Tankut Ilter
Ege University
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Featured researches published by Tankut Ilter.
Digestive Diseases and Sciences | 2007
Zeki Karasu; Fatih Tekin; Galip Ersoz; Fulya Gunsar; Yücel Batur; Tankut Ilter; U.S. Akarca
Thrombocytopenia is a common complication of chronic liver diseases, but its pathogenesis is not clear. Although generally attributed to hypersplenism, other factors should also be considered. We investigated the relationship between the peripheral platelet count and the degree of fibrosis in patients with chronic viral hepatitis. In an effort to avoid the effects of hypersplenism, we excluded patients with splenomegaly and/or bi- or pan-cytopenia. Seven hundred eighty-four patients (265 chronic viral hepatitis C and 519 chronic viral hepatitis B) were included in the study. Univariate analysis showed that the peripheral platelet count had a negative correlation with fibrosis score, necroinflammatory activity, and age in both groups. In multivariate analysis, the peripheral platelet count had a similar correlation with the fibrosis score and age, but not with necroinflammatory activity, in both groups. The peripheral platelet count decreased more significantly in females with chronic hepatitis C but not in the chronic hepatitis B group. In conclusion, a decrease in peripheral platelet count may be a sign of an increase in the degree of fibrosis during the course of chronic viral hepatitis B and C and factors other than hypersplenism may play a role in this decrease in the peripheral platelet count.
Journal of Clinical Gastroenterology | 2007
Goktug Onder; Ahmet Aydin; U.S. Akarca; Fatih Tekin; Omer Ozutemiz; Tankut Ilter
Goals To assess the resistance of Helicobacter pylori to clarithromycin in Turkey. Background Recent studies have emphasized the remarkable reduction in H. pylori eradication rates. Resistance to clarithromycin is the most important factor affecting the success of H. pylori eradication therapies. Study The study involved 110 consecutive adult dyspeptic patients infected with H. pylori. Resistance to clarithromycin was studied by real-time polymerase chain reaction method on gastric biopsy specimens. Results Of the 110 patients, 56 (50.9%) were male and mean age (±SD) was 45.1±13.1 years. Overall, 53 (48.2%) patients were found to be resistant to clarithromycin. Resistance to clarithromycin was not statistically associated with age, sex, previous macrolide use, residence (urban/rural), education status, and presence of peptic ulcer. Conclusions The rate of resistance to clarithromycin was found to be markedly high. This result may explain the recently reported low success rates of H. pylori eradication therapies with clarithromycin.
Experimental and Toxicologic Pathology | 2010
Nevin Oruç; Omer Ozutemiz; Deniz Nart; Gül Yüce; Handan Ak Celik; Tankut Ilter
OBJECTIVE Pancreatic renin-angiotensin system has been implied to play a role in the regulation of pancreatic functions and could be a new therapeutic target in acute pancreatitis. The aim of this study was to evaluate the therapeutic potential of angiotensin-converting-enzyme inhibition by captopril and angiotensin II type 1 receptor inhibition by L-158809 and losartan experimentally in acute pancreatitis. DESIGN Rats were randomly divided into 15 groups. Acute edematous pancreatitis was induced by injection of cerulein 20microg/kg SC four times at hourly intervals. Severe necrotizing pancreatitis was induced by retrograde injection of 3% taurocholate into the biliary-pancreatic duct. INTERVENTIONS Captopril, L-158809 and losartan were given intraperitoneally. Main outcome features: pancreatic pathology, pancreatic myeloperoxidase activity and serum amylase activity were assessed. RESULTS Captopril decreased serum amylase (10,809+/-1867 vs. 4085+/-1028U/L, p<0.01), myeloperoxidase activity (3.5+/-0.5 vs. 1.5+/-0.1, p<0.05) and histopathological score (5.0+/-0.4 vs. 1.1+/-0.5, p<0.01) in acute edematous pancreatitis. In taurocholate induced severe necrotizing pancreatitis captopril ameliorated histopathological score (10.1+/-1.2 vs. 3.4+/-0.5, p<0.01), pancreatic parenchymal necrosis (4.5+/-0.6 vs. 0.0+/-0.0, p<0.001), fatty necrosis (2.8+/-0.9 vs. 0.1+/-0.1, p<0.01) and edema (2.1+/-0.3 vs. 1.4+/-0.3, p<0.05). However, L-158809 did not have similar beneficial effects on acute pancreatitis in rats while losartan decreased pancreatic parenchymal necrosis and neutrophil infiltration. CONCLUSIONS This study not only demonstrated the differential effects of captopril, losartan and L-158809 in acute pancreatitis but also showed that there is still much to investigate about pancreatic renin-angiotensin system. Inhibition of angiotensin-converting enzyme should be evaluated carefully as a potential new therapeutic target in acute pancreatitis.
