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NCT Number: NCT06571084

New Screening and Diagnostic Cut-off Points of PA Patients

This study aims to establish the screening and diagnostic cut-off points for primary aldosteronism patients by a novel small molecule "sandwich method" aldosterone and renin chemiluminescent immunoassay.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Primary aldosteronism (PA) is the most common causes of secondary hypertension. The diagnostic workup for PA is composed of multiple steps and requires measurement of both plasma aldosterone and renin. In terms of assay of aldosterone, most of currently available chemiluminescence assays are based on competitive methods. What is actually detected is the sum of aldosterone and its metabolite aldosterone 3C glucuronide, which causes the value to be about 50%~100% higher than the actual value. This study aims to establish a new ARR (aldosterone/renin ratio) cutoff point for PA screening and a new cutoff point for PA diagnosis, using a recently developed two-site sandwich chemiluminescence method (Snibe, China) for aldosterone and renin assay.

Hypertensive patients referred to hospitals for screening of PA will be included. All the participants proceed to seated saline infusion test (SIT) and captopril challenge test (CCT) for confirmation. Aldosterone and renin will be measured using chemiluminescent immunoassay on the Liaison analyzer (DiaSorin, Italy) and MAGLUMI X8 (Snibe, China), as well as liquid chromatography-tandem mass spectrometry (LC-MS/MS) platform. According to the experience of Fuwai Hospital, the following diagnosis criteria are proposed: Based on the results of currently used (DiaSorin, Italy), aldosterone > 8.5ng/dL and renin < 15μIU/mL after sitting saline infusion conform PA, and aldosterone ≤ 8.5ng/dL excludes PA.

The total number of cases to be enrolled in this study is planned to be 770, including at least 77 positive subjects and at least 406 negative subjects. By drawing the ROC curve, the point corresponding to the maximum value of the Youden index will be selected as the cutoff value, and the corresponding sensitivity, specificity, positive predictive value, negative predictive value, positive likelihood ratio, negative likelihood ratio, etc. will be calculated.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18-75y;
  • persistent hypertension (BP >150/100 mm Hg), or drug-resistant hypertension;
  • newly diagnosed hypertension;
  • hypertension and spontaneous or diuretic-induced hypokalemia;
  • hypertension with adrenal incidentaloma;
  • hypertension and a family history of early-onset hypertension or cerebrovascular accident at a young age (<40 years);
  • status as a hypertensive first-degree relative of patients with PA;
  • patients with hypertension and obstructive sleep apnea.

Exclusion criteria

  • age <18; BMI ≤ 18.0kg/m2 or ≥ 35.0 kg/m2;
  • a diagnosis of secondary hypertension other than PA;
  • chronic cardiac dysfunction (NYHA III-IV);
  • medium and several kidney dysfunction (Ccr<30ml/min);
  • liver cirrhosis;
  • terminal malignant tumor;
  • recent use of steroids or oral contraceptives;
  • pregnancy or lactation.

Treatment and study plan

Primary outcomes

  1. Preliminary confirmation positive for primary aldosteronism

    Time frame: 1 month

    Aldosterone ≥ 85pg/ml after sitting saline test

Study contacts

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

Jun Cai

CONTACT

[email protected]

Zhou Zhou

CONTACT

[email protected]

+86 10 88398055

Sponsors and collaborators

Lead sponsor

China National Center for Cardiovascular Diseases

Other Gov

Collaborators

  • Beijing Anzhen Hospital
  • Chinese Academy of Medical Sciences, Fuwai Hospital
  • First Affiliated Hospital of Chongqing Medical University
  • Wuhan Asia Heart Hospital

Registry information

Official study title

Establishment and Clinical Application Evaluation of Screening and Diagnostic Cut-off Points With Aldosterone and Renin for Primary Aldosteronism Patients

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Aug 26, 2024
Registry last updated
Aug 26, 2024

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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