Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/143897
Campo DC Valoridioma
dc.contributor.authorGarcía Cantón, Césaren_US
dc.contributor.authorRivero, Yaizaen_US
dc.contributor.authorBosch, Elviraen_US
dc.contributor.authorBatista, Fatimaen_US
dc.contributor.authorGonzalez-Martin, Jesus M.en_US
dc.contributor.authorGonzalez, Seleneen_US
dc.contributor.authorGuinea, Soniaen_US
dc.contributor.authorTugores, Antonioen_US
dc.contributor.authorAladro, Saraen_US
dc.contributor.authorAfonso, Saraen_US
dc.contributor.authorFernandez, Sauloen_US
dc.contributor.authorHernandez, Domingoen_US
dc.contributor.authorBoronat Cortés, Mauroen_US
dc.date.accessioned2025-07-28T10:15:29Z-
dc.date.available2025-07-28T10:15:29Z-
dc.date.issued2025en_US
dc.identifier.issn1660-8151en_US
dc.identifier.otherWoS-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/143897-
dc.description.abstractIntroduction: Metabolic dysfunction-associated fatty liver disease (MAFLD) is a prevalent liver condition commonly associated with obesity, metabolic syndrome, and type 2 diabetes mellitus. It has also been linked to an increased risk of cardiovascular events and overall mortality. Recent studies have established pathophysiological connections between MAFLD and chronic kidney disease (CKD). This study aimed to determine the prevalence of MAFLD in patients with advanced chronic kidney disease (ACKD), identify associated factors, and evaluate its impact on patient survival. Methods: A retrospective longitudinal cohort study was conducted with incident patients diagnosed with stage 4 or 5 CKD, not on dialysis, who initiated care for ACKD between 2011 and 2015. Clinical and laboratory data were collected, and the presence of MAFLD was estimated using the Fatty Liver Index (FLI). To assess the impact of FLI and other variables on survival, Kaplan-Meier univariate analysis and Cox regression multivariate analysis were performed, with follow-up through February 2024. Results: Among 367 patients, 60.2% had diabetes, and 70.8% had an FLI >= 60. Age and diabetes mellitus were significant factors associated with a higher likelihood of FLI >= 60. FLI was identified as an independent risk factor for decreased survival in patients with diabetes, after adjusting for other variables (HR, 1.015; 95% CI 1.004-1.027; p = 0.009). However, in non-diabetic patients, FLI was not a significant predictor of lower survival in multivariate Cox regression analysis. Conclusions: MAFLD is highly prevalent in patients with ACKD, particularly among those with diabetes, for whom it may represent an independent risk factor for reduced survival. This association was not observed in non-diabetic ACKD patients. These results suggest the need to design preventive and treatment strategies for MAFLD in this population.en_US
dc.languageengen_US
dc.relation.ispartofNephron - Clinical Practiceen_US
dc.sourceNephron [ISSN 1660-8151], (2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject320506 Nefrologíaen_US
dc.subject.otherRisken_US
dc.subject.otherMetabolic Dysfunction-Associated Fatty Liver Diseaseen_US
dc.subject.otherAdvanced Chronic Kidney Diseaseen_US
dc.subject.otherDiabetes Mellitusen_US
dc.subject.otherSurvival Analysisen_US
dc.titleMetabolic Dysfunction-Associated Fatty Liver Disease in Advanced Chronic Kidney Disease: Impact on Patient Survivalen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1159/000546525en_US
dc.identifier.isi001530099500001-
dc.identifier.eissn2235-3186-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid48757643-
dc.contributor.daisngid13623802-
dc.contributor.daisngid5213281-
dc.contributor.daisngid19429132-
dc.contributor.daisngid29494273-
dc.contributor.daisngid22364616-
dc.contributor.daisngid79018277-
dc.contributor.daisngid79109766-
dc.contributor.daisngid4228804-
dc.contributor.daisngid79003911-
dc.contributor.daisngid8235762-
dc.contributor.daisngid52468985-
dc.contributor.daisngid78624882-
dc.description.numberofpages12en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Garcia-Cantón, C-
dc.contributor.wosstandardWOS:Rivero, Y-
dc.contributor.wosstandardWOS:Bosch, E-
dc.contributor.wosstandardWOS:Batista, F-
dc.contributor.wosstandardWOS:Gonzalez-Martin, JM-
dc.contributor.wosstandardWOS:González, S-
dc.contributor.wosstandardWOS:Guinea, S-
dc.contributor.wosstandardWOS:Tugores, A-
dc.contributor.wosstandardWOS:Aladro, S-
dc.contributor.wosstandardWOS:Afonso, S-
dc.contributor.wosstandardWOS:Fernandez, S-
dc.contributor.wosstandardWOS:Hernandez, D-
dc.contributor.wosstandardWOS:Boronat, M-
dc.date.coverdate2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr2,3
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds11,0
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0001-8535-8543-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameGarcía Cantón, César-
crisitem.author.fullNameBoronat Cortés, Mauro-
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