To estimate the prevalence and risk factors for abnormal liver enzymes in a large age- and gender stratified population-based sample of apparently healthy individuals with or without alcohol consumption and other health-related risk factors (adiposity, physical inactivity, smoking).
Data on alcohol use, smoking, diet and physical activity were recorded using structured questionnaires from 13,976 subjects (6513 men, 7463 women, aged 25–74 years) in the national FINRISK studies. Alcohol data was used to categorize the participants into abstainers, light drinkers, moderate drinkers and heavy drinkers. Serum gamma-glutamyltransferase (GGT) and alanine aminotransferase (ALT) activities were measured using standard kinetic methods.
Male light drinkers, moderate drinkers and heavy drinkers showed significantly higher relative risks of abnormal GGT than abstainers: 1.37 (95% confidence interval 1.11 to 1.71, p < 0.01), 2.72 (2.08 to 3.56, p < 0.0005), and 6.10 (4.55 to 7.17, p < 0.0005), respectively. Corresponding values for women were 1.22 (0.99 to 1.51, p = 0.065), 1.90 (1.44 to 2.51, p < 0.0005), and 5.91 (3.80 to 9.17, p < 0.0005). Estimated threshold doses for a significant GGT elevation was 14 standard weekly alcohol doses for men and 7 for women. Excess body weight and age over 40 years modulated the thresholds towards smaller quantities of alcohol. The risk of abnormal GGT was also significantly influenced by physical inactivity and smoking. The relative risks of abnormal ALT activities were increased in male heavy drinkers, especially in those presenting with adiposity and sedentary lifestyle.
Citation: Niemelä O, Niemelä M, Bloigu R, Aalto M, Laatikainen T (2017) Where should the safe limits of alcohol consumption stand in light of liver enzyme abnormalities in alcohol consumers? PLoS ONE 12(12): e0188574. https://doi.org/10.1371/journal.pone.0188574
Editor: John Green, University Hospital Llandough, UNITED KINGDOM
Received: June 7, 2017; Accepted: November 9, 2017; Published: December 5, 2017
Copyright: © 2017 Niemelä et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are available for application from FINRISK at https://www.thl.fi/en/web/thl-biobank/for-researchers/apply/. The data contain potentially identifying information and are restricted by the Personal Data Act (Finlex 523/1999). The authors did not receive any special access privileges when applying for the data. Interested, qualified researchers may apply for this data in the same manner as the the authors did.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Alcohol consumption accounts for a significant proportion of life years lost to disability [1–3]. Based on scientific evidence about the harmful consequences of alcohol drinking, the definition of heavy or at-risk drinking has been rapidly evolving over the past two decades. The data gathered so far has also prompted revisions of governmental guidelines in several countries [2, 4–6]. In current societies approximately every sixth adult individual have been estimated to drink alcohol in amounts, which exceed the limits that are known to increase the risk of multiple medical problems (24 standard drinks of alcohol per week for men and 16 drinks for women) [1, 4, 5]. However, the health risks resulting from consumption of more modest amounts of alcohol and the issue of safe limits of alcohol use have remained as matters of long-standing controversy.
Recently, evidence has accumulated to indicate that even light to moderate alcohol drinking may increase the risk of certain cancers [6–8] and adverse brain outcomes in long-term follow-ups . Studies have further indicated that the activities of common liver enzymes, ALT and GGT, may increase from baseline as a result of relatively low alcohol drinking levels especially in individuals with adiposity [10–13]. With epidemic levels of both obesity and excessive alcohol intake doctors are currently encountering increasing numbers of abnormal liver function tests which may indicate silent liver disease [2, 10, 14]. The early changes in the activities of liver enzymes in such patients may also predict both hepatic and extra-hepatic health risks, including metabolic syndrome, and cardio- or cerebrovascular events [15–17]. Changes in GGT activities appear to be mechanistically linked with the activation of oxidative stress [18–20], whereas serum ALT rather marks disturbed liver cell integrity or cellular adaptation to maintain energy homeostasis [21, 22].
