The Metabolites We Test

Using just a pinprick of blood, Ixcela measures gut-specific metabolites to provide a personalized wellness plan that helps you feel and look great. Below is a list of metabolites we test. These metabolites are either produced by, or used by your gut microbiome. Since reporting indivdual values is not that helpful for most people, Ixcela results show how these metabolite levels impact five areas of health: Gastrointestinal Fitness, Immuno Fitness, Cognitive Acuity, Emotional Balance, and Energetic Efficiency.


Ixcela Tests Key Metabolites in Your Gut

Metabolite Name

Indole-3-Propionic Acid

Indole-3-Propionic Acid

Indole-3-Propionic Acid

Indole-3-Propionic Acid

Indole-3-Propionic Acid

Indole-3-Lactic Acid

Indole-3-Lactic Acid

Indole-3-Lactic Acid

Indole-3-Lactic Acid

Indole-3-Lactic Acid

Indole-3-Acetic Acid

Indole-3-Acetic Acid

Indole-3-Acetic Acid

Indole-3-Acetic Acid

Indole-3-Acetic Acid

Tryptophan

Tryptophan

Tryptophan

Tryptophan

Tryptophan

Serotonin

Serotonin

Serotonin

Serotonin

Serotonin

Kynurenine

Kynurenine

Kynurenine

Kynurenine

Kynurenine

Total Indoxyl Sulfate

Total Indoxyl Sulfate

Total Indoxyl Sulfate

Total Indoxyl Sulfate

Total Indoxyl Sulfate

Tyrosine

Tyrosine

Tyrosine

Tyrosine

Tyrosine

Xanthine

Xanthine

Xanthine

Xanthine

Xanthine

3-Methylxanthine

3-Methylxanthine

3-Methylxanthine

3-Methylxanthine

3-Methylxanthine

Uric Acid

Uric Acid

Uric Acid

Uric Acid

Uric Acid

Our test is backed by scientific studies. Learn more about the metabolites we test as well as relevant references.

Learn More About Each Metabolite

Indole-3-Propionic Acid (IPA)

  • Indole-3-propionic acid (IPA), a strong neuroprotective antioxidant, is a key indicator of a healthy gut microbiome.[1,2]
  • IPA plays a crucial role in regulating intestinal permeability.[3] Healthy intestines allow nutrients to pass into the bloodstream, but prevent potentially harmful substances from migrating to areas of the body where they could cause inflammation and gastrointestinal (GI) distress.
  • Low levels of IPA may indicate a weak population of the bacterial colony Clostridium sporogenes, a beneficial bacterial strain in the gut.[3]

Indole-3-Lactic Acid (ILA)

  • Indole-3-lactic acid (ILA) is found in fermented foods and produced by some gut bacteria from the amino acid tryptophan.
  • Proper levels of ILA are important for the production of other essential metabolites, like indole-3-propionic acid (IPA).[6]
  • Low or high levels of ILA may indicate gut bacteria dysbiosis (bacterial imbalance), which can lead to a variety of adverse symptoms, including gastrointestinal (GI) distress, inflammation, poor immune system, sleep disturbances, skin inflammation, and negative health outcomes.[7]

Indole-3-Acetic Acid (IAA)

  • Indole-3-acetic acid (IAA) is a naturally occurring plant hormone that is also produced by some gut bacteria.[4] Proper levels of IAA maintain beneficial Lactobacillus species of gut bacteria.
  • IAA is a precursor to other important metabolites, like indole-3-propionic acid (IPA).[5,6]
  • Both high and low levels of IAA can indicate a potential dysbiosis (bacterial imbalance), which can lead to a variety of adverse symptoms, including gastrointestinal (GI) distress, inflammation, poor immune system, sleep disturbances, skin inflammation, and negative health outcomes.

