Pyroluria

What is Pyroluria, Pyrrole Disorder & Kryptopyrroles?

Pyroluria is known by many different names including Pyrrole Disorder, Kryptopyrrole, Kryptopyrroluria, Pyrroluria, Pyrolle Disorder, Mauve Factor and Hemepyrrole. Pyroluria can best be described as the abnormal synthesis and metabolism of the oxygen carrying molecule in your blood, called haemoglobin. As with all cells in your body there are waste or by-products produced and the by-product of haemoglobin is a metabolite called hydroxyhemopyrrolin-2-one (HPL) also known as Pyrrole. The metabolite was originally thought to be a Kryptopyrrole but further studies have proven this not to be the case.

People who suffer from Pyroluria produce excessive amounts of these Pyrroles which bind to or inhibit the nutrients; Zinc (1-7), Biotin 8, and the Omega 6 Fat GLA from reaching their targets within your body. This effectively renders these nutrients unavailable to you.

Supplementation with these nutrients not only helps to reduce your Pyrrole levels but also the severity of the conditions, signs and symptoms listed below.

Conditions Associated With Pyroluria

Acute Intermittent Porphyria Criminal Behaviour Neurosis/Neurotic
ADD/ADHD Depression Post Natal Depression
Alcoholism Down Syndrome Schizophrenia
Allergies Epilepsy Substance Abuse
Asperger’s Syndrome Learning Difficulties Tourette’s Syndrome
Autism Lung Cancer Violent Offenders
Bi-Polar Disorder Manic Depression

Signs & Symptoms Of Pyroluria

Kryptopyrrole/Polyuria Test Kit

Kryptopyrrole Test - Pyroluria Test
More Info

There are many signs and symptoms that may indicate the presence of elevated Pyrroles in your blood. The list below may give you an indication that you may have a Pyrrole disorder, however it is not a diagnosis for Pyroluria. For a correct diagnosis we recommend having a Kryptopyrroles Test which can be ordered through our online store.

Abdominal pain Lack of hair on head, eyebrows and eyelashes areas
Abnormal body fat distribution Lack of regular menstrual cycles
Acne Loss of appetite
Allergies Low libido
Amnesia spells Low tolerance to stress
Anger – explosive Migraines
Anxiety/anxious Mood swings
Argumentative - likes to argue Morning nausea
Cold hands and feet Motion sickness
Constipation Much higher capability in the evening than mornings
Creaking in joints Nervous exhaustion
Delayed puberty Nervousness
Delusions Overwhelmed in stressful situations
Depression Pale skin, poor tanning or burn easy in the sun
Difficulty remembering dreams Panic attacks
Dramatic Paranoia
Dyslexia Pessimism
Early greying of hair Poor memory
Eczema Poor morning appetite/tendency to skip breakfast
Elevated eosinophil’s Preference for spicy or heavily flavoured foods
Emotionally unstable Prone to stitches when running now or as a child
Fatigue Reading difficulties
Fluid retention Seizures
Frequent colds, fevers, and chills Sensitivity to bright light
Frequent ear infections as a child Sensitivity to smells
Hallucinations Severe inner tension
Hyperactivity Skin rashes
Hypersensitivity to noise Significant growth after the age of 16
Hyper-pigmentation of the skin Social withdrawal
Hypoglycaemia Substance abuse
Inability to think clearly Temper tantrums
Insomnia Tendency towards iron deficient anaemia
Intolerance to alcohol Tingling in the arms and legs
Intolerance to drugs Tremors
Intolerance to some protein foods Unusual smelling body odour
Joint pain Unusual smelling breath
Knee pain

Unusual Body Appearances Associated with Pyroluria

Pyroluria Positive Treatment Plan

View Plans

Some people who suffer from Pyroluria may also have abnormalities in their physical appearance such as;

  • If your family has black skin yours will be the lightest skin in your family
  • Lack of hair on your head, eyebrows and eyelashes- Skin which is prone to stretch marks
  • Teeth in your upper jar will often be overcrowded (unless orthodontic treatments have taken place)
  • White spots on your fingernails
  • You may suffer from acne, eczema or herpes
  • Your tooth enamel has a poor appearance
  • Your skin will appear paper thin

What Causes Pyroluria?

