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  • 1
    Online Resource
    Online Resource
    Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc. | New York, NY : Elsevier Science | Oxford : Blackwell | Malden, Mass. : Wiley-Blackwell | London [u.a.] : Nature ; Nachgewiesen 93.1998 -
    UID:
    (DE-627)320426386
    Format: Online-Ressource
    ISSN: 1572-0241
    Note: Gesehen am 26.01.2024
    Additional Information: Supplement The American journal of gastroenterology. Supplements
    Additional Edition: 0002-9270
    Additional Edition: Erscheint auch als DVD-ROM-Ausgabe, 1998-2018 The American journal of gastroenterology [London] : [Springer Nature], 2019
    Additional Edition: Erscheint auch als Druck-Ausgabe The American journal of gastroenterology Hagerstown, MD : Wolters Kluwer Health, Inc., 1954 0002-9270
    Language: English
    Keywords: Zeitschrift
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  • 2
    E-Resource
    E-Resource
    [London] : [Springer Nature] ; Vol. 93, no. 1 (1998)-113 (2018)
    UID:
    (DE-627)1669217264
    Format: DVD-ROMs
    Note: Archivzeitraum nach Verlagswechsel zu WoltersKluwer (via Ovid) nur auf Anforderung bei SpringerNature als DVD-ROMs erhältlich , DVD-ROM 2 of 2 enthält außer Vol. 93, no. 1 (1998)-113 (2018) auch zum Zeitpunkt des Verlagswechsels bereits erschienene Online First-Artikel
    Additional Edition: 1572-0241
    Additional Edition: 0002-9270
    Additional Edition: Erscheint auch als Online-Ausgabe The American journal of gastroenterology Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998 1572-0241
    Additional Edition: Erscheint auch als Druck-Ausgabe The American journal of gastroenterology Hagerstown, MD : Wolters Kluwer Health, Inc., 1954 0002-9270
    Language: English
    Keywords: Zeitschrift ; DVD-ROM
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  • 3
    Journal/Serial
    Journal/Serial
    Hagerstown, MD : Wolters Kluwer Health, Inc. | New York, NY : Coll. | Baltimore, Md. : Williams & Wilkins | New York, NY : Elsevier | Malden, Mass. : Blackwell | Malden, Mass. : Wiley-Blackwell | New York, NY : Nature Publ. Group ; 21.1954 -
    UID:
    (DE-627)129933759
    Format: 28 cm
    ISSN: 0002-9270
    Additional Information: Suppl InfoPOEMs for gastroenterologist
    Additional Information: Supplement The American journal of gastroenterology / Supplements
    Additional Edition: 1572-0241
    Additional Edition: Erscheint auch als Online-Ausg The American journal of gastroenterology Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998 1572-0241
    Additional Edition: Erscheint auch als DVD-ROM-Ausgabe, 1998-2018 The American journal of gastroenterology [London] : [Springer Nature], 2019
    Former: Vorg The Review of gastroenterology
    Language: English
    Keywords: Gastroenterologie ; Krankheit ; Verdauungskanal ; Medizin ; Zeitschrift
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  • 4
    Journal/Serial
    Journal/Serial
    Hagerstown, MD : Wolters Kluwer Health, Inc. | New York, NY : Coll. | Baltimore, Md. : Williams & Wilkins | New York, NY : Elsevier | Malden, Mass. : Blackwell | Malden, Mass. : Wiley-Blackwell | New York, NY : Nature Publ. Group ; 21.1954 -
    UID:
    (DE-602)gbv_129933759
    Format: 28 cm
    ISSN: 0002-9270
    Additional Information: Suppl InfoPOEMs for gastroenterologist
    Additional Information: Supplement The American journal of gastroenterology / Supplements
    Additional Edition: ISSN 1572-0241
    Additional Edition: Erscheint auch als Online-Ausg The American journal of gastroenterology Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998 ISSN 1572-0241
    Additional Edition: Erscheint auch als DVD-ROM-Ausgabe, 1998-2018 The American journal of gastroenterology [London] : [Springer Nature], 2019
    Former: Vorg The Review of gastroenterology
    Language: English
    Keywords: Gastroenterologie ; Krankheit ; Verdauungskanal ; Medizin ; Zeitschrift
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  • 5
    Online Resource
    Online Resource
    London : Springer Nature ; Volume 1, issue 1 (July 2012)-volume 3, issue 3 (December 2016) ; damit Erscheinen eingestellt
    UID:
    (DE-627)1009610333
    Format: Online-Ressource