Tryptophan

Serotonin

Kynurenine

  • Kynurenine (KYN) is a tryptophan metabolite made in the liver.[16] Gut bacteria influence the conversion of tryptophan into kynurenine.[18]
  • Due to kynurenine’s critical role in the body’s inflammatory response, high levels of kynurenine can indicate chronic infection and/or deficiency of vitamin B6, a vitamin important for the creation of red blood cells.[19,21]
  • Beacuse B vitamins influence kynurenine production and metabolism, high or low levels of kynurenine may be due to vitamin B deficiencies.[21]

Total Indoxyl Sulfate

Tyrosine

Xanthine

  • Xanthine is a metabolite of the purine pathway.[26]
  • In the digestive tract, xanthine induces hydrochloric acid production and promotes secretion of pepsin from cells lining the stomach, which aids in digestion.[28] However, elevated xanthine can lead to oxidative stress and increase risk of inflammation.
  • Elevated xanthine may be the result of caffeine intake, cardiovascular overtraining, and/or physical and emotional stress.[29]
  • Xanthine accumulation during strenuous cardiovascular exercise can limit energy output, in turn affecting performance.

3-Methylxanthine

Uric Acid (UA)

About the Five Areas of Health

Ixcela: Gastrointestinal Fitness

What is Gastrointestinal Fitness?

The gastrointestinal (GI) tract is an organ system comprising the esophagus, stomach, and the large and small intestines. The GI tract is responsible for the swallowing and digestion of food, absorption of nutrients, and generation of waste. The GI tract is also home to trillions of microbes, known as the gut microbiome, which has been found to be vital to GI and systemic health, modulation of the immune system, and regulation of brain function.1–3 GI health and fitness revolves around maintaining the structural integrity of the intestinal wall and maintaining optimal levels of biochemicals and gut microbes. A number of metabolites associated with gut health are measured using the Ixcela Internal Fitness™ test kit, resulting in your Gastrointestinal Fitness score.

Ixcela: Immuno Fitness

What is Immuno Fitness?

The immune system’s response to various physiological perturbations plays a significant role in maintaining optimal internal health. Additionally, research has shown that the relationship between the body’s immune system and the gut microbiome is inter-dependent, with both systems producing compounds that affect each other.1,6–9 A healthy gut improves the body’s ability to fight infection. Growth and development of the gut microbiome over the human lifespan, especially postnatally and through infancy, also influences development of the immune system and vice versa.1,10 Normal levels of antibodies and immune cells, stable gut wall integrity, and lack of food allergies are some characteristics of a healthy immune system. The Immuno Fitness score is a measure of immune health and is modulated by certain key metabolites.

Ixcela: Emotional Balance

What is Emotional Balance?

Emotional well-being is one of the most important factors in the overall health of an individual. The body’s response to stress—physical, physiological, or psychological—is a key determinant in regulation of emotional state,3,14 and studies increasingly support that the gut microbiome is a major contributor to stress response3,14,15 and thus emotional well-being. Through various biochemicals, the gut microbiome has been linked to affecting mood, anxiety, and other conditions modified by stress.3,14-16 Your Emotional Balance score is a measure of emotional health and is modified by the composition of microbes and levels of metabolites in the gut.

Ixcela: Cognitive Acuity

What is Cognitive Acuity?

In the last decade, there has been tremendous research about the complex bidirectional communication between the brain and gut microbiome. Through numerous studies, it has become evident that the gut microbiome regulates, and is itself regulated by, the brain via various hormones and signaling molecules.3,5,14,15 Effects of the gut microbiome on the brain have been linked to certain types of microbial species residing in the gut.3,20 Through mechanisms such as stimulation of the nervous system, production of toxic metabolites, and change in intestinal wall permeability, the gut microbiome influences neurological chemistry and function, enhancing cognitive function.3,5,14–16 Cognitive Acuity is a measure of gut-mediated neurological health.

Ixcela: Energetic Efficiency

What is Energetic Efficiency?

Major functions of the gut are digestion of food and absorption of nutrients, and the gut microbiome plays a critical part in these processes.1,4,11,21 Microbes in the gut synthesize molecules known as short-chain fatty acids from nondigestible dietary components.1,22,23 These molecules act as a source of energy for the body and promote cellular mechanisms that maintain tissue integrity. Additionally, studies have found that harvesting energy from food is a microbial species-dependent process.24,25 Thus, having the right microbes in your gut will improve your daily energy levels. Your Energetic Efficiency score is reflective of the gut microbiome’s ability to effectively harness energy for the body.