Pyrrole Support

Pyrrole Support
More Info

There is evidence to suggest that Pyroluria is a genetically based ailment. Statistics and research indicates that if a parent, grandparent, aunt, uncle, brother or sister has suffered from major Depression, Bi-Polar Disorder, Alcoholism, Schizophrenia or has suicided, there is a greater risk of Pyroluria in other family members.

Research has discovered that stress increases the production of these Pyrroles in your blood, which in turn causes a worsening of your symptoms (2,6,43). A US navy study conducted in 1992 found a very rapid increase in Pyrrole levels in male volunteers who were subjected to the stress of a brief cold-water immersion (44)

Poor dietary choices and poor digestive health can lead to an increase in Pyrrole levels (9) This makes sense as a poor diet and digestion robs your body of essential nutrients. This causes deficiencies to occur and results in various aspects of your health operating below par. It’s a downward spiral as without the correct nutrients you can’t function properly, this increases the stresses placed on your body and further drives up blood Pyrrole levels.

Leaky Gut Syndrome also known as intestinal permeability, is a condition whereby microscopic holes occur in your intestinal wall and allow undigested food, bacterial by-products, poisons and toxins to pass into your bloodstream. Leaky Gut Syndrome is widespread in sufferers of Pyroluria and a common factor in driving up blood Pyrrole levels.

Studies have shown that zinc deficiency increases bowel permeability (Leaky Gut syndrome) in animal and humans  (10-16).

Laxatives especially magnesium sulphate and bisacodyl (laxative drug) increases Leaky Gut Syndrome (17-19). Enemas (especially soap suds and tap water), result in loss of the intestinal lining, which then leads to Leaky Gut Syndrome (20).

It is a well known fact that stress damages the intestinal wall and causes intestinal inflammation. Both of which lead to an increase in Leaky Gut Syndrome  (9, 21-23).

Dysbiosis, an overgrowth of detrimental bacteria in the intestinal tract, has also been linked to an increase in blood pyrrole levels as well as contributing to Leaky Gut Syndrome (17, 24). Stress increases the adherence of bad bacteria to the intestinal wall within 30 minutes (25).

Alcohol, smoking, drugs and heavy metal exposure can dramatically increase blood pyrrole levels. This is why sufferers of Pyroluria tend to get a worsening of their symptoms 24 to 48 hours after a big night on the grog or recreational drug use.

What Damage Can Elevated Pyrrole Levels Cause?

Pyrrole Support Packs

Pyrrole Support Pack View Packs

Pyrroles are classed as 'nerve poisons' (26) and as such can cause damage to your nerves, nerve cells and tissue, your brain and they can interrupt messages being sent along your nerves especially within your brain.

Heme is a substance found in your body that has an iron atom at its core. The most commonly know heme is haemoglobin, the oxygen carrying red pigment of your blood. Heme is not only found in your blood but in other areas of your body such as your liver and nerves. Your nerves metabolic activity is highly dependent on heme for their function and low levels of heme leads to a metabolic crisis occurring in your nerves resulting in neuronal (nerve) cell death (27-29). The by-product of haemoglobin metabolism, Hydroxyhemopyrrolin-2-one (HPL) or pyrrole, is believed to decrease heme levels in humans. Animal studies have shown that HPL caused a decrease in liver heme, and the heme containing detoxifying enzyme cytochrome P450, by up to 55% over a 48 hour period (30). Vitamin B6, biotin and zinc are all required for the production of heme and a reduction in these nutrients results in sub normal heme levels (28,31).  Heme levels are further depressed by stress and heavy metal exposure  28) .  Low levels of heme result in an excess production of the toxic free radical nitric oxide, which can cause serious damage to brain tissue and is suspected to play a role in schizophrenia, autism and Down Syndrome(38-42).

