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Performance of non-invasive tests and histology for the prediction of clinical outcomes in patients with non-alcoholic fatty liver disease: an individual participant data meta-analysis

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dc.contributor.authorMozes, Ferenc E.-
dc.contributor.authorLee, Jenny A.-
dc.contributor.authorVali, Yasaman-
dc.contributor.authorAlzoubi, Osama-
dc.contributor.authorStaufer, Katharina-
dc.contributor.authorTrauner, Michael-
dc.contributor.authorPaternostro, Rafael-
dc.contributor.authorStauber, Rudolf E.-
dc.contributor.authorHolleboom, Adriaan G.-
dc.contributor.authorvan Dijk, Anne-Marieke-
dc.contributor.authorMak, Anne Linde-
dc.contributor.authorBoursier, Jerome-
dc.contributor.authorLoup, Marc de Saint-
dc.contributor.authorShima, Toshihide-
dc.contributor.authorBugianesi, Elisabetta-
dc.contributor.authorGaia, Silvia-
dc.contributor.authorArmandi, Angelo-
dc.contributor.authorShalimar-
dc.contributor.authorLupsor-Platon, Monica-
dc.contributor.authorWong, Vincent Wai-Sun-
dc.contributor.authorLi, Guanlin-
dc.contributor.authorWong, Grace Lai-Hung-
dc.contributor.authorCobbold, Jeremy-
dc.contributor.authorKarlas, Thomas-
dc.contributor.authorWiegand, Johannes-
dc.contributor.authorSebastiani, Giada-
dc.contributor.authorTsochatzis, Emmanuel-
dc.contributor.authorLiguori, Antonio-
dc.contributor.authorYoneda, Masato-
dc.contributor.authorNakajima, Atsushi-
dc.contributor.authorHagstrom, Hannes-
dc.contributor.authorAkbari, Camilla-
dc.contributor.authorHirooka, Masashi-
dc.contributor.authorChan, Wah-Kheong-
dc.contributor.authorMahadeva, Sanjiv-
dc.contributor.authorRajaram, Ruveena-
dc.contributor.authorZheng, Ming-Hua-
dc.contributor.authorGeorge, Jacob-
dc.contributor.authorEslam, Mohammed-
dc.contributor.authorPetta, Salvatore-
dc.contributor.authorPennisi, Grazia-
dc.contributor.authorVigano, Mauro-
dc.contributor.authorRidolfo, Sofia-
dc.contributor.authorAithal, Guruprasad Padur-
dc.contributor.authorPalaniyappan, Naaventhan-
dc.contributor.authorLee, Dae Ho-
dc.contributor.authorEkstedt, Mattias-
dc.contributor.authorNasr, Patrik-
dc.contributor.authorCassinotto, Christophe-
dc.contributor.authorde Ledinghen, Victor-
dc.contributor.authorBerzigotti, Annalisa-
dc.contributor.authorMendoza, Yuly P.-
dc.contributor.authorNoureddin, Mazen-
dc.contributor.authorTruong, Emily-
dc.contributor.authorFournier-Poizat, Celine-
dc.contributor.authorGeier, Andreas-
dc.contributor.authorMartic, Miljen-
dc.contributor.authorTuthill, Theresa-
dc.contributor.authorAnstee, Quentin M.-
dc.contributor.authorHarrison, Stephen A.-
dc.contributor.authorBossuyt, Patrick M.-
dc.contributor.authorPavlides, Michael-
dc.date.accessioned2024-01-16T12:30:55Z-
dc.date.available2024-01-16T12:30:55Z-
dc.date.issued2023-08-
dc.identifier.issn2468-1253-
dc.identifier.issn2468-1253-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/90120-
dc.description.abstractBackground Histologically assessed liver fibrosis stage has prognostic significance in patients with non-alcoholic fatty liver disease (NAFLD) and is accepted as a surrogate endpoint in clinical trials for non-cirrhotic NAFLD. Our aim was to compare the prognostic performance of non-invasive tests with liver histology in patients with NAFLD. Methods This was an individual participant data meta-analysis of the prognostic performance of histologically assessed fibrosis stage (F0-4), liver stiffness measured by vibration-controlled transient elastography (LSM-VCTE), fibrosis-4 index (FIB-4), and NAFLD fibrosis score (NFS) in patients with NAFLD. The literature was searched for a previously published systematic review on the diagnostic accuracy of imaging and simple non-invasive tests and updated to Jan 12, 2022 for this study. Studies were identified through PubMed/MEDLINE, EMBASE, and CENTRAL, and authors were contacted for individual participant data, including outcome data, with a minimum of 12 months of follow-up. The primary outcome was a composite endpoint of all-cause mortality, hepatocellular carcinoma, liver transplantation, or cirrhosis complications (ie, ascites, variceal bleeding, hepatic encephalopathy, or progression to a MELD score >= 15). We calculated aggregated survival curves for trichotomised groups and compared them using stratified log-rank tests (histology: F0-2 vs F3 vs F4; LSM: <10 vs 10 to <20 vs >= 20 kPa; FIB-4: <1<middle dot>3 vs 1<middle dot>3 to <= 2<middle dot>67 vs >2<middle dot>67; NFS: <-1<middle dot>455 vs -1<middle dot>455 to <= 0<middle dot>676 vs >0<middle dot>676), calculated areas under the time-dependent receiver operating characteristic curves (tAUC), and performed Cox proportional-hazards regression to adjust for confounding. This study was registered with PROSPERO, CRD42022312226.Findings Of 65 eligible studies, we included data on 2518 patients with biopsy-proven NAFLD from 25 studies (1126 [44<middle dot>7%] were female, median age was 54 years [IQR 44-63), and 1161 [46<middle dot>1%] had type 2 diabetes). After a median follow-up of 57 months [IQR 33-91], the composite endpoint was observed in 145 (5<middle dot>8%) patients. Stratified log-rank tests showed significant differences between the trichotomised patient groups (p<0<middle dot>0001 for all comparisons). The tAUC at 5 years were 0<middle dot>72 (95% CI 0<middle dot>62-0<middle dot>81) for histology, 0<middle dot>76 (0<middle dot>70-0<middle dot>83) for LSM-VCTE, 0<middle dot>74 (0<middle dot>64-0<middle dot>82) for FIB-4, and 0<middle dot>70 (0<middle dot>63-0<middle dot>80) for NFS. All index tests were significant predictors of the primary outcome after adjustment for confounders in the Cox regression.Interpretation Simple non-invasive tests performed as well as histologically assessed fibrosis in predicting clinical outcomes in patients with NAFLD and could be considered as alternatives to liver biopsy in some cases.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER INC-
dc.titlePerformance of non-invasive tests and histology for the prediction of clinical outcomes in patients with non-alcoholic fatty liver disease: an individual participant data meta-analysis-
dc.typeArticle-
dc.identifier.wosid001084590000001-
dc.identifier.doi10.1016/S2468-1253(23)00141-3-
dc.identifier.bibliographicCitationLANCET GASTROENTEROLOGY & HEPATOLOGY, v.8, no.8, pp 704 - 713-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-85162866470-
dc.citation.endPage713-
dc.citation.startPage704-
dc.citation.titleLANCET GASTROENTEROLOGY & HEPATOLOGY-
dc.citation.volume8-
dc.citation.number8-
dc.type.docTypeArticle-
dc.publisher.locationUnited States-
dc.subject.keywordPlusFIBROSIS STAGE-
dc.subject.keywordPlusNAFLD-
dc.subject.keywordPlusMORTALITY-
dc.subject.keywordPlusBIOPSY-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusSCORE-
dc.subject.keywordPlusTIME-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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