# Lactobacillus helveticus UA881 Improves Body Composition, Lipid Profiles, and Gut Microbiota in Overweight Adults: A Randomized Double-Blind Placebo-Controlled Trial

**Authors:** Yu-Wei Chang, Yin-Chin Liu, Pin-Chao Huang, Shao-Yu Lee, Meei-Yn Lin, Chin-Lin Hsu

PMC · DOI: 10.3390/biomedicines14020276 · Biomedicines · 2026-01-26

## TL;DR

This study shows that a specific probiotic, Lactobacillus helveticus UA881, can help overweight adults lose weight and improve their lipid profiles and gut health.

## Contribution

The study demonstrates the novel metabolic and microbiota-modulating effects of Lactobacillus helveticus UA881 in overweight individuals.

## Key findings

- UA881 reduced body weight, BMI, and body fat mass in overweight adults.
- The probiotic decreased serum triglycerides and attenuated increases in uric acid and LDL-C.
- Gut microbiota alpha diversity improved, with increased Anaerostipes and Blautia and reduced Collinsella.

## Abstract

Background: Overweight and metabolic disorders are strongly associated with gut microbiota dysbiosis. Probiotics represent a safe dietary strategy to improve metabolic health, although strain-specific effects remain unclear. This study evaluated the metabolic and gut microbiota-modulating effects of Lactobacillus helveticus (UA881) in overweight adults. Methods: In a randomized, double-blind, placebo-controlled trial, 50 overweight adults (Body mass index, BMI 25–27 kg/m2) were assigned to receive UA881 (5 × 109 CFU/day) or placebo for 28 days. Anthropometric parameters, body composition, serum biochemical markers, inflammatory cytokines, fecal short-chain fatty acids (SCFAs), and gut microbiota composition (16S rRNA sequencing) were assessed at baseline and after 28 days. Statistical analyses included paired t-tests and ANCOVA adjusted for baseline values. Results: After 28 days of supplementation, UA881 significantly reduced body weight, BMI, and body fat mass. The primary endpoint, serum triglycerides, was significantly decreased, and the increases in uric acid, total cholesterol, and Low density lipoprotein-cholesterol (LDL-C) observed in the placebo group were attenuated. No significant changes were observed in interleukin-6 (IL-6) or tumor necrosis factor-α (TNF-α) levels. Fecal butanoic acid showed an increasing trend, and gut microbiota alpha diversity was significantly improved. At the genus level, Anaerostipes and Blautia were enriched, while Collinsella was reduced. Conclusions: A 28-day supplementation with L. helveticus UA881 (5 × 109 CFU/day) improved body composition and lipid-related metabolic parameters and favorably modulated gut microbiota composition in overweight adults, supporting its potential as a probiotic candidate for metabolic health.

## Linked entities

- **Species:** Lactobacillus helveticus (taxon 1587)

## Full-text entities

- **Genes:** PRKAA2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 5563] {aka AMPK, AMPK2, AMPKa2, PRKAA}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** metabolic dysregulation (MESH:D021081), metabolic (MESH:D008659), Overweight (MESH:D050177), systemic (MESH:D015619), cardiac disease (MESH:D006331), type 2 diabetes mellitus (MESH:D003924), adiposity (MESH:D018205), Obesity (MESH:D009765), weight loss (MESH:D015431), insulin resistance (MESH:D007333), Aging (MESH:D019588), non-alcoholic fatty liver disease (MESH:D065626), cardiovascular disease (MESH:D002318), infections (MESH:D007239), Dysbiosis (MESH:D064806), cancer (MESH:D009369), milk allergy (MESH:D016269), dyslipidemia (MESH:D050171), atherosclerosis (MESH:D050197), injury to (MESH:D014947), inflammation (MESH:D007249), metabolic syndrome (MESH:D024821)
- **Chemicals:** Creatinine (MESH:D003404), Glucose (MESH:D005947), ether (MESH:D004986), cholesterol (MESH:D002784), isocaproic acid (MESH:C034527), NaOH (MESH:D012972), SCFA (MESH:D005232), sulfuric acid (MESH:C033158), acetate (MESH:D000085), acetic acid (MESH:D019342), Lipid (MESH:D008055), urea nitrogen (MESH:C530477), propanoic acid (MESH:C029658), Vit B12 (MESH:D014805), water (MESH:D014867), butanoic acid (MESH:D020148), TG (MESH:D014280), propanoic acids (MESH:D011422), carbohydrate (MESH:D002241), fatty acid (MESH:D005227), Butyrate (MESH:D002087), AC (MESH:D000186), UA (MESH:D014527), isobutanoic acid (MESH:C020380), nitrogen (MESH:D009584), maltodextrin (MESH:C008315), PTFE (MESH:D011138), K2EDTA (-), bile acid (MESH:D001647), pentanoic acid (MESH:D010421)
- **Species:** Blautia (genus) [taxon 572511], Anaerostipes (genus) [taxon 207244], Lactobacillus helveticus (species) [taxon 1587], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Collinsella (genus) [taxon 102106]
- **Cell lines:** UA881 — Homo sapiens (Human), Fabry disease, Finite cell line (CVCL_7305)

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938260/full.md

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Source: https://tomesphere.com/paper/PMC12938260