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Rationale, design and baseline characteristics of the Microbiome and Insulin Longitudinal Evaluation Study (MILES).
Jensen, Elizabeth T; Bertoni, Alain G; Crago, Osa L; Hoffman, Kristi L; Wood, Alexis C; Arzumanyan, Zorayr; Lam, Lok-Sze Kelvin; Roll, Kathryn; Sandow, Kevin; Wu, Martin; Rich, Stephen S; Rotter, Jerome I; Chen, Yii-Der I; Petrosino, Joseph F; Goodarzi, Mark O.
Affiliation
  • Jensen ET; Department of Epidemiology and Prevention, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Bertoni AG; Department of Epidemiology and Prevention, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Crago OL; Department of Epidemiology and Prevention, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Hoffman KL; Department of Molecular Virology and Microbiology, Alkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, Texas, USA.
  • Wood AC; USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine, Houston, Texas, USA.
  • Arzumanyan Z; Department of Pediatrics, Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation and Harbor-UCLA Medical Center, Torrance, California, USA.
  • Lam LK; Department of Pediatrics, Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation and Harbor-UCLA Medical Center, Torrance, California, USA.
  • Roll K; Department of Pediatrics, Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation and Harbor-UCLA Medical Center, Torrance, California, USA.
  • Sandow K; Department of Pediatrics, Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation and Harbor-UCLA Medical Center, Torrance, California, USA.
  • Wu M; Department of Biology, University of Virginia, Charlottesville, Virginia, USA.
  • Rich SS; Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia, USA.
  • Rotter JI; Department of Pediatrics, Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation and Harbor-UCLA Medical Center, Torrance, California, USA.
  • Chen YI; Department of Pediatrics, Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation and Harbor-UCLA Medical Center, Torrance, California, USA.
  • Petrosino JF; Department of Molecular Virology and Microbiology, Alkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, Texas, USA.
  • Goodarzi MO; Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Diabetes Obes Metab ; 22(11): 1976-1984, 2020 11.
Article in En | MEDLINE | ID: mdl-32687239
ABSTRACT

AIM:

To investigate the role of the gut microbiome in regulating key insulin homeostasis traits (insulin sensitivity, insulin secretion and insulin clearance) whose dysfunction leads to type 2 diabetes (T2D). MATERIALS AND

METHODS:

The Microbiome and Insulin Longitudinal Evaluation Study (MILES) focuses on African American and non-Hispanic white participants aged 40-80 years without diabetes. Three study visits are planned (at baseline, 15 and 30 months). Baseline measurements include assessment of the stool microbiome and administration of an oral glucose tolerance test, which will yield indexes of insulin sensitivity, insulin secretion and insulin clearance. The gut microbiome profile (composition and function) will be determined using whole metagenome shotgun sequencing along with analyses of plasma short chain fatty acids. Additional data collected include dietary history, sociodemographic factors, health habits, anthropometry, medical history, medications and family history. Most assessments are repeated 15 and 30 months following baseline.

RESULTS:

After screening 875 individuals, 129 African American and 224 non-Hispanic white participants were enrolled. At baseline, African American participants have higher blood pressure, weight, body mass index, waist and hip circumferences but similar waist-hip ratio compared with the non-Hispanic white participants. On average, African American participants are less insulin-sensitive and have higher acute insulin secretion and lower insulin clearance.

CONCLUSIONS:

The longitudinal design and robust characterization of potential mediators will allow for the assessment of glucose and insulin homeostasis and gut microbiota as they change over time, improving our ability to discern causal relationships between the microbiome and the insulin homeostasis traits whose deterioration determines T2D, setting the stage for future microbiome-directed therapies to prevent and treat T2D.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Insulin Resistance / Diabetes Mellitus, Type 2 / Gastrointestinal Microbiome Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Diabetes Obes Metab Journal subject: ENDOCRINOLOGIA / METABOLISMO Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Insulin Resistance / Diabetes Mellitus, Type 2 / Gastrointestinal Microbiome Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Diabetes Obes Metab Journal subject: ENDOCRINOLOGIA / METABOLISMO Year: 2020 Type: Article Affiliation country: United States