Plasma lncRNA Biomarkers for Early MCI Detection

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Solution Overview

Problem

Current diagnostic methods for Alzheimer's disease and mild cognitive impairment are time-consuming, labor-intensive, and lack effective peripheral blood biomarkers for early detection, relying on expensive and inaccessible imaging techniques.

Innovation Solution

Development of a diagnostic marker using specific long non-coding RNA (lncRNA) molecules, such as ENST000000549762, NR_024049, and ENST000000567919, in plasma for screening and diagnosing mild cognitive impairment, integrated into a diagnostic kit for measuring their expression levels.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If professional doctors use medical history consultation and scale scores for diagnosis, then diagnostic accuracy can be maintained, but the evaluation becomes time-consuming and labor-intensive

Engineering Contradiction:
Improvediagnostic accuracyVSAvoidevaluation time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent performs preliminary screening using lncRNA biomarker detection in peripheral blood before comprehensive clinical evaluation. This preliminary action identifies high-risk individuals who then receive full diagnostic workup, reducing the time and resources needed for population-wide screening while maintaining diagnostic accuracy for those who need it.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent introduces lncRNA biomarkers as an intermediary between initial patient presentation and full clinical diagnosis. These biomarkers serve as a mediator that provides objective, quantifiable data to support clinical judgment, reducing the time required for subjective scale assessment while maintaining or improving diagnostic accuracy.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If brain structure imaging examination is used for auxiliary diagnosis, then macroscopic brain structure changes can be observed, but it cannot detect early stage MCI characteristic changes and is expensive

Engineering Contradiction:
Improvedetection capabilityVSAvoidcost
Core Design Contradiction:
Measurement precisionVSQuantity of substance

Solution Approach 1:

The patent employs peripheral blood samples as a cheap, easily obtainable biological material instead of expensive brain imaging. The blood-based lncRNA detection provides a low-cost alternative that can be performed repeatedly over time to track disease progression, making early detection accessible without the high costs of MRI or PET imaging.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Solution Approach 2:

The patent substitutes mechanical/physical imaging methods (MRI, CT, PET) with a biochemical detection method based on lncRNA analysis. This replacement uses molecular biology techniques to detect disease-related RNA molecules in blood, achieving early detection capability without the expense and complexity of advanced imaging equipment.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

3Measurement precision

If senile plaque imaging is used for AD diagnosis, then pathological changes can be visualized, but it is expensive and has no clinical application in China

Engineering Contradiction:
Improvepathological detection accuracyVSAvoidclinical accessibility
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The patent extracts the diagnostic function from complex, expensive imaging procedures and concentrates it into a simple blood test. By taking out the essential diagnostic information (presence of disease markers) and delivering it through a minimal-invasive blood sample analysis, the patent makes accurate diagnosis accessible in routine clinical settings without requiring specialized imaging facilities.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent creates a functional copy of the diagnostic capability found in expensive imaging procedures. Instead of requiring actual PET or MRI scans to detect pathological changes, the patent uses lncRNA biomarkers in blood as a surrogate indicator that copies the diagnostic information, providing equivalent clinical value at a fraction of the cost and with much greater accessibility.

Inventive Principle:
Principle #26Copying

4Ease of operation

If peripheral blood biomarkers are used for screening, then early diagnosis can be achieved with simple operation and minimal trauma, but no effective biomarkers have been identified yet

Engineering Contradiction:
Improvesample collection simplicityVSAvoidbiomarker effectiveness
Core Design Contradiction:
Ease of operationVSMeasurement precision

Solution Approach 1:

The patent uses a composite approach by analyzing multiple lncRNA biomarkers simultaneously rather than relying on a single marker. This composite biomarker panel combines several RNA molecules with different expression patterns, creating a more robust and accurate diagnostic tool that overcomes the limitations of individual markers while maintaining the simplicity of blood-based testing.

Inventive Principle:
Principle #40Composite materials

Data Source

PatentUS20240076740A1MCI diagnostic marker, MCI diagnostic kit and corresponding detection method
Publication Date: 2024.03.07 SHANGHAI MENTAL HEALTH CENT (SHANGHAI PSYCHOLOGICAL COUNSELLING TRAINING CENT)
  • US20240076740A1 patent drawing
  • US20240076740A1 patent drawing
  • US20240076740A1 patent drawing

AI summary

A diagnostic marker for prodromal stage Mild Cognitive Impairment (MCI) of the Alzheimer's disease is provided. The marker is plasma long-chain non-coding ribonucleic acid (lncRNA), including one or more of ENST00000549762, NR_024049, T324988 or ENST00000567919. Also disclosed are an application of the marker and a corresponding kit.