A Study Of Arginine On Glucagon Secretion In Humans

Overview

About this study

The purpose of this study is to determine the effect of arginine on amino acids-stimulated glucagon secretion and amino acids clearance.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Obese group with IFG

    • Aged between 25 and 70 years of age

    • BMI > 28 Kg/M2 and < 40 Kg/M2

    • Impaired Fasting Glucose (IFG – fasting glucose >100 but <126 mg/dL)

    • Reside within a 100-mile radius of Mayo Clinic, Rochester, MN

  • Control group (Lean)

    • BMI > 19 Kg/M2 and < 25 Kg/M2

    • Fasting glucose < 100mg/dL

    • Reside within a 100-mile radius of Mayo Clinic, Rochester, MN

 

  • T1DM group

    • BMI > 28 Kg/M2 and < 40 Kg/M2

    • Type 1 diabetes (T1DM)

    • Reside within a 100-mile radius of Mayo Clinic, Rochester, MN

 

  • Obese group with NFG

    • BMI > 28 Kg/M2 and < 40 Kg/M2

    • Fasting glucose < 100mg/dL

    • Reside within a 100-mile radius of Mayo Clinic, Rochester, MM

Exclusion Criteria:

  • Obese group with IFG

    • Age < 25 (to ensure that we are not studying subjects with latent type 1 diabetes as people in Olmsted County presenting before age 25 have a high incidence of T1DM) or > 70 years (to avoid extreme age as a factor in islet function)

    • BMI < 28 Kg/M2 or > 40 Kg/M2

    • HbA1c > 6.5% or fasting glucose < 100mg/dL or > 126 mg/dL

    • Use of any glucose-lowering agents

    • For female subjects: positive pregnancy test at the time of enrollment or study

    • History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy

    • Active systemic illness or malignancy

    • Symptomatic macrovascular or microvascular disease

 

  • Control group (Lean)

    • Age < 25 or > 70 years (to enable matching to the Obese group with IFG)

    • BMI < 19 Kg/M2 or > 25 Kg/M2

    • HbA1c > 5.8% or fasting glucose > 100mg/dL.

    • (Use of any glucose-lowering agents

    • For female subjects: positive pregnancy test at the time of enrollment or study

    • History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy

    • Active systemic illness or malignancy

    • Symptomatic macrovascular or microvascular disease

 

  • T1DM group

    • Age < 25 or > 70 years (to enable matching to the Obese group with IFG)

    • BMI < 28 Kg/M2 or > 40 Kg/M2 (to enable matching to the Obese group with IFG)

    • HbA1c < 5.8 or > 9.0%

    • Use of any glucose-lowering agents beyond insulin

    • For female subjects: positive pregnancy test at the time of enrollment or study

    • History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy

    • Active systemic illness or malignancy

    • Symptomatic macrovascular or microvascular disease

 

  • Obese group with NFG

    • Age < 25 or > 70 years (to enable matching to the Obese group with IFG)

    • BMI < 28 Kg/M2 or > 40 Kg/M2 (to enable matching to the Obese group with IFG)

    • HbA1c > 5.8% or fasting glucose > 100mg/dL

    • Use of any glucose-lowering agents

    • For female subjects: positive pregnancy test at the time of enrollment or study

    • History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy

    • Active systemic illness or malignancy

    • Symptomatic macrovascular or microvascular disease

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 07/21/2026. Questions regarding updates should be directed to the study team contact.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Adrian Vella, M.D.

Contact us for the latest status

More information

Publications

Publications are currently not available
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CLS-20611464

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