*These statements have not been evaluated by the FDA. These products are not intended to diagnose, treat, cure or prevent any disease.


References

  1. Chyan, Yau-Jan, et al. “Potent Neuroprotective Properties against the Alzheimer β-Amyloid by an Endogenous Melatonin-Related Indole Structure, Indole-3-Propionic Acid.” Journal of Biological Chemistry, vol. 274, no. 31, 1999, pp. 21937-21942. doi: 10.1074/jbc.274.31.21937. www.jbc.org/content/274/31/21937.
  2. Wikoff, William R., et al. “Metabolomics Analysis Reveals Large Effects of Gut Microflora on Mammalian Blood Metabolites.” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 10, 2009, pp. 3698-3703. doi: 10.1073/pnas.0812874106. www.ncbi.nlm.nih.gov/pmc/articles/PMC2656143/.
  3. Kaufmann, Stefan H. E. “Indole Propionic Acid: a Small Molecule Links between Gut Microbiota and Tuberculosis.” Antimicrobial Agents and Chemotherapy, vol. 62, no. 5, 2018. doi: 10.1128/AAC.00389-18. aac.asm.org/content/62/5/e00389-18.
  4. Patten, Cheryl L., et al. “Activity, Distribution and Function of Indole-3-Acetic Acid Biosynthetic Pathways in Bacteria.” Critical Reviews in Microbiology, vol. 39, no. 4, 2012, pp. 395-415. https://doi.org/10.3109/1040841X.2012.716819.
  5. Abdul Rahim, M., et al. “Diet-Induced Metabolic Changes of the Human Gut Microbiome: Importance of Short-Chain Fatty Acids, Methylamines and Indoles.” Acta Diabetologica, vol. 56, no. 5, 2019, pp. 493-500. doi: 10.1007/s00592-019-01312-x. www.ncbi.nlm.nih.gov/pmc/articles/PMC6451719/.
  6. Gao, Jing, et al. “Impact of the Gut Microbiota on Intestinal Immunity Mediated by Tryptophan Metabolism.” Frontiers in Cellular and Infection Microbiology, vol. 8, no. 13, 2018. doi: 10.3389/fcimb.2018.00013. www.ncbi.nlm.nih.gov/pmc/articles/PMC5808205/.
  7. Roager, Henrik M., et al. “Microbial Tryptophan Catabolites in Health and Disease.” Nature Communications, vol. 9, no. 3294, 2018. https://doi.org/10.1038/s41467-018-05470-4.
  8. Davis, Ian and Liu, Aimin. “What Is the Tryptophan Kynurenine Pathway and Why Is It Important to Neurotherapy?” Expert Review of Neurotherapeutics, vol. 15, no. 7, 2015, pp. 719-721. doi: 10.1586/14737175.2015.1049999. www.ncbi.nlm.nih.gov/pmc/articles/PMC4482796.
  9. Hinz, Marty, et al. “5-HTP Efficacy and Contraindications.” Neuropsychiatric Disease and Treatment, vol. 8, 2012, pp. 323-328. doi: 10.2147/NDT.S33259. www.ncbi.nlm.nih.gov/pmc/articles/PMC3415362/.
  10. O’Mahony, S.M., et al. “Serotonin, Tryptophan Metabolism and the Brain-Gut-Microbiome Axis.” Behavioural Brain Research, vol. 277, 2015, pp. 32-48. https://doi.org/10.1016/j.bbr.2014.07.027.
  11. Griffiths, William J., et al. “Tryptophan and Sleep in Young Adults.” Society for Psychophysiological Research, vol. 9, no. 3, 1972, pp. 345-356. https://doi.org/10.1111/j.1469-8986.1972.tb03218.x.
  12. Bornstein, Joel C. “Serotonin in the Gut: What Does It Do?” Frontiers in Neuroscience, vol. 6, no. 16, 2012. doi: 10.3389/fnins.2012.00016. www.ncbi.nlm.nih.gov/pmc/articles/PMC3272651/.
  13. Frazer, Alan and Hensler, Julie G. “Serotonin Involvement in Physiological Function and Behavior.” Basic Neurochemistry: Molecular, Cellular and Medical Aspects, 6th Edition, 1999, www.ncbi.nlm.nih.gov/books/NBK27940/.
