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NCT Number: NCT05216042

GENESIS: Genotype Guided - Natriuretic Peptides - Cardiometabolic Health Study

Natriuretic Peptides (NP) are hormones produced by the heart, and they have a wide range of favorable metabolic benefits. Lower levels of these hormones are associated with an increased likelihood of the development of diabetes and poor cardiometabolic health. Obese and Black individuals have ~30% lower levels of NP and are at a greater risk of developing cardiovascular (CV) events as compared to lean and White counterparts. Some people have common genetic variations that cause them to have ~20% lower NP levels. Similar to other low NP populations, these individuals with low NP genotype (i.e., carrying a common genetic variation called rs5068) are at a greater risk of developing cardiometabolic diseases. By understanding the NP response following the exercise challenge and the glucose challenge in individuals with genetically lower NP levels will help us understand how to improve cardiometabolic health in them.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35294, United States

Location status: Recruiting

Location contact

Nehal Vekariya, MS

CONTACT

[email protected]

205-934-7173

Pankaj Arora, MD

PRINCIPAL_INVESTIGATOR

About this study

The heart plays an endocrine role by secreting hormones called Natriuretic Peptides (NPs). NPs directly regulates blood pressure (BP) by causing dilation of blood vessels and removing sodium and water from the body. Apart from blood pressure regulation, previous experimental data suggest that NPs has a wide range of favorable metabolic effects and regulates energy homeostasis, fatty acid oxidation, lipid metabolism, glucose intolerance, insulin sensitivity, and obesity. Investigators have demonstrated that low levels of NPs can increase the risk of developing cardiovascular (CV) events (such as heart failure [HF], stroke, myocardial infarction [MI], or heart attack).

Former studies by the investigators have shown that the NP deficient states such as obese and black individuals contributes to lower energy expenditure, poor metabolic profile and promotes the onset of diabetes. Certain genetic factors contribute to the higher predisposition to cardiometabolic disease in individuals with relative atrial natriuretic peptide (ANP) deficiency. PI and others have identified a common genetic variant, rs5068 is associated with higher plasma ANP levels.

The lack of the rs5068 variant has a comparable effect on ANP levels as seen in obese and black individuals and plays a causal role in cardiometabolic health regulation. The rs5068 variant is only present in 10-12% of the population, thereby leaving nearly 90% of adults vulnerable to the potential adverse cardiometabolic impact of having a relative ANP deficiency. This indicates that a low ANP genotype is associated with a poor metabolic health profile.

Our earlier study, in normotensive healthy young adults, demonstrated that a high glucose meal results in reduce ANP levels by 20-30%, which indicates that ANP is a glucose-responsive hormone. The preliminary data from our ongoing clinical trial has shown increased ANP levels with response to the exercise. The impact of genetically determined low ANP levels on the differences in exercise-induced ANP (beneficial) increase and glucose load-induced suppression of ANP (detrimental) is not known in humans.

Micro-RNA-425 (miR-425) is a negative regulator of ANP and acts in a genotype-specific manner. In our previous study, the investigators have demonstrated that miR-425 levels decreased by 71% following one week on a high-salt diet compared with a low-salt diet in individuals with low ANP genotype, and no change was seen in high ANP genotype individuals. In vitro experiments in animals showed an increase in cardiac miR-425 levels by 22-30%. The negative regulator of ANP also independently negatively regulates the control of energy expenditure. The responsiveness of mir-425 to glucose challenge and exercise challenge (metabolic perturbations) has not been previously evaluated in humans.

Individuals with genetically reduced amounts of ANP will be the focus of our present genotype-guided physiological investigation. Following the glucose and exercise challenges, the investigators will additionally investigate the extent to which miR-425 mediated control of ANP suppression occurs. This study will help in understanding how ANP regulates cardiometabolic health in individuals with genetically lower ANP levels.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults: Age more than or equal to 18; an equal number of Males and Females
  • Consent to the collection of genetic material
  • Willing to adhere to the study protocol

Exclusion criteria

  • Age <18, at screening.
  • BMI >45 kg/m2.
  • Blood pressure more than 140/90 mmHg.
  • Participants who are taking more than 2 hypertension medications.
  • History of diabetes or fasting plasma glucose >126 mg/dl or HbA1C>=6.5% or prior treatment with antidiabetic medication.
  • Have any past or present history of cardiovascular diseases (stroke, seizure, myocardial infarction, heart failure, transient ischemic attack, angina, or cardiac arrhythmia)
  • 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);
  • 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
  • Anemia (men, Hct < 38%; women, Hct <36%)
  • Inability to exercise on a treadmill

Treatment and study plan

Study diet

Dietary Supplement

Participants will consume the study diet for 5 days provided by the clinical research unit's metabolic kitchen (at UAB)

Exercise capacity VO2 max determination

Other

Each participant's maximal oxygen capacity will be determined using a modified Bruce treadmill protocol and will also undergo a DEXA scan to determine the body mass.

