External validation of the fatty liver index and lipid accumulation product indices, using 1H-magnetic resonance spectroscopy, to identify hepatic steatosis in healthy controls and obese, insulin-resistant individuals

被引:139
作者
Cuthbertson, Daniel J. [1 ,2 ]
Weickert, Martin O. [3 ,4 ,5 ]
Lythgoe, Daniel [6 ]
Sprung, Victoria S. [1 ,2 ]
Dobson, Rebecca [1 ,2 ]
Shoajee-Moradie, Fariba [7 ]
Umpleby, Margot [7 ]
Pfeiffer, Andreas F. H. [8 ,9 ]
Thomas, E. Louise [10 ]
Bell, Jimmy D. [10 ]
Jones, Helen [11 ]
Kemp, Graham J. [12 ]
机构
[1] Aintree Univ Hosp NHS Fdn Trust, Ctr Clin Sci, Dept Obes & Endocrinol, Liverpool L9 7AL, Merseyside, England
[2] Univ Liverpool, Inst Ageing & Chron Dis, Dept Obes & Endocrinol, Liverpool L9 7AL, Merseyside, England
[3] Univ Hosp Coventry, Warwickshire Inst Study Diabet Endocrinol & Metab, Coventry, W Midlands, England
[4] Warwickshire NHS Trust, Coventry, W Midlands, England
[5] Univ Warwick, Warwick Med Sch, Div Metab & Vasc Hlth, Warwick, England
[6] Univ Liverpool, Canc Res UK Liverpool Canc Trials Unit, Liverpool L69 3BX, Merseyside, England
[7] Univ Surrey, Fac Hlth & Med Sci, Dept Diabet & Metab Med, Guildford GU2 5XH, Surrey, England
[8] German Inst Human Nutr, Dept Clin Nutr, Potsdam, Germany
[9] Charite, Dept Endocrinol Diabet & Nutr, D-13353 Berlin, Germany
[10] Univ London Imperial Coll Sci Technol & Med, MRC, Ctr Clin Sci, Metab & Mol Imaging Grp, London, England
[11] Liverpool John Moores Univ, Res Inst Sport & Exercise Sci, Liverpool L3 5UX, Merseyside, England
[12] Univ Liverpool, Magnet Resonance & Image Anal Res Ctr, Inst Ageing & Chron Dis, Dept Musculoskeletal Biol, Liverpool L69 3BX, Merseyside, England
关键词
CARDIOVASCULAR-DISEASE; TRIGLYCERIDE CONTENT; METABOLIC SYNDROME; INCREASED RISK; PREVALENCE; POPULATION;
D O I
10.1530/EJE-14-0112
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: Simple clinical algorithms including the fatty liver index (FLI) and lipid accumulation product (LAP) have been developed as surrogate markers for non-alcoholic fatty liver disease (NAFLD), constructed using (semi-quantitative) ultrasonography. This study aimed to validate FLI and LAP as measures of hepatic steatosis, as determined quantitatively by proton magnetic resonance spectroscopy (H-1-MRS). Methods: Data were collected from 168 patients with NAFLD and 168 controls who had undergone clinical, biochemical and anthropometric assessment. Values of FLI and LAP were determined and assessed both as predictors of the presence of hepatic steatosis (liver fat>5.5%) and of actual liver fat content, as measured by H-1-MRS. The discriminative ability of FLI and LAP was estimated using the area under the receiver operator characteristic curve (AUROC). As FLI can also be interpreted as a predictive probability of hepatic steatosis, we assessed how well calibrated it was in our cohort. Linear regression with prediction intervals was used to assess the ability of FLI and LAP to predict liver fat content. Further validation was provided in 54 patients with type 2 diabetes mellitus. Results: FLI, LAP and alanine transferase discriminated between patients with and without steatosis with an AUROC of 0.79 (IQR=0.74, 0.84), 0.78 (IQR=0.72, 0.83) and 0.83 (IQR=0.79, 0.88) respectively although could not quantitatively predict liver fat. Additionally, the algorithms accurately matched the observed percentages of patients with hepatic steatosis in our cohort. Conclusions: FLI and LAP may be used to identify patients with hepatic steatosis clinically or for research purposes but could not predict liver fat content.
引用
收藏
页码:561 / 569
页数:9
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