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dc.contributor.authorValenzuela-Vallejo, L.-
dc.contributor.authorChrysafi, P.-
dc.contributor.authorKouvari, M.-
dc.contributor.authorGuatibonza-Garcia, V.-
dc.contributor.authorMylonakis, S. C.-
dc.contributor.authorKatsarou, A.-
dc.contributor.authorVerrastro, O.-
dc.contributor.authorMarkakis, G.-
dc.contributor.authorEslam, Mohammed-
dc.contributor.authorPapatheodoridis, G.-
dc.contributor.authorMingrone, G.-
dc.contributor.authorGeorge, Jacob-
dc.contributor.authorMantzoros, C. S.-
dc.date.accessioned2024-03-12T04:05:31Z-
dc.date.available2024-03-12T04:05:31Z-
dc.date.issued2023-
dc.identifier.citationMetabolism: Clinical and Experimental 148:155694, 2023-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9060-
dc.description.abstractBACKGROUND: The role of metabolic/inflammatory hormonal systems in metabolic dysfunction associated steatotic liver disease (MASLD) remains to be fully elucidated. Purpose(s): To report the levels of the novel total and H-specific growth differentiation factor-15 (GDF-15) and other established hormonal systems and to describe hormonal patterns in controls and patients with MASLD and its stages. METHODS: This is a multicenter study from two Gastroenterology-Hepatology Departments (Greece and Australia) and one Bariatric-Metabolic Surgery Department (Italy). Overall, n = 455 serum samples of patients with biopsy-proven MASLD (n = 374) and Controls (n = 81) were recruited. RESULTS: We report for the first time that total and H-specific GDF-15 levels are higher in MASLD, at-risk metabolic dysfunction associated steatohepatitis (MASH), and severe fibrosis than in Controls. In addition, follistatin-like-3 (FSTL-3), free insulin-like growth factor-1 (IGF-1), leptin, and insulin levels were higher in MASLD patients than in Controls, while adiponectin levels were lower in MASLD subjects than in Controls. Activin-A, follistatin (FST), FSTL-3, and insulin levels significantly increased in severe fibrosis compared to no/mild fibrosis, while free IGF-1 decreased. In addition, adiponectin levels were lower in subjects without fibrosis vs. any fibrosis. Moreover, GDF-15 presented a strong positive association for the likelihood of having MASLD and at-risk MASH, while in adjusted analyses, FST and adiponectin showed inverse associations. Two different patterns of at-risk MASH were revealed through unsupervised analysis (total variation explained=54%). The most frequent pattern met in our sample (34.3%) was characterized by higher levels of total and H-specific GDF-15, follistatins, and activins, as well as low adiponectin levels. The second pattern revealed was characterized by high levels of free IGF-1, insulin, and leptin, with low levels of activin-A and adiponectin. Similar patterns were also generated in the case of overall MASLD. CONCLUSIONS: Total and H-specific GDF-15 levels increase as MASLD severity progresses. FSTL-3, free IGF-1, leptin, and insulin are also higher, whereas adiponectin and activin-A levels are lower in the MASLD group than in Controls. Hormonal systems, including GDF-15, may not only be involved in the pathophysiology but could also prove useful for the diagnostic workup of MASLD and its stages and may potentially be of therapeutic value.-
dc.subjectHepatology-
dc.titleCirculating hormones in biopsy-proven steatotic liver disease and steatohepatitis: A multicenter observational study-
dc.typeJournal Article-
dc.identifier.doihttps://dx.doi.org/10.1016/j.metabol.2023.155694-
dc.subject.keywordsbariatric surgery-
dc.subject.keywordsdiabetes mellitus-
dc.subject.keywordsfatty liver-
dc.subject.keywordsfibrosis-
dc.subject.keywordsgastroenterology-
dc.subject.keywordsinsulin blood level-
dc.subject.keywordsmetabolic disorder-
dc.subject.keywordsnonalcoholic fatty liver-
dc.subject.keywordsnonalcoholic steatohepatitis-
dc.subject.keywordsobesity-
dc.subject.keywordsprotein expression-
dc.subject.keywordssurgery-
dc.subject.keywordsadiponectin-
dc.subject.keywordsendogenous compound-
dc.subject.keywordsfollistatin-
dc.subject.keywordsgrowth differentiation factor 15-
dc.subject.keywordshormone-
dc.subject.keywordsinsulin-
dc.subject.keywordsleptin-
dc.subject.keywordssomatomedin C-
dc.identifier.journaltitleMetabolism: Clinical and Experimental-
dc.identifier.departmentGastroenterology and Hepatology-
dc.identifier.departmentStorr Liver Centre-
dc.contributor.wslhdEslam, Mohammed-
dc.contributor.wslhdGeorge, Jacob-
dc.type.studyortrialControlled Study-
dc.type.studyortrialMajor Clinical Study-
dc.type.studyortrialMulticentre Study-
dc.identifier.pmid37757973-
dc.identifier.affiliationDepartment of Medicine, Beth-Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States-
dc.identifier.affiliationDepartment of Gastroenterology, Universita Cattolica del Sacro Cuore, Rome, Italy-
dc.identifier.affiliationDepartment of Gastroenterology, Medical School of National and Kapodistrian University of Athens, General Hospital of Athens "Laiko", Athens, Greece-
dc.identifier.affiliationStorr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Sydney, NSW, Australia-
dc.identifier.affiliationDepartment of Medicine, Boston VA Healthcare System, Boston, MA, United States-
dc.identifier.facilityBlacktown-
dc.identifier.facilityWestmead-
Appears in Collections:Blacktown Mount Druitt Hospital

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