Gastrointestinal Microflora Studies in Late‐Onset Autism

Sydney M. Finegold(West Los Angeles College), Denise Molitoris(West Los Angeles College), Yuli Song(West Los Angeles College), Chengxu Liu(West Los Angeles College), Marja–Liisa Väisänen(West Los Angeles College), Ellen R Bolte(Rush Children's Hospital), M. McTeague(West Los Angeles College), Richard H. Sandler(Rush Children's Hospital), Hannah M. Wexler(West Los Angeles College), Elizabeth M. Marlowe(West Los Angeles College), Matthew D. Collins(University of Reading), Paul A. Lawson(University of Reading), Paula Summanen(West Los Angeles College), Mehmet Baysallar(West Los Angeles College), Thomas J. Tomzynski(West Los Angeles College), Erik K. Read(West Los Angeles College), Eric A. Johnson(University of Wisconsin–Madison), Rial D. Rolfe(Texas Tech University), Palwasha Nasir, Haroun N. Shah, David A. Haake(University of California, Los Angeles), Patricia Manning(Cincinnati Children's Hospital Medical Center), Ajay Kaul(Cincinnati Children's Hospital Medical Center)
Clinical Infectious Diseases
September 1, 2002
Cited by 732Open Access
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Abstract

Some cases of late-onset (regressive) autism may involve abnormal flora because oral vancomycin, which is poorly absorbed, may lead to significant improvement in these children. Fecal flora of children with regressive autism was compared with that of control children, and clostridial counts were higher. The number of clostridial species found in the stools of children with autism was greater than in the stools of control children. Children with autism had 9 species of Clostridium not found in controls, whereas controls yielded only 3 species not found in children with autism. In all, there were 25 different clostridial species found. In gastric and duodenal specimens, the most striking finding was total absence of non-spore-forming anaerobes and microaerophilic bacteria from control children and significant numbers of such bacteria from children with autism. These studies demonstrate significant alterations in the upper and lower intestinal flora of children with late-onset autism and may provide insights into the nature of this disorder.


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