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Study protocol P-MAPS: microbiome as predictor of severity in acute pancreatitis-a prospective multicentre translational study.
Ammer-Herrmenau, C; Asendorf, T; Beyer, G; Buchholz, S M; Cameron, S; Damm, M; Frost, F; Henker, R; Jaster, R; Phillip, V; Placzek, M; Ratei, C; Sirtl, S; van den Berg, T; Weingarten, M J; Woitalla, J; Mayerle, J; Ellenrieder, V; Neesse, A.
Afiliação
  • Ammer-Herrmenau C; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany.
  • Asendorf T; Department of Medical Statistics, University Medical Center, Göttingen, Germany.
  • Beyer G; Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.
  • Buchholz SM; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany.
  • Cameron S; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany.
  • Damm M; Department of Medicine I, University Hospital Halle, Halle, Germany.
  • Frost F; Department of Medicine A, University Medicine Greifswald, Greifswald, Germany.
  • Henker R; Division of Gastroenterology, Medical Department II, University Hospital of Leipzig, Leipzig, Germany.
  • Jaster R; Department of Medicine II, University Hospital Rostock, Rostock, Germany.
  • Phillip V; Department of Medicine II, University Hospital rechts der Isar, Technical University Munich, Munich, Germany.
  • Placzek M; Department of Medical Statistics, University Medical Center, Göttingen, Germany.
  • Ratei C; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany.
  • Sirtl S; Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.
  • van den Berg T; Department of Medical Bioinformatics, University Medical Center, Göttingen, Germany.
  • Weingarten MJ; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany.
  • Woitalla J; Department of Medicine II, University Hospital Rostock, Rostock, Germany.
  • Mayerle J; Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.
  • Ellenrieder V; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany.
  • Neesse A; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Robert-Kochsstraße 40, 37075, Göttingen, Germany. albrecht.neesse@med.uni-goettingen.de.
BMC Gastroenterol ; 21(1): 304, 2021 Jul 31.
Article em En | MEDLINE | ID: mdl-34332533
BACKGROUND: Acute pancreatitis (AP) is an inflammatory disorder that causes a considerable economic health burden. While the overall mortality is low, around 20% of patients have a complicated course of disease resulting in increased morbidity and mortality. There is an emerging body of evidence that the microbiome exerts a crucial impact on the pathophysiology and course of AP. For several decades multiple clinical and laboratory parameters have been evaluated, and complex scoring systems were developed to predict the clinical course of AP upon admission. However, the majority of scoring systems are determined after several days and achieve a sensitivity around 70% for early prediction of severe AP. Thus, continued efforts are required to investigate reliable biomarkers for the early prediction of severity in order to guide early clinical management of AP patients. METHODS: We designed a multi-center, prospective clinical-translational study to test whether the orointestinal microbiome may serve as novel early predictor of the course, severity and outcome of patients with AP. We will recruit 400 AP patients and obtain buccal and rectal swabs within 72 h of admission to the hospital. Following DNA extraction, microbiome analysis will be performed using 3rd generation sequencing Oxford Nanopore Technologies (ONT) for 16S rRNA and metagenomic sequencing. Alpha- and beta-diversity will be determined and correlated to the revised Atlanta classification and additional clinical outcome parameters such as the length of hospital stay, number and type of complications, number of interventions and 30-day mortality. DISCUSSION: If AP patients show a distinct orointestinal microbiome dependent on the severity and course of the disease, microbiome sequencing could rapidly be implemented in the early clinical management of AP patients in the future. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04777812.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pancreatite / Microbiota Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pancreatite / Microbiota Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article