Recent advances in individualized medicine have also emphasized a more systematic use of biomarker data for the assessment of lifestyle and dietary interventions aimed at reducing disorders caused by hazardous drinking or excess body weight [1, 10, 23]. A more widespread use of laboratory tests has, however, been hampered by the lack of uniform definitions of biomarker normal ranges for even the most commonly used biomarkers, such as liver enzymes, and lack of knowledge on the safe limits of alcohol intake [24, 25]. There is also a paucity of studies observing the relationships between mild to moderate levels of alcohol drinking and the early-phase changes in liver enzymes in large populations stratified by key covariates [10, 25].
In the present study we collected data from a large national FINRISK population health survey to determine the relative risks of abnormal liver enzyme findings in apparently healthy individuals with detailed records on alcohol consumption, diet and other health-related behaviour, including physical activity. The recently established ULNs for liver enzymes based on abstainers with normal body weight were used as reference . The purpose of the study was to offer new perspectives on the relationships between alcohol use, adiposity, sedentary life style and liver enzyme abnormalities, which would have important implications for public health.
Materials and methods
Data was collected from a cross-sectional population health survey (The National FINRISK study) carried out in six different geographic areas in Finland in years 1997, 2002, and 2007. This survey was originally set out to examine risk factors of chronic, non-communicable diseases and modifiable behavioural risk factors. For this purpose, an age- and gender stratified random sample was drawn from the population register according to an international WHO MONICA (Monitoring trends and determinants in cardiovascular disease) protocol . The clinical examinations included physical measurements, laboratory tests and detailed questionnaires encompassing alcohol intake, current health status, diet, smoking, current physical activity, medical history and socioeconomic factors [26–28]. Body weight and height were measured to the nearest 0.1 kg and 0.1 cm, respectively. Body mass index (BMI, kg/m2) was calculated as a measure of relative body weight. Waist circumference was measured to the nearest 0.5 cm between the lowest rib and the iliac crest while the subject was at minimal respiration.
The subjects included were devoid of any clinical signs of liver disease, ischaemic heart or brain disease, diabetes or abnormal glucose tolerance test, hypertension or active infection at the time of the study. The final study population consisted of 13,976 apparently healthy individuals: 6513 men and 7463 women (mean age 45 ± 13 years, range 25–74 years) who completed the questionnaires and attended the medical examinations. The response rates in the 1997, 2002 and 2007 surveys were 73.4%, 71.4% and 66.9%, respectively. Alcohol consumption was assessed with structured questionnaires including information on the type of beverage consumed and the quantity and frequency of consumption using a retrospective recall method registering consumption from the past weeks and one year prior to blood sampling [28, 29]. The amount of ethanol in different beverages was quantitated based on defined portion sizes as follows: regular beer 12 grams (1/3 L), strong beer 15.5 grams (1/3 L), long drink 15.5 grams (1/3 L), spirit 12 grams (4 cL), wine 12 grams (12 cL) and cider 12 grams (1/3 L). A dose of 12 grams of pure ethanol was considered as one standard drink.
The data on alcohol consumption was subsequently used to categorize the population by gender and drinking habits as follows: 1. persons who reported no current alcohol consumption were referred to as non-drinkers (abstainers), 2. light drinkers consumed between 1–13 drinks (men) or 1–6 drinks (women), 3. moderate drinkers consumed 14–23 drinks (men) or 7–15 drinks (women) and 4. heavy drinkers consumed more than 23 drinks (men) or more than 15 drinks (women) per week. In the assessment of relative risks of abnormal liver enzyme activities in more detail the category of light drinkers was further separated into subgroups of very light drinkers: men < 7 (n = 2166), women < 3.5 (n = 2092) drinks per week and light drinkers men ≥ 7 and < 14 (n = 1436), women ≥ 3.5 and < 7 (n = 1200) drinks per week.
Smoking and coffee consumption were assessed with a set of standardized questions and expressed as the amount of cigarettes per day and as the intake of standard servings of coffee (cups) per day, respectively. Physical activity and the number and total time used for physical exercises were registered using structured questionnaires [28, 30]. The data was used to classify the population into the subgroups of 1. moderate or vigorous activity (over 4 hours of activity per week including brisk running, walking, cross-country skiing, swimming or other strenuous exercises) 2. light (0.5–4 hours per week including walking, cycling, gardening or other moderate activities), and 3. sedentary activity (less than 0.5 hours per week).
