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Effect of Renin Angiotensin Aldosterone System Genetic Polymorphism on the Pharmacological Effect of Mineralocorticoid Receptor Antagonists in Patients With Myocardial Infarction

Effect of Renin Angiotensin Aldosterone System Genetic Polymorphism on the Pharmacological Effect of Mineralocorticoid Receptor Antagonists in Patients With Myocardial Infarction

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05873400
Enrollment
102
Registered
2023-05-24
Start date
2022-08-01
Completion date
2024-04-01
Last updated
2023-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction

Keywords

Aldosterone Antagonist, Myocardial Infarction, Cardiac remodeling, Gene polymorphism, Remodeling Marker, Stress Marker

Brief summary

Early treatment of Myocardial Infarction patients with mineralocorticoid receptor antagonist with help reduces the incidence of cardiac remodeling and development into heart failure. Also studying aldosterone synthase (CYP11B2) and mineralocorticoid receptor (NR3C2) gene polymorphisms in Egyptian Myocardial Infarction patients will help tailor medication therapy and optimize therapeutic effects with the least adverse effects.

Interventions

None listed

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* ST- segment elevation patients. * Patients who are candidate for add-on treatment with Mineralocorticoid receptor antagonists (MRAs) to improve cardiac remodeling. * Age of 18 years to 80 years. * Written informed consent of the subject to participate in the study.

Exclusion criteria

* Contraindications to Mineralocorticoid receptor antagonists (MRA) including: serum potassium \>5.5 mEq/L at initiation; CrCl ≤30 mL/minute; concomitant use of strong CYP3A4 inhibitors; concomitant use with potassium supplements or potassium-sparing diuretics. * Mild-to-severe valvular stenosis or severe (grade III/IV) valvular regurgitation * Pregnant or nursing women. * Non cardiac disorders associated with increased growth factor (e.g., HIV, Alzheimer, Crohn's disease, Cancer, glomerulonephritis, glomerulosclerosis, diabetic nephropathy, muscle atrophy, fibrotic conditions and burns). * Patients with chronic heart failure with reduced ejection fraction (LVEF \<40%).

Design outcomes

Primary

MeasureTime frameDescription
Genetic polymorphism3 monthsTo investigate impact of genetic polymorphism in aldosterone synthase (CYP11B2), mineralocorticoid receptor (NR3C2) on pharmacological effect of MRAs in patients with STEMI through measurement of biochemical serum markers such as serum aldosterone, oxidative stress markers and cardiac remodeling markers.

Secondary

MeasureTime frameDescription
Gene Interaction3 monthsTo investigate the potential interaction between these target gene polymorphisms and the overall patients' clinical outcome in response to treatment with Mineralocorticoid receptor antagonists (MRAs).
Gene incidence3 monthsTo detect the incidence of aldosterone synthase (CYP11B2) and mineralocorticoid receptor (NR3C2) gene polymorphisms in Egyptian patients with ST- segment elevation (STEMI).

Countries

Egypt

Contacts

Primary ContactIsel Al-ansary, Bachelor Degree
isele.alansary@gmail.com01098173054
Backup ContactNeven Sarhan, PhD
sarhanneven@gmail.com01021944422

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026