  14. Yano, Jessica M., et al. “Indigenous Bacteria from the Gut Microbiota Regulate Host Serotonin Biosynthesis.” Cell, vol. 161, no. 2, 2015, pp. 264-276. doi: 10.1016/j.cell.2015.02.047. www.ncbi.nlm.nih.gov/pmc/articles/PMC4393509/.
  15. Gardier, Alain. “Mechanism of Action of Antidepressant Drugs: Importance of Genetically Modified Mice in the Pharmacological in Vivo Approach.” Therapie, vol. 60, no. 5, 2005, pp. 469-476. https://doi.org/10.2515/therapie:2005067.
  16. Davis, Ian and Liu, Aimin. “What Is the Tryptophan Kynurenine Pathway and Why Is It Important to Neurotherapeutics?” Expert Review of Neurotherapeutics, vol. 15, no. 7, 2015, pp. 719-721. doi: 10.1586/14737175.2015.1049999. www.ncbi.nlm.nih.gov/pmc/articles/PMC4482796/.
  17. Gao, Jing, et al. “Impact of the Gut Microbiota on Intestinal Immunity Mediated by Tryptophan Metabolism.” Frontiers in Cellular and Infection Microbiology, vol. 8, no. 13, 2018. doi: 10.3389/fcimb.2018.00013. www.ncbi.nlm.nih.gov/pmc/articles/PMC5808205/.
  18. Waclawiková, Barbora and El Aidy, Sahar. “Role of Microbiota and Tryptophan Metabolites in the Remote Effect of Intestinal Inflammation on Brain and Depression.” Pharmaceuticals (Basel, Switzerland), vol. 11, no. 3, 2018. doi: 10.3390/ph11030063. www.ncbi.nlm.nih.gov/pmc/articles/PMC6160932/.
  19. Rudzki, Leszek, et al. “Probiotic Lactobacillus Plantarum 299v Decreases Kynurenine Concentration and Improves Cognitive Functions in Patients with Major Depression: A Double-Blind, Randomized, Placebo-Controlled Study.” Psychoneuroendocrinology, vol. 100, 2019, pp. 213-222. www.sciencedirect.com/science/article/abs/pii/S0306453018302695.
  20. Rogers, G.B., et al. “From Gut Dysbiosis to Altered Brain Function and Mental Illness: Mechanisms and Pathways.” Molecular Psychiatry, vol. 21, 2016, pp. 738-748. https://doi.org/10.1038/mp.2016.50.
  21. Majewski, M., et al. “Overview of the Role of Vitamins and Minerals on the Kynurenine Pathway in Health and Diseases.” Journal of Physiology and Pharmacology, vol. 67, no. 1, 2016, pp. 3-19. www.researchgate.net/publication/284717312.
  22. Huć, T., et al. “Indole and Indoxyl Sulfate, Gut Bacteria Metabolites of Tryptophan, Change Arterial Blood Pressure via Peripheral and Central Mechanisms in Rats.” Pharmacological Research, vol. 130, 2018, pp. 172-179. https://doi.org/10.1016/j.phrs.2017.12.025.
  23. Leong, Sheldon C. and Sirich, Tammy L. “Indoxyl Sulfate-Review of Toxicity and Therapeutic Strategies.” Toxins (Basel), vol. 8, no. 12, 2016, pp. 358. doi: 10.3390/toxins8120358. www.ncbi.nlm.nih.gov/pmc/articles/PMC5198552/.
  24. Hénaut, Lucie, et al. “The Impact of Uremic Toxins on Vascular Smooth Muscle Cell Function.” Toxins (Basel), vol. 10, no. 6, 2018, pp. 218. doi: 10.3390/toxins10060218. www.ncbi.nlm.nih.gov/pmc/articles/PMC6024314/.
  25. Praschberger, Monika, et al. “The Uremic Toxin Indoxyl Sulfate Acts as a pro- or Antioxidant on LDL Oxidation.” Free Radical Biology & Medicine, U.S. National Library of Medicine, Oct. 2014, doi.org/10.1016/j.freeradbiomed.2014.10.778.
  26. “Xanthine - Topic Overview.” ScienceDirect, https://www.sciencedirect.com/topics/medicine-and-dentistry/xanthine.
