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Gene polymorphism detection kit for guiding psychiatric medication

A gene polymorphism and detection kit technology, applied in the field of biomedicine, can solve the problems of long detection period, high cost, complicated operation, etc., and achieve the effect of easy promotion and low cost

Pending Publication Date: 2021-11-02
ZHENGZHOU UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, the detection of genes related to psychotropic drugs mainly includes PCR-Sanger sequencing method, fluorescent quantitative PCR method, and gene chip method. Factors such as long cycle, low detection throughput, and high cost limit its rapid and accurate screening in clinical laboratories, so it is not suitable for the detection of multiple genes and multiple sites; and the gene chip method is due to high cost and complicated operation. and other factors limit its rapid and accurate screening in clinical laboratories; fluorescent quantitative PCR method has the advantages of high sensitivity, accurate typing, simple and fast operation, etc., and is currently widely used in clinical genotyping detection

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  • Gene polymorphism detection kit for guiding psychiatric medication
  • Gene polymorphism detection kit for guiding psychiatric medication
  • Gene polymorphism detection kit for guiding psychiatric medication

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0085] Example 1: A gene polymorphism detection kit for guiding psychiatric medication, which includes detection of CYP2D6 gene rs1065852 site, HTR2C gene rs1414334 site, ANKK1 gene rs1800497 site, CYP1A2 gene rs762551 site, MC4R gene rs489693 site

[0086] The primer set includes two forward primers and a shared reverse primer for detecting the rs1065852 site of the CYP2D6 gene, two forward primers and a shared reverse primer for detecting the rs1414334 site of the HTR2C gene, and a primer for detecting the rs1800497 site of the ANKK1 gene. Two forward primers and one common reverse primer, two forward primers and one common reverse primer for detection of CYP1A2 gene rs762551 site, two forward primers and one common reverse primer for detection of MC4R gene rs489693 site, Two forward primers and one shared reverse primer for detecting the rs1799978 site of the DRD2 gene.

[0087] The base sequence of the forward primer and common reverse primer for detecting the rs1065852 si...

Embodiment 2

[0161] Embodiment 2: Consistency comparison experiment

[0162] Randomly select 16 clinical samples to carry out genotyping of these 6 loci using the method of the present invention (qPCR), and at the same time use the first-generation sequencing method to verify the results, and find that the qPCR typing results and the first-generation sequencing results are consistent with all loci. The rates were all 100%. The qPCR typing results and the first-generation sequencing results are shown in Table 3:

[0163] Table 3: Comparison of 16 clinical samples using this method for locus typing and next-generation sequencing results

[0164]

[0165] It can be seen from the consistency experiment that the present invention can quickly and accurately type the relevant genes of psychotropic drugs, so as to provide better personalized medication guidance to patients.

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Abstract

The invention discloses a gene polymorphism detection kit for guiding psychiatric medication. The kit comprises a specific primer group and a fluorescent probe group, wherein the specific primer group and the fluorescent probe group are used for detecting the rs1065852 site of a CYP2D6 gene, the rs1414334 site of an HTR2C gene, the rs1800497 site of an ANKK1 gene, the rs762551 site of a CYP1A2 gene, the rs489693 site of an MC4R gene and the rs1799978 site of a DRD2 gene. According to the invention, the primer group and the fluorescent probe group are utilized, and the template DNA is specifically amplified by using a fluorescent PCR amplification technology, so that the polymorphism of a plurality of sites of a plurality of genes related to psychotropic drugs can be accurately detected at the same time; ARMS primer design is adopted, mismatched bases are introduced, the specificity of primer amplification is improved, the sensitivity is high, and accurate genotyping can be conducted on human template DNA at the lowest DNA initial amount of 10 ng; the detection speed is high and the efficiency is high: the PCR reaction only needs less than 1 hour to complete the amplification reaction, the cost is lower, the required reagent consumables are all clinically common reagents, the cost is lower, and the clinical popularization is convenient.

Description

technical field [0001] The invention relates to the technical field of biomedicine, in particular to a gene polymorphism detection kit for guiding psychiatric medication. Background technique [0002] At present, the clinical treatment methods and methods of mental illness are still mainly based on drug treatment. Schizophrenia is one of the most serious mental illnesses. Schizophrenic patients generally need long-term or even life-long medication, that is, the patient's dependence on drugs and High viscosity. Therefore, while psychotropic drugs are used clinically to treat and save patients, the adverse reactions caused by them cannot be ignored. Clinical practice shows that in different stages of drug metabolism, transport, receptors, etc., when different individuals receive the same drug treatment, there are obvious differences in its therapeutic effect, side effects and drug tolerance. difference. Gene polymorphism is the essential cause of individual differences in d...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/6883C12Q1/6858
CPCC12Q1/6883C12Q1/6858C12Q2600/156C12Q2600/106C12Q2600/166C12Q2531/113C12Q2545/101C12Q2563/107
Inventor 郭建成占闽宁冯帅升朱丹丹孙晓晓张悦史健翔许红恩刘海芳薛夏柳丹华秦亚平薛滨雨
Owner ZHENGZHOU UNIV
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