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Dive into the research topics where Anastasia Kourikou is active.

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Featured researches published by Anastasia Kourikou.


World Journal of Gastrointestinal Endoscopy | 2011

Endoscopic ultrasonography for gastric submucosal lesions

Ioannis S. Papanikolaou; Konstantinos Triantafyllou; Anastasia Kourikou; Thomas Rösch

Gastric submucosal tumors (SMTs) are a rather frequent finding, occurring in about 0.36% of routine upper GI-endoscopies. EUS has emerged as a reliable investigative procedure for evaluation of these lesions. Diagnostic Endoscopic ultrasonography (EUS) has the ability to differentiate intramural tumors from extraluminal compressions and can also show the layer of origin of gastric SMTs. Tumors can be further characterized by their layer of origin, echo pattern and margin. EUS-risk criteria of their malignant potential are presented, although the emergence of EUS-guided fne needle aspiration (EUS-FNA) has opened new indications for transmural tissue diagnosis and expanded the possibilities of EUS in SMTs of the stomach. Tissue diagnosis should address whether the SMT is a Gastrointestinal stromal tumour (GIST) or another tumor type and evaluate the malignant potential of a given GIST. However, there seems to be a lack of data on the optimal strategy in SMTs suspected to be GISTs with a negative EUS-FNA tissue diagnosis. The current management strategies, as well as open questions regarding their treatment are also presented.


Hepatology | 2017

The risk of hepatocellular carcinoma decreases after the first 5 years of entecavir or tenofovir in Caucasians with chronic hepatitis B

George V. Papatheodoridis; Ramazan Idilman; George N. Dalekos; Maria Buti; Heng Chi; Florian van Boemmel; Jose Luis Calleja; Vana Sypsa; John Goulis; Spilios Manolakopoulos; A. Loglio; Spyros I. Siakavellas; Onur Keskin; Nikolaos K. Gatselis; Bettina E. Hansen; Maria Lehretz; Juan de la Revilla; Savvoula Savvidou; Anastasia Kourikou; Ioannis Vlachogiannakos; Kostantinos Galanis; Cihan Yurdaydin; T. Berg; Massimo Colombo; Rafael Esteban; Harry L.A. Janssen; P. Lampertico

Whether there is a change of hepatocellular carcinoma (HCC) incidence in chronic hepatitis B patients under long‐term therapy with potent nucleos(t)ide analogues is currently unclear. We therefore assessed the HCC incidence beyond year 5 of entecavir/tenofovir (ETV/TDF) therapy and tried to determine possible factors associated with late HCC occurrence. This European, 10‐center, cohort study included 1,951 adult Caucasian chronic hepatitis B patients without HCC at baseline who received ETV/TDF for ≥1 year. Of them, 1,205 (62%) patients without HCC within the first 5 years of therapy have been followed for 5‐10 (median, 6.8) years. HCCs have been diagnosed in 101/1,951 (5.2%) patients within the first 5 years and 17/1,205 (1.4%) patients within 5‐10 years. The yearly HCC incidence rate was 1.22% within and 0.73% after the first 5 years (P = 0.050). The yearly HCC incidence rate did not differ within and after the first 5 years in patients without cirrhosis (0.49% versus 0.47%, P = 0.931), but it significantly declined in patients with cirrhosis (3.22% versus 1.57%, P = 0.039). All HCCs beyond year 5 developed in patients older than 50 years at ETV/TDF onset. Older age, lower platelets at baseline and year 5, and liver stiffness ≥12 kPa at year 5 were independently associated with more frequent HCC development beyond year 5 in multivariable analysis. No patient with low Platelets, Age, Gender‐Hepatitis B score at baseline or year 5 developed HCC. Conclusion: The HCC risk decreases beyond year 5 of ETV/TDF therapy in Caucasian chronic hepatitis B patients, particularly in those with compensated cirrhosis; older age (especially ≥50 years), lower platelets, and liver stiffness ≥12 kPa at year 5 represent the main risk factors for late HCC development. (Hepatology 2017;66:1444–1453).