All surveys were conducted in accordance with the Declaration of Helsinki according to the ethical rules of the National Public Health Institute. Written informed consent was obtained from all participants. The approval for this study was received from the Coordinating Ethics Committee of the Helsinki Hospital District.
Serum ALT and GGT were measured by standard kinetic methods following recommendations of the European Committee for Clinical Laboratory Standards (ECCLS) on an Abbott Architect clinical chemistry analyser (Abbott Laboratories, Abbott Park, IL, USA).
Values are expressed as mean ± SD or mean ± 95% confidence interval (CI). Comparisons in the distribution of the data were carried out with a chi square test for trend and pr-test on the equality of proportions using Stata statistical data analysis software (StataCorp LP, TX, USA). For comparisons between groups, Student’s t-test or ANOVA with Tukey’s HSD as a post hoc test for multiple factors were used. ANOVA with Dunnett post hoc test was used to determine the threshold levels of alcohol doses for initiating a significant elevation in liver enzymes based on the data with a separate category for each weekly standard drink. Logistic regression was used to assess whether drinking status and the covariates associated with the abnormal liver enzyme levels. Both univariable and multivariable analyses were performed and the results of multivariable analyses are reported. In the analyses the participants with missing data were listwise excluded. The analyses were carried out with IBM SPSS Statistics 22.0 (Armonk, NY: IBM Corp.). A p-value < 0.05 was considered statistically significant.
The main demographic characteristics and lifestyle factors of the participants classified to subgroups according to alcohol consumption and gender are summarized in Table 1. Among men, 26.0% of the population were abstainers, 55.3% were light drinkers, 12.0% were moderate drinkers and 6.7% were heavy drinkers. In women the corresponding percentages were 41.2%, 44.1%, 12.7%, and 2.0%.
The upper normal limits used for ALT and GGT were based on previously described values defined by calculating 97.5th percentiles of the data based on normal weight non-drinkers . The amount of alcohol (mean ± SD) consumed in those exceeding the ULNs in GGT analyses in the present population was 170 ± 206 grams per week for men and 55 ± 78 grams per week for women (Table 2). For ALT, the corresponding levels were 144 ± 194 grams per week for men and 42 ± 63 grams per week for women (Table 2).
Fig 1 shows the frequencies of abnormal liver enzymes from the different subgroups classified according to drinking status. In men, abnormal GGT findings were significantly more frequent in light drinkers (10.9%) (p < 0.01), moderate drinkers (21.8%) (p < 0.001) and heavy drinkers (40.6%) (p < 0.001) than in abstainers (8.7%). In women, the likelihood of abnormal GGT findings was increased in moderate drinkers (10.6%) (p < 0.001) and in heavy drinkers (31.2%) (p < 0.001) when compared to abstainers (6.7%) or light drinkers (7.2%) (p < 0.001 for each comparison). For ALT, the group of heavy drinkers showed abnormal values more frequently than the group of abstainers (p < 0.001 for men, p < 0.01 for women) (Fig 1).
In the analyses of the incidences of abnormal liver enzyme values based on alcohol consumption reported from the past 12 months, the estimates of weekly alcohol consumption were found to be in good agreement with the estimates obtained from the data on more recent drinking (r = 0.664, p < 0.0001). The incidences of elevated liver enzymes were, however, higher in the subgroups classified as heavy drinkers based on the latter approach (Fig 1) than in the corresponding subgroups formed based on 12-mo data (GGT: 31.4% men, 26.5% women; ALT 21.1% men, 12.8% women). No significant differences occurred in the corresponding comparisons of abstainers, light drinkers or moderate drinkers. The individuals who could be classified as former drinkers (n = 314, 159 men, 155 women) reporting previous alcohol consumption but no alcohol consumption from the past 12 months showed low rates of elevated liver enzyme values (GGT: 7.1% men, 2.4% women; ALT 6.0% men, 1.4% women).
The estimated threshold alcohol doses for initiating a significant elevation in GGT activities were 14 standard drinks of weekly alcohol consumption for men and 7 drinks for women (Fig 2). Excess body weight and increasing age were found to modulate the thresholds towards smaller quantities (Fig 3).
