The effect of probiotic administration on metabolomics and glucose metabolism in CF patients

Pediatr Pulmonol. 2022 Oct;57(10):2335-2343. doi: 10.1002/ppul.26037. Epub 2022 Jun 15.

Abstract

Background and objectives: Cystic fibrosis (CF)-related diabetes (CFRD) affects 50% of CF adults. Gut microbial imbalance (dysbiosis) aggravates their inflammatory response and contributes to insulin resistance (IR). We hypothesized that probiotics may improve glucose tolerance by correcting dysbiosis.

Methods: A single-center prospective pilot study assessing the effect of Vivomixx® probiotic (450 billion/sachet) on clinical status, spirometry, lung clearance index (LCI), and quality of life (QOL) questionnaires; inflammatory parameters (urine and stool metabolomics, blood cytokines); and glucose metabolism (oral glucose tolerance test [OGTT]), continuous glucose monitoring [CGM], and homeostasis model assessment of IR (HOMA-IR) in CF patients.

Results: Twenty-three CF patients (six CFRD), mean age 17.7 ± 8.2 years. After 4 months of probiotic administration, urinary cysteine (p = 0.018), lactulose (p = 0.028), arabinose (p = 0.036), mannitol (p = 0.041), and indole 3-lactate (p = 0.046) significantly increased, while 3-methylhistidine (p = 0.046) and N-acetyl glutamine (p = 0.047) decreased. Stool 2-Hydroxyisobutyrate (p = 0.022) and 3-methyl-2-oxovalerate (p = 0.034) decreased. Principal component analysis, based on urine metabolites, found significant partitions between subjects at the end of treatment compared to baseline (p = 0.004). After 2 months of probiotics, the digestive symptoms domain of Cystic Fibrosis Questionnaire-Revised improved (p = 0.007). In the nondiabetic patients, a slight decrease in HOMA-IR, from 2.28 to 1.86, was observed. There was no significant change in spirometry results, LCI, blood cytokines and CGM.

Conclusions: Changes in urine and stool metabolic profiles, following the administration of probiotics, may suggest a positive effect on glucose metabolism in CF. Larger long-term studies are needed to confirm our findings. Understanding the interplay between dysbiosis, inflammation, and glucose metabolism may help preventing CFRD.

Keywords: CFRD; cystic fibrosis; glucose metabolism; metabolomics; probiotics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Arabinose
  • Blood Glucose / metabolism
  • Blood Glucose Self-Monitoring / methods
  • Child
  • Cysteine
  • Cystic Fibrosis*
  • Cytokines
  • Diabetes Mellitus* / diagnosis
  • Dysbiosis
  • Glucose Intolerance* / diagnosis
  • Glutamine
  • Humans
  • Indoles
  • Insulin Resistance*
  • Lactates
  • Lactulose
  • Mannitol
  • Pilot Projects
  • Probiotics* / therapeutic use
  • Prospective Studies
  • Quality of Life
  • Young Adult

Substances

  • Blood Glucose
  • Cytokines
  • Indoles
  • Lactates
  • Glutamine
  • Mannitol
  • Lactulose
  • Arabinose
  • Cysteine