CYP2J2: Arachidonic Acid, Inflammation, and Heart Disease
The CYP2J2 gene is important in the metabolism of arachidonic acid into either pro- or anti-inflammatory lipid signals.
Phase I Detoxification
Phase I detoxification is the first step in the body’s process of metabolizing and eliminating toxins, drugs, and other harmful substances. This phase primarily takes place in the liver and involves a group of enzymes known as the CYP450 (cytochrome P450) family.
The CYP enzymes work to modify the chemical structure of the toxins to make the toxins more polar and reactive, preparing them for Phase II detoxification and elimination. However, in some cases, Phase I reactions can lead to the formation of intermediate metabolites that are more toxic than the original compounds.
The CYP450 enzymes are important in how well medications work for people. For some medications, a slow or fast CYP enzyme can drastically change the effect. Understanding your CYP variants can help you dial in which medications may work better, and it can also help you know which toxins may be important to avoid.
CYP2C9: Warfarin Dosing, NSAIDs, THC, and Drug Metabolism
Wonder why warfarin, ibuprofen, THC, or other drugs hit you harder than others? CYP2C9 genetic variants affect drug metabolism, side‑effect risk, and interactions with supplements and other medications.
CYP2C19 Gene: SSRIs, Medications, and Toxin Metabolism
CYP2C19 variants can affect how you respond to SSRIs, clopidogrel, oral progesterone, diazepam, and PPIs. Learn more about how your genes interact with toxins and medications.
CYP2B6: Genetic Variants That Interact with Medications
The CYP2B6 enzyme is part of the body’s first line of defense in detoxifying and breaking down certain and important for metabolizing several medications. Genetic variants of this enzyme can either speed up or slow down its function.
CYP2C8 Pharmacogenetics: Ibuprofen, NSAID Risk, and Arachidonic Acid
CYP2C8 pharmacogenomics: see how variants in this detox gene change the metabolism of ibuprofen and other drugs, influence bleeding risk, and interact with CYP2C9 and supplements.
CYP1A2 Gene: Fast or Slow Caffeine Metabolizer and More
The CYP1A2 gene breaks down caffeine, melatonin, several major prescription drugs, and interacts with smoking. Learn how your genes influence caffeine metabolism and more.
CYP2D6: Medication Interactions, Natural Inhibitors, and Anxiety Traits
The CYP2D6 enzyme is responsible for metabolizing about 25% of commonly used medications. There are several fairly common genetic variants in CYP2D6 that affect how quickly you will break down a drug.
CYP2E1: Breaking down alcohol and more
The CYP2E1 enzyme is part of the phase I detoxification system. Discover how variants might affect your alcohol metabolism and more.
CYP3A4 Gene: Impacting Prescription Drugs, Vitamin D, and Grapefruits
The CYP3A family of genes is involved in metabolizing about half of the drugs on the market today. Check your genes to see if you carry variants that impact the speed at which you metabolize medications.
CYP2A6: Breaking down nicotine and other medications
CYP2A6 gene variants shape how fast you break down nicotine and key medications, influencing smoking habits, chemo response, and drug side effects.
CYP1A1: Detoxifying Cigarette Smoke and Estrogen
This phase I detoxification gene is important in the breakdown of the hydrocarbons produced in smoke and air pollution. It also affects the metabolism of estrogen.