Redefining the alanine aminotransferase upper limit of normal improves the prediction of metabolic syndrome risk

被引:5
作者
Janicko, Martin [1 ]
Veseliny, Eduard [1 ]
Orencak, Radoslav [1 ]
Hust'ak, Rastislav [1 ]
Fedacko, Jan [1 ]
Drazilova, Sylvia [5 ]
Madarasova-Geckova, Andrea [2 ]
Marekova, Maria [3 ]
Pella, Daniel [1 ]
Kristian, Pavol [4 ]
Rac, Marek [1 ]
Jarcuska, Peter [1 ]
机构
[1] Pavol Jozef Safarik Univ Kosice, Dept Internal Med 1, Kosice 04011, Slovakia
[2] Pavol Jozef Safarik Univ Kosice, Dept Publ Hlth, Kosice 04011, Slovakia
[3] Pavol Jozef Safarik Univ Kosice, Dept Med Biochem, Kosice 04011, Slovakia
[4] Pavol Jozef Safarik Univ Kosice, Dept Infect Dis, Kosice 04011, Slovakia
[5] Poprad Hosp, Dept Internal Med, Poprad, Slovakia
关键词
alanine aminotransferase; metabolic syndrome; upper limit of normal; FATTY LIVER-DISEASE; TRANSAMINASE-ACTIVITY; INSULIN-RESISTANCE; KOREAN POPULATION; PREVALENCE; ALT; ATHEROSCLEROSIS; ADOLESCENTS; DEFINITION; VALUES;
D O I
10.1097/MEG.0000000000000297
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Multiple studies have recently proposed the lowering of upper limit of normal (ULN) for alanine aminotransferase (ALT) to improve the diagnostic sensitivity for viral hepatitides and metabolic syndrome (MS). We have tried to validate some of the proposed ULNs in the diagnosis of MS. Methods We used data from the HepaMeta Study conducted in 2011 in Slovakia, which explored the prevalence of MS in eastern Slovakia. Patients were tested for the criteria of MS and ALT. Different, previously published, ALT cutoffs were then used to calculate odds' ratios, sensitivity, specificity, and accuracy of MS and its components. Results Manufacturers' recommended ULN used in our institution (0.8 mu kat/l, 47 U/l for men and 0.6 mu kat/l, 35 U/l for women) failed to predict any significant risk of MS. Lowered cutoff (72% of the original ULN) identified the patients with the highest age-adjusted probability of MS (odds ratio 3.194, 95% confidence interval 1.398-7.295). ALT was significantly associated with elevated levels of triacylglycerols, hyperglycemia, and obesity. Conclusion In patients with MS, one must consider liver involvement if the patient has ALT levels in the upper third of the reference range. There is the need for discussion about the feasibility of lower ALT ULN in clinical practice. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:405 / 411
页数:7
相关论文
共 35 条
[1]   Metabolic syndrome - a new world-wide definition. A consensus statement from the international diabetes federation [J].
Alberti, KGMM ;
Zimmet, P ;
Shaw, J .
DIABETIC MEDICINE, 2006, 23 (05) :469-480
[2]   Prevalence of and risk factors for nonalcoholic fatty liver disease: The Dionysos Nutrition and Liver Study [J].
Bedogni, G ;
Miglioli, L ;
Masutti, F ;
Tiribelli, C ;
Marchesini, G ;
Bellentani, S .
HEPATOLOGY, 2005, 42 (01) :44-52
[3]  
Bergmeyer H.U., 1980, CLIN CHIM ACTA, V105, pF145
[4]   Systematic review with meta-analysis: the proportion of chronic hepatitis B patients with normal alanine transaminase ≤40 IU/L and significant hepatic fibrosis [J].
Chao, D. T. ;
Lim, J. K. ;
Ayoub, W. S. ;
Nguyen, L. H. ;
Nguyen, M. H. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2014, 39 (04) :349-358
[5]   Prospective evaluation of unexplained chronic liver transaminase abnormalities in asymptomatic and symptomatic patients [J].
Daniel, S ;
Ben-Menachem, T ;
Vasudevan, G ;
Ma, CK ;
Blumenkehl, M .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 1999, 94 (10) :3010-3014
[6]   Current therapeutic strategies in non-alcoholic fatty liver disease [J].
Dowman, J. K. ;
Armstrong, M. J. ;
Tomlinson, J. W. ;
Newsome, P. N. .
DIABETES OBESITY & METABOLISM, 2011, 13 (08) :692-702
[7]   Variability in the Upper Limit of Normal for Serum Alanine Aminotransferase Levels: A Statewide Study [J].
Dutta, Anand ;
Saha, Chandan ;
Johnson, Cynthia S. ;
Chalasani, Naga .
HEPATOLOGY, 2009, 50 (06) :1957-1962
[8]   Prevalence of elevated alanine aminotransferase among US adolescents and associated factors: NHANES 1999-2004 [J].
Fraser, Abigail ;
Longnecker, Matthew P. ;
Lawlor, Debbie A. .
GASTROENTEROLOGY, 2007, 133 (06) :1814-1820
[9]  
HAFKENSCHEID JCM, 1979, CLIN CHEM, V25, P55
[10]   Liver markers and development of the metabolic syndrome - The insulin resistance atherosclerosis study [J].
Hanley, AJG ;
Williams, K ;
Festa, A ;
Wagenknecht, LE ;
D'Agostino, RB ;
Haffner, SM .
DIABETES, 2005, 54 (11) :3140-3147