World Journal of Gastroenterology | 2015

Gene polymorphisms associated with functional dyspepsia

Anastasia Kourikou; George Karamanolis; George Dimitriadis; Konstantinos Triantafyllou

Functional dyspepsia (FD) is a constellation of functional upper abdominal complaints with poorly elucidated pathophysiology. However, there is increasing evidence that susceptibility to FD is influenced by hereditary factors. Genetic association studies in FD have examined genotypes related to gastrointestinal motility or sensation, as well as those related to inflammation or immune response. G-protein b3 subunit gene polymorphisms were first reported as being associated with FD. Thereafter, several gene polymorphisms including serotonin transporter promoter, interlukin-17F, migration inhibitory factor, cholecystocynine-1 intron 1, cyclooxygenase-1, catechol-o-methyltransferase, transient receptor potential vanilloid 1 receptor, regulated upon activation normal T cell expressed and secreted, p22PHOX, Toll like receptor 2, SCN10A, CD14 and adrenoreceptors have been investigated in relation to FD; however, the results are contradictory. Several limitations underscore the value of current studies. Among others, inconsistencies in the definitions of FD and controls, subject composition differences regarding FD subtypes, inadequate samples, geographical and ethnical differences, as well as unadjusted environmental factors. Further well-designed studies are necessary to determine how targeted genes polymorphisms, influence the clinical manifestations and potentially the therapeutic response in FD.


Hepatology | 2018

Significance of definitions of relapse after discontinuation of oral antivirals in HBeAg‐negative chronic hepatitis B

George V. Papatheodoridis; Spilios Manolakopoulos; Tung-Hung Su; Spyros I. Siakavellas; Chun-Jen Liu; Anastasia Kourikou; Hung-Chih Yang; Jia-Horng Kao

Relapses are observed in most hepatitis B e antigen (HBeAg)‐negative chronic hepatitis B patients who discontinue treatment with nucleos(t)ide analogues (NAs); however, the rates of relapse vary widely among studies, and whether all patients with relapse need retreatment is unclear. The aim of this study was to assess the impact of different definitions on the rates of posttreatment relapse and therefore on the probability of retreatment in patients who have discontinued effective long‐term NA therapy. In total, 130 HBeAg‐negative chronic hepatitis B patients without cirrhosis and before NA treatment were included. All had on‐therapy virological remission for ≥24 months and close follow‐up for ≥12 months after stopping NA treatment or until retreatment, which started on stringent predefined criteria. Relapses rates based on several predetermined definitions of virological and perhaps biochemical criteria were assessed. The median duration of therapy was 60 months and the median duration of on‐therapy virological remission was 43 months. During a median off‐NAs follow‐up of 15 months, no patient experienced liver decompensation or died. Cumulative relapse rates were 2%‐49%, 4%‐73%, 11%‐82%, and 16%‐90% at 3, 6, 12, and 24 months, respectively, whereas cumulative retreatment rates were 15%, 22%, and 40% at 6, 12, and 24 months, respectively, after discontinuation of NA therapy. No patient characteristic was independently associated with the probability of relapse based on at least two definitions or of retreatment. Conclusion: In HBeAg‐negative chronic hepatitis B patients who discontinue NA therapy, the definition of relapse has a great impact on off‐NAs relapse rates and potentially on the probability of retreatment. Regardless of definition, off‐NAs relapses cannot be easily predicted by patient characteristics. A substantial proportion of such patients may not require retreatment if stringent criteria are adopted. (Hepatology 2017).


Liver International | 2017

Hepatitis B s antigen kinetics during treatment with nucleos(t)ides analogues in patients with hepatitis B e antigen‐negative chronic hepatitis B

Athanasia Striki; Spilios Manolakopoulos; Melanie Deutsch; Anastasia Kourikou; George Kontos; Hariklia Kranidioti; Emilia Hadziyannis; George V. Papatheodoridis

Serum hepatitis B s antigen (HBsAg) levels might be used as a predictor of virological breakthrough or of sustained off‐treatment virological response in hepatitis B e antigen (HBeAg)‐negative chronic hepatitis B (CHB) patients. We evaluated the changes of HBsAg in those patients under nucleos(t)ide analogue(s) [NA(s)] therapy for ≥12 months.


Journal of Hepatology | 2018

Eight-year survival in chronic hepatitis B patients under long-term entecavir or tenofovir therapy is similar to the general population

George V. Papatheodoridis; Vana Sypsa; George N. Dalekos; Cihan Yurdaydin; Florian van Boemmel; Maria Buti; John Goulis; Jose Luis Calleja; Heng Chi; Spilios Manolakopoulos; A. Loglio; Spyros I. Siakavellas; Nikolaos K. Gatselis; Onur Keskin; Maria Lehretz; Savvoula Savvidou; Juan de la Revilla; Bettina E. Hansen; Anastasia Kourikou; Ioannis Vlachogiannakos; Kostantinos Galanis; Ramazan Idilman; Massimo Colombo; Rafael Esteban; Harry L.A. Janssen; T. Berg; P. Lampertico

