VITAL-IMPACT: Improving Cardiometabolic Health in Black Individuals Through Therapeutic Augmentation of Cyclic Guanosine Mono-Phosphate Signaling Pathway

Obesity Clinical Trial

— VITAL-IMPACT  

Official title:

Improving Cardiometabolic Health in Black Individuals Through Therapeutic Augmentation of Cyclic Guanosine Mono-Phosphate Signaling Pathway

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06320951
• Other study ID #: 300012681
• Secondary ID: Pending
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: May 1, 2025
• Est. completion date: April 30, 2029

Study information

• Verified date: May 2024
• Source: University of Alabama at Birmingham
• Contact: Nehal Vekariya, MS
• Phone: 2059347173
• Email: nvekariya[@]uabmc.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study investigates the potential of vericiguat, a soluble guanylate cyclase stimulator, to improve cardiometabolic health in obese Black individuals with insulin resistance by directly enhancing cyclic guanosine monophosphate (cGMP) activity. Given that this population has been shown to have lower cGMP activity and the association of lower cGMP activity with increased cardiometabolic disease risk, the proposed study hypothesizes that augmenting cGMP activity in obese individuals will improve insulin sensitivity and energy expenditure. This study is a placebo-controlled randomized trial involving 200 Black obese participants with insulin resistance, assessing the effects of vericiguat on insulin sensitivity, resting, and exercise-induced energy expenditure over 12 weeks. Additionally, it will explore changes in brown adipose tissue and gene expression related to energy metabolism in white adipose tissue, aiming to provide insights into how increasing cGMP activity may improve cardiometabolic health in Black obese individuals.

Description:

Obese Black individuals have a higher prevalence of insulin resistance, which is linked to an elevated risk of cardiometabolic diseases and cardiovascular disease. The reasons behind the increased insulin resistance in this group are not fully understood. Key to regulating glucose metabolism and the overall balance of energy, the cyclic guanosine monophosphate (cGMP) pathway is crucial for maintaining cardiometabolic health. Research indicates that both Black race and obesity are associated with reduced levels of upstream regulators of cGMP activity, including natriuretic peptides (NPs) and nitric oxide (NO). This reduced level of NPs and NO predisposes Black obese individuals to decreased cGMP activity, potentially contributing to the higher occurrence of cardiometabolic diseases seen in this population. Vericiguat, a drug that stimulates the soluble guanylate cyclase, thereby enhancing cGMP activity independently of NO, presents a novel approach to improving cardiometabolic health in those most at risk due to low cGMP activity. This study hypothesizes that directly augmenting cGMP levels with vericiguat will improve cardiometabolic health parameters including insulin sensitivity and energy expenditure in Black obese adults with insulin resistance. Investigators plan to execute a placebo-controlled randomized trial targeting Black obese participants with insulin resistance to examine whether vericiguat can (1) improve insulin sensitivity and (2) increase resting energy expenditure. For the first aim, Investigators aim to enroll 200 Black obese (BMI≥30 kg/m^2) individuals with a HOMA-IR of ≥2.5, randomizing them to either vericiguat 10 mg once daily or a placebo once daily in a double-blind setup for 12 weeks. Investigators will assess improvements in insulin sensitivity through euglycemic hyperinsulinemic clamp and compare the results between the vericiguat and placebo groups after 12 weeks. For the second aim, Investigators will evaluate changes in resting and exercise energy expenditure across both groups over the same period. An exploratory objective will investigate changes in brown adipose tissue volume and activity using PET-MRI, as well as UCP1 gene expression in white adipose tissue, in a subset of 100 participants after 12 weeks of vericiguat treatment. This will offer insights into the mechanisms by which cGMP augmentation may facilitate improvements in cardiometabolic health. By focusing on the direct enhancement of cGMP activity in Black obese individuals, this study proposes a novel targeted therapeutic strategy aimed at improving cardiometabolic health and addressing the increasing prevalence of cardiometabolic disease in the Black population.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 200
• Est. completion date: April 30, 2029
• Est. primary completion date: April 30, 2028
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Adults: Age more than or equal to 18 years of age

