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Autism Studies and Related Medical Conditions, January 2009 - TACA

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207. Fedorak RN, Madsen KL. Probiotics <strong>and</strong> the management of inflammatory bowel<br />

disease. Inflamm Bowel Dis. 2004 May;10(3):286-99. PMID: 15290926<br />

"The demonstration that immune <strong>and</strong> epithelial cells can discriminate between different<br />

microbial species has extended our underst<strong>and</strong>ing of the actions of probiotics beyond<br />

simple barrier <strong>and</strong> antimicrobial concepts. Several probiotic mechanisms of action,<br />

relative to inflammatory bowel disease, have been elucidated: (1) competitive<br />

exclusion, whereby probiotics compete with microbial pathogens for a limited number of<br />

receptors present on the surface epithelium; (2) immunomodulation <strong>and</strong>/or stimulation<br />

of an immune response of gut-associated lymphoid <strong>and</strong> epithelial cells; (3) antimicrobial<br />

activity <strong>and</strong> suppression of pathogen growth; (4) enhancement of barrier function; <strong>and</strong><br />

(5) induction of T cell apoptosis in the mucosal immune compartment. The unraveling<br />

of these mechanisms of action has led to new support for the use of probiotics in the<br />

management of clinical inflammatory bowel disease. Though level 1 evidence now<br />

supports the therapeutic use of probiotics in the treatment of postoperative pouchitis,<br />

only levels 2 <strong>and</strong> 3 evidence is currently available in support of the use of probiotics in<br />

the treatment of ulcerative colitis <strong>and</strong> Crohn's disease. Nevertheless, one significant <strong>and</strong><br />

consistent finding has emerged during the course of research in the past year: not all<br />

probiotic bacteria have similar therapeutic effects. Rigorously designed, controlled<br />

clinical trials are vital to investigate the unresolved issues related to efficacy, dose,<br />

duration of use, single or multi-strain formulation, <strong>and</strong> the concomitant use of<br />

prebiotics, synbiotics, or antibiotics."<br />

208. Nardone G, Rocco A. Probiotics: a potential target for the prevention <strong>and</strong><br />

treatment of steatohepatitis. J Clin Gastroenterol. 2004 Jul;38(6 Suppl):S121-2. PMID:<br />

15220676<br />

"The accumulation of fat in hepatocytes with a necroinflammatory componentsteatohepatitis-that<br />

may or may not have associated fibrosis is becoming a frequent<br />

lesion. Although steatohepatitis is currently recognized to be a leading cause of<br />

cryptogenic cirrhosis, the pathogenesis has not been fully elucidated. Among the<br />

various factors implicated, intestinal bacterial overgrowth may play a role. Indeed,<br />

various rat models of intestinal bacterial overgrowth have been associated with liver<br />

lesions similar to NASH, <strong>and</strong> bacterial overgrowth has been observed significantly more<br />

often in patients with NASH compared with control subjects. The authors discuss the<br />

relationship among intestinal bacterial overgrowth, steatohepatitis development, <strong>and</strong><br />

probiotic treatment."<br />

209. Saggioro A. Probiotics in the treatment of irritable bowel syndrome. J Clin<br />

Gastroenterol. 2004 Jul;38(6 Suppl):S104-6. PMID: 15220671<br />

"Irritable Bowel Syndrome (IBS) may be diagnosed on the presence of symptoms,<br />

according to Rome II criteria <strong>and</strong> some studies have shown that abnormal colonic<br />

fermentation may be an important factor in the development of symptoms in some<br />

<strong>Autism</strong> <strong>Studies</strong> & <strong>Related</strong> <strong>Medical</strong> <strong>Conditions</strong> – <strong>TACA</strong> © Page 356

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