6 results on '"Farzaneh, Motamed"'
Search Results
2. Association of Interleukin-6 and Interleukin-1 Family Gene Polymorphisms in Autoimmune Hepatitis
- Author
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Azizollah Yousefi, Mehri Najafi, Farzaneh Motamed, Elham Mahmoudi, Alireza Zare Bidoki, Maryam Sadr, Farzaneh Rahmani, Fatemeh Farhmand, Ahmad Khodadad, Gholamhossein Fallahi, and Nima Rezaei
- Subjects
Chronic autoimmune hepatitis ,Single nucleotide polymorphism ,Proinflammatory cytokines ,Genetic predisposition ,Hepatocyte destruction ,Specialties of internal medicine ,RC581-951 - Abstract
Introduction and aim. Autoimmune hepatitis (AIH) is an immune-mediated destruction of liver cells, in recognition of interface hepatitis, seropositivity for autoantibodies, and interface hepatitis in histology sections. Hepatocyte destruction in AIH is the direct result of CD4+ T-cell destruction. Yet, Th17 mediated immune attach and a diversity of cytokine networks, including pro-inflammatory cytokines such as Interleukin 1 (IL-1) and Interleukin 6 (IL-6), set the stage for the destructive liver damage.Material and method. Peripheral blood samples from 57 patients, with AIH, recruited from referrals to the main pediatric hospital in Tehran. Single nucleotide polymorphisms for the following cytokines genes, were evaluated through, polymerase chain reaction with sequence-specific primers (PCR-SSP) assay: IL-1a (C/T -889), IL-Ια (C/T -511), IL-1 β (C/T +3962), IL-1 receptor (IL-1R; C/T Pst-I 1970), IL-1RA (C/T Mspa-I 11100), and IL-6 (C/G -174 and A/G nt565).Results. Significant higher frequency of genotype AA was detected in patients in IL-6 at position nt565 (15.8% in AIH patients vs. 2.9% in controls, p = 0.003). The haplotype GA of IL-6 at -174 and nt565, was significantly overrepresented in the AIH group, compared to (20.9% of AIH vs. 1.4% in controls p < 0.0001).Conclusion. Results of our study, indicate significant deviation toward high yield IL-6 polymorphisms, in AIH patients. These data could bring new insights in pathophysiology of disease, which could contribute to developing novel treatments for AIH.
- Published
- 2018
- Full Text
- View/download PDF
3. Evaluation of liver diseases in Iranian patients with primary antibody deficiencies
- Author
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Farzaneh Motamed, Asghar Aghamohammadi, Mahmoud Soltani, Mahboubeh Mansouri, Nima Rezaei, Shahram Teimourian, Nima Pouladi, Sina Abdollahzadeh, and Nima Parvaneh
- Subjects
Liver disease ,Primary antibody deficiency ,HCV infection ,Chronic active hepatitis ,Specialties of internal medicine ,RC581-951 - Abstract
Introduction. Patients with primary antibody deficiency (PAD) can complicate with liver disease. This study was performed in order to study the prevalence and causes of hepatobiliary diseases in Iranian patients with PAD.Material and methods. Sixty-two patients with PAD were followed-up and signs and symptoms of liver disease were recorded. All patients were screened for hepatitis C virus (HCV-RNA) and those patients with any sign of liver disease or gastrointestinal complaints were tested for Cryptosporidium parvum.Results. Clinical evidences of liver disease, including hepatomegaly, were documented in 22 patients (35.5%). Eight patients (13%) had clinical and/or laboratory criteria of chronic liver disease. Only one patient was HCV-RNA positive; he had stigmata of chronic liver disease and pathologic evidence of chronic active hepatitis with cirrhosis. Cryptosporidium parvum test was positive for one patient with hyper-IgM syndrome. In liver biopsy of patients with liver involvement, one had histological findings related to sclerosing cholangitis, and five had mild to moderate chronic active hepatitis with unknown reason.Conclusions. Chronic active hepatitis is the most common pathologic feature of liver injury in Iranian patients with PAD. Liver disease in PAD usually accompanies with other organ involvements and could increase the mortality of PAD. Whether this high rate of liver disease with unknown origin (75%) is the result of an unidentified hepatotropic virus or other mechanisms such as autoimmunity, is currently difficult to understand.
- Published
- 2009
- Full Text
- View/download PDF
4. Whipple surgery for eosinophilic gastroenteritis in a child
- Author
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Shokoufeh Ahmadipour and Farzaneh Motamed
- Subjects
medicine.medical_specialty ,Gastrointestinal ,lcsh:Surgery ,digestive system ,03 medical and health sciences ,0302 clinical medicine ,Eosinophilia ,medicine ,Eosinophilic gastroenteritis ,Unusual case ,medicine.diagnostic_test ,business.industry ,Esophagogastroduodenoscopy ,digestive, oral, and skin physiology ,lcsh:RJ1-570 ,lcsh:Pediatrics ,lcsh:RD1-811 ,medicine.disease ,Surgery ,Endoscopy ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Pediatrics, Perinatology and Child Health ,Duodenum ,Adhesion ,030211 gastroenterology & hepatology ,business ,Pancreas - Abstract
Herein, we present an unusual case of the involvement of pancreas and duodenum in eosinophilic gastroenteritis (EoG), revealed in esophagogastroduodenoscopy (EGD). Owing to patients’ condition and findings from endoscopy, Whipple surgery was performed to remove the part of pancreas and duodenum. Long-term therapeutic efficacy was achieved through this intervention.