    ISSN: 1948-9501
    Note: Gesehen am 27.04.2020
    Additional Information: Supplement zu The American journal of gastroenterology
    Additional Edition: 1948-9498
    Additional Edition: Erscheint auch als Druck-Ausgabe The American journal of gastroenterology / Supplements New York, NY : Nature Publ. Group, 2012 1948-9498
    Language: English
    Keywords: Zeitschrift
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  • 6
    UID:
    (DE-627)1780396201
    Format: 11
    ISSN: 1572-0241
    Content: INTRODUCTION: Incidence of colorectal cancer (CRC) in young adults has been increasing in recent decades in many countries for still widely unclear reasons. Suspected candidates include increasing prevalence of overweight and obesity, but specific evidence on their role for early-onset CRC (EOCRC) is sparse. We conducted a systematic review and meta-analysis to summarize available evidence on the association of body mass index (BMI) with EOCRC. METHODS: We systematically searched PubMed, EMBASE, and Web of Science up to February 2021 for studies that evaluated the association of BMI (before diagnosis but not near diagnosis) with CRC risk and reported specific results for EOCRC. Results from studies with similar BMI groupings were summarized in meta-analyses using random-effects models. RESULTS: Twelve studies were eligible and included. Results of 6 studies were pooled in meta-analyses, which yielded a higher risk of EOCRC for overweight and obesity (BMI ≥25 kg/m2) compared with normal weight (odds ratio [OR] 1.42, 95% confidence interval [CI] 1.19-1.68). An increasing risk with increasing BMI was observed, with much higher risk for obesity (OR 1.88, 95% CI 1.40-2.54) than for overweight (OR 1.32, 95% CI 1.19-1.47). DISCUSSION: Obesity is a strong risk factor for EOCRC, and its increasing prevalence in younger generations is likely to substantially contribute to the increase in EOCRC. Efforts to limit the obesity epidemic in adolescents and younger adults may be crucial for reducing CRC incidence in future generations of adults.
    Note: Gesehen am 06.12.2021
    In: The American journal of gastroenterology, Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998, 116(2021), 11, Seite 2173-2183, 1572-0241
    In: volume:116
    In: year:2021
    In: number:11
    In: pages:2173-2183
    In: extent:11
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 7
    UID:
    (DE-627)1814705686
    Format: 12
    ISSN: 1572-0241
    Content: OBJECTIVES: Autoimmune pancreatitis (AIP) is thought to be an immune-mediated inflammatory process, directed against the epithelial components of the pancreas. The objective was to identify novel markers of disease and to unravel the pathogenesis of AIP. - METHODS: To explore key targets of the inflammatory process, we analyzed the expression of proteins at the RNA and protein level using genomics and proteomics, immunohistochemistry, western blot, and immunoassay. An animal model of AIP with LP-BM5 murine leukemia virus-infected mice was studied in parallel. RNA microarrays of pancreatic tissue from 12 patients with AIP were compared with those of 8 patients with non-AIP chronic pancreatitis. - RESULTS: Expression profiling showed 272 upregulated genes, including those encoding for immunoglobulins, chemokines and their receptors, and 86 downregulated genes, including those for pancreatic proteases such as three trypsinogen isoforms. Protein profiling showed that the expression of trypsinogens and other pancreatic enzymes was greatly reduced. Immunohistochemistry showed a near-loss of trypsin-positive acinar cells, which was also confirmed by western blotting. The serum of AIP patients contained high titers of autoantibodies against the trypsinogens PRSS1 and PRSS2 but not against PRSS3. In addition, there were autoantibodies against the trypsin inhibitor PSTI (the product of the SPINK1 gene). In the pancreas of AIP animals, we found similar protein patterns and a reduction in trypsinogen. - CONCLUSIONS: These data indicate that the immune-mediated process characterizing AIP involves pancreatic acinar cells and their secretory enzymes such as trypsin isoforms. Demonstration of trypsinogen autoantibodies may be helpful for the diagnosis of AIP.
