C. Van Steenkiste
Ghent University
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Publication
Featured researches published by C. Van Steenkiste.
Journal of Viral Hepatitis | 2017
Rob Bielen; Christophe Moreno; H. Van Vlierberghe; Stefan Bourgeois; Jean-Pierre Mulkay; Thomas Vanwolleghem; W. Verlinden; C. Brixco; J. Decaestecker; C de Galocsy; F Janssens; L Van Overbeke; C. Van Steenkiste; F. D'Heygere; Mike Cool; K. Wuyckens; Frederik Nevens; Geert Robaeys
Recently, concerns were raised of high rates of HCC recurrence in patients treated with direct‐acting antivirals (DAA) for hepatitis C infection. We investigated the HCC occurrence and recurrence rates within 6 months after treatment with DAA with or without pegylated interferon (PEG‐IFN) in real life. This is a retrospective, multicenter cohort trial, executed in 15 hospitals distributed across Belgium. Populations were matched based on fibrosis score (Metavir F3‐F4). Patients with a Child‐Pugh score ≥ B were excluded. In total, 567 patients were included, of whom 77 were treated with PEG‐IFN+DAA between 2008 and 2013 and 490 with DAA without PEG‐IFN between 2013 and 2015. Patients treated with PEG‐IFN+DAA (53±9y) were younger than patients treated with DAA without PEG‐IFN (59±12y) (P=.001). 47% of patients treated with PEG‐IFN+DAA were in the F4 stage vs 67% of patients treated with DAA without PEG‐IFN (P=.001). Screening was inadequate in 20% of both patient groups (P=.664). The early occurrence rate of HCC was 1.7% and 1.1% in patients treated with DAA with and without PEG‐IFN, respectively (P=.540). The early recurrence rate was 0% in patients treated with PEG‐IFN+DAA and 15.0% in patients treated with DAA without PEG‐IFN (P=.857). There is no difference in early occurrence of new HCC between patients treated with DAA with and without PEG‐IFN. We did observe a high early recurrence rate of HCC in patients treated with DAA without PEG‐IFN. However, these patients were at baseline more at risk for HCC. Finally, in 20%, screening for HCC was inadequate.
International Journal of Obesity | 2017
Sander Lefere; F. Van De Velde; Lindsey Devisscher; Marlies Bekaert; Sarah Raevens; Xavier Verhelst; Y. Van Nieuwenhove; Marleen Praet; Anne Hoorens; C. Van Steenkiste; H. Van Vlierberghe; Bruno Lapauw; Anja Geerts
Background:Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease worldwide and is strongly associated with obesity, dyslipidemia and insulin resistance. NAFLD often presents as simple steatosis (NAFL) but can progress to non-alcoholic steatohepatitis (NASH) and fibrosis. Current non-invasive biomarkers are not tailored to identify significant (⩾F2) fibrosis, although recent guidelines recommend a stringent follow-up of this patient population. We and others have reported on the role of pathological angiogenesis in the pathogenesis of NAFLD, highlighting pro-angiogenic factors as potential diagnostic markers.Objective:To investigate the applicability of angiogenic and endothelial dysfunction markers as non-invasive diagnostic tools for NASH or NASH-associated fibrosis in obese patients.Methods:In a prospective cross-sectional study, male patients undergoing bariatric surgery (n=61) and control patients (n=35) were recruited. Serum protein levels and visceral adipose tissue gene expression of endothelial dysfunction and angiogenic markers were analyzed by multiplex bead-based assay and quantitative RT-PCR, respectively. For validation, we recruited a second cohort of patients undergoing bariatric surgery (n=40) and a cohort of NAFLD patients from our outpatient clinic (n=30).Results:We identified serum vascular cell adhesion molecule-1 (VCAM-1) as an independent predictor for ⩾F2 fibrosis (median 14.0 vs 8.7 ng ml−1 in patients with and without significant fibrosis; P<0.0001) with an area under the receiver-operating characteristics (AUROC) curve of 0.80. The cutoff point of 13.2 ng ml−1 showed a sensitivity of 80% and specificity of 83%. In line with these results, VCAM-1 visceral adipose tissue gene expression was also elevated in patients with fibrosis (P=0.030). In the bariatric surgery and clinical validation cohorts, VCAM-1 displayed similar AUROCs of 0.89 and 0.85, respectively.Conclusions:VCAM-1 levels are able to accurately predict significant (⩾F2) fibrosis in NAFLD patients.
