فهرست مطالب

Gastroenterology and Hepatology From Bed to Bench Journal
Volume:10 Issue: 1, Winter 2017

  • تاریخ انتشار: 1395/12/25
  • تعداد عناوین: 14
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  • Gabriel Samasca, Genel Sur, Iulia Lupan, Peter Makovicky, Hugh James Freeman Page 1
  • Nahal Eshghifar, Naser Farrokhi, Tahereh Naji, Mohammad Reza Zali Page 3
  • Faegheh Behboudi Farahbakhsh, Ehsan Nazemalhosseini Mojarad, Faezeh Goudarzi, Pedram Azimzadeh, Amir Houshang Mohammad Alizadeh, Mehrdad Haghazali, Reza Mahmoudi Lamoki, Hamid Asadzadeh Aghdaei Page 14
  • Mostafa Rezaei, Tavirani, Majid Rezaei, Tavirani, Vahid Mansouri, Mohammad Rostami, Nejad, Reza Valizadeh, Seyed Mohammad Mahdavi, Mohammad Reza Zali Page 21
    Aim: Since interactome analysis of diseases can provide candidate biomarker panel related to the diseases, in this research, protein-protein interaction (PPI) network analysis is used to introduce the involved crucial proteins in Gastric adenocarcinoma (GA).
    Background
    Gastric adenocarcinoma (GA) is the most common type of stomach cancer. There is no efficient diagnostic molecular method for GA.
    Method
    Applying Cytoscape software 3.4.0 and String Database, the PPI network was constructed for 200 genes. Based on centrality parameters, the critical nodes were screened. Gene ontology of the key proteins for pathway analysis and molecular function processing were done and the highlighted pathways and activities were discussed.
    Results
    The results indicated that among 200 initial genes, 141 one were included in a main connected network. Seven crucial proteins including tumor protein p53, epidermal growth factor receptor, albumin, v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian), v-akt murine thymoma viral oncogene homolog 1, v-src sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog (avian) and catenin (cadherin-associated protein), beta 1, 88kDa , and Myogenic differentiation 1, were introduced as key nodes of the network. These identified proteins are mostly involved in pathways and activities related to cancer.
    Conclusion
    In conclusion, the finding is corresponding to the significant roles of these introduced proteins in GA disease. This protein panel may be a useful probe for diagnostic proposes in management of GA.
  • Behta Keshavarz, Pakseresht, Seyed Ataollah Sadat Shandiz, Fahimeh Baghbani, Arani Page 29
  • Mohammad Al Kadi, Fawza Monem Page 34
    Background
    There is an accumulating evidence indicating that the inadequate immune responses are responsible for HBV persistency. Therefore, polymorphisms in genes encoding the cytokines, which are responsible for regulation of the immune response, can affect the course and outcome of the infection. The IFN-?  T/A polymorphism affects the expression of IFN-?, which shown to be crucial to HBV clearance.
    The Aim: This study aimed to investigate the association of IFN- ?  (T/A) Polymorphism with the HBV infection outcome in Syrian population. Patients and
    Methods
    In this prospective cross-sectional study, 113 samples were collected (43 healthy individuals, 69 chronic HBV patients). Genomic DNA was isolated. Sequencing and ARMS-PCR were performed to genotype the IFN-?  T/A polymorphism.
    Results
    Results of this study showed an association between IFN- ?  T/A polymorphism with the chronic HBV infection (P
    Conclusion
    Results of this study might conclude that the IFN- ?  T/A polymorphism is associated with the chronic HBV infection, according to the genetic model AA vs. AT&TT.
    Keywords: IFN, ?, Hepatitis B, Chronic, Polymorphism, Single Nucleotide, Syria
  • Abbas Esmaeelzadeh, Hassan Saadatnia, Bahram Memar, Elham Mokhtari Amirmajdi, Azita Ganji, Ladan Goshayeshi, Zahra Meshkat, Alireza Pasdar, Hassan Vosoughinia, Mohammadreza Farzanehfar, Shahrzad Tehranian, Kamran Ghaffarzadehgan, Farnood Rajabzadeh, Mitra Ahadi Page 39
    Introduction
    Chronic hepatitis B infection (CHB) is a major global health problem. Hepatitis B e antigen (HBeAg)-negative is a common type of CHB in Iran. Liver damage in HBeAg-negative CHB leads to progressive form of the liver disease with poor prognosis. Therefore, it seems necessary to perform a comprehensive evaluation of different spectrum of laboratory measurements accompanying histological findings. The aim of this study was to evaluate the association between the biochemical, virologic and histologic features in HBeAg-negative CHB. Furthermore, we assessed the application of new cut-off values for alanine aminotransferase in HBeAg-negative CHB patients.
    Materials And Methods
    HBeAg- negative CHB patients referring to hepatology clinics at Ghaem and Imam Reza hospitals during two years period were enrolled. Patients with alcohol consumption, liver mass, fatty liver and whom with positive results of Anti HDV, Anti HCV or Anti HIV were excluded. Liver enzymes were requested and Hepatitis B viral loads were measured by real time polymerase chain reaction (RT-PCR) in all patients. Liver biopsies were assessed by two expert pathologists. The relationship between viral loads, liver enzymes and histopathological features was analyzed using descriptive and analytic statistical methods.