    Note: Gesehen am 18.08.2022
    In: The American journal of gastroenterology, Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998, 105(2010), 9, Seite 2060-2071, 1572-0241
    In: volume:105
    In: year:2010
    In: number:9
    In: pages:2060-2071
    In: extent:12
    Additional Edition: Erscheint auch als Druck-Ausgabe Löhr, J.-Matthias Autoantibodies against the exocrine pancreas in autoimmune pancreatitis 2010
    Language: English
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  • 8
    UID:
    (DE-627)1750223341
    Format: 10
    ISSN: 1572-0241
    Content: INTRODUCTION: - In previous studies, the protective effect of colonoscopy was generally stronger for distal colorectal cancer than for proximal colorectal cancer (CRC). This study aimed to investigate whether reduction of CRC risk through colonoscopy varies according to major tumor markers and pathways of CRC. - METHODS: - This is a population-based case-control study from Germany, including 2,132 patients with a first diagnosis of CRC and information on major molecular tumor markers and 2,486 control participants without CRC. Detailed participant characteristics were collected by standardized questionnaires. Information on previous colonoscopy was derived from medical records. Polytomous logistic regression was used to calculate adjusted odds ratios (ORs) and 95% confidence intervals (CIs) for the association between previous colonoscopy and subtypes of CRC. - RESULTS: - Overall, we observed strong risk reduction of CRC after colonoscopy that was weaker for microsatellite instable (MSI) than for non-MSI CRC (OR 0.70, 95% CI 0.50-0.97 vs OR 0.28, 95% CI 0.24-0.33), for CpG island methylator phenotype high CRC than for CpG island methylator phenotype low/negative CRC (OR 0.45, 95% CI 0.34-0.59 vs OR 0.29, 95% CI 0.25-0.34), for BRAF-mutated than for BRAF nonmutated CRC (OR 0.62, 95% CI 0.42-0.91 vs OR 0.30, 95% CI 0.25-0.35), for KRAS nonmutated than for KRAS-mutated CRC (OR 0.34, 95% CI 0.29-0.40 vs OR 0.26, 95% CI 0.20-0.32), and for CRC classified into the sessile serrated pathway than for CRC of the traditional pathway (OR 0.57, 95% CI 0.36-0.91 vs OR 0.30, 95% CI 0.25-0.37). After colonoscopy with the detection of adenomas or hyperplastic polyps, no risk reduction was found for sessile serrated pathway CRC, MSI, and BRAF-mutated subtypes. - DISCUSSION: - Our study extends the molecular understanding of existing differences in risk reduction of proximal and distal CRCs reported by previous studies and may imply important information for improving strategies for timely detection of relevant precursors.