Acta Clinica Belgica | 2014
F. de Clerck; P. Pletinckx; D. Claeys; F. Muysoms; V. Vergucht; P. Burvenich; E Vanderstraeten; Daniël Baert; Els Monsaert; K. Rasquin; G. De Cock; C. Van Steenkiste
Abstract We report the case of a 56-year-old male patient who was admitted to the emergency department with crescendo abdominal pain since 2 weeks. In the past 2 years, similar but less pronounced episodes were present, each time resolving spontaneously after spasmolytic drugs. Abdominal ultrasound revealed an ileocecal intussusception. An attempt for preoperative reduction was partially successful. A colonoscopy was performed and showed a tubulovillous adenomatous polyp with high-grade dysplasia, but subsequent right hemicolectomy revealed an underlying cecal adenocarcinoma. The combination of the low incidence and the non-specific symptoms of ileocecal intussusception in the adult makes this entity difficult to diagnose. In most cases, modern imaging techniques such as CT scan, ultrasound, or MRI make the correct preoperative diagnosis. Especially when colonic involvement is present, suspicion of a malignant lead point (i.e. culprit lesion) is primordial. The therapeutic strategy depends on several variables and asks for a patient-tailored, selective approach mostly involving surgery. Based on this case and a short review of literature, we discuss the clinical presentation, diagnostic tools, treatment, and challenges of adult ileocecal intussusception.
Journal of Hepatology | 2015
Yves-Paul Vandewynckel; Debby Laukens; Lindsey Devisscher; Annelies Paridaens; Eliene Bogaerts; Xavier Verhelst; A. Van den Bussche; Sarah Raevens; C. Van Steenkiste; M. Van Troys; Christophe Ampe; Benedicte Descamps; Chris Vanhove; Olivier Govaere; Louis Libbrecht; A. Geerts; H. Van Vlierberghe
Journal of Hepatology | 2016
Yves-Paul Vandewynckel; C. Coucke; Debby Laukens; Lindsey Devisscher; Annelies Paridaens; Eliene Bogaerts; A. Vandierendonck; Sarah Raevens; Xavier Verhelst; C. Van Steenkiste; Louis Libbrecht; Anja Geerts; H. Van Vlierberghe
Journal of Hepatology | 2017
Sarah Raevens; Annelies Paridaens; Sander Lefere; Christophe Casteleyn; Bart Jonckx; Xavier Verhelst; H. Van Vlierberghe; C. Van Steenkiste; Anja Geerts; Lindsey Devisscher; Isabelle Colle
Journal of Hepatology | 2017
Rob Bielen; Christophe Moreno; H. Van Vlierberghe; Stefan Bourgeois; Jean-Pierre Mulkay; Sven Francque; W. Verlinden; Christian Brixko; J Decaestecker; C de Galocsy; F Janssens; Mike Cool; C. Van Steenkiste; François D’Heygere; K. Wuyckens; Frederik Nevens; Geert Robaeys
Journal of Hepatology | 2008
C. Van Steenkiste; Ben Schroyen; A. Geerts; Eline Vanheule; H. Van Vlierberghe; Debby Laukens; Kim Olievier; Herwig Reynaert; Albert Geerts; Peter Carmeliet; M. De Vos; Isabelle Colle
Acta Gastro-enterologica Belgica | 2018
S. Francque; Nicolas Lanthier; Len Verbeke; Herwig Reynaert; C. Van Steenkiste; Luisa Vonghia; Wilhelmus J. Kwanten; Joost Weyler; Eric Trepo; David Cassiman; Françoise Smets; Mina Komuta; Eveline Dirinck; Etienne Danse; B Op de Beeck; E van Creanenbroeck; T Van Nieuwenhove; G. Hubens; A. Geerts; Christophe Moreno; A. Driessen
Journal of Hepatology | 2017
Sander Lefere; F. Van De Velde; Lindsey Devisscher; Marlies Bekaert; Sarah Raevens; Xavier Verhelst; Y. Van Nieuwenhove; Marleen Praet; Anne Hoorens; C. Van Steenkiste; H. Van Vlierberghe; Bruno Lapauw; Anja Geerts