Angiotensin-(1-7) and Energy Expenditure in Human Obesity

Description

The objective of this study is to better define the role of the hormone angiotensin-(1-7) in energy balance. We will test the overall hypothesis that angiotensin-(1-7) increases resting energy expenditure and promotes markers of heat production (thermogenesis) in white adipose tissue in human obesity.

Conditions

Obesity

Study Overview

Study Details

Study overview

The objective of this study is to better define the role of the hormone angiotensin-(1-7) in energy balance. We will test the overall hypothesis that angiotensin-(1-7) increases resting energy expenditure and promotes markers of heat production (thermogenesis) in white adipose tissue in human obesity.

Angiotensin-(1-7) and Energy Expenditure in Human Obesity

Angiotensin-(1-7) and Energy Expenditure in Human Obesity

Condition
Obesity
Intervention / Treatment

-

Contacts and Locations

Hershey

Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania, United States, 17033

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Men and women of all races
  • * Capable of giving informed consent
  • * Age 18-60 years
  • * Body mass index (BMI) between 30-40 kg/m2
  • * Satisfactory history and physical exam
  • * Age ≤ 17 or ≥ 61 years
  • * Pregnant, nursing, or postmenopausal women
  • * Decisional impairment
  • * Prisoners
  • * Alcohol or drug abuse
  • * Current smokers
  • * Highly trained athletes
  • * Claustrophobia
  • * Subjects with \>5% weight change in the past 3 months
  • * Evidence of type I or type II diabetes (fasting glucose \> 126 mg/dL or use of anti-diabetic medications)
  • * History of serious cardiovascular disease other than hypertension (e.g. myocardial infarction within 6 months, symptomatic coronary artery disease, presence of angina pectoris, significant arrhythmia, congestive heart failure, deep vein thrombosis, pulmonary embolism, second or third degree heart block, mitral valve stenosis, aortic stenosis, hypertrophic cardiomyopathy) or cerebrovascular disease (e.g. cerebral hemorrhage, stroke, transient Ischemic attack).
  • * History or presence of immunological or hematological disorders
  • * Impaired hepatic function (aspartate aminotransferase or alanine aminotransferase levels \>2 times upper limit of normal range)
  • * Impaired renal function (serum creatinine \>2.0 mg/dl)
  • * Anemia
  • * Treatment with anticoagulants (e.g. warfarin)
  • * Treatment with chronic systemic glucocorticoid therapy (\>7 consecutive days in 1 month)
  • * Treatment with medications influencing energy expenditure (e.g. psychostimulants)
  • * Treatment with any investigational drug in the 1-month preceding the study
  • * Inability to give, or withdraw, informed consent

Ages Eligible for Study

18 Years to 60 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Amy Arnold,

Amy C Arnold, PhD, PRINCIPAL_INVESTIGATOR, Pennsylvania State University College of Medicine

Study Record Dates

2025-12