The levels leading to GGT increases especially in those above 40 years of age are markedly lower than the current limits of heavy drinking in many Western countries (men: 24 drinks, women: 16 drinks) (dashed line).
Data are shown as median and interquartile ranges.
Table 3 summarizes the multivariable relative risks of abnormal GGT and ALT findings according to drinking habits, age, waist circumference, physical activity and smoking. When compared with abstainers, male light drinkers, moderate drinkers and heavy drinkers had relative risks of abnormal GGT activities of 1.37 (95% confidence interval 1.11 to 1.71, p < 0.01), 2.72 (2.08 to 3.56, p < 0.0005), and 6.10 (4.55 to 7.17, p < 0.0005), respectively. Corresponding values for women were 1.22 (0.99 to 1.51, p = 0.065), 1.90 (1.44 to 2.51, p < 0.0005), and 5.91 (3.80 to 9.17, p < 0.0005). When the category of light drinkers was further separated into subgroups of very light drinkers (men < 7, women < 3.5 drinks per week) and light drinkers (men ≥ 7 and < 14, women ≥ 3.5 and < 7 drinks per week) the relative risks for abnormal activities were not found to be increased in any of the comparisons among very light drinkers (data not shown).
The risk of abnormal GGT was found to be significantly influenced by age, adiposity, physical activity and smoking (Table 3). For ALT, the relative risks of abnormal activities were increased only in male heavy drinkers. Adiposity and sedentary lifestyle also increased the likelihood of abnormal ALT levels (Table 3). The individuals with low or sedentary physical activity showed markedly higher relative risks for elevated liver enzymes than those engaged in physically demanding activities for at least 3 hours per week.
The analysis of the associations between coffee consumption and the risk for elevated liver enzyme values showed that GGT activities in those classified as heavy drinkers (whereas not in other drinking categories) were also significantly influenced by coffee drinking. Heavy drinkers consuming ≥ 4 cups of coffee showed significantly lower GGT levels (men 65 ± 74 U/L, women 41 ± 76 U/L) than the corresponding groups consuming 1–3 cups (men 91 ± 90 U/L, women 62 ± 120 U/L) or no coffee (men 120 ± 171 U/L, women 76 ± 95 U/L) (p < 0.001 for comparisons in both genders).
In this large cross-sectional population-based sample of apparently healthy individuals, we showed that the relative risk of abnormal liver enzyme activities is increased in individuals consuming alcohol in amounts considered as light to moderate drinking levels. In light of recent findings indicating that the early changes in the activities of GGT and ALT should also be regarded as important prognostic markers of both hepatic and extra-hepatic health risks [17, 19, 22], it may be assumed that the risk categories of alcohol drinking and associated individual health-related behaviour need further attention.
The large number of well-characterized study subjects offered us with the possibility to perform a comprehensive analysis of the relative risks of abnormal biomarker findings across all levels of alcohol consumption and other factors of lifestyle. Our study relied largely on the data obtained from common liver enzymes, ALT and GGT, both of which are readily induced by excessive alcohol consumption and are associated with relevant clinical outcomes. These liver enzymes may also be considered biomarkers of choice since they are easily measurable, cost-effective and easy to interpret by clinicians. Although current progress in clinical laboratories and quality control regimes has led to more consistent measurement procedures, several practical problems have remained unresolved including definitions of universal normal ranges. The ULNs for even the most commonly used biomarkers for liver status, ALT and GGT, currently show significant variation between individual laboratories and geographic areas [11, 25, 31, 32]. Thus, there is a continuing need for additional biomarker validation to translate the numerical values into clinically meaningful information, which would also allow more efficient international comparisons of the data.
Over the past decades reduction of harmful alcohol drinking has been an important target for public health policies. Although heavy alcohol use is known to be causally linked to over 60 distinct diseases, the association between light to moderate drinking and the overall risk of health problems has remained unclear [1, 5]. The concepts of beneficial, safe or harmful levels of ethanol intake have also remained as topics of great interest and lively debate. While other studies have suggested that light to moderate drinking is associated with beneficial health effects especially in those following a Mediterranean diet , other groups of investigators have not reached similar conclusions [34–36]. The questions on the dose-effect relationships between ethanol intake, biomarker changes and possible tissue injury have also remained unresolved. The present data supports the view that biochemical responses in the sequence of events leading to health problems may be expected to occur even in association with light to moderate drinking levels especially in those with precipitating risk factors. Recent findings by other groups of investigators have also emphasized the view that light to moderate drinking could be associated with an elevated risk of cancer [6–8], atrial fibrillation , left ventricular diastolic dysfunction , adverse brain outcomes  and an increase in all-cause mortality . Although reductions in alcohol-attributable disease burden may obviously be expected to be achieved through a more efficient identification of high-risk individuals, alcohol-consuming patients seem rarely receive specific intervention in current clinical practice unless the situation is complicated by comorbidity.
