BMP10 Peptide Biomarker for Atrial Fibrillation Assessment

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Solution Overview

Problem

Current methods lack reliable biomarkers for assessing atrial fibrillation, diagnosing its severity, and predicting stroke risk associated with the condition.

Innovation Solution

Determining the amount of BMP10-type peptide in a subject's sample, optionally combined with other biomarkers like natriuretic peptides, ESM-1, Ang2, and FABP3, and comparing these levels to reference amounts to assess atrial fibrillation, diagnose heart failure, and predict hospitalization risk.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If current diagnostic methods are used for atrial fibrillation, then simplicity and clinical relevance are maintained, but reliability of assessment and diagnosis is insufficient

Engineering Contradiction:
Improvereliability of atrial fibrillation assessmentVSAvoidcomplexity of diagnostic method
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies parameter changes by introducing new measurable parameters (BMP10-type peptide levels, N-terminal prosegment levels) to improve the reliability of atrial fibrillation assessment. The diagnostic method measures specific biochemical parameters in blood samples that correlate with atrial fibrillation severity and stroke risk, thereby enhancing diagnostic reliability without requiring complex procedural changes

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent implements universality by creating a multi-functional diagnostic approach using BMP10-type peptides that can simultaneously assess atrial fibrillation presence, differentiate between paroxysmal and persistent forms, and predict stroke risk. This single biomarker system serves multiple diagnostic functions, improving reliability while maintaining practical simplicity

Inventive Principle:
Principle #6Universality (Multi-functionality)

2Measurement precision

If current biomarker methods are used, then ease of operation is maintained, but measurement precision for stroke risk prediction is insufficient

Engineering Contradiction:
Improveprecision of stroke risk predictionVSAvoidease of diagnostic operation
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The patent improves measurement precision by introducing specific biochemical parameters (BMP10-type peptide concentrations, N-terminal prosegment levels) that provide more accurate stroke risk stratification. The method establishes reference ranges and cutoff values for these parameters, enabling precise risk prediction while maintaining ease of operation through standard blood sampling and immunoassay techniques

Inventive Principle:
Principle #35Parameter changes

3Reliability

If traditional classification methods are used, then simplicity is maintained, but ability to differentiate AF severity and predict outcomes is insufficient

Engineering Contradiction:
Improvereliability of AF classificationVSAvoidcomplexity of classification system
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent enhances classification reliability by introducing quantitative biochemical parameters (BMP10 levels, N-terminal prosegment ratios) that objectively differentiate between paroxysmal and persistent atrial fibrillation. These parameter-based classifications provide more reliable stratification than traditional clinical criteria alone, enabling better prediction of stroke risk and treatment response

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS20210190801A1Circulating BMP10 (bone morphogenic protein 10) in the assessment of atrial fibrillation
Publication Date: 2021.06.24 ROCHE DIAGNOSTICS OPERATIONS INC
  • US20210190801A1 patent drawing
  • US20210190801A1 patent drawing
  • US20210190801A1 patent drawing

AI summary

The present invention relates to a method for assessing atrial fibrillation in a subject, said method comprising the steps of determining the amount of BMP 10 in a sample from the subject, and comparing the amount of BMP 10 to a reference amount, whereby atrial fibrillation is to be assessed. Moreover, the present invention relates to a method for diagnosing heart failure based on the determination of BMP 10 in a sample from a subject. Further, the present invention relates to a method for predicting the risk of a subject of hospitalization due to heart failure based on the determination of a BMP 10-type peptide in a sample from a subject.