• Self-identified race/ethnicity as African-American or Black

• BMI = 30 kg/m2

• HOMA-IR = 2.5

• Blood pressure: 120-160/80-100 mmHg (untreated or 1 week of washout in those treated with up to two classes of antihypertensives)

• Willing to adhere to study protocol

Exclusion Criteria:

• Women who are pregnant or breastfeeding or who can become pregnant and not practicing an acceptable method of birth control during the study (including abstinence)

• Have any past or present history of cardiovascular diseases (stroke, myocardial infarction, heart failure, transient ischemic attack, angina, seizure or cardiac arrhythmia)

• BP more than 160/100 mmHg or those treated with three or more classes of antihypertensives

• BMI >45 kg/m2

• History of diabetes or fasting plasma glucose >=126 mg/dL or HbA1C>=6.5% or prior treatment with antidiabetics

• Estimated GFR < 60 ml/min/1.73 m2; albumin-creatinine ratio =30 mg/g

• Hepatic Transaminase (AST and ALT) levels >3x the upper limit of normal

• Significant psychiatric illness (assessed using validated MINI questionnaire)

• Anemia (men, Hb<13 g/dL; women, Hb <12 g/dL)

• Inability to exercise on a treadmill

Related Conditions & MeSH terms

• Cardiovascular Diseases
• Energy Expenditure
• Hypersensitivity
• Insulin Resistance
• Insulin Sensitivity/Resistance
• Metabolic Disease
• Metabolic Diseases
• Metabolism
• Obesity

Intervention

Drug:
• Vericiguat 10 MG
The subject will be randomized, in a double-blind manner to vericiguat 10 mg once daily for a period of 12 weeks.

Other:
• Placebo
The subject will be randomized, in a double-blind manner to placebo once daily for a period of 12 weeks.
• Insulin Sensitivity Test
An assessment of the insulin sensitivity will be done using the Euglycemic Hyperinsulinemic Clamp, at baseline and after 12 weeks of pharmacological interventions.
• Resting Energy and Exercise Energy Expenditure Assessment
Each participant's Energy Expenditure will be determined using a metabolic cart, at baseline and after 12 weeks of pharmacological interventions.
• White Adipose Tissue Biopsy
Participants who consent to participate in the exploratory aim will undergo WAT biopsy to assess UCP1 gene expression from the collected biospecimens, at baseline and after 12 weeks of pharmacological interventions.
• MRI-PET Scan for Brown Adipose Tissue Volume Assessment
Participants who consent to participate in the exploratory aim will undergo PET/MR to BAT volume at baseline and after 12 weeks of pharmacological interventions.

Locations

Country	Name	City	State
United States	University of Alabama at Birmingham	Birmingham	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in insulin sensitivity after vericiguat in Black obese individuals with insulin resistance.	The difference in change in insulin sensitivity between baseline and post-intervention between two arms.	12 weeks
Primary	Change in resting energy expenditure (REE) after vericiguat in Black obese individuals with insulin resistance.	The difference in change in REE between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in BAT volume after vericiguat in Black obese individuals with insulin resistance.	The difference in change in BAT volume between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in BAT activity after vericiguat in Black obese individuals with insulin resistance.	The difference in change in BAT activity between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in UCP1 gene expression after vericiguat in Black obese individuals with insulin resistance.	The difference in change in UCP1 gene expression between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in exercise energy expenditure (EEE) after vericiguat in Black obese individuals with insulin resistance.	The difference in change in EEE between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in glycosylated hemoglobin (HbA1C) after vericiguat in Black obese individuals with insulin resistance.	The difference in change in HbA1C between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in Body Mass Index (BMI) after vericiguat in Black obese individuals with insulin resistance.	The difference in change in BMI between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in Total Cholesterol (TC) after vericiguat in Black obese individuals with insulin resistance.	The difference in change in TC between baseline and post-intervention between two arms.	12 weeks
Secondary	Change in low-density lipoprotein-cholesterol (LDL-C) after vericiguat in Black obese individuals with insulin resistance.	The difference in change in LDL-C between baseline and post-intervention between two arms.	12 weeks