The present data indicates that the influence of ethanol on liver enzymes is significantly driven by factors such as gender, age, excess body weight, physical inactivity or smoking, which should all be taken into account when discussing individually on the most appropriate levels of drinking. Although the primary mechanisms underlying such observations remain unknown at this time it is possible that all these conditions stimulate oxidative stress in an additive, gender- and age-dependent manner. GGT enzyme plays a pivotal role in the metabolism of glutathione (GSH), and elevated activities could sign a need to maintain intracellular GSH levels during oxidative stress [11, 15, 40–44]. While alcohol use and related harm are more prevalent in men, women seem to show elevated liver enzyme activities following consumption of smaller amounts of alcohol. In accordance with previous findings, alcohol consumption in those above 40 years of age appears to pose a higher risk towards elevated GGT levels , which could indicate a greater sensitivity towards oxidative stress upon aging or more prolonged alcohol exposure in such individuals [41, 45]. Unfortunately, quantitative data on lifetime exposure to ethanol was not available in this survey to test this hypothesis.
The presence of adiposity was also found to be an important driving force for abnormal liver enzymes. There may also be additive effects of excess body weight and alcohol use [46–48]. Recent studies have shown that the risk of non-alcoholic fatty liver disease (NAFLD) increases with both increasing levels of average daily alcohol consumption and increasing BMI . The adverse effects of ethanol on the liver are also aggravated by high-fat-diets in experimental animal models . Since in real life situations alcohol use often co-exists with obesity, synergistic health problems and metabolic comorbidities due to these two triggers may be expected to occur in an ever-increasing manner together with an increasing occurrence of abnormal liver function tests in the affected individuals [12, 13, 47, 51, 52]. Lifestyle and dietary therapies play a pivotal role in reversing the course of such conditions and consequently, there may be an increasingly important role of liver enzymes in monitoring treatment based on behavior change. There may also be emerging new applications for these enzymes as overall health indicators including health problems outside the liver . Increases in ALT and GGT levels have been shown to predict deposition of triglycerides and fat in tissues and to increase extra-hepatic health risks, such as type 2 diabetes, metabolic syndrome, insulin resistance and cardio- or cerebrovascular events [15, 17, 19, 52–58]. Due to the ability of GGT to trigger iron-dependent oxidation of LDL in coronary plaques, studies have also proposed a role for GGT as a mechanistic link between fatty liver and atherosclerosis .
Physical inactivity is an increasingly common contributor to poor health across the world [59, 60]. Here physical inactivity and sedentary behaviour were found to markedly increase the risk for elevated liver enzymes supporting also the view that improvement of metabolic health through physical exercise could serve as a therapeutic approach to provide protection from the harmful consequences of alcohol and diet-induced adverse metabolic and obesogenic effects. The individuals engaged in physically demanding activities for at least 3 hours per week showed markedly lower risks for elevated liver enzymes than those with low or sedentary activity. It remains to be established whether physical exercise could also confer long-term benefits to hepatic health and alcohol-attributable disease burden in general [61–63].
In accordance with recent data by other groups of investigators  the present observations also point to a significant synergistic effect of smoking and alcohol use in increasing GGT levels. Smoking was more common in heavy drinkers of alcohol and it appears that the combination of heavy drinking and smoking also leads to additive hepatotoxic effects, especially in men [64, 65]. In addition, coffee consumption was found to interact with alcohol consumption and GGT levels such that a high intake of coffee in heavy alcohol drinkers was more likely to be associated with lower GGT levels than those in the corresponding group of heavy drinkers consuming no coffee. This observation points to a possible protective effect of coffee drinking towards alcohol-induced liver damage [66, 67]. However, in the present material the amount of coffee intake required for significant effects in GGT activities in heavy drinkers was higher (≥ 4 cups per day) than the recent estimates for the hepatoprotective effects of coffee in U.S. National Health and Nutrition Examination Survey (≥ 3 cups per day) Xiao et al.  or in the Singapore Chinese Health study (≥ 2 cups per day) .