European Journal of Gastroenterology & Hepatology | 2010
Murat Akyildiz; Fulya Gunsar; Deniz Nart; Osman Sahin; Funda Yilmaz; Sinan Akay; Galip Ersoz; Zeki Karasu; Tankut Ilter; Yücel Batur; Afig Berdeli; Ulus Salih Akarca
Aim To investigate the macrophage migration inhibitory factor (MIF) expression and −173 G/C polymorphism of the MIF gene in nonalcoholic fatty liver disease (NAFLD). Method Ninety-one patients with diagnosis of NAFLD and 104 healthy controls were included in the study. MIF −173 G/C polymorphism was detected using the PCR–restriction fragment length polymorphism based method. NAFLD was stratified as nonalcoholic steatohepatitis (NASH), probable NASH and steatosis, respectively in groups 1, 2 and 3, according to NAFLD Activity Score. MIF expression was detected by immunohistochemistry staining. Results Mean age of the patients was 50.1±9.6 years, and 54 of them were male. Serum alanine aminotransferase and aspartate aminotransferase were 50/83, 42/63 and 31/32, respectively in groups 1, 2 and 3, (P<0.05). Both the MIF expression of hepatocytes and mononuclear cells were more prominent in groups 1 and 2 than group 3. There was no correlation between MIF expression of hepatocytes and fibrosis stage. However, MIF expression of mononuclear cells significantly increased according to fibrosis stage (P<0.05, R : 0.2). There was no significant correlation between MIF genotype and MIF expression in the liver. Conclusion MIF expression is significantly increased especially by mononuclear cells in liver tissue of patients with NASH secondary to inflammation. Thus, it should be considered as a consequence not a causal factor.
Digestive Diseases and Sciences | 2006
Nevin Oruç; Yaman Tokat; Refik Killi; Murat Tombuloglu; Tankut Ilter
Qualitative and quantitative abnormalities of fibrinogen can result in hemostatic disorders (1). Congenital afibrinogenemia is a rare coagulation disorder transmitted as an autosomal recessive trait (2). The incidence of afibrinogenemia is 1–2 cases per million population (3). It is more common in populations with a high rate of consanguinity (3). Symptoms of afibrinogenemia vary from mild hemorrhagic events to severe bleeding episodes, though thrombotic events are very rare. We report an afibrinogenemic patient who presented with hepatic venous thrombosis at 16 years old. Evaluation of all hemostatic parameters and coagulation factors revealed no other pathology except afibrinogenemia. Paradoxically, afibrinogenemia may be a risk factor for vascular thrombotic events like Budd–Chiari Syndrome (BCS).
Journal of Gastroenterology and Hepatology | 2007
Zeki Karasu; Murat Akyildiz; Murat Kilic; Murat Zeytunlu; Unal Aydin; Fatih Tekin; Funda Yilmaz; Tijen Özacar; Ulus Salih Akarca; Galip Ersoz; Fulya Gunsar; Tankut Ilter; Michael R. Lucey
Background and Aim: Living donor liver transplantation (LDLT) has particular advantages for Turkey where hepatitis B virus (HBV) infection is the most common cause of cirrhosis, both because LDLT circumvents the difficulties encountered in the emerging world in providing deceased donor organs, and because it allows preemptive antiviral therapy. The aim of this study was to review one institutions experience with LDLT in patients with chronic HBV infection.
The Turkish journal of gastroenterology | 2015
Ilker Turan; Özden Dedeli; Serhat Bor; Tankut Ilter
BACKGROUND/AIMS Although probiotics have been extensively studied in irritable bowel syndrome, data on the impact of probiotics on chronic constipation are scarce. We aimed to evaluate the effects of kefir, which is a probiotic fermented milk product, on the symptoms, colonic transit, and bowel satisfaction scores of patients with chronic constipation. MATERIALS AND METHODS Twenty consecutive patients with functional constipation according to the Rome II criteria were divided into two groups based on their colon transit studies: 1. The normal transit (NT) group (n=10); and 2. The slow transit (ST) group (n=10). After a baseline period, 500 mL/day of a probiotic kefir beverage was administered to all patients for 4 weeks. Defecation parameters (stool frequency, stool consistency, degree of straining, laxative consumption) were recorded in diaries daily by the patients. Bowel satisfaction scores were assessed using a visual analog scale. The colon transit study was repeated in the ST group at the end of the study. RESULTS At the end of the study, the patients showed an increased stool frequency (p<0.001), improved stool consistency (p=0.014), and decreased laxative consumption (p=0.031). The degree of straining during evacuation showed a tendency to improve after kefir administration; however, this was not statistically significant (p=0.18). A repeat transit study showed an acceleration of colonic transit in the ST group (p=0.013). Bowel satisfaction scores also improved (p<0.001). CONCLUSION This pilot study shows that kefir has positive effects on the symptoms of constipation. Our results also suggest that kefir improves bowel satisfaction scores and accelerates colonic transit. Controlled trials are warranted to confirm these findings.
