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AmpliSNiP Dementia Medication Metabolism Panel (qPCR)

SNP29

The aging society presents us with challenges related to the diagnosis and therapy of dementia-related diseases. In Poland, approximately 500,000 people suffer from dementia, including 300,000 individuals with Alzheimer’s disease. Moreover, it is estimated that the number of patients will double in the next 20-25 years. Currently, only 15-20% of patients are correctly diagnosed and treated. Both the effectiveness and complications of therapies depend significantly on the genetic background.
The complex nature of dementia-related diseases and the lack of effective therapeutic schemes result in medications aimed at symptomatic relief or stabilization of cognitive decline over periods ranging from several months to several years. The main goal of pharmacotherapy for dementia-related diseases is to increase cholinergic transmission in the brain, offering the potential to halt cognitive decline. Optimizing drug doses and adjusting treatment regimens based on knowledge of the individual metabolic abilities of each patient allows for better therapeutic outcomes and reduces the risk of adverse effects. This applies not only to the use of acetylcholinesterase inhibitors and memantine but also to other medications that patients must take for accompanying symptoms of associated conditions.

The AmpliSNiP Dementia Medication Metabolism Panel (qPCR) kit enables the analysis of 16 polymorphisms that influence the rate of metabolism of medications used to alleviate symptoms and/or slow the progression of dementia.
The AmpliSNiP Dementia Medication Metabolism Panel (qPCR) kit contains 32 qPCR reaction setups allowing for the analysis of individual polymorphisms within the human genes under examination (two setups for each polymorphism analyzed). The kit includes a multi-well plate, where the analysis of individual allelic variants of the studied polymorphisms is conducted in separate wells of the plate. The qPCR reaction is duplex. Detection of individual variants is performed on the FAM channel. The second channel (HEX) is used for the detection of human DNA.

The table below lists all the polymorphisms and their allelic variants that are subjected to analysis.

GenePolymorphismAllelic variant
ABCA1rs2230806A>G
CHATrs2177370T>C
CHATrs3793790G>A
CYP2C8rs1058930G>C
CYP2C8rs11572080G>A
CYP2C8rs10509681T>C
CYP2C9rs1057910A>C
CYP2C9rs1799853C>T
GenePolymorphismAllelic variant
CYP2C19rs12248560C>T
CYP2D6rs1065852C>T
CYP2D6rs5030655T>delT
CYP2D6rs35742686A>delA
CYP3A4rs2740574A>G
NAT2rs1799929C>T
NAT2rs1799930G>A
NAT2rs1799931G>A
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