383 A COMPARISON OF FATTY LIVER INDEX WITH THREE NON-INVASIVE METHODS FOR THE DETECTION AND QUANTIFICATION OF LIVER STEATOSIS: REGULAR ULTRASOUND, HEPATORENAL ULTRASOUND INDEX AND STEATOTEST

2010 ◽  
Vol 52 ◽  
pp. S158
Author(s):  
S. Zelber-Sagi ◽  
M. Webb ◽  
M. Leshno ◽  
L. Blendis ◽  
H. Yeshua ◽  
...  
2019 ◽  
Vol 29 (Supplement_4) ◽  
Author(s):  
T Barré ◽  
C Protopopescu ◽  
F Bani-Sadr ◽  
L Piroth ◽  
P Sogni ◽  
...  

Abstract Background Thanks to innovation in treatment, people living with HIV and/or HCV now live longer but are growingly facing non-communicable disease burden. HIV-HCV co-infected patients are at high risk of metabolic complications and liver-related events, which are both associated with hepatic steatosis and its progressive form, non-alcoholic steatohepatitis (NASH), a known risk factor for mortality. The fatty liver index (FLI), a non-invasive steatosis biomarker, has recently drawn attention for its clinical prognostic value, but has never been applied to HIV-HCV co-infected patients. We aimed at testing whether elevated FLI (≥60) was associated with all-cause mortality in co-infected patients. Methods Our study is based on data from ANRS CO13 HEPAVIH, a French national prospective cohort of HIV-HCV co-infected patients. Socio-behavioral and clinical data from patients clinically followed-up were used in the analysis. Using a Cox proportional hazards model for mortality from all causes (983 patients; 4,432 visits), we computed hazard ratios associated with risk factors and confounders. Results After multiple adjustment, individuals with FLI≥60 had almost double the risk of all-cause mortality (adjusted hazard ratio [95% confidence interval]: 1.91 [1.17-3.12], p = 0.009), independently of HCV cure (0.21 [0.07-0.61], p = 0.004), advanced fibrosis (1.77 [1.00-3.14], p = 0.05), history of hepatocellular carcinoma and/or liver transplantation (7.74 [3.82-15.69], p < 10-3), history of indirect clinical signs of cirrhosis (2.80 [1.22-6.41], p = 0.015), and HIV CDC clinical stage C (2.88 [1.74-4.79], p < 10-3). Conclusions An elevated fatty liver index is a risk factor for all-cause mortality in HIV-HCV co-infected patients independently of liver fibrosis and HCV cure. In the present era of nearly 100% HCV cure rates, these findings encourage the more systematic use of non-invasive steatosis biomarkers to help identify co-infected patients with higher mortality risk. Key messages A FLI≥60 is strongly associated with mortality in HIV-HCV co-infected patients. FLI could be calculated routinely to identify most at-risk patients.


Author(s):  
Julie A. Pasco ◽  
Sophia X. Sui ◽  
Emma C. West ◽  
Kara B. Anderson ◽  
Pamela Rufus-Membere ◽  
...  

AbstractAccumulation of fat in the liver and skeletal muscle is associated with obesity and poor health outcomes. Liver steatosis is a characteristic of non-alcoholic fatty liver disease (NAFLD) and myosteatosis, of poor muscle quality in sarcopenia. In this study of 403 men (33–96 years), we investigated associations between the fatty liver index (FLI) and muscle density, as markers of fat accumulation in these organs. We also investigated associations between the FLI and parameters of sarcopenia, including DXA-derived appendicular lean mass (ALM) and handgrip strength by dynamometry. Muscle density was measured using pQCT at the radius and tibia. FLI was calculated from BMI, waist circumference, and levels of triglycerides and gamma-glutamyltransferase. There was a pattern of decreasing muscle density across increasing quartiles of FLI. After adjusting for age and lifestyle, mean radial muscle density in Q4 was 2.1% lower than Q1 (p < 0.001) and mean tibial muscle density was 1.8% lower in Q3 and 3.0% lower in Q4, compared to Q1 (p = 0.022 and < 0.001, respectively). After adjusting for age and sedentary lifestyle, participants in the highest FLI quartile were sixfold more likely to have sarcopenia. In conclusion, our results suggest that fat accumulation in the liver co-exists with fat infiltration into skeletal muscle.


2012 ◽  
Vol 7 (2) ◽  
pp. 592-599 ◽  
Author(s):  
Meredith A. Borman ◽  
Farah Ladak ◽  
Pam Crotty ◽  
Aaron Pollett ◽  
Richard Kirsch ◽  
...  

Diabetes ◽  
2019 ◽  
Vol 68 (Supplement 1) ◽  
pp. 1907-P
Author(s):  
JUANA CARRETERO GÓMEZ ◽  
JOSE CARLOS AREVALO LORIDO ◽  
RICARDO GÓMEZ-HUELGAS ◽  
JOSÉ MIGUEL SEGUÍ-RIPOLL ◽  
MANUEL SUAREZ TEMBRA ◽  
...  

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 2306-PUB
Author(s):  
YURIKO MATSUSHITA ◽  
YUTAKA HASEGAWA ◽  
NORIKO TAKEBE ◽  
YASUSHI ISHIGAKI

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