- Published
- 2020
5. Association of Interleukin-6 and Interleukin-1 Family Gene Polymorphisms in Autoimmune Hepatitis
- Author
-
Nima Rezaei, Alireza Zare Bidoki, Farzaneh Rahmani, Gholamhossein Fallahi, Elham Mahmoudi, Mehri Najafi, Fatemeh Farhmand, Farzaneh Motamed, Ahmad Khodadad, Azizollah Yousefi, and Maryam Sadr
- Subjects
0301 basic medicine ,Male ,Genotype ,Specialties of internal medicine ,Single-nucleotide polymorphism ,Autoimmune hepatitis ,Iran ,Polymerase Chain Reaction ,Polymorphism, Single Nucleotide ,Chronic autoimmune hepatitis ,Proinflammatory cytokine ,03 medical and health sciences ,0302 clinical medicine ,Immune system ,Hepatocyte destruction ,Reference Values ,Confidence Intervals ,Medicine ,Humans ,Prospective Studies ,Interleukin 6 ,Child ,Proinflammatory cytokines ,Hepatology ,biology ,business.industry ,Interleukin-6 ,Genetic predisposition ,Haplotype ,Autoantibody ,Interleukin ,General Medicine ,medicine.disease ,Hospitals, Pediatric ,Single nucleotide polymorphism ,Hepatitis, Autoimmune ,030104 developmental biology ,Gene Expression Regulation ,Haplotypes ,RC581-951 ,Case-Control Studies ,Immunology ,biology.protein ,030211 gastroenterology & hepatology ,Female ,business ,Interleukin-1 - Abstract
Introduction and aim. Autoimmune hepatitis (AIH) is an immune-mediated destruction of liver cells, in recognition of interface hepatitis, seropositivity for autoantibodies, and interface hepatitis in histology sections. Hepatocyte destruction in AIH is the direct result of CD4+ T-cell destruction. Yet, Th17 mediated immune attach and a diversity of cytokine networks, including pro-inflammatory cytokines such as Interleukin 1 (IL-1) and Interleukin 6 (IL-6), set the stage for the destructive liver damage. Material and method. Peripheral blood samples from 57 patients, with AIH, recruited from referrals to the main pediatric hospital in Tehran. Single nucleotide polymorphisms for the following cytokines genes, were evaluated through, polymerase chain reaction with sequence-specific primers (PCR-SSP) assay: IL-1a (C/T -889), IL-Ια (C/T -511), IL-1 β (C/T +3962), IL-1 receptor (IL-1R; C/T Pst-I 1970), IL-1RA (C/T Mspa-I 11100), and IL-6 (C/G -174 and A/G nt565). Results. Significant higher frequency of genotype AA was detected in patients in IL-6 at position nt565 (15.8% in AIH patients vs. 2.9% in controls, p = 0.003). The haplotype GA of IL-6 at -174 and nt565, was significantly overrepresented in the AIH group, compared to (20.9% of AIH vs. 1.4% in controls p Conclusion. Results of our study, indicate significant deviation toward high yield IL-6 polymorphisms, in AIH patients. These data could bring new insights in pathophysiology of disease, which could contribute to developing novel treatments for AIH.
- Published
- 2018
6. The efficacy of a 1-week triple therapy for eradication of Helicobacter pylori infection in children.
- Author
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Mehri N, Kambiz E, Ahmad K, Fatemeh F, Farzaneh M, Hossein FG, and Fatemeh M
- Subjects
- Adolescent, Amoxicillin administration & dosage, Anti-Bacterial Agents administration & dosage, Anti-Ulcer Agents administration & dosage, Biopsy, Breath Tests, Child, Child, Preschool, Clarithromycin administration & dosage, Drug Administration Schedule, Drug Therapy, Combination, Endoscopy, Gastrointestinal, Female, Gastric Mucosa pathology, Helicobacter Infections pathology, Humans, Male, Omeprazole administration & dosage, Treatment Outcome, Amoxicillin therapeutic use, Anti-Bacterial Agents therapeutic use, Anti-Ulcer Agents therapeutic use, Clarithromycin therapeutic use, Helicobacter Infections drug therapy, Omeprazole therapeutic use
- Abstract
Background and Study Aims: Poor compliance to therapy and antibiotic resistance are the main causes for failure of anti-Helicobacter pylori (H. pylori) therapy. The purpose of this study was to assess the effectiveness of omeprazole-based triple therapy in Iranian children., Patients and Methods: Fifty-seven children with H. pylori-related gastroduodenal disease received 1-week triple therapy with a combination of omeprazole, amoxicillin and clarithromycin (according to the susceptibility test). Success of eradication was assessed by (13)C-urea breath test and endoscopy., Results: Sixty-four patients (mean age 11.3years; range 2.7-16years) were included. Eradication was successful in 84.2% (95% confidence interval, 72.8% intention to treat)., Conclusion: One-week triple therapy was effective for the eradication of H. pylori infection in children., (Copyright © 2011 Arab Journal of Gastroenterology. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2011
- Full Text
- View/download PDF
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