Aldosterone-Angiotensin II Ratio for Primary Hyperaldosteronism Diagnosis

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current diagnostic methods for primary hyperaldosteronism (PHA) face challenges due to interference from anti-hypertensive treatments and limited predictive power, leading to false positive and false negative results, and require complex and costly confirmation testing.

Innovation Solution

Measuring the aldosterone-to-angiotensin II ratio (AA2R) in biological samples, which is less prone to interference from anti-hypertensive treatments and provides improved diagnostic performance compared to the aldosterone-to-renin ratio (ARR) by offering higher discrimination between PHA and non-PHA patients.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If the aldosterone-to-renin ratio (ARR) is used for diagnosis of primary hyperaldosteronism, then the diagnostic specificity and sensitivity can be improved compared to measuring aldosterone alone, but the diagnostic power remains insufficient leading to false positive and false negative results

Engineering Contradiction:
Improvediagnostic accuracyVSAvoiddiagnostic reliability
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The patent changes the diagnostic parameter from ARR (aldosterone-to-renin ratio) to AAR (aldosterone-to-angiotensin II ratio). This parameter substitution resolves the contradiction by using angiotensin II levels instead of renin levels, providing both improved measurement precision and diagnostic reliability for detecting primary hyperaldosteronism.

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If confirmation testing is performed to improve diagnostic accuracy, then false results can be reduced, but the testing protocol becomes complex and costly

Engineering Contradiction:
Improvediagnostic accuracyVSAvoidtesting protocol complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent merges the screening and confirmation functions into a single AAR measurement. By combining these functions that were previously separate, the testing protocol becomes simpler and less costly while maintaining high diagnostic accuracy, thus resolving the contradiction between diagnostic precision and protocol complexity.

Inventive Principle:
Principle #5Merging (Combining)

3Reliability

If anti-hypertensive treatments are administered to patients, then blood pressure control is improved, but the diagnostic power of ARR is interfered with leading to false results

Engineering Contradiction:
Improveblood pressure controlVSAvoiddiagnostic precision
Core Design Contradiction:
ReliabilityVSMeasurement precision

Solution Approach 1:

The patent uses angiotensin II as an intermediary parameter that is less affected by anti-hypertensive medications compared to renin. This intermediary approach allows diagnostic measurement to proceed accurately even when patients are on blood pressure medication, resolving the contradiction between blood pressure control and diagnostic precision.

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentEP3058374B1Method for diagnosis of primary hyperaldosteronism
Publication Date: 2019.06.26 ATTOQUANT DIAGNOSTICS
  • EP3058374B1 patent drawingFigure 1
  • EP3058374B1 patent drawingFigure 2
  • EP3058374B1 patent drawingFigure 3

AI summary

The present invention relates to methods and kits for the diagnosis of primary hyperaldosteronism (PHA). In particular, the present invention relates to the use of a new diagnostic parameter that is composed of the ratio between the Ang II level, in particular the steady state equilibrium Ang II level, and the aldosterone level in a biological sample, such as e.g. plasma. The ratio of the two measured parameters is used to diagnose PHA in patients and has clear advantages over currently used diagnostic methods.