Free radicals or oxidative stress are substances that can damage and destroy your cells. Antioxidants are substances produced by your body and found in foods that protect your cells from oxidative stress or free radical damage, much like the way galvanised paint protects iron from rusting. Your body has three major antioxidant systems; Glutathione, Catalase and Superoxide Dismutase and these all need either zinc or vitamin B6 in some part to assist in their production. A marginal deficiency of vitamin B6 is associated with lower levels of Glutathione production and cell mitochondrial (cell battery) decay (32-34). Catalase consists of four protein subunits, each requiring heme, and since HPL suppresses heme, we can assume that pyroluria is associated with lower catalase levels, as is the case in schizophrenia and autism (35-37).

Additional Roles Of Vitamin B6, Zinc, Biotin & GLA In Keeping You Healthy

Leaky Gut Syndrome Test

Leaky Gut Syndrome Test
More Info

There are many additional illnesses and diseases that may result from a single or combined deficiency of vitamin B6, zinc, biotin and the omega fat GLA (gamma-linolenic acid).......read more

Pyroluria The Statistics

Below is a table that shows neuro-behavioural disorders and the percentages of high hydroxyhemopyrrolin-2-one (HPL) or pyrroles associated with those disorders (9).

Diagnosed Ailment % of HPL
Acute intermittent porphyria 100
Latent acute intermittent porphyria 70
Down syndrome 71
Schizophrenia acute 59-80
Schizophrenia chronic 40-50
Criminal behaviour
  -Adults with sudden deviance 71
  -Youths, violent offenders 33
Manic Depression 47-50
Depression (non schizophrenic) 12-46
Autism 46-48
Epilepsy 44
Learning Disabilities 40-47
ADD/ADHD 40-47
Neuroses 20
Alcoholism 20-84

The reason for the variance in some of the above figures is that it depends which study the results have come from. For example one study may have found only 20% of alcoholics had high levels of HPL whereas another study found that 84% of alcoholics had high levels of HPL.

Why Isn’t Pyroluria More Accepted By Mainstream Medicine?

Unfortunately Pyroluria falls outside the realm of mainstream medicine due to the fact that the only way to rectify the problem is by improving the sufferer’s nutritional status, diet, digestion and stress levels. Mainstream medicine relies on drugs to suppress a symptom or relieve suffering and this form of treatment will not work for a person who has a Pyrrole disorder. Sadly sufferers of Pyroluria fall through the cracks and are often misdiagnosed and given medication or drugs that do nothing to rectify the underlying problem. Unfortunately these medications can lead to further deterioration of a persons health.

What to do next?

As you can see pyroluria is a complex health issue and whereas treatment with the relevant nutrients will help to reduce the symptoms associated with pyroluria, it hasn’t addressed the underlying causes. So any treatment protocol for pyroluria needs to not only support the nutritional deficiencies caused by an elevation of pyrroles, but to also identify and treat what has caused these in the first place. The first step is to assess whether or not you are suffering from pyrrole disorder is to get yourself tested.

Pyroluria or Kryptopyrrole Test

We understand that it may be difficult for you to come and see us at our clinic so we have made it easy for you to find out whether you may be suffering from Pyroluria by ordering a Kryptopyrroles Test through our online store. We simply send you a test kit with full instructions on how to collect your urine sample and send it off to pathology for testing. Once your results are received we will analyse these and send you a detailed results report including suggested nutritional supplements and dietary advice to rectify your body’s underlying imbalances. It’s that easy.

What treatment do you recommend if I have already been tested for Kryptopyrroles / Pyroluria?

If you have already been tested we can offer the following services to you;

Pyroluria Treatment Plan - Online Download PDF (16 Page) and Audio File (mp3)

 

Skype Consultation - If you would like a more comprehensive overview of your health a Skype consultation can also be arranged.

References:

