P. Janssen
Katholieke Universiteit Leuven
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Publication
Featured researches published by P. Janssen.
Alimentary Pharmacology & Therapeutics | 2011
P. Janssen; P. Vanden Berghe; Sofie Verschueren; Anders Lehmann; Inge Depoortere; Jan Tack
Aliment Pharmacol Ther 2011; 33: 880–894
Clinical Gastroenterology and Hepatology | 2012
Jan Tack; P. Janssen; Tatsuhiro Masaoka; Ricard Farré; Lukas Van Oudenhove
BACKGROUND & AIMS Impaired accommodation and hypersensitivity to gastric distention are believed to be involved in the development of functional dyspepsia (FD). Buspirone, a 5-hydroxytryptamine 1A receptor agonist, relaxes the proximal stomach in healthy individuals. We studied the effects of buspirone on symptoms and mechanisms of FD. METHODS We performed a randomized, double-blind, placebo-controlled, crossover study of 17 patients (13 women; mean age, 38.5 ± 2.4 years). The study included 2 treatment periods of 4 weeks each, separated by a 2-week washout period. In the first period, 7 participants were given buspirone (10 mg, 3 times daily for 4 weeks) and 10 were given placebo 15 minutes before meals; patients switched groups for the second period. We assessed meal-related symptoms and severity, along with gastric sensitivity, accommodation, and emptying (by using barostat and breath tests) before and after 4 weeks of treatment. RESULTS Buspirone significantly reduced the overall severity of symptoms of dyspepsia (7.5 ± 1.3 vs 11.5 ± 1.2 for placebo; P < .005) and individual symptoms of postprandial fullness, early satiation, and upper abdominal bloating, whereas placebo had no significant effect (all P < .05). Buspirone did not alter the rate of gastric emptying of solids or sensitivity to gastric distention, but it significantly increased gastric accommodation, compared with placebo (229 ± 28 vs 141 ± 32 mL, respectively; P < .05), and delayed gastric emptying of liquids (half-life = 64 ± 5 vs 119 ± 24 minutes, respectively). Adverse events were similar when patients were given buspirone or placebo. CONCLUSIONS In patients with FD, 4 weeks of administration of buspirone significantly improved symptoms and gastric accommodation, compared with placebo, whereas gastric emptying of liquids was delayed.
The American Journal of Gastroenterology | 2013
P. Janssen; M. Scott Harris; Michael P. Jones; Tatsuhiro Masaoka; Ricard Farré; Hans Törnblom; Lukas Van Oudenhove; Magnus Simren; Jan Tack
OBJECTIVES:The relationship between symptom improvement (SI) and acceleration of gastric emptying (GE) for different drugs used in the treatment of idiopathic and diabetic gastroparesis is uncertain. In this paper we examined the study-specific correlations between SI and GE, and we performed a meta-regression analysis of the association across multiple studies.METHODS:The MEDLINE database (1,946 to present) was searched, and only controlled trials or trials with an established effective comparator that compared both SI and GE were included.RESULTS:Studies were identified for metoclopramide (n=6), domperidone (n=6), cisapride (n=14), erythromycin (n=3), botulinum toxin (n=2), and levosulpiride (n=3). Even though most drugs concomitantly improved symptoms and accelerated GE, no study reported a significant correlation between SI and GE. Moreover, a correlation analysis over all studies using meta-regression did not show a significant relationship between SI and GE. Our findings need to be qualified by inconsistencies in study methods, which is a limitation but also suggests that our findings are robust to methodological factors.CONCLUSIONS:In this review, no evidence of a relationship between SI and GE was identified for different drugs used for the treatment of gastroparesis. This finding questions the use of GE measurement to direct drug development for gastroparesis.
Alimentary Pharmacology & Therapeutics | 2013
P. Janssen; Alessandra Rotondo; F. Mulé; J. Tack
Recent advancements in understanding the roles and functions of glucagon‐like peptide 1 (GLP‐1) and 2 (GLP‐2) have provided a basis for targeting these peptides in therapeutic strategies.
Neurogastroenterology and Motility | 2011
P. Janssen; Sofie Verschueren; H. Giao Ly; Robin Vos; L. Van Oudenhove; J. Tack
Background The stomach relaxes upon food intake and thereby provides a reservoir while keeping the intragastric pressure (IGP) low. We set out to determine whether we could use IGP as a measurement for stomach accommodation during food intake.
Alimentary Pharmacology & Therapeutics | 2011
D Ang; Nicholas J. Talley; Magnus Simren; P. Janssen; Guy E. Boeckxstaens; Jan Tack
Aliment Pharmacol Ther 2011; 33: 634–649
Alimentary Pharmacology & Therapeutics | 2010
K. Ameloot; P. Janssen; Emidio Scarpellini; Robin Vos; Werend Boesmans; Inge Depoortere; P. Vanden Berghe; J. Tack
Aliment Pharmacol Ther 31, 1123–1131
Alimentary Pharmacology & Therapeutics | 2011
P. Janssen; Hans Pottel; Robin Vos; Jan Tack
Aliment Pharmacol Ther 2011; 33: 607–614
Neurogastroenterology and Motility | 2013
A. Papathanasopoulos; A. Rotondo; P. Janssen; Werend Boesmans; Ricard Farré; P. Vanden Berghe; J. Tack
Menthol reduces intestinal motility in animal studies, an effect that is probably mediated by transient receptor potential channels. Peppermint oil (PO), with menthol as a major constituent, is widely used as a spasmolytic agent in irritable bowel syndrome. In the current study, we investigated the effect of acute PO administration on intragastric pressure (IGP) profiles and gastric sensorimotor functions in health.
Neurogastroenterology and Motility | 2012
P. Janssen; Sofie Verschueren; Jan Tack
Background Different studies indicated a correlation between intragastric pressure (IGP) and satiation. Our aim was to investigate this correlation while artificially increasing the IGP.