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Racial Differences in Vagal Control of Glucose Homeostasis (RDVCGH)

Vanderbilt University Medical Center logo

Vanderbilt University Medical Center

Status and phase

Completed
Phase 2
Phase 1

Conditions

Obesity

Treatments

Drug: Placebo Oral Capsule
Drug: Galantamine
Drug: Intralipid
Drug: Heparin

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators will test the hypothesis that acute central acetylcholinesterase inhibition will restore PNS activity and reduce oxidation in AAW compared to whites.

Full description

Obesity has a greater detrimental impact on the health of African American women (AAW) than on any other racial or gender group. Nearly 80% of AAW are overweight or obese. Reduced insulin sensitivity is more prevalent among AAW as compared to white women and men of both races. This condition puts AAW at increased risk for the development of type 2 diabetes mellitus. The exact mechanism underlying these pathophysiological differences remains unknown. The investigators have found that obese AAW have decreased parasympathetic nerve (PNS) activity compared to whites and recent studies in animal models showed that the PNS confers protection against oxidative stress. In our AA cohort, PNS activity was directly correlated with insulin sensitivity in obese AAW even after controlling for differences in age, blood pressure and visceral adiposity. Equally important, the investigators also showed that the decrease in insulin sensitivity was associated with increased oxidative stress as measured by plasma levels of F2-isoprostanes. Taken together these findings lead us to hypothesize that the decreased PNS activity in obese AAW compared to white women has deleterious effects on oxidative stress and insulin sensitivity.The investigators will test the hypothesis that acute central acetylcholinesterase inhibition will restore PNS activity and reduce oxidation in AAW compared to whites.

Enrollment

23 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female
  • African American or white (race will be self-defined, but only subjects who report both parents of the same race will be included)
  • 18-60 years old
  • BMI 30-45 Kg/m2
  • Not pregnant or breastfeeding

Exclusion criteria

  • Pregnant or breastfeeding
  • Diabetes diagnosis (defined by the American Diabetes Association (ADA) criteria)38
  • Cardiovascular disease such as myocardial infarction within 6 months prior to enrollment, presence of angina pectoris, significant arrhythmia, congestive heart failure (LV hypertrophy acceptable), deep vein thrombosis, pulmonary embolism, mitral valve stenosis, aortic stenosis, or hypertrophic cardiomyopathy.
  • Arrhythmia (first-, second-, and third-degree atrioventricular (AV) block)
  • Significant weight change >5% in the past 3 months
  • Impaired hepatic function (AST and/or Alanine transaminase (ALT) > one and one half times (1.5X) upper limit of normal range)
  • Impaired renal function (eGFR <60ml/min)
  • Users of strong inhibitors of Cytochrome P450 3A4 (CYP3A4) or cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6)
  • Users of other acetylcholinesterase inhibitors such as pyridostigmine or bethanechol
  • History of alcohol or drug abuse
  • Mental conditions rendering the subject unable to understand the nature, scope, and possible consequences of the study
  • Inability to comply with the protocol, e.g., uncooperative attitude, inability to return for follow-up visits, and unlikelihood of completing the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

23 participants in 2 patient groups, including a placebo group

Galantamine 16 mg then placebo
Experimental group
Description:
Galantamine 16 mg po one time dose then placebo on 2nd visit
Treatment:
Drug: Intralipid
Drug: Heparin
Drug: Galantamine
Drug: Placebo Oral Capsule
Placebo then Galantamine 16 mg
Placebo Comparator group
Description:
Placebo capsule po one time dose then Galantamine 16 mg on 2nd visit
Treatment:
Drug: Intralipid
Drug: Heparin
Drug: Galantamine
Drug: Placebo Oral Capsule

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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