  27. Boekema, P.J., et al. “Coffee and Gastrointestinal Function: Facts and Fiction. A Review.” Scandinavian Journal of Gastroenterology, Supplement, vol. 230, 1999, pp. 35-39. doi: 10.1080/003655299750025525. www.ncbi.nlm.nih.gov/pubmed/10499460.
  28. Sanchis-Gomar, F., et al. “Effects of Acute Exercise and Xanthine Oxidase Inhibition on Novel Cardiovascular Biomarkers.” Translational Research: The Journal of Laboratory and Clinical Medicine, vol. 162, no. 2, 2013, pp. 102-109. doi: 10.1016/j.trsl.2013.02.006. www.ncbi.nlm.nih.gov/pubmed/23507375.
  29. Ashihara, Hiroshi, et al. “Metabolism of Caffeine and Related Purine Alkaloids in Leaves of Tea ( Camellia Sinensis L.).” Plant and Cell Physiology, vol. 38, no. 4, 1997, pp. 413-419. https://doi.org/10.1093/oxfordjournals.pcp.a029184.
  30. “Compound Summary 3-Methylxanthine.” National Center for Biotechnology Information: PubChem Compound Database, https://pubchem.ncbi.nlm.nih.gov/compound/3-Methylxanthine.
  31. Liszt, Kathrin Ingrid, et al. “Caffeine Induces Gastric Acid Secretion via Bitter Taste Signaling in Gastric Parietal Cells.” Proceedings of the National Academy of Sciences of the United States of America, vol. 114, no. 30, 2017, pp. 6260-6269. doi: 10.1073/pnas.1703728114. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544304/.
  32. Maiuolo, Jessica, et al. “Regulation of Uric Acid Metabolism and Excretion.” International Journal of Cardiology, vol. 213, 2016, pp. 8-14. https://doi.org/10.1016/j.ijcard.2015.08.109.
  33. Yu, Yiran, et al. “Alterations of the Gut Microbiome Associated With the Treatment of Hyperuricaemia in Male Rats.” Frontiers in Microbiology, vol. 9, no. 2233, 2018. doi: 10.3389/fmicb.2018.02233. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156441/.
  34. Garcia-Gil, M., et al. “Emerging Role of Purine Metabolizing Enzymes in Brain Function and Tumors.” International Journal of Molecular Sciences, vol. 19, no. 11, 2018. doi: 10.3390/ijms19113598. https://www.ncbi.nlm.nih.gov/pubmed/30441833.
  35. Ames, BN, et al. “Uric Acid Provides an Antioxidant Defense in Humans against Oxidant- and Radical-Caused Aging and Cancer: a Hypothesis.” Proceedings of the National Academy of Sciences of the United States of America, U.S. National Library of Medicine, Nov. 1981, doi.org/10.1073/pnas.78.11.6858.
  36. Fernstrom, J.D. “Dietary Amino Acids and Brain Function.” Journal of the American Dietetic Association, vol. 94, no. 1, 1994, pp. 71-77. https://doi.org/10.1016/0002-8223(94)92045-1.
  37. Van Kessel, Sebastiaan P., et al. “Gut Bacterial Tyrosine Decarboxylases Restrict the Bioavailability of Levodopa, the Primary Treatment in Parkinson's Disease.” Nature Communications, vol. 10, no. 1, 2019, pp. 310. doi: 10.1038/s41467-019-08294-y. https://www.biorxiv.org/content/10.1101/356246v1.
  38. Khaliq, W., et al. “Reductions in Tyrosine Levels Are Associated with Thyroid Hormone and Catecholamine Disturbances in Sepsis.” Intensive Care Medicine Experimental, vol. 3, 2015. doi: 10.1186/2197-425X-3-S1-A686. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798095/.
  39. “NIH - Genetics Home Reference - Tyrosinemia.” U.S. National Library of Medicine, https://ghr.nlm.nih.gov/condition/tyrosinemia.