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Advanced liver fibrosis and the metabolic syndrome in a primary care setting.
Schreiner, Andrew D; Zhang, Jingwen; Durkalski-Mauldin, Valerie; Livingston, Sherry; Marsden, Justin; Bian, John; Mauldin, Patrick D; Moran, William P; Rockey, Don C.
Afiliação
  • Schreiner AD; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Zhang J; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Durkalski-Mauldin V; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Livingston S; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Marsden J; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Bian J; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Mauldin PD; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Moran WP; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Rockey DC; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
Diabetes Metab Res Rev ; 37(8): e3452, 2021 11.
Article em En | MEDLINE | ID: mdl-33759300
AIMS: The fibrosis-4 index (FIB-4) and NAFLD fibrosis score (NFS) are noninvasive and accessible methods for assessing advanced liver fibrosis risk in primary care. We evaluated the distribution of FIB-4 and NFS scores in primary care patients with clinical signals for nonalcoholic fatty liver disease (NAFLD). MATERIALS AND METHODS: This retrospective cohort study of electronic record data between 2007 and 2018 included adults with at least one abnormal aminotransferase and no known (non-NAFLD) liver disease. We calculated patient-level FIB-4 and NFS scores, the proportion of patients with mean values exceeding advanced fibrosis thresholds (indeterminate risk: FIB-4 > 1.3, NFS > -1.455; high-risk: FIB-4 > 2.67, NFS > 0.676), and the proportion of patients with a NAFLD International Classification of Diseases-9/10 code. Logistic regression models evaluated the associations of metabolic syndrome (MetS) components with elevated FIB-4 and NFS scores. RESULTS: The cohort included 6506 patients with a median of 6 (interquartile range: 3-13) FIB-4 and NFS scores per patient. Of these patients, 81% had at least two components of MetS, 29% had mean FIB-4 and NFS scores for indeterminate fibrosis risk, and 11% had either mean FIB-4 or NFS scores exceeding the high advanced fibrosis risk thresholds. Regression models identified associations of low high-density lipoprotein, hyperglycemia, Black race and male gender with high-risk FIB-4 and NFS values. Only 5% of patients had existing diagnoses for NAFLD identified. CONCLUSIONS: Many primary care patients have FIB-4 and NFS scores concerning for advanced fibrosis, but rarely a diagnosis of NAFLD. Elevated FIB-4 and NFS scores may provide signals for further clinical evaluation of liver disease in primary care settings.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome Metabólica / Hepatopatia Gordurosa não Alcoólica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome Metabólica / Hepatopatia Gordurosa não Alcoólica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article