1. Pfeiffer CC, Iliev V. Pyroluria, urinary mauve factor, cases double deficiency of B6 and zinc in schizophrenics. Fed Am Soc Exp Biol. 1973;32:276.
2. Pfeiffer CC, Sholer A, Jenny EH, et al. Treatment of pyroluric schizophrenia with large doses of pyridoxine and a dietary supplement of zinc. J Appl Nut. 1974;26:21-28.
3. Pfeiffer CC, Bacchi D, copper, zinc, manganese niacin and pyridoxine in schizophrenia J Appl Nutr. 1975;27:9-39.
4. Pfeiffer CC. Mental and elemental nutrients. New Canaan, CT: Keats publishing 1976.
5. Pfeiffer CC. The schizophrenia’s ’76. Biol Psychiatry. 1976;11(6):773-775.
Pfeiffer CC. Extra nutrients and mental illness. Biol Psychiatry. 1981;16(9):797-799
6. Pfeiffer CC, Holford P. Mental Illness and Schizophrenia: The Nutritional Connection. Harper Collins Publishers, Great Britain;1987.
7. Pfeiffer CC. Nutrition and Mental Illness: An Orthomolecular Approach to Balancing Body Chemistry. Rochester, VT: Healing Arts Press;1987.
8. Kruesi O. Low plasma biotin levels in high mauve patients. Oral Communication 2005
9. Discercing the mauve factor, part 1: Alt Theapies, Mar/Apr 2008. Vol.14, No.2
10. Rohweder J, Runkel N, Fromm M, Schulzke JD, Buhr HJ. Zinc acts a protective agent on the mucosal barrier in experimental TNBS colitis [in German]. Langenbecks Arch Chir Suppl Kongressbd. 1998;115(Suppl 1):223-227.
11. Rodriguez P, Darmon N, Chappuis P, et al. Intestinal paracellular permeability during malnutrition in guinea pigs: effect of high dietary zinc. Gut. 1996;39(3):416-422.
12. Sturniolo GC, Fries W, Mazzon E, Di Leo V, Barollo M, D’inca R. Effect of zinc supple- mentation on intestinal permeability in experimental colitis. J Lab Clin Med. 2002;139(5):311-315.
13. Mahmood A, Fitzgerald AJ, Marchbank T, et al. Zinc carnosine, a health food supple- ment that stabilizes small bowel integrity and stimulates gut repair processes. Gut. 2007;56(2):168-175. Epub 2006 Jun 15.
14. Bates CJ, Evans PH, Dardenne M, et al. A trial of zinc supplementation in young rural Gambian children. Br J Nutr. 1993;69(1):243-255.
15. Chen P, Soares AM, Lima AA, et al. Association of vitamin A and zinc status with altered intestinal permeability: analyses of cohort data from northeastern Brazil. J Health Popul Nutr. 2003;21(4):309-315.
16. Sturniolo GC, Di Leo V, Ferronato A, D’Odorico A, D’Incà R. Zinc supplementation tightens “leaky gut” in Crohn’s disease. Inflamm Bowel Dis. 2001;7(2):94-98.
17. Irvine DG. Kryptopyrrole in molecular psychiatry. In: Hawkins D, Pauling L, eds. Orthomolecular Psychiatry: Treatment of Schizophrenia. San Francisco: WH Freeman and Company; 1973:146-178.
18. Sakurai E, Fukuse G, Ueda M, Murata R, Hikichi N, Niwa H. Alteration of biogenic amines, serotonin, histamine and polyamines, in cases of diarrhea induced by various cathartics [in Japanese]. Nippon Yakurigaku Zasshi. 1980;76(5):293-299.
19. Farack UM, Nell G. Mechanism of action of diphenolic laxatives: the role of adenylate cyclase and mucosal permeability. Digestion. 1984;30(3):191-194.
20. Schmelzer M, Schiller LR, Meyer R, Rugari SM, Case P. Safety and effectiveness of large-volume enema solutions. Appl Nurs Res. 2004;17(4):265-274.
21. Hart A, Kamm MA. Review article: mechanisms of initiation and perpetuation of gut inflammation by stress. Ailment Pharmacol Ther. 2002;16(12):2017-2028.
22. Martínez-Augustín O, Sánchez de Medina F Jr, Sánchez de Medina F. Effect of psycho- genic stress on gastrointestinal function. J Physiol Biochem. 2000;56(3):259-274.
23. Bhatia V, Tandon RK. Stress and the gastrointestinal tract. J Gastroenterol Hepatol. 2005;20(3):332-339.