The primary strengths of the current study include the large number of participants, detailed assessments of risk factors, standardized evaluation of alcohol consumption and other risk profiles as well as parallel assessments in men and women. The cross-sectional setting of the survey can be kept as a limitation of this study since lack of follow-up data prevents analyses on the specific relationships between changes in liver enzyme activities and duration of drinking or indices of adiposity. It is also possible that the alcohol recall techniques may lead to underestimation of alcohol intake and overestimate the proportion of those not drinking alcohol at all [29, 69]. This would, however, rather lead to diluting effects to the observed results and the real associations and interactions might be even stronger. It should further be noted that previous studies have emphasized the importance of differentiating between former drinkers, current drinkers and abstainers in studies evaluating health-related effects of alcohol drinking . In our analyses, the individuals who could be classified as former drinkers with no alcohol consumption during the past one year prior to sampling showed low rates of abnormal values underscoring the impact of successful behavioural changes in improving liver health.
Taken together, our study provides a comprehensive assessment of the relationships between alcohol intake and risk of abnormal liver enzyme levels, which may occur even at light to moderate levels of drinking in an age-, gender-, BMI-, and physical activity dependent manner. Current data should be considered in public health recommendations and in the definition of safe limits of ethanol intake.
- 1. Connor JP, Haber PS, Hall WD. Alcohol use disorders. Lancet. 2016;387: 988–998. pmid:26343838
- 2. Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012;380: 2224–2260. pmid:23245609
- 3. Wittchen HU. The burden of mood disorders. Science. 2012;338: 15. pmid:23042853
- 4. Gunzerath L, Faden V, Zakhari S, Warren K. National Institute on Alcohol Abuse and Alcoholism report on moderate drinking. Alcohol Clin Exp Res. 2004;28: 829–847. pmid:15201626
- 5. Rehm J, Samokhvalov AV, Shield KD. Global burden of alcoholic liver diseases. J Hepatol. 2013;59: 160–168. pmid:23511777
- 6. Cao Y, Willett WC, Rimm EB, Stampfer MJ, Giovannucci EL. Light to moderate intake of alcohol, drinking patterns, and risk of cancer: results from two prospective US cohort studies. BMJ. 2015;351: h4238. pmid:26286216
- 7. Choi YJ, Myung SK, Lee JH. Light alcohol drinking and risk of cancer: a meta-analysis of cohort studies. Cancer Res Treat. 2017; Epub ahead of print. pmid:28546524
- 8. Bagnardi V, Rota M, Botteri E, Tramacere I, Islami F, Fedirko V et al. Light alcohol drinking and cancer: a meta-analysis. Ann Oncol. 2013;24: 301–308. pmid:22910838
- 9. Topiwala A, Allan CL, Valkanova V, Zsoldos E, Filippini N, Sexton C et al. Moderate alcohol consumption as risk factor for adverse brain outcomes and cognitive decline: longitudinal cohort study. BMJ. 2017;357: j2353. pmid:28588063
- 10. Niemelä O. Biomarker-based approaches for assessing alcohol use disorders. Int J Environ Res Public Health. 2016;13: 166. pmid:26828506
- 11. Danielsson J, Kangastupa P, Laatikainen T, Aalto M, Niemelä O. Impacts of common factors of life style on serum liver enzymes. World J Gastroenterol. 2014;20: 11743–11752. pmid:25206278
