# Serum metabolomics of diabetic dogs treated with daily administration of a commercially available lyophilized feces preparation

**Authors:** Jose D. J. Ruiz Romero, Patrick Barko, Jan S. Suchodolski, David A. Williams, Holly H. Ganz, Arnon Gal

PMC · DOI: 10.1007/s11259-026-11181-9 · Veterinary Research Communications · 2026-03-27

## TL;DR

This study found that a fecal preparation improved some metabolic markers in diabetic dogs, though glycemic control improved only slightly.

## Contribution

The study is the first to investigate serum metabolomic changes in diabetic dogs treated with a commercial lyophilized feces preparation.

## Key findings

- LFP-treated dogs showed lower interstitial glucose levels at most time points compared to placebo.
- LFP significantly reduced 24-hour water intake in diabetic dogs.
- Metabolomic analysis revealed metabolic changes in carbohydrate, protein, and lipid pathways in LFP-treated dogs.

## Abstract

Enteric microbial dysbiosis can contribute to the pathobiology of canine diabetes mellitus (DM) by interfering with host metabolism, promoting inflammation, and altering incretin hormone responses. Enriching and diversifying an unbalanced gastrointestinal microbiome with microbiome-based interventions such as lyophilized fecal preparations (LFP) can help improve gut function and glycemic control of diabetic dogs. This study aimed to determine the differences in the serum metabolomes, levels of interstitial glucose (IG), and 24-hour water intake of diabetic dogs treated with daily administration of LFP or placebo. A prospective, randomized, double-masked, placebo-controlled clinical trial was conducted using six DM dogs in the LFP group and six DM dogs in the placebo group. Dogs had physical examinations and 24-hour water intake assessments at admission, 2, 4, 6, and 8 weeks, with continuous IG monitoring performed throughout the study. Serum samples were collected longitudinally at baseline and during follow-up for untargeted metabolomic analysis. The marginal mean of IG after 8 weeks was lower in the LFP group (286 ± 22 mg/dL vs. 309 ± 22 mg/dL; p = 0.468), with the LFP group showing lower marginal mean IG at each time point except week five. Marginal mean log 24-hour water intake was significantly lower in the LFP group compared to placebo (mean difference − 0.24 ± 0.10, p = 0.024). Treatment groups significantly differed in metabolites with important roles in carbohydrate, protein, and lipid metabolism. Overall, our results show that LFP induced measurable metabolic alterations, with patterns generally consistent with a more favorable metabolic profile, but only minimal improvement in glycemic control.

The online version contains supplementary material available at 10.1007/s11259-026-11181-9.

## Linked entities

- **Diseases:** diabetes mellitus (MONDO:0005015)
- **Species:** Canis lupus familiaris (taxon 9615)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 488629], INS (insulin) [NCBI Gene 483665], UOX (urate oxidase) [NCBI Gene 490189], SCD (stearoyl-CoA desaturase) [NCBI Gene 486839], GCG (glucagon) [NCBI Gene 403571] {aka GLP-1}
- **Diseases:** vascular dysfunction (MESH:D002561), beta-cell dysfunction (MESH:D007340), malabsorption (MESH:D008286), inadequate insulin (MESH:D012892), insulin deficiency (MESH:D007333), impaired (MESH:D060825), metabolic disease (MESH:D008659), Clostridioides difficile infection (MESH:D003015), ulcerative colitis (MESH:D003093), poorly regulated (MESH:C564833), Dysbiosis (MESH:D064806), polydipsia (MESH:D059606), hyperglycemia (MESH:D006943), metabolic syndrome (MESH:D024821), DM (MESH:D003920), mitochondrial dysfunction (MESH:D028361), inflammation (MESH:D007249), DNL (MESH:D005862)
- **Chemicals:** purine (MESH:C030985), Citric acid (MESH:D019343), Allantoin (MESH:D000481), lysine (MESH:D008239), unsaturated fatty acids (MESH:D005231), uric acid (MESH:D014527), DIAL (-), luminal (MESH:D010634), 9,12-octadecadienoic acid (MESH:D019787), phenols (MESH:D010636), homoarginine (MESH:D006709), sialic acids (MESH:D012794), Tricarboxylic acid (MESH:D014233), fatty acid (MESH:D005227), amino acid (MESH:D000596), sucrose (MESH:D013395), Kynurenine (MESH:D007737), acylcarnitine (MESH:C116917), carbohydrate (MESH:D002241), LPS (MESH:D008070), steroids (MESH:D013256), monosaccharides (MESH:D009005), palmitate (MESH:D010168), SCFA (MESH:D005232), 11-octadecenoic acid (MESH:C050413), TCA (MESH:D014238), free fatty acids (MESH:D005230), water (MESH:D014867), cornstarch (MESH:D013213), tryptophan (MESH:D014364), palmitoyl-carnitine (MESH:D010172), N-acetylneuraminic acid (MESH:D019158), Butyrate (MESH:D002087), Lipid (MESH:D008055), glucose (MESH:D005947)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Canis lupus familiaris (dog, subspecies) [taxon 9615], gut metagenome (species) [taxon 749906], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031211/full.md

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Source: https://tomesphere.com/paper/PMC13031211