Fibroscan and low-density lipoprotein as determinants of severe liver fibrosis in diabetic patients with nonalcoholic fatty liver disease.


Journal

European journal of gastroenterology & hepatology
ISSN: 1473-5687
Titre abrégé: Eur J Gastroenterol Hepatol
Pays: England
ID NLM: 9000874

Informations de publication

Date de publication:
Dec 2019
Historique:
pubmed: 29 5 2019
medline: 29 10 2020
entrez: 29 5 2019
Statut: ppublish

Résumé

Fibroscan is an effective and noninvasive tool to quantify fibrosis and steatosis in liver diseases including nonalcoholic fatty liver disease (NAFLD). Type-2-diabetes is a known risk factor for worse prognosis in NAFLD. In this study, we compare liver status in NAFDL diabetic and nondiabetic patients, identify potential risk factors, and determine the usefulness of Fibroscan in this population. The charts of all patients with NAFLD who underwent Fibroscan at our institution were reviewed. Fibroscan results, demographics, and clinical data were collected and analyzed using SPSS software. Of the 248 NAFLD patients, 73 (29.4%) were diabetic and 175 (70.6%) were nondiabetic. As detected by the NAFLD' liver stiffness measure, 35 (47.94%) diabetic patients had severe liver fibrosis (F4) in contrast to only 46 (26.3%) nondiabetics. Diabetic patients also presented more with hypertension, dyslipidemia, coronary artery disease, and chronic kidney disease. Liver steatosis, liver function tests, and noninvasive scores did not vary significantly between the two groups, except for γ-glutamyltransferase, prothrombin time-international normalized ratio, and BMI-alanine aminotransferase ratio-diabetes score. Diabetic patients had significantly lower high-density lipoproteins and low-density lipoproteins. Fibroscan results and low-density lipoprotein are potential diagnostic factors of liver fibrosis in diabetic patients with NAFLD. Further studies are necessary to verify liver fibrosis diagnostic tools and prognostic and genetic markers in diabetic patients.

Sections du résumé

BACKGROUND BACKGROUND
Fibroscan is an effective and noninvasive tool to quantify fibrosis and steatosis in liver diseases including nonalcoholic fatty liver disease (NAFLD). Type-2-diabetes is a known risk factor for worse prognosis in NAFLD. In this study, we compare liver status in NAFDL diabetic and nondiabetic patients, identify potential risk factors, and determine the usefulness of Fibroscan in this population.
PATIENTS AND METHODS METHODS
The charts of all patients with NAFLD who underwent Fibroscan at our institution were reviewed. Fibroscan results, demographics, and clinical data were collected and analyzed using SPSS software.
RESULTS RESULTS
Of the 248 NAFLD patients, 73 (29.4%) were diabetic and 175 (70.6%) were nondiabetic. As detected by the NAFLD' liver stiffness measure, 35 (47.94%) diabetic patients had severe liver fibrosis (F4) in contrast to only 46 (26.3%) nondiabetics. Diabetic patients also presented more with hypertension, dyslipidemia, coronary artery disease, and chronic kidney disease. Liver steatosis, liver function tests, and noninvasive scores did not vary significantly between the two groups, except for γ-glutamyltransferase, prothrombin time-international normalized ratio, and BMI-alanine aminotransferase ratio-diabetes score. Diabetic patients had significantly lower high-density lipoproteins and low-density lipoproteins.
CONCLUSION CONCLUSIONS
Fibroscan results and low-density lipoprotein are potential diagnostic factors of liver fibrosis in diabetic patients with NAFLD. Further studies are necessary to verify liver fibrosis diagnostic tools and prognostic and genetic markers in diabetic patients.

Identifiants

pubmed: 31135513
doi: 10.1097/MEG.0000000000001461
doi:

Substances chimiques

Biomarkers 0
Lipoproteins, LDL 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1540-1544

Commentaires et corrections

Type : CommentIn

Auteurs

Rola F Jaafar (RF)

Department of Surgery, Faculty of Medicine.

Adel M Hajj Ali (AM)

Department of Surgery, Faculty of Medicine.

Ahmad M Zaghal (AM)

Department of Surgery, Faculty of Medicine.

Mariam Kanso (M)

Department of Surgery, Faculty of Medicine.

Salim G Habib (SG)

Liver Transplantation and Hepatopancreaticobiliary Surgery, Department of General Surgery.

Adham F Halaoui (AF)

Liver Transplantation and Hepatopancreaticobiliary Surgery, Department of General Surgery.

Fady Daniel (F)

Department of Internal Medicine, Faculty of Medicine, American University of Beirut Medical Center Beirut 11-0236, Lebanon.

Farah Mokaddem (F)

Department of Surgery, Faculty of Medicine.

Mohamad J Khalife (MJ)

Department of Surgery, Faculty of Medicine.

Deborah M Mukherji (DM)

Department of Internal Medicine, Faculty of Medicine, American University of Beirut Medical Center Beirut 11-0236, Lebanon.

Walid G Faraj (WG)

Department of Surgery, Faculty of Medicine.

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Classifications MeSH