Identification of Helicobacter pylori DNA in Iranian patients with gallstones.

In order to identify Helicobacter in gallstones of Iranian patients with biliary disease, gallstone and bile samples from 33 patients were subjected to rapid urease test, culture and Multiplex PCR using primers based on 16s rRNA and isocitrate dehydrogenase genes for the identification of Helicobact...

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Publicado en:Epidemiology & Infection Vol. 132; no. 6; pp. 1185 - 1190
Autores principales: Farshad SH, Alborzi A, Hosseini SAM, Oboodi B, Rasouli M, Japoni A, Nasiri J, Farshad, Sh, Alborzi, A, Malek Hosseini, S A, Oboodi, B, Rasouli, M, Japoni, A, Nasiri, J
Formato: pictorial research Journal Article
Publicado: Cambridge University Press Dec2004
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Dec2004
      vid: 132
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      pub: Cambridge University Press
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        10.1017/s0950268804002985
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        atl: Identification of Helicobacter pylori DNA in Iranian patients with gallstones.
      aug:
        au:
          Farshad SH
          Alborzi A
          Hosseini SAM
          Oboodi B
          Rasouli M
          Japoni A
          Nasiri J
          Farshad, Sh
          Alborzi, A
          Malek Hosseini, S A
          Oboodi, B
          Rasouli, M
          Japoni, A
          Nasiri, J
        affil: Professor Alborzi Clinical Microbiology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran
      sug:
        subj:
          Cholelithiasis
          DNA Iran
          Helicobacter Infections Familial and Genetic
          Adult
          Aged
          Funding Source
          Iran
          Middle Age
          Polymerase Chain Reaction
          Human
          Adult: 19-44 years
          Aged: 65+ years
          Middle Aged: 45-64 years
      ab: In order to identify Helicobacter in gallstones of Iranian patients with biliary disease, gallstone and bile samples from 33 patients were subjected to rapid urease test, culture and Multiplex PCR using primers based on 16s rRNA and isocitrate dehydrogenase genes for the identification of Helicobacter genus and H. pylori respectively. This PCR was also done on bile samples from 40 autopsied gallbladders with normal pathology (control group). In 18.1% of stone and 12.1% of bile samples, H. pylori DNA was detected using PCR. Rapid urease and culture tests were negative for all samples. The PCR was negative in the control group. In conclusion, H. pylori DNA was detected in stone samples of Iranian patients with gallstones but we are not sure of their viability. To clarify the clinical role of Helicobacter in gallbladder diseases, studies using accurate tests on larger patient and control groups are needed to ascertain whether this microorganism is an innocent bystander or active participant in gallstone formation.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        Journal Article
      ougenre: Article
    language: English
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