    Results
    One hundred and fifty HBeAg-negative and HBe Ab-positive CHB patients (males=110, mean age=38.44±11.34 years) were assessed. Serum ALT levels had a significant relation with the logarithm of serum HBV-DNA levels (P
    Conclusions
    In HBeAg-negative CHB patients, serum AST levels had a better predicting value for liver necrosis and inflammation. Moreover, age could be regarded as an independent predictor of the stage of liver fibrosis. This study revealed that the new cutoff values for ALT had superiority over the conventional values to identify patients with a higher risk of liver fibrosis.
    Keywords: Hepatitis B, HBeAg, grade, stage, viral load, AST, ALT
  • Akram Ahangarpour, Ali Akbar Oroojan, Mohsen Rezaei, Mohammad Javad Khodayar, Soheila Alboghobeish, Marzieh Zeinvand Page 44
    Aim: The aim of present study was to evaluate the different doses of Butyric acid (BA) and Arsenic (As) on mouse liver mitochondria oxidative stress and pancreatic islets insulin secretion.
    Background
    BA is found in many foods and As is a toxic metal in drinking water. They can induce oxidative stress in some tissue.
    Materials And Methods
    In this experimental study, Liver mitochondria were isolated by administration of different centrifugation method and pancreatic islets of mice were isolated by a collagenase method. Mitochondria by BA (35, 75, 150, 300 ?M) and As (20, 50, 100, 200 ?M) and the islets were incubated by BA (250, 500, 1000, 1500 ?M) and As (0, 50, 100, 200 ?M) for 1 hour. At the end of experiment mitochondrial viability and membrane potential, ROS, MDA, GSH and islets insulin secretion were measured by their specific methods.
    Results
    BA and As administration increased mitochondrial levels of ROS, MDA and decreased GSH and pancreatic islet insulin secretion in a dose dependent manner (p
    Conclusion
    Alone or in combination administration of BA and As induced oxidative stress in liver mitochondria and decreased insulin secretion of pancreatic islets.
    Keywords: Butyric acid, Arsenic, Liver mitochondria, Islet
  • Soraya Moamer, Ahmad Reza Baghestani, Mohammad Amin Pourhoseingholi, Nastaran Hajizadeh, Farzaneh Ahmadi, Mohsen Norouzinia Page 54
    Aim: The aim of this study was to assess the association between survival of patients with colorectal cancer and prognostic factors in a competing risks parametric model using Weibull distribution.
    Background
    The prognosis of colorectal cancer is relatively good in terms of survival time. In many prognostic studies, patients may be exposed to several types of competing events. These different causes of death are called competing risks.
    Methods
    Data recorded from 372 patients with colorectal cancer who registered in Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences (Tehran, Iran) from 2004 to 2015 in a retrospective study. Analysis was performed using competing risks model and Weibull distribution. Software used for data analysis was R, and significance level was regarded as 0.05.
    Results
    The result indicated that, at the end of follow-up, 111 (29.8%) death was from colorectal cancer and 14 (3.8%) death was due to other diseases. The average body mass index (BMI) was 24.61(SD 3.98). The mean survival time for a patient in 372 was 62.05(SD 48.78) month with median equals to 48 months. According to competing-risks method, only stageIII ( HR, 1.69; 95% CI, 1.246-2.315 ), stageIV( HR, 4.51; 95% CI,2.91-6.99 ) and BMI( HR, 0.96; 95% CI, 0.96-0.975) have a significant effect on patient’s survival time.
    Conclusion
    This study indicated pathologic stage(III,IV) and BMI as the prognosis, using Weibull model with competing risks analysis, while other model without the competing events leads to significant predictors which may due to over-estimation.
    Keywords: Survival analysis, Competing, risks, Colorectal cancer, Weibull model
  • Reza Safdari, Elham Maserat, Hamid Asadzadeh Aghdaei, Amir Hossein Javan Amoli, Hamid Moheghegh Shalmani Page 60
  • Ainkaran Santhirasekaram, Sherif Latif, Easha Arooj, Kamran Rostami, Sauid Ishaq Page 66
    It is not clear in guidelines whether it would be is necessary to organise a CT angiogram (CTA) prior to these procedures in patients with an acute lower GI bleed. While there are studies which recommend the use of a CTA, there are other studies against using CTA in these circumstances. Here we present a case of a patient with an acute lower GI bleed who became haemodynamically unstable. We show in this case study, the catheter angiogram not being able to identify the site of bleeding without the aid of the CTA prior.
    Keywords: (GI) bleed, colonoscopy, CT angiogram, catheter angiography
  • Mosayeb Shahryar, Iraj Shahramian, Seyed Mohsen Dehghani, Noormohammad Noori, Maryam Ataollahi Page 70
  • James Alexander Nott, Asad Khan, Ravi Madhotra, George Macfaul, Kamran Rostami Page 73
  • Dominic King, David Al Dulaimi Page 75