BACKGROUND & AIMS The effects of long-term antiviral therapy on survival have not been adequately assessed in chronic hepatitis B (CHB). In this 10-centre, ongoing cohort study, we evaluated the probability of survival and factors affecting survival in Caucasian CHB patients who received long-term entecavir/tenofovir therapy. METHODS We included 1,951 adult Caucasians with CHB, with or without compensated cirrhosis and without hepatocellular carcinoma (HCC) at baseline, who received entecavir/tenofovir for ≥12 months (median, six years). Kaplan-Meier estimates of cumulative survival over time were obtained. Standardized mortality ratios (SMRs) were calculated by comparing death rates with those in the Human Mortality Database. RESULTS The one-, five-, and eight-year cumulative probabilities were 99.7, 95.9, and 94.1% for overall survival, 99.9, 98.3, and 97.4% for liver-related survival, and 99.9, 97.8, and 95.8% for transplantation-free liver-related survival, respectively. Overall mortality was independently associated with older age and HCC development, liver-related mortality was associated with HCC development only, and transplantation-free liver-related mortality was independently associated with HCC development and lower platelet levels at baseline. Baseline cirrhosis was not independently associated with any type of mortality. Compared with the general population, in all CHB patients mortality was not significantly different (SMR 0.82), whereas it was lower in patients without HCC regardless of baseline cirrhosis (SMR 0.58) and was higher in patients who developed HCC (SMR 3.09). CONCLUSION Caucasian patients with CHB and compensated liver disease who receive long-term entecavir/tenofovir therapy have excellent overall and liver-related eight-year survival, which is similar to that of the general population. HCC is the main factor affecting their overall mortality, and is the only factor affecting their liver-related mortality. LAY SUMMARY Caucasian patients with chronic hepatitis B with or without compensated cirrhosis who receive long-term entecavir or tenofovir therapy have excellent overall eight-year survival, which is similar to that of the general population. Hepatocellular carcinoma is the main factor affecting their overall mortality, and is the only factor affecting liver-related mortality in this setting.


Obesity Facts | 2012

Intragastric balloon left in the stomach for more than a year: two case reports.

Athanasios D. Sioulas; Dimitrios Polymeros; Anastasia Kourikou; Ioannis S. Papanikolaou; Konstantinos Triantafyllou

Objective: Intragastric balloon (IGB) is often used to achieve short-term weight reduction in morbidly obese patients. It is placed endoscopically for a 6-month-period either in the pre-bariatric surgery setting and also in cases where no bariatric surgery is planned. Prolonged implantation may be accompanied by serious complications. Case Reports: We herein report two cases of extraction of intact IGBs long time after their placement. Conclusion: Although no adverse events were observed, adherence to manufacturers’ recommendations is definitely suggested.


Endoscopy | 2012

Fatal perforation with subcutaneous emphysema complicating ERCP.

Iosif Beintaris; Dimitrios Polymeros; Ι. S. Papanikolaou; C. Kontopoulou; Anastasia Kourikou; Athanasios D. Sioulas; N. G. Danias; George Dimitriadis; Konstantinos Triantafyllou


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Journal of Hepatology | 2017

POSTER PRESENTATIONS: Posters Friday, 21 April 2017: Viral hepatitis: Hepatitis C – Clinical (therapy)FRI-209 - Platelets represent an independent predictor of sustained virological response (SVR) in patients with advanced chronic hepatitis C (CHC) treated with current direct acting antiviral(s) (DAA). HERACLIS: Hellenic multicenter real-life cohort study

George V. Papatheodoridis; A. Kapatais; E. Sinakos; I. Elefsiniotis; John Goulis; Melanie Deutsch; John Vlachogiannakos; George N. Dalekos; John Koskinas; S. Karatapanis; M. Schina; Emanuel K. Manesis; I. Ketikoglou; V. Sevastianos; Christos Triantos; Evangelos Cholongitas; M.-V. Papageorgiou; Anastasia Kourikou; T. Karaoulani; E. Evangelidou; A. Koukoufiki; D. Karagiannakis; Nikolaos K. Gatselis; M. Tampaki; G. Ntetskas; C. Tsolias; T. Voulgaris; P. Ioannidou; Evangelos Akriviadis; Spilios Manolakopoulos

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George V. Papatheodoridis

National and Kapodistrian University of Athens

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Konstantinos Triantafyllou

National and Kapodistrian University of Athens

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Evangelos Akriviadis

Aristotle University of Thessaloniki

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John Vlachogiannakos

National and Kapodistrian University of Athens

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