Publication:
Prevalence of non-alcoholic fatty liver disease (NAFLD) in a cohort of patients with type 2 diabetes: the PHIGNA-DM2 study.

dc.contributor.authorMartínez-Ortega, Antonio Jesús
dc.contributor.authorPiñar Gutiérrez, Ana
dc.contributor.authorLara-Romero, Carmen
dc.contributor.authorRemón Ruiz, Pablo Jesús
dc.contributor.authorAmpuero-Herrojo, Javier
dc.contributor.authorde Lara-Rodríguez, Irene
dc.contributor.authorRomero-Gómez, Manuel
dc.contributor.authorGarcía Luna, Pedro P
dc.contributor.authorSoto-Moreno, Alfonso
dc.date.accessioned2023-05-03T14:31:54Z
dc.date.available2023-05-03T14:31:54Z
dc.date.issued2022
dc.description.abstractBackground: type 2 diabetes (T2D) is a risk factor for nonalcoholic fatty liver disease (NAFLD). Objective: to evaluate the prevalence of NAFLD in a cohort of patients with T2D. Methods: an observational, descriptive study performed between May 2018 and December 2019 at the Endocrinology and Nutrition Unit. The χ² test was performed for qualitative variables and a non-parametric test for the comparison of medians of quantitative variables. Steatosis degree was defined by the coefficient attenuated parameter (CAP): (S0: 288 dB/m) or stiffness: F0-F1: 15 kPa, using transient elastography (TE) (FibroScan®). A univariate analysis was performed and subsequently a multivariate analysis with statistically significant variables used to study the predictive factors of intense steatosis and advanced fibrosis. Results: n = 104 patients with T2D; 84 (80.7 %) were obese. TE demonstrated advanced fibrosis in 20 % and intense steatosis (S3) in more than 50 %. Lower total bilirubin (OR: 0.028; 95 % CI: (0.002-0.337); p = 0.005) was found to be an independent factor for S3 steatosis in the multivariate analysis. BMI ((OR: 1.497; 95 % CI: (1.102-2.034); p = 0.01)) was a predictive factor for advanced fibrosis in a multivariate analysis. Conclusions: NAFLD-associated intense steatosis and NAFLD-associated fibrosis were commonly found in patients with T2DM and obesity. Diabetic patients should be screened for liver disease as one more target organ.
dc.identifier.doi10.20960/nh.03969
dc.identifier.essn1699-5198
dc.identifier.pmid36134588
dc.identifier.unpaywallURLhttps://doi.org/10.20960/nh.03969
dc.identifier.urihttp://hdl.handle.net/10668/21761
dc.issue.number5
dc.journal.titleNutricion hospitalaria
dc.journal.titleabbreviationNutr Hosp
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number1012-1018
dc.pubmedtypeJournal Article
dc.pubmedtypeObservational Study
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectDiabetes de tipo 2. Diabetes mellitus. Enfermedad de hígado graso no alcohólico. Fibrosis hepática. Esteatosis hepática. Elastografía.
dc.subject.meshBilirubin
dc.subject.meshDiabetes Mellitus, Type 2
dc.subject.meshFibrosis
dc.subject.meshHumans
dc.subject.meshLiver
dc.subject.meshLiver Cirrhosis
dc.subject.meshNon-alcoholic Fatty Liver Disease
dc.subject.meshObesity
dc.subject.meshPrevalence
dc.titlePrevalence of non-alcoholic fatty liver disease (NAFLD) in a cohort of patients with type 2 diabetes: the PHIGNA-DM2 study.
dc.title.alternativePrevalencia de la hepatopatía grasa no alcohólica (HGNA) en una cohorte de pacientes con diabetes de tipo 2: el estudio PHIGNA-DM2.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number39
dspace.entity.typePublication

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