- 12. Alatalo PI, Koivisto HM, Hietala JP, Puukka KS, Bloigu R, Niemelä OJ. Effect of moderate alcohol consumption on liver enzymes increases with increasing body mass index. Am J Clin Nutr. 2008;88: 1097–1103. pmid:18842799
- 13. Ruhl CE, Everhart JE. Joint effects of body weight and alcohol on elevated serum alanine aminotransferase in the United States population. Clin Gastroenterol Hepatol. 2005;3: 1260–1268. pmid:16361053
- 14. Younossi ZM, Koenig AB, Abdelatif D, Fazel Y, Henry L, Wymer M. Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology. 2016;64: 73–84. pmid:26707365
- 15. Lee TH, Kim WR, Benson JT, Therneau TM, Melton LJ III. Serum aminotransferase activity and mortality risk in a United States community. Hepatology. 2008;47: 880–887. pmid:18302294
- 16. Ruhl CE, Everhart JE. Elevated serum alanine aminotransferase and gamma-glutamyltransferase and mortality in the United States population. Gastroenterology. 2009;136: 477–485. pmid:19100265
- 17. Ruttmann E, Brant LJ, Concin H, Diem G, Rapp K, Ulmer H et al. Gamma-glutamyltransferase as a risk factor for cardiovascular disease mortality: an epidemiological investigation in a cohort of 163,944 Austrian adults. Circulation. 2005;112: 2130–2137. pmid:16186419
- 18. Caro AA, Cederbaum AI. Oxidative stress, toxicology, and pharmacology of CYP2E1. Annu Rev Pharmacol Toxicol. 2004;44: 27–42. pmid:14744237
- 19. Kazemi-Shirazi L, Endler G, Winkler S, Schickbauer T, Wagner O, Marsik C. Gamma glutamyltransferase and long-term survival: is it just the liver? Clin Chem. 2007;53: 940–946. pmid:17384006
- 20. Lee DH, Blomhoff R, Jacobs DR Jr. Is serum gamma glutamyltransferase a marker of oxidative stress? Free Radic Res. 2004;38: 535–539. pmid:15346644
- 21. Gerhart-Hines Z, Rodgers JT, Bare O, Lerin C, Kim SH, Mostoslavsky R et al. Metabolic control of muscle mitochondrial function and fatty acid oxidation through SIRT1/PGC-1alpha. EMBO J. 2007;26: 1913–1923. pmid:17347648
- 22. Kim WR, Flamm SL, Di Bisceglie AM, Bodenheimer HC. Serum activity of alanine aminotransferase (ALT) as an indicator of health and disease. Hepatology. 2008;47: 1363–1370. pmid:18366115
- 23. Conigrave KM, Degenhardt LJ, Whitfield JB, Saunders JB, Helander A, Tabakoff B et al. CDT, GGT, and AST as markers of alcohol use: the WHO/ISBRA collaborative project. Alcohol Clin Exp Res. 2002;26: 332–339. pmid:11923585
- 24. Gluud C, Gluud LL. Evidence based diagnostics. BMJ. 2005;330: 724–726. pmid:15790646
- 25. Ruhl CE, Everhart JE. Upper limits of normal for alanine aminotransferase activity in the United States population. Hepatology. 2012;55: 447–454. pmid:21987480
- 26. The World Health Organization MONICA Project (Monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators. J Clin Epidemiol. 1988;41: 105–114. pmid:3335877
- 27. Kuulasmaa K, Tolonen H, Cepaitis Z, Laatikainen T, Nissinen A et al. European Health Risk Monitoring Project. Accessed from: http://www.thl.fi/ehrm/. Accessed on: June 1, 2017.
- 28. Peltonen M, Saarikoski L, Lund L, Salminen I, Laatikainen T et al. Kansallinen FINRISKI 2007 -terveystutkimus: Tutkimuksen toteutus ja tulokset: Menetelmät. Kansanterveyslaitoksen julkaisuja B36 / 2008. Accessed from: http://urn.fi/URN:ISBN:978-951-740-907-0. Accessed on: October 12, 2017.