Exercise Challenge

Other

Each participant will walk at 70 % of his/her VO2max for 20 minutes on treadmill and will also undergo a resting energy expenditure test.

Glucose Challenge

Other

Participants will come in fasting state on day 6th and will be given 75 gm oral glucose solution to drink, followed by blood collection every hour for next 8 hours.

Primary outcomes

  1. Change in MRproANP levels following a standardized oral glucose challenge between the high genotype group and low genotype group.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  2. Change in Exercise Energy Expenditure between the high genotype and low genotype group.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  3. Change in miR-425 levels following a standardized oral glucose challenge in those with low ANP genotype.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  4. Change in miR-425 levels following a standardized exercise challenge in those with low ANP genotype.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

Secondary outcomes

  1. Change in the NPs (ANP, BNP, NTproBNP) following the glucose challenge between the high genotype group and low genotype group.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  2. Change in the serum glucose following the glucose challenge between the high genotype group and low genotype group.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  3. Change in the serum insulin following the glucose challenge between the high genotype group and low genotype group.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  4. Change in Resting Energy Expenditure (REE) between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  5. Change in the NPs (ANP, BNP, NTproBNP) with standardized exercise protocol between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  6. Change in the serum glucose levels with standardized exercise protocol between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  7. Change in the serum insulin levels with standardized exercise protocol between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  8. Change in the free fatty acid levels with standardized exercise protocol between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  9. Change in the glycerol levels with standardized exercise protocol between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  10. Change in miR-425 levels with change in NP levels (ANP, MRproANP, BNP, and NTproBNP) following glucose challenge.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  11. Change in miR-425 levels with change in NP levels (ANP, MRproANP, BNP, and NTproBNP) following exercise challenge.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  12. Change in miR-425 levels with change in serum glucose levels following glucose challenge.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  13. Change in miR-425 levels with change in serum insulin levels following glucose challenge.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  14. Change in miR-425 levels with change in serum glucose levels following exercise challenge.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  15. Change in miR-425 levels with change in serum insulin levels following exercise challenge.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  16. Correlation of resting miR-425 levels with REE

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

    Levels of miR-425 measured in 2-ΔΔCT will be assessed and will be related to REE measured in kcal/min

  17. Change in miR-425 levels with change in NP levels (ANP, MRproANP, BNP, and NTproBNP) following glucose challenge between the two genotype groups.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  18. Change in miR-425 levels with change in NP levels (ANP, MRproANP, BNP, and NTproBNP) following exercise challenge between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  19. Change in miR-425 levels with change in serum glucose levels following glucose challenge between the two genotype groups.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  20. Change in miR-425 levels with change in serum insulin levels following glucose challenge between the two genotype groups.

    Time frame: From 1st hour to 8th hour on the main study visit day after consuming study meals for 5 days

  21. Change in miR-425 levels with change in serum glucose levels following exercise challenge between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  22. Change in miR-425 levels with change in serum insulin levels following exercise challenge between the two genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

  23. Correlation of resting miR-425 levels with REE between the genotype groups.

    Time frame: About 3 hours on the exercise challenge visit day after consuming study meals for 4 days

    Levels of miR-425 levels measured in 2-ΔΔCT will be related to the REE measured in kcal/min and will be compared between the genotype groups

Study contacts

Contact information is provided by the study sponsor or research team.

Nehal Vekariya, MS

CONTACT

[email protected]

205-934-7173

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Official study title

Atrial Natriuretic Peptide and Regulation of Cardiometabolic Health: A Genotype-Guided Human Physiological Study

Important dates

Study start
2022
Primary completion
2026
Study completion
2027
First posted
Jan 31, 2022
Registry last updated
Apr 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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