ALS Diagnosis via Biomarker Panel Extraction

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for diagnosing amyotrophic lateral sclerosis (ALS) are slow and require extensive specialist consultations, resulting in a mean time of 13-18 months from symptom onset to confirmation of diagnosis.

Innovation Solution

A method involving the determination of the quantitative or qualitative level of specific biomarkers such as PDIA3, CCDC80, HSPA8, and DAG1 in biological samples to diagnose or prognose ALS, utilizing a panel of biomarkers to facilitate quicker diagnosis.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional specialist consultation methods are used for ALS diagnosis, then diagnostic accuracy can be maintained through comprehensive evaluation, but diagnostic time increases to 13-18 months

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

Solution Approach 1:

The patent extracts and measures specific biomarkers (DAG1, PLEC, HSPA5, NCL, TPM1, TNC, IGFBP3, COL5A1, CLEC11A, MAP1B, NACA, PSMA2, RPL5, MYL6, CTSB, HSPD1, PTRF, NUCB1, PDIA4, P4HB, ACTN4, EEF1D, TPI1, SSBP1, PSMB8, PSAP, PSMB7, CAPZA1, PRDX1, PODN, MMP1, NUCB2, HMGB1, AHNAK, FNDC1, DENR, PENK, S100A11, RPL29, RPL27, RPL8, SRSF2, SF3B4, SBSN, LYAR, NUDC, CRLF1, TGFB1, CAT, CTSD, DLD, EPB41L2, PSMB9, RPS14, RPL7A, COLEC12, SMARCC2, TAGLN2, CCT4, ASPH, GPS1, CDK13, SH3GL2, HBA1, APEX1, PSMB5, TXN, AXL, RPS8, SET, RPS18, CFL1, DMKN, RPL22, RPL6, FKBP10, PAFAH1B1, S100A13, PSMA6, SERPINE1, CAPRIN1, SEPT7, VTN, ENPP2, NEO1, DKC1, CHI3L1, SKOR1, SSRP1, COL4A2, NME1, CFB, EIF2S3, DPYSL2, NUMA1, KTN1, CHID1, EFEMP1, YWHAZ, LDHB, SDCBP, TLN1, DES, APP) from biological samples to diagnose ALS, replacing the need for prolonged specialist consultations while maintaining diagnostic accuracy

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent uses biomarkers as intermediary substances that mediate the diagnosis process. These biomarkers serve as measurable indicators that bridge the gap between clinical symptoms and definitive diagnosis, enabling faster identification of ALS cases without requiring extended specialist evaluation periods

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If a comprehensive panel of biomarkers is measured to improve diagnostic accuracy, then measurement complexity and cost increase

Engineering Contradiction:
Improvediagnostic accuracyVSAvoidmeasurement complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent segments the diagnostic process into measuring multiple individual biomarkers (DAG1, PLEC, HSPA5, NCL, TPM1, TNC, IGFBP3, COL5A1, CLEC11A, MAP1B, NACA, PSMA2, RPL5, MYL6, CTSB, HSPD1, PTRF, NUCB1, PDIA4, P4HB, ACTN4, EEF1D, TPI1, SSBP1, PSMB8, PSAP, PSMB7, CAPZA1, PRDX1, PODN, MMP1, NUCB2, HMGB1, AHNAK, FNDC1, DENR, PENK, S100A11, RPL29, RPL27, RPL8, SRSF2, SF3B4, SBSN, LYAR, NUDC, CRLF1, TGFB1, CAT, CTSD, DLD, EPB41L2, PSMB9, RPS14, RPL7A, COLEC12, SMARCC2, TAGLN2, CCT4, ASPH, GPS1, CDK13, SH3GL2, HBA1, APEX1, PSMB5, TXN, AXL, RPS8, SET, RPS18, CFL1, DMKN, RPL22, RPL6, FKBP10, PAFAH1B1, S100A13, PSMA6, SERPINE1, CAPRIN1, SEPT7, VTN, ENPP2, NEO1, DKC1, CHI3L1, SKOR1, SSRP1, COL4A2, NME1, CFB, EIF2S3, DPYSL2, NUMA1, KTN1, CHID1, EFEMP1, YWHAZ, LDHB, SDCBP, TLN1, DES, APP) separately, allowing for systematic and standardized measurement of each biomarker to improve overall diagnostic accuracy while managing measurement complexity through structured analysis

Inventive Principle:
Principle #1Segmentation

Data Source

PatentEP3788379B1A method of diagnosing or prognosing a neurological disorder
Publication Date: 2022.06.22 UNIVERSITY OF ULSTER
  • EP3788379B1 patent drawingFigure 1A~1B
  • EP3788379B1 patent drawingFigure 2A~2C
  • EP3788379B1 patent drawingFigure 3A~4

AI summary

The present invention relates to a method of diagnosing or prognosing a neurological disorder in a subject. The method comprises determining the quantitative or qualitative level of one or more biomarkers in a biological sample from the subject; and diagnosing or prognosing the neurological disorder in the subject based on the quantitative or qualitative level of the or each biomarker in the biological sample.