Psoriasis Genetic Markers and SNP Detection Methods
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Solution Overview
Problem
Current methods lack reliable genetic markers for diagnosing and treating psoriasis, as existing studies have not consistently identified effective markers for disease susceptibility and treatment response.
Innovation Solution
Identification of novel single nucleotide polymorphisms (SNPs) associated with psoriasis, along with methods for detecting these SNPs and using them to develop diagnostic reagents and therapeutic agents, allowing for personalized treatment strategies.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If current genetic marker studies are used for psoriasis diagnosis, then diagnostic methods are available, but the markers lack reliability and consistency
Solution Approach 1:
The patent segments the complex psoriasis genetic analysis into specific manageable SNP loci (IL12B, IL23R, and other identified polymorphisms). By focusing on discrete, well-defined genetic markers rather than broad genomic regions, the patent achieves more reliable and consistent diagnostic measurements while maintaining the ability to detect psoriasis susceptibility.
2Reliability
If generic psoriasis treatment is applied, then treatment can be provided, but treatment efficacy is suboptimal and side effects increase
Solution Approach 1:
The patent applies local quality by tailoring treatment to the specific genetic profile of each patient. By identifying particular SNP variants (such as IL12B rs3212227 and IL23R rs7530511) that predict treatment response, the patent enables clinicians to select therapies targeted to the patient's specific genetic characteristics, thereby improving efficacy while reducing exposure to ineffective treatments and their associated side effects.
3Loss of time
If early detection methods are implemented, then psoriasis risk can be identified, but reliable genetic markers are currently lacking
Solution Approach 1:
The patent enables preliminary action by identifying genetic markers (SNPs in IL12B, IL23R, and other genes) that predict psoriasis susceptibility before clinical symptoms manifest. By detecting these genetic variants in advance, the patent allows for early intervention and prevention strategies to be implemented before the disease develops or progresses, thereby reducing future health burdens.
Data Source
AI summary
The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.