24. Irvine DG. Mauve factor and 6-sulfatoxy skatole: two biochemical abnormalities asso- ciated with specific measures of psychiatric disease. Clin Chem. 1963;9:444-445.
25. Chen C, Lyte M, Stevens MP, Vulchanova L, Brown DR. Mucosally-directed adrenergic nerves and sympathomimetic drugs enhance non-intimate adherence of Escherichia coli O157:H7 to porcine cecum and colon. Eur J Pharmacol. 2006;539(1-2):116-124.
26. Corwin A M, et al. Encylopaedia Britannica 1960;18:801
27. Atamna H, Killilea DW, Killilea AN, Ames BN. Heme deficiency may be a factor in the mitochondrial and neuronal decay of aging. Proc Nat Acad Sci U S A. 2002;99(23):14807-14812.
28. Atamna H. Heme, iron, and the mitochondrial decay of ageing. Ageing Res Rev. 2004;(3)3:303-318.
29. Lill R, Kispal G. Maturation of cellular Fe-S proteins: an essential function of mitochon- dria. Trends Biochem Sci. 2000;25(8):352-356.
30. Graham DJM, Thompson GG, Moore MR, Goldberg AA. The effects of selected monopyrroles on various aspects of heme biosynthesis and degradation in the rat. Arch
Biochem Biophys. 1979;65(1):132-138.
31. Ames BN, Atamna H, Killilea DW. Mineral and vitamin deficiencies can accelerate the mitochondrial decay of aging. Mol Aspects Med. 2005;26(4-5):363-378.
32. Cabrini L, Bergami R, Fiorentini D, Marchetti M, Landi L, Tolomelli B. Vitamin B6 deficiency affects antioxidant defences in rat liver and heart. Biochem Mol Biol Int.1998;46(4):689-697. 107.
33. Park LC, Zhang H, Sheu KF, et al. Metabolic impairment induces oxidative stress, com-promises inflammatory responses, and inactivates key mitochondrial enzyme in micro-glia. J Neurochem. 1999;72(5):1948-1958. 108.
34. Atamna H, Walter PB, Ames BN. The role of heme and iron-sulfur clusters in mito-chondrial biogenesis, maintenance, and decay with age. Archiv Biochem Biophys.2002;397(2):345-353.
35. Fendri C, Mechri A, Khiari G, Othman A, Kerkeni A, Gaha L. Oxidative stress involve- ment in schizophrenia pathophysiology: a review [in French]. Encephale. 2006;32(2 Pt 1):244-252.
36. Ranjekar PK, Hinge A, Hegde MV, et al. Decreased antioxidant enzymes and mem-brane essential polyunsaturated fatty acids in schizophrenic and bipolar mood disor-der patients. Psychiatry Res. 2003;121(2):109122.
37. Zoroglu SS, Armutcu F, Ozen S, et al. Increased oxidative stress and altered activities of erythrocyte free radical scavenging enzymes in autism. Eur Arch Psychiatry ClinNeurosci. 2004;254(3):143-147.
38. Liu S, Kawai K, Tyurin VA, et al. Nitric oxide-dependent pro-oxidant and pro-apoptoticeffect of metallothioneins in HL-60 cells challenged with cupric nitrilotiracetate.Biochem J. 2001;354(pt 2):397-406.
39. Smith KJ, Kapoor R, Felts PA. Demyelination: the role of reactive oxygen and nitrogen species. Brain Path. 1999;9(1):69-92.
40. Shinkai T, Ohmori O, Hori H, Nakamura J. Allelic association of the neuronal nitricoxide synthatse (NOS1) gene with schizophrenia. Mol Psychiatry. 2002;7(6):560-563.
41. Sögüt S, Zoroglu SS, Ozyurt H, et al. Changes in nitric oxide levels and antioxidant enzyme activities may have a role in the pathophysiological mechanisms involved inautism. Clin Chim Acta. 2003;331(1-2):111-117.
42. De la Monte SM, Bloch KD. Aberrant expression of the constituitive endothelial nitricoxide synthase gene in Alzheimer disease Mol Chem Neuropathol. 1997;30(1-2):139-159.
43. Ward JL. Relationship of kryptopyrrole, zinc and pyridoxine in schizophrenics. JOrthomolec Psychiatr. 1975;4:27-31.
44. Discerning the Mauve Factor by Woody R. McGinnis MD, Tapan Audhya  Ph.D. and William J Walsh Ph.D.