESH:D058617), hypoglycemic (MESH:C000721848), weight gain (MESH:D015430), Obese (MESH:D009765), nausea (MESH:D009325), retinopathy (MESH:D058437), cardiovascular disease (MESH:D002318), hypoglycemia (MESH:D007003), infection (MESH:D007239), uremic (MESH:D006463), ischemic heart disease (MESH:D017202), ESRD (MESH:D007676), gastrointestinal adverse effects (MESH:D005767), weight loss (MESH:D015431), cerebrovascular disease (MESH:D002561), impaired insulin clearance (MESH:D007333), death (MESH:D003643), hypertension (MESH:D006973), DKD (MESH:D003928), neuropathy (MESH:D009422), nausea and/or vomiting (MESH:D020250), T2DM (MESH:D003924), adiposity (MESH:D018205), heart failure (MESH:D006333), coronary artery disease (MESH:D003324)
- **Chemicals:** meglitinides (MESH:C030516), water (MESH:D014867), iDPP4 (-), sodium (MESH:D012964), glucose (MESH:D005947), RAs (MESH:D011883)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942463/full.md

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Source: https://tomesphere.com/paper/PMC12942463