# Effect of Calcium Hydroxy-Methyl-Butyrate-Enriched Diabetes-Specific Oral Nutritional Supplementation on Patients with Heterogeneous Diabetes Mellitus Population with Disease Related Malnutrition Assessed with AI-Assisted Ultrasound Imaging

**Authors:** Juan J. López-Gómez, Jaime González-Gutiérrez, Paloma Pérez-López, Olatz Izaola-Jauregui, Ángela Cebriá, Lucía Estévez-Asensio, David Primo-Martín, Mario Alfredo Saavedra-Vasquez, Beatriz Ramos-Bachiller, Daniel Rico-Bargues, Eduardo Jorge Godoy, Daniel Antonio De Luis-Román

PMC · DOI: 10.3390/nu17203208 · Nutrients · 2025-10-13

## TL;DR

This study found that adding calcium hydroxy-methyl-butyrate to diabetes-specific nutritional supplements improved muscle mass in patients at risk of malnutrition.

## Contribution

The novel contribution is demonstrating that CaHMB-enriched supplements specifically enhance muscle mass in diabetic patients with malnutrition risk.

## Key findings

- The CaHMB group showed a significant increase in muscle area and thickness compared to the non-CaHMB group.
- The odds of increased muscle mass were higher in the CaHMB group, with adjusted odds ratios of 9.31 for thickness and 3.96 for area.

## Abstract

Background/Objectives: Sarcopenia is common in patients with diabetes mellitus. The use of branched-chain amino acids may influence muscle mass. The aim of this study is to evaluate the effect of a diabetes-specific formula enriched with calcium hydroxy-methyl-butyrate (CaHMB) on muscle mass in patients with diabetes and high risk of malnutrition. Methods: A prospective observational study in 95 patients divided into two cohorts of patients with diabetes, treated with a tailored diet, dietary counseling, and diabetes-specific oral nutritional supplements (ONSs) administered between meals: one enriched with CaHMB (CaHMB Diabetes ONS) 44 (46.32%) patients; and another without CaHMB (Diabetes-Specific ONS) 51 (53.68%) patients. Anthropometric parameters, bioimpedance, artificial intelligence (AI)-assisted ultrasound of the rectus femoris muscle (PIIXMEDTM), and handgrip strength were assessed. Evaluations were conducted at baseline and after 3 months. Results: The mean age was 71.05 (10.67) years; 56.8% were male. After three months, both groups increased their nutritional intake with no differences in dietary protein content between groups. The CaHMB group showed a greater increase in muscle mass as measured by ultrasound, both in muscle area (CaHMB ONS: +5.84 (−3.3 ± 21.58)% vs. Diabetes-Specific ONS: −9.34% (−25.78 ± 12.02)%; p < 0.01) and muscle thickness (CaHMB ONS: +9.17 (−4.40 ± 21.05)% vs. Diabetes-Specific ONS −6.30 (−18.57 ± 12.56)%; p < 0.01). The CaHMB ONS group showed a higher likelihood of increased muscle mass compared to the Diabetes-Specific ONS, with an odds ratio (OR) of 9.31 (95%CI: 2.16–40.13) for thickness and 3.96 (95%CI: 1.11–14.13) for area, adjusted for gender, age, serum albumin, and baseline glycated hemoglobin. Conclusions: Supplementation with Ca-HMB in patients with diabetes and high risk of malnutrition showed significant improvements in muscle mass as assessed by AI-assisted ultrasound. Both groups increased nutritional intake, but only the CaHMB group showed specific benefits in muscle parameters.

## Linked entities

- **Chemicals:** calcium hydroxy-methyl-butyrate (PubChem CID 9860341), CaHMB (PubChem CID 9860341)
- **Diseases:** diabetes mellitus (MONDO:0005015), malnutrition (MONDO:0006873)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** Diabetes (MESH:D003920), Sarcopenia (MESH:D055948), muscle mass (MESH:C536030), Malnutrition (MESH:D044342), Disease Related (MESH:D000077733)
- **Chemicals:** Ca-HMB (-), branched-chain amino acids (MESH:D000597)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12566804/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12566804/full.md

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Source: https://tomesphere.com/paper/PMC12566804