- 29. Lemmens P, Tan ES, Knibbe RA. Measuring quantity and frequency of drinking in a general population survey: a comparison of five indices. J Stud Alcohol. 1992;53: 476–486. pmid:1405641
- 30. Männistö S, Harald K, Kontto J, Lahti-Koski M, Kaartinen NE, Saarni SE et al. Dietary and lifestyle characteristics associated with normal-weight obesity: the National FINRISK 2007 Study. Br J Nutr. 2014;111: 887–894. pmid:24229475
- 31. Mu R, Chen W, Pan B, Wang L, Hao X, Huang X et al. First definition of reference intervals of liver function tests in China: a large-population-based multi-center study about healthy adults. PLoS One. 2013;8: e72916. pmid:24058449
- 32. Rustad P, Felding P, Franzson L, Kairisto V, Lahti A, Mårtensson A et al. The Nordic Reference Interval Project 2000: recommended reference intervals for 25 common biochemical properties. Scand J Clin Lab Invest. 2004;64: 271–284. pmid:15223694
- 33. Di Castelnuovo A, Costanzo S, Bagnardi V, Donati MB, Iacoviello L, de Gaetano G. Alcohol dosing and total mortality in men and women: an updated meta-analysis of 34 prospective studies. Arch Intern Med. 2006;166: 2437–2445. pmid:17159008
- 34. Holmes MV, Dale CE, Zuccolo L, Silverwood RJ, Guo Y, Ye Z et al. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data. BMJ. 2014;349: g4164. pmid:25011450
- 35. Klatsky AL. Alcohol and cardiovascular diseases: where do we stand today? J Intern Med. 2015;278: 238–250. pmid:26158548
- 36. Stockwell T, Zhao J, Panwar S, Roemer A, Naimi T, Chikritzhs T. Do "Moderate" Drinkers Have Reduced Mortality Risk? A Systematic Review and Meta-Analysis of Alcohol Consumption and All-Cause Mortality. J Stud Alcohol Drugs. 2016;77: 185–198. pmid:26997174
- 37. McManus DD, Yin X, Gladstone R, Vittinghoff E, Vasan RS, Larson MG et al. Alcohol consumption, left atrial diameter, and atrial fibrillation. J Am Heart Assoc. 2016;5. pmid:27628571
- 38. Catena C, Colussi G, Verheyen ND, Novello M, Fagotto V, Soardo G et al. Moderate alcohol consumption is associated with left ventricular diastolic dysfunction in nonalcoholic hypertensive patients. Hypertension. 2016;68: 1208–1216. pmid:27672023
- 39. Sipilä P, Rose RJ, Kaprio J. Drinking and mortality: long-term follow-up of drinking-discordant twin pairs. Addiction. 2016;111: 245–254. pmid:26359785
- 40. Emdin M, Pompella A, Paolicchi A. Gamma-glutamyltransferase, atherosclerosis, and cardiovascular disease: triggering oxidative stress within the plaque. Circulation. 2005;112: 2078–2080. pmid:16203922
- 41. Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature. 2000;408: 239–247. pmid:11089981
- 42. Lança AJ, Israel Y. Histochemical demonstration of sinusoidal gamma-glutamyltransferase activity by substrate protection fixation: comparative studies in rat and guinea pig liver. Hepatology. 1991;14: 857–863. pmid:1718834
- 43. Speisky H, Shackel N, Varghese G, Wade D, Israel Y. Role of hepatic gamma-glutamyltransferase in the degradation of circulating glutathione: studies in the intact guinea pig perfused liver. Hepatology. 1990;11: 843–849. pmid:1971805
- 44. Zhang H, Forman HJ. Redox regulation of gamma-glutamyl transpeptidase. Am J Respir Cell Mol Biol. 2009;41: 509–515. pmid:19684307
- 45. Sturgill MG, Lambert GH. Xenobiotic-induced hepatotoxicity: mechanisms of liver injury and methods of monitoring hepatic function. Clin Chem. 1997;43: 1512–1526. pmid:9265903
- 46. Carmiel-Haggai M, Cederbaum AI, Nieto N. Binge ethanol exposure increases liver injury in obese rats. Gastroenterology. 2003;125: 1818–1833. pmid:14724834
- 47. Day CP, James OF. Steatohepatitis: a tale of two "hits"? Gastroenterology. 1998;114: 842–845. pmid:9547102
- 48. Loomba R, Bettencourt R, Barrett-Connor E. Synergistic association between alcohol intake and body mass index with serum alanine and aspartate aminotransferase levels in older adults: the Rancho Bernardo Study. Aliment Pharmacol Ther. 2009;30: 1137–1149. pmid:19737152
- 49. Lau K, Baumeister SE, Lieb W, Meffert PJ, Lerch MM, Mayerle J et al. The combined effects of alcