Author/Authors :
Moradi, Abdolvahab Golestan Research Center of Gastroenterology and Hepatology - Golestan University of Medical Sciences, Gorgan , Fazlollahi, Narges Autoimmune and Motility Disorders Research Center - Digestive Diseases Research Institute - Tehran University of Medical Sciences, Tehran , Eshraghi, Amid Autoimmune and Motility Disorders Research Center - Digestive Diseases Research Institute - Tehran University of Medical Sciences, Tehran , Gholipour, Mahin Golestan Research Center of Gastroenterology and Hepatology - Golestan University of Medical Sciences, Gorgan , Khoshnia, Masoud Golestan Research Center of Gastroenterology and Hepatology - Golestan University of Medical Sciences, Gorgan , Javid, Naeme Department of Microbiology - Golestan University of Medical Sciences, Gorgan , Montazeri, Ali Liver and Pancreatobiliary Diseases Research Center - Digestive Diseases Research Institute - Tehran University of Medical Sciences, Tehran , Mikaeli, Javad Autoimmune and Motility Disorders Research Center - Digestive Diseases Research Institute - Tehran University of Medical Sciences, Tehran
Abstract :
BACKGROUND Achalasia, as an incurable disease is defined by the lack of normal esophageal peristalsis and loss of lower esophageal sphincter relaxation due to impaired myenteric neural plexus. The exact cause of myenteric neural cells degeneration in achalasia is still unknown. One hypothesis is that certain neurotropic viruses and autoimmune factors cause the inflammatory response in myenteric
network, which consequently destroy neural cells. This study was designed to find the evidence of viral causes of achalasia. METHODS In this case-control study, 52 patients with achalasia and 50 controls referred to Shariati Hospital, were evaluated for the genome of neurotropic viruses, HPV, and adenovirus by polymerase chain reaction (PCR) and reverse transcription (RT) PCR techniques. RESULTS Genome assessment of neurotropic DNA viruses turned out negative in the patients, however, the genome of HSV-1 (Herpes simplex virus) was found in tissues of six controls. No neurotropic
RNA viruses were observed in the tissue samples and whole blood of both the patients and controls. Among non-neurotropic viruses, adenovirus genome was positive in tissues of two out of 52 patients and three out of 50 controls. In addition, one out of 52 patients and two out of 50 controls were positive for HPV infection in tissues. CONCLUSION We could not detect any significant relationship between achalasia and HPV, adenovirus, and neurotropic viruses in the cases. Nevertheless, it does not exclude the hypothesis of either an alternate viral species or resolved viral infection as the etiology of achalasia.
Keywords :
Achalasia , DNA neurotropic viruses , RNA neurotropic viruses , HPV , Adenovirus