A. Makristathis et al., DETECTION OF HELICOBACTER-PYLORI IN STOOL SPECIMENS BY PCR AND ANTIGEN ENZYME-IMMUNOASSAY, Journal of clinical microbiology, 36(9), 1998, pp. 2772-2774
A highly sensitive seminested PCR assay to detect Helicobacter pylori
DNA in feces was developed. PCR with stool specimens and a novel antig
en enzyme immunoassay (EIA) for H. pylori detection in feces were eval
uated as diagnostic tools and in follow-up with samples from 63 infect
ed and 37 noninfected persons. Infected individuals received eradicati
on therapy followed by endoscopic follow-up 35 days after the start of
treatment. At that time, a second stool specimen was obtained from 55
of these patients. Before eradication, the sensitivity of BCR was 93.
7% and that of EIA 88.9%. Specificities were 100 and 94.6%, respective
ly. Of the 55 follow-up specimens, 41 originated from patients from wh
om H. pylori had been eradicated. Of these, 21 were still positive by
PCR and 13 were positive by EPA, indicating that 1 month may be too sh
ort a period for follow-up evaluation of stool specimens by these test
s.