Epidemiology and genetic epidemiology of the liver function test proteins (VSports注册入口)
- PMID: 19209234
- PMCID: VSports app下载 - PMC2636884
- DOI: V体育2025版 - 10.1371/journal.pone.0004435
Epidemiology and genetic epidemiology of the liver function test proteins
Abstract
Background: The liver function test (LFT) is among the most commonly used clinical investigations to assess hepatic function, severity of liver diseases and the effect of therapies, as well as to detect drug-induced liver injury (DILI). VSports手机版.
Aims: To determine the relative contribution of genetic and environmental factors as well as test and quantify the effects of sex, age, BMI and alcohol consumption to variation in liver function test proteins--including alanine amino transaminase (ALT), Albumin, gamma glutamyl transpeptidase (GGT), total bilirubin, total protein, total globulin, aspartate transaminase (AST), and alkaline phosphotase (ALP)--using the classical twin model. V体育安卓版.
Methods: Blood samples were collected from a total of 5380 twin pairs from the TwinsUK registry. We measured the expression levels of major proteins associated with the LFT, calculated BMI from measured weight and height and questionnaires were completed for alcohol consumption by the twins. The relative contribution of genetic and environmental factors to variation in the LFT proteins was assessed and quantified using a variance components model fitting approach V体育ios版. .
Results: Our results show that (1) variation in all the LFTs has a significant heritable basis (h(2) ranging from 20% to 77%); (2) other than GGT, the LFTs are all affected to some extent by common environmental factors (c(2) ranging from 24% to 54%); and (3) a small but significant proportion of the variation in the LFTs was due to confounding effects of age, sex, BMI, and alcohol use. VSports最新版本.
Conclusions: Variation in the LFT proteins is under significant genetic and common environmental control although sex, alcohol use, age and BMI also contribute significantly to inter-individual variation in the LFT proteins. Understanding the underlying genetic contribution of liver function tests may help the interpretation of their results and explain wide variation among individuals V体育平台登录. .
Conflict of interest statement
V体育安卓版 - References
-
- Lazo M, Selvin E, Clark JM. Brief communication: clinical implications of short-term variability in liver function test results. Ann Intern Med. 2008;148:348–52. - PubMed
-
- Sheehan M, Haythorn P. Predictive values of various liver function tests with respect to the diagnosis of liver disease. Clin Biochem. 1979;12:262–3. - PubMed
-
- Drivdal M, Trydal TA, Bergstad I, et al. Prognosis, with evaluation of general biochemistry, of liver disease in lymphoedema cholestasis syndrome 1 (LCS1/Aagenaes syndrome). Scand J Gastroenterol. 2006;41:465–71. - PubMed
-
- Tromm A, May B, Klein R, et al. Long-term response of primary biliary cirrhosis (stage I) to therapy with ursodeoxycholic acid. Hepatogastroenterology. 2005;52:753–6. - VSports手机版 - PubMed
-
- Shankar S, Hosking DJ. Biochemical assessment of Paget's disease of bone. J Bone Miner Res. 2006;21(suppl 2):P22–7. - PubMed
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