Effect of Rifaximin Treatment on Endotoxemia and Insulin Sensitivity in Humans.

insulin resistance lipopolysaccharide obesity rifaximin

Journal

Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997

Informations de publication

Date de publication:
01 Sep 2019
Historique:
received: 16 04 2019
accepted: 20 06 2019
entrez: 21 8 2019
pubmed: 21 8 2019
medline: 21 8 2019
Statut: epublish

Résumé

The gut microbiome is a source of inflammatory factors such as lipopolysaccharide (LPS; endotoxin) that influence metabolic homeostasis. Rifaximin is a well-tolerated antibiotic that may reduce LPS. We sought to develop a method to accurately assess postprandial endotoxemia and to determine whether rifaximin treatment improves metabolic homeostasis in obese humans with metabolic syndrome. Plasma LPS, adipose inflammation, glucose and lipid metabolism, and insulin sensitivity were evaluated in a clinical research setting. Twelve obese human research participants with prediabetes or three features of metabolic syndrome participated. The research participants were randomized to placebo control or rifaximin soluble solid dispersion (80 mg/d) treatment groups and treated for 12 weeks. We evaluated changes in insulin sensitivity with a euglycemic clamp; changes in lipid and glucose metabolism with oral lipid and glucose tolerance tests; changes in plasma LPS during the lipid tolerance test; and changes in adipose tissue and systemic inflammation by measuring inflammatory cytokines. Rifaximin treatment slightly worsened insulin sensitivity ( Rifaximin treatment did not lower plasma LPS or improve metabolic homeostasis in obese humans.

Identifiants

pubmed: 31428718
doi: 10.1210/js.2019-00148
pii: jes_201900148
pmc: PMC6691337
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1641-1651

Subventions

Organisme : NIDDK NIH HHS
ID : R21 DK100258
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001998
Pays : United States

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Auteurs

Brian S Finlin (BS)

The Department of Internal Medicine, Division of Endocrinology, and the Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, Kentucky.

Beibei Zhu (B)

The Department of Internal Medicine, Division of Endocrinology, and the Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, Kentucky.

Tania Boyechko (T)

The Department of Internal Medicine, Division of Endocrinology, and the Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, Kentucky.

Philip M Westgate (PM)

College of Public Health, University of Kentucky, Lexington, Kentucky.

Chee W Chia (CW)

Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland.

Josephine M Egan (JM)

Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland.

Philip A Kern (PA)

The Department of Internal Medicine, Division of Endocrinology, and the Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, Kentucky.

Classifications MeSH