    Note: Gesehen am 03.03.2021
    In: The American journal of gastroenterology, Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998, 115(2020), 12, Seite 2007-2016, 1572-0241
    In: volume:115
    In: year:2020
    In: number:12
    In: pages:2007-2016
    In: extent:10
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 9
    UID:
    (DE-627)1751323382
    Format: 11
    ISSN: 1572-0241
    Content: In colorectal cancer screening, implementing risk-adapted screening might be more effective than traditional screening strategies. We aimed to compare the effectiveness of a risk-adapted screening strategy with colonoscopy and fecal immunochemical test (FIT) in colorectal cancer screening. - METHODS: - A randomized controlled trial was conducted in 6 centers in China since May 2018. Nineteen thousand five hundred forty-six eligible participants aged 50-74 years were recruited and randomly allocated into 1 of the 3 screening groups in a 1:2:2 ratio: (i) one-time colonoscopy (n = 3,916), (ii) annual FIT (n = 7,854), and (iii) annual risk-adapted screening (n = 7,776). Based on the risk-stratification score, high-risk subjects were referred for colonoscopy and low-risk ones were referred for FIT. All subjects with positive FIT were referred for diagnostic colonoscopy. The detection rate of advanced neoplasm was the primary outcome. The study is registered with the China Clinical Trial Registry (www.chictr.org.cn Identifier: ChiCTR1800015506). - RESULTS: - For baseline screening, the participation rates of the colonoscopy, FIT, and risk-adapted screening groups were 42.5% (1,665/3,916), 94.0% (7,386/7,854), and 85.2% (6,628/7,776), respectively. For the intention-to-screen analysis, the detection rates of advanced neoplasm were 2.40% (94/3,916), 1.13% (89/7,854), and 1.66% (129/7,776), with odds ratios (95% confidence intervals) of 2.16 (1.61-2.90; P 〈 0.001) for colonoscopy vs FIT, 1.45 (1.10-1.90; P 〈 0.001) for colonoscopy vs risk-adapted screening, and 1.49 (1.13-1.97; P 〈 0.001) for risk-adapted screening vs FIT, respectively. The numbers of subjects who required a colonoscopic examination to detect 1 advanced neoplasm were 18 in the colonoscopy group, 10 in the FIT group, and 11 in the risk-adapted screening group. - DISCUSSION: - For baseline screening, the risk-adapted screening approach showed a high participation rate, and its diagnostic yield was superior to that of FIT at a similarly low load of colonoscopy.
    Note: Gesehen am 03.11.2021
    In: The American journal of gastroenterology, Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998, 115(2020), 8, Seite 1264-1274, 1572-0241
    In: volume:115
    In: year:2020
    In: number:8
    In: pages:1264-1274
    In: extent:11
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 10
    UID:
    (DE-627)1726998622
    Format: 9
    ISSN: 1572-0241
    Content: OBJECTIVES: -Randomized trials have shown that annual or biannual screening by guaiac-based fecal occult blood tests (gFOBTs) reduces colorectal cancer (CRC) mortality. Few clinical studies have evaluated diagnostic performance of gFOBT through validation by colonoscopy in all participants. We aimed for a comprehensive evaluation of diagnostic performance of gFOBT by age and sex under routine screening conditions. - METHODS: -Our analysis is based on 20,884 colonoscopies following up a positive gFOBT and 182,956 primary screening colonoscopies documented in a state-wide quality assurance program in Bavaria, Germany, in 2007-2009. Positive likelihood ratios (LR+), which represent an integrative measure of diagnostic performance, were derived, by age groups (55-59, 60-64, 65-69, 70-74 years) and sex, from a joint and comparative analysis of prevalences of colorectal neoplasms in both groups. - RESULTS: -Overall LR+ (95% confidence intervals) were 1.11 (1.06-1.15), 1.80 (1.72-1.88), and 5.04 (4.64-5.47) for non-advanced adenoma, advanced adenoma, and cancer, respectively. Assuming a specificity of gFOBT of 95.2%, as recently observed in a German study among 2,235 participants of screening colonoscopy, these LR+ would translate to sensitivities of 5.3%, 8.6%, and 24.2% for the three outcomes, respectively. Diagnostic performance was similarly poor among women and men and across age groups. - CONCLUSIONS: - The performance of gFOBT under routine screening conditions is even worse than previously estimated from clinical studies. In routine screening application, gFOBTs are expected to miss more than 9 out of 10 advanced adenomas and 3 out of 4 cancers. These results underline the need and the potential for better noninvasive CRC screening tests.
    Note: Online 17 December 2013 , Gesehen am 13.08.2020
    In: The American journal of gastroenterology, Alphen aan den Rijn, The Netherlands : Wolters Kluwer Health, Inc., 1998, 109(2014), 3, Seite 427-435, 1572-0241
    In: volume:109
    In: year:2014
    In: number:3
    In: pages:427-435
    In: extent:9
    Additional Edition: Erscheint auch als Druck-Ausgabe Diagnostic performance of guaiac-based fecal occult blood test in routine screening 2014
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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