Background: Primary aldosteronism (PA) is the most common cause of secondary hypertension, associated with increased cardiovascular morbidity and mortality. This study evaluated biochemical and clinical responses to mineralocorticoid receptor antagonist (MRA) therapy and identified predictors of treatment success based on the Primary Aldosteronism Medical Outcomes (PAMO) consensus. Methods: This observational study analyzed data from the TAIPAI database linked to the National Health Insurance Research Databases, including 1,305 PA patients between June 2007 and June 2021. After excluding those who underwent surgery during the study period or had relevant disease, 269 patients were classified according to their clinical and biochemical responses to MRA therapy based on the PAMO criteria. Results: Among the 269 patients (mean age: 54.9±11.5 years, 40.9% male), 22.3% achieved clinical success, 55.4% partial success, and 22.3% failed. Biochemically, 56.9% of patients achieved success, 37.5% partial success, and 5.6% failed. Notably, 14.1% of patients achieved both clinical and biochemical success. After a mean follow-up period of six years, clinical success was significantly associated with a reduction in major adverse cardiovascular events (p=0.020), whereas biochemical success alone did not show the same association. Cox proportional hazards analysis demonstrated a significant association between Charlson comorbidity score (HR=1.28, p=0.003), clinical success (HR=0.29, p=0.047), and cardiovascular outcomes. Conclusions: MRA therapy achieved clinical success in 22.3% and biochemical success in 56.9% of PA patients. After a mean 6 years follow-up, clinical success independently reduced MACE risk, regardless of whether biochemical success is achieved. This highlights the importance of prioritizing clinical outcomes in PA treatment.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementNeither I nor my co-authors have a conflict of interest that is relevant to the subject matter or materials included in this work.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
This study complied with the Declaration of Helsinki and received approval from the Institutional Review Board of National Taiwan University Hospital, Taipei, Taiwan (No. 200611031R). All experimental protocols research was approved by the Institute Research Ethical Committee of National Taiwan University Hospital (NTUH) (Http://doi.org/10.6084/m9.figshare.21730985).
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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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Data AvailabilityThe datasets generated and analyzed during the present study are available from the corresponding authors on request.
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