Digestive Diseases and Sciences | 2007
Sinan Akay; Zeki Karasu; Aysin Noyan; Semanur Pala; Ahmet Musoglu; Tankut Ilter; Yücel Batur
Although percutaneous liver biopsy (PLB) has very low mortality and morbidity rates, it often is considered painful and frightening by the patients. This study was designed to grade the intensity of pain expected before the procedure and experienced during the procedure, and whether there is any correlation between pain and the emotional state of the patient. A total of 118 consecutive patients (aged 19–68 (mean, 44) years), who were undergoing PLB for the first time, were included in the study. Visual Analogue Scale (VAS) was used before the procedure, after the procedure to grade the degree of pain expected, and the degree of the pain experienced respectively. All the patients were evaluated by a questionnaire for their personality and emotional situation by using the Minnesota Multiphasic Personality Inventory Somatization Sub-scale (MMPI-SS). Mean VAS score for expected pain before the procedure was 60±20 and for the pain experienced during the procedure was 22±16 (P < 0.0001). Although the expected pain scores of female patients were significantly higher than males (66±22 vs. 55±17; P=0.003), there was no difference between female and male patients in the experienced pain scores. The procedure of PLB is expected to be more painful than it really is by the patients, especially by females. Calming the patients by informing them about the procedure and their diseases will probably diminish the expected pain.
Digestive Diseases and Sciences | 2006
Murat Akyildiz; Ilker Turan; Omer Ozutemiz; Yücel Batur; Tankut Ilter
Upper gastrointestinal bleeding (UGIB) is a life-threatening complication of cirrhosis that develops from esophageal varices in almost 70% of patients. The mortality rate from the bleeding episodes is reported to be 30% [1–4]. Standard management of UGIB of cirrhotic patients is vasoactive therapy combined with endoscopic procedures such as endoscopic sclerotherapy and band ligation [5]. Currently, it is reported that recombinant activated fVIIa (Novoseven, NovoNordisc) can correct the prothrombin time in decompensated cirrhotic patients and also can be used safely in Childs B and C cirrhotic patients with UGIB [6–8]. Herein, we describe the first case report in the literature of a cerebrovascular event after the administration of a single dose of fVIIa in a cirrhotic patient with esophageal variceal bleeding.
Alimentary Pharmacology & Therapeutics | 2005
Fatih Tekin; Omer Ozutemiz; Tankut Ilter
Sirs, We read with interest the article by Muller et al. on the 5-aminosalicylate (5-ASA) nephrotoxicity in patients with inflammatory bowel disease (IBD). They have estimated that clinical nephrotoxicity occurs in about one in 4000 patients/year taking 5-ASA therapy. Among them, tubulointerstitial nephritis (TIN) was found to be the most common one. In cases with TIN, withdrawal of 5-ASA leads to restoration of renal function in 85% of cases where the diagnosis is made within 10 months of starting treatment, however, further delay in diagnosis is associated with poor outcome. Thus, regular monitoring of creatinine level will provide better outcome in these patients. It was recommended that in patients under 5-ASA therapy who had a normal baseline creatinine level, monitoring of renal function should be carried out monthly for the first 3 months, 3-monthly for the next 9 months and annually after 5 years of treatment. On the contrary, there exists the lack of data in the literature about the safety of 5-ASA compounds in patients with IBD and chronic renal failure (CRF). In the prospective study by Muller et al., two of 59 patients were known to have pre-existing renal impairment, however, details of these two patients (differences, if any, in dosage of 5ASA, clinical outcome, etc.) have not been mentioned. We believe that more attention may be needed for patients with CRF and IBD using 5-ASA. Patients with IBD are usually dehydrated during the acute episode because of diarrhoea. In addition, it is well known that patients with CRF are more likely to be affected by prerenal uraemia and nephrotoxic agents. Furthermore, the kidney can be an extraintestinal target of IBD, and CRF can be observed prior to starting 5-ASA therapy. Thus, we suggest that these circumstances have to be kept in mind when treatment with 5-ASA is started in patients with CRF and IBD.