1 / 31

Optimizing GI Function and Heavy Metal Burden in Lyme Disease

Learn how to optimize GI function and reduce heavy metal burden in Lyme disease. Topics include antibiotic-induced diarrhea, intestinal dysbiosis, liver/gallbladder support, heavy metals, and treatment options.

marywalter
Download Presentation

Optimizing GI Function and Heavy Metal Burden in Lyme Disease

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Optimizing GI Function and Heavy Metal Burden in Lyme Disease Raj Patel, MD Medical Options for Wellness Los Altos, CA 650-964-6700 www.DrRajPatel.net Raj Patel, M.D.

  2. Overview • Optimize GI Function • Antibiotic induced diarrhea • Intestinal dysbiosis (definition, causes, treatment) • Liver/GB Support • B. Heavy Metals • Prevalence • Signs & symptoms • Testing • Treatment options • Methylation in non-responders • C. Conclusion Raj Patel, M.D.

  3. A. Optimize GI Function • 1. Antibiotic Induced Diarrhea (AID) • Common complication from extended antibiotic use • Probability increases with use of >2 antibiotics • Doxy + Flagyl for 10 d caused a significant increase • in GI and vaginal candida counts than either alone. • Maraki S. J Chemother. 2003 Aug;15(4):369-73. • Certain antibiotics more commonly associated with • AID (Cephalosporins and Penicillins) • Clostridium difficile induced enterocolitis • Symptoms: diarrhea, abdominal pain, fevers • Incidence: only accounts for 10-20% of all AID cases • E. Bergogne-Bérézin Int J Antimicrob Agents. 2000 Dec;16(4):521-6 Raj Patel, M.D.

  4. Non-Clostridium AID Common pathogens include Clostridium perfringens, Staphylococcus aureus, Klebsiella oxytoca, Candida species, and Salmonella species. Accounts for 80-90% of all AID cases • Clin Infect Dis. 1998 Oct;27(4):702-10 • AID Treatment Options Mild Symptoms: Saccharomyces boulardii • Probiotics • Bland diet • Drug holiday/Change antibiotics • Elmer GW. et al JAMA. 1996 Jul 3 ;276(1):29-30 Biotherapeutic agents. A neglected • modality for the treatment and prevention of selected intestinal and vaginal infections. Severe Symptoms: Metronidazole • Vancomycin Raj Patel, M.D.

  5. 2. Intestinal Dysbiosis • a. Definition: • Term originally coined by Metchnikoff to describe altered pathogenic • bacteria in gut. Today, abnormal milieu due to bacterial and fugal • imbalance. • These abnormal bacteria have been shown to produce: • toxic products- endotoxins, phenols, ammonia, & indoles • Macfarlane C et al. Proteolysis and amino acid fermentation. In: Gibson GR, Macfarlane GT, eds. • Human Colonic Bacteria: Role in Nutrition, Physiology, and Pathology. Boca Raton, FL: • CRC Press; 1995:75-100. • Chronic degenerative diseases - inflammatory bowel disease, • ankylosing spondylitis, & RA • Peltonen R, Nenonen M, Helve T, et al. Br J Rheumatol 1997;36:64-68. • Brandtzaeg P. Review article: Aliment Pharmacol Ther 1997;11:24-37. Raj Patel, M.D.

  6. Intestinal Dysbiosis (con’t) • b. Functions of the microflora • Immune stimulation • Vitamin synthesis (B group & K) • Enhancement of gut motility, digestion & nutrient absorption • Improve epithelial function via increased SCFA production, • decreased apoptosis, increased barrier integrity • Inhibit pathogenic bacteria via decreasing luminal pH, decreasing • epithelial binding, and decreasing epithelial invasion • Metabolism of certain drugs • Holzapfel WH, et al. Int J Food Microbiol 1998;41:85-101. • Noack J, et al. J Nutr 1998;128:1385-1391. • Gibson GR, Roberfroid MB. J Nutr 1995;125:1401-1412. • Sartor, RB. J. Clin. Gastro 2007;41:537-543 Raj Patel, M.D.

  7. Intestinal Dysbiosis (con’t) c. Causes of Intestinal Dysbiosis I. Antibiotics-based on spectrum of activity, route of excretion, dosage, & length of use. Hawrelak, JA Alternative Medicine Review Vol 9, No 2 2004 Raj Patel, M.D.

