Human Growth Hormone Biomarker for Cardiovascular Risk Stratification

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for stratifying patients at risk for cardiovascular disease for pharmacologic intervention are limited to biomarkers associated with vasoactive or inflammatory activities, and human growth hormone (hGH) has not been previously described in this context, despite elevated levels being associated with increased cardiac event risk.

Innovation Solution

Determining the level of hGH and/or its isoforms in a blood sample and comparing it to a pre-determined threshold to identify vascular risk reduction potential with antihypertensive drugs such as ACE inhibitors, ARBs, Beta-blockers, and statins.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional biomarkers (vasoactive or inflammatory) are used for patient stratification, then the stratification method is well-established, but it cannot identify all patients who would benefit from antihypertensive therapy

Engineering Contradiction:
Improveaccuracy of patient stratificationVSAvoidscope of identifiable patients
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent changes the biomarker parameter from traditional vasoactive or inflammatory markers to human growth hormone (hGH) levels. This parameter change enables identification of a broader patient population (including those with normal traditional markers) who would benefit from antihypertensive therapy, thereby resolving the contradiction between established methodology and expanded applicability

Inventive Principle:
Principle #35Parameter changes

2Adaptability or versatility

If hGH level determination is added to patient stratification, then more patients can be identified for therapy, but the diagnostic process becomes more complex

Engineering Contradiction:
Improvescope of identifiable patientsVSAvoidcomplexity of diagnostic process
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent segments the patient population into distinct groups based on hGH levels (elevated vs. normal), allowing targeted therapy recommendations. This segmentation approach simplifies the complex diagnostic process by creating clear, actionable categories rather than requiring continuous assessment of multiple overlapping biomarkers

Inventive Principle:
Principle #1Segmentation

3Adaptability or versatility

If hGH level determination is added to patient stratification, then more patients can be identified for therapy, but the testing procedure becomes more involved

Engineering Contradiction:
Improvescope of identifiable patientsVSAvoidcomplexity of testing procedure
Core Design Contradiction:
Adaptability or versatilityVSDifficulty of detecting and measuring

Solution Approach 1:

The patent uses hGH level measurement as an intermediary biomarker that mediates between traditional risk assessment and therapy selection. This intermediary approach simplifies the overall testing procedure by providing a single, clear indicator that complements rather than replaces existing assessment methods, making the extended diagnostic process more manageable

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentEP3201631B1Hgh determination for use to guide prevention of a major adverse cardiac event or a cardiovascular disease in a subject
Publication Date: 2021.05.26 SPHINGOTEC GMBH
  • EP3201631B1 patent drawingFigure 1~2
  • EP3201631B1 patent drawingFigure 3~4
  • EP3201631B1 patent drawingFigure 5~6

AI summary

Subject matter of the present invention is a method of determining whether a subject has a vascular risk that can be reduced by blood pressure lowering therapy with antihypertensive drugs (e.g. Angiotensin converting enzyme inhibitor (ACE inhibitor), Angiotensin Receptor Blocker (ARB), Beta-Adrenoreceptor Blocker (Beta-blocker) and/or statins) comprising the steps: • determining the level of hGH, and/or its isoforms in a blood sample of said subject and • comparing the determined level of hGH, and/or its isoforms in said blood sample with a pre-determined threshold and • wherein in case the determined level of hGH, and/or its isoforms is above said pre-determined threshold then the subject is identified as having a vascular risk that can be reduced by blood pressure lowering therapy with antihypertensive drugs (e.g. Angiotensin converting enzyme inhibitor (ACE inhibitor), Angiotensin Receptor Blocker (ARB), Beta-Adrenoreceptor Blocker (Beta-blocker) and/or statins) and wherein in case the determined level of hGH, and/or its isoforms is below said pre-determined threshold then the subject is identified as not having a vascular risk that can be reduced by blood pressure lowering therapy with antihypertensive drugs (e.g. Angiotensin converting enzyme inhibitor (ACE inhibitor), Angiotensin Receptor Blocker (ARB), Beta- Adrenoreceptor Blocker (Beta-blocker) and/or statins).