  8. Effects of Antibiotics on Intestinal Flora Raj Patel, M.D. Hawrelak, JA Alternative Medicine Review Vol 9, No 2 2004

  9. c. Causes of Intestinal Dysbiosis (con’t) • II. Stress: • Altered gut motility and increased bicarbonate production • potentially leading to decreased survival/adherence/replication of • healthy flora • Lenz HJ. Et al. Gastroenterology 1988;94:598-602. • Lenz HJ. Proc Natl Acad Sci U S A 1989;86:1417-1420. • Decreased mucin and mucopolysaccharide production leading to • increased adherence and replication of dysbiotic flora Raj Patel, M.D.

  10. c.Causes of Intestinal Dysbiosis (con’t) • III. Lyme and Coinfections • Lyme is well documented to invade and multiply in the GI tract • Fried MD, et al Gastrointestinal pathology in children with Lyme disease. Jour. of Spirochetal • & Tick-Borne Diseases 1996; 3:101-04 • Lyme and more commonly ehrlichiosis, tick borne relapsing fever, • & Rocky Mountain Spotted Fever are commonly associated with • diarrhea and intestinal dysbiosis. • Reisinger EC. et al. Nat. Clin. Pract. Gastrenterol. Hepatol. 2005 May; 2(5):216-22. • Zaidi SA. et al. Clin. Infect. Dis. 2002 May 1;34(9):1206-12 Raj Patel, M.D.

  11. c. Causes of Intestinal Dysbiosis (con’t) • IV. Maldigestion • Pancreatic exocrine deficiency Fecal elastase marker for pancreatic enzyme production • Gallbladder dysfunction with decreased bile production -> fat • maldigestion • Consider fecal fat testing • Increased intestinal permeability/inflammation • Microscopically characterized by blunting/loss of micro-villi and • compromised tight junctions between cells • Corresponding loss of disaccharidases resulting in carbohydrate • maldigestion, increased disaccharide load to colon, and resulting • dysbiosis. • Diagnosed by Lactulose/Mannitol test (increased ratio indicates • increased permeability) Raj Patel, M.D.

  12. c. Causes of Intestinal Dysbiosis (con’t) • V. Diet - Composition of diet affects type and metabolic activity of • gut flora • Gibson GR. Dietary modulation of the human gut microflora using prebiotics. Br J Nutr • 1998;80:S209-S212. • High Protein Diet: Typical American diet contains 100g of protein per day. Up to 12g can escape digestion & become available for fermentation by colonic bacteria. • The resulting harmful byproducts include ammonia, • sulfides, indoles, phenols & amines-> migraines, • carcinogens, damage lining, contribute to portal • encephalopathy. • Significant issue in Lyme patients with • compromised GI function Raj Patel, M.D.

  13. c.Causes of Intestinal Dysbiosis (con’t) • V. Diet (con’t) • High Carbohydrate Diet: • High refined carbohydrate diet • -> slows bowel transit time • -> increases bacterial fermentation • -> increases exposure to potentially toxic bowel contents (96) • -> promotion of fungal overgrowth (esp. in presence of multiple • antibiotics) • Lewis SJ, Heaton KW. Am J Gastroenterol 1999;94:2010-2016. • High carbohydrate diet (esp gluten and casein) • -> increases disaccharide load to colon (due to intestinal • inflammation and disaccharidase deficiency) • -> abnormal bacterial overgrowth and fermentation Raj Patel, M.D.

  14. Intestinal Dysbiosis (con’t) • d. Treatment Options for Intestinal Dysbiosis • Antibiotics: All things being equal choose antibiotics with less effect on • gut flora. • Support intestinal flora-probiotics (research carefully) • prebiotics (FOS, etc.) • fermented foods • Stress: Help patients manage stress effectively • Support endocrine systems esp. adrenals and thyroid as covered • earlier • Treat insommnia aggressively (melatonin, 5HTP, Ramelteon, • Trazodone, etc.) • Treat depression/anxiety if needed Raj Patel, M.D.

  15. Intestinal Dysbiosis (con’t) • d. Treatment Options for Intestinal Dysbiosis • Lyme: Expect improvement in gut issues as load of Lyme and • coinfections reduced • Maldigestion: Digestive enzmes-Use broad spectrum digestive aids • that include protease, lipase, & amylase as well as • disaccharidases (lactase, maltase, and sucrase) • Gallbladder support-Taurine, ox bile, and bile salts can • aid in bile production and fat digestion • Intestinal inflammation/permeability-Glutamine, • slippery elm, and DGL aid in reducing gut • inflammation. Eliminate allergenic/intolerant foods • & consider desensitization Raj Patel, M.D.

  16. Intestinal Dysbiosis (con’t) • d. Treatment Options for Intestinal Dysbiosis (con’t) • Diet: Consider decreasing protein intake if excessive • Eliminate gluten, casein, and refined carbohydrates • Consider Specific Carbohydrate Diet (SCD) in those severely • carbohydrate intolerant • Gottschall, E (1994). Breaking the Vicious Cycle: Intestinal Health Through Diet, • Revised edition, Kirkton Press.. Raj Patel, M.D.

  17. Intestinal Dysbiosis (con’t) • 3. Liver/Gallbladder Function • Dysfunction/Inflammation of liver and gallbladder • I. Lyme and coinfections • II. Antibiotics: Elevate liver function tests • Those with biliary excretion can result in GB dysfunction • Testing • I. Comprehensive liver detoxification screen to evaluate phase I & II • function • II. Genomic testing • Hepatic nutritional support Raj Patel, M.D.

  18. Hepatic Nutritional Support Patrick Hanaway, MD Genova Diagnostic Laboratories Raj Patel, M.D.

  19. B. Heavy Metals • 1. Heavy Metals - Hg, Cd, Pb, & Ar are the best studied • a. Hg • I. Sources: • Thimersol (50% Hg by volume) was the preservative in most vaccines until approx 2001. • Cumulative dose in vaccines from birth to age 5 years exceeded the EPA guidelines for safety. • Large population of older children and young adults have had significant exposure. • Study on NYC adult population revealed 24.8% had bloodlevels at or exceeding 5ug/l, the NY State reportable level. McKelvey W. Environ Health Perspect. 2007 Oct;115(10):1435-41 • Seafood, dental amalgams, and industrial output account for the major sources of exposure today. (26,27) • WHO. Methyl Mercury. Environmental Health Criteria, vol. 101. Geneva: World Health Organization, 1990 Sallsten G, et.al., J Dent Res 1996; 75: 594–8 Raj Patel, M.D.

  20. 1. Heavy Metals(con’t) • a. Hg • II. Toxicity: • Low level chronic exposure can lead to nervous system • damage resulting in depression, anxiety & cognitive loss • Weiss B, Clarkson TW, Simon W. Environ Health Perspect 2002; 110 (Suppl 5): 851–4 • Autoimmunity • Hultman, P. et al. The FASEB Journal Nov 1994; 1183-90 • Paresthesias, insommnia, cognitive difficulties, • neuromuscular changes, headaches and anxiety. • http://www.epa.gov/iris/subst/0692.htm Raj Patel, M.D.

  21. 1. Heavy Metals(con’t) b. Cd I. Sources: Color pigment (dyes & paints) Cigarette smoke Ni-Cd batteries Phosphate fertilizers Jarup L et al. Health effects of cadmium exposure—a review of the literature and a risk estimate. Scand J Work Environ Health 1998; 24 (Suppl 1): 1–51 WHO. Cadmium. Environmental Health Criteria, vol. 134. Geneva: World Health Organization, 1992 II. Toxicity: Kidney damage Osteoporosis Cancer Jarup, L. Br. Med. Bull. 68:167-182 (2003) Raj Patel, M.D.

  22. 1. Heavy Metals (con’t) c. Pb I. Sources: Gasoline (Worldwide major source but not in US) Lead in drinking water primarily dueto the presence of lead in certain pipes, solder, and fixtures. In kids toys and lead based paints in old homes II. Toxicity: Decreased IQ Memory deterioration Cancer Anemia Peripheral nerve symptoms WHO. Lead. Environmental Health Criteria, vol. 165. Geneva: World Health Organization, 1995 Steenland K, Boffetta P. Am J Ind Med 2000; 38: 295–9 Raj Patel, M.D.

  23. 1. Heavy Metals (con’t) d. Ar I. Sources: Wood preservative Fish Pesticides/food Industrial exposure II. Toxicity: Cancer-lung, bladder, & kidney Peripheral neuropathy Anemia GI Effects WHO. Arsenic and Arsenic Compounds. Environmental Health Criteria, vol. 224. Geneva: World Health Organization, 2001 Chilvers DC, Peterson PJ. Global cycling of arsenic. In: Hutchinson TC, Meema KM (eds) Lead, Mercury, Cadmium and Arsenic in the Environment. Chichester: John Wiley & Sons, 1987; 279–303 www.epa.gov/ttn/atw/hlthef/arsenic.html Raj Patel, M.D.

  24. B. Heavy Metals (con’t) • 2. Testing for Heavy Metals • Blood levels useful for acute exposure, but unreliable tool for chronic low level exposures. • Mercury has affinity for fatty tissue. Rarely seen in blood. • The half-life of Pb in blood is about one month whereas the • half-life in bone is 20-30 years. (35) • WHO. Lead. Environmental Health Criteria, vol. 165. Geneva: World Health Organization, 1995 • Difficult to accurately assess total body burden. Urinary porphyrins have some utility – currently probably the best clinical test available. • Hair Mineral Analysis may be helpful, but show false negative in • individuals with compromised detoxification pathways • Provocative challenge-involves administering a test dose of a chelator • (DMPS, DMSA, or EDTA) and measuring pre- and post- fecal &/or • urine for heavy metals. Raj Patel, M.D.

  25. B. Heavy Metals (con’t) • 3. Treatment - best done once Lyme/coinfection load reduced • Pharmacological Chelators: DMPS • DMSA • EDTA • Penicillamine • Non-pharmacological chelators: Sauna • Alginate/Chlorella • Zeolite Raj Patel, M.D.

  26. B. Heavy Metals (con’t) • 3. Treatment (con’t) • Nutritional support during chelation essential • I. Gut binding agents-Bentonite • Charcoal • Cholestyramine • II. Mineral replacement-depending on the chelator used, replace • minerals aggressively with special attention to Ca & Mg • with EDTA and Cu & Zn with DMPS/DMSA • III. Antioxidant support-necessary to quench free radicals generated • during heavy metal removal. Supplement with A, C, E, Zn, • selenium, and reduced glutathione. • IV. Hepatic support-as outlined earlier Raj Patel, M.D.

  27. B. Heavy Metals • 4. Assess methylation function in non-responders • Definition: Methylation involves transfer of methyl group • Methylation plays a role in: • Neurotransmitter synthesis and breakdown • Renal disease • Cardiovascular disease • Cancer • Heavy metal detoxification • Anti-viral immune modulation Raj Patel, M.D.

  28. Zn P5P P5P Mg B12 Methylation Cycle 5,10 MTHF Methionine SAM MSR Methionine Synthase MTHR SAH 5 MTHF Homocysteine Homocysteine CBS Cystathione Cysteine Glutathione Taurine Raj Patel, M.D.

  29. B. Heavy Metals • 4. Assess methylation in non-responders (con’t) • Single Nucleotide Polymorphisms (SNPs): Can impair methylation Commonly found in the general population SNPs involving MTHFR C677T have a 47% incidence among Caucasians • Ulrich CM. et al.Cancer Epidemiol Biomarkers Prev. 1999 Aug;8(8):659-68 • Heavy metals at low levels can suppress key enzymes involved in methylation Raj Patel, M.D.

  30. B. Heavy Metals • 4. Assess methylation in non-responders (con’t) • Testing to assess methylation: genomic testing • urine/serum amino acid analysis • Nutritional Support to open/bypass areas of impairment: • Methyl B12 / Cyano B12 • TMG (or DMG) • Folic/Folinic acid • P5P/B6 • Reduced Glutathione Raj Patel, M.D.

  31. C. Conclusion 1. Aggressive GI support before, during and after antibiotic treatment can greatly assist in reducing complications and improve outcome 2. Heavy metals are ubiquitous. They can compromise immune functioning, promote overgrowth of candida as well as dysbiotic flora. Judicial heavy metal detoxification, once the lyme/coinfection load has been reduced, with appropriate methylation support as needed, may improve outcome and potentially reduce the likelihood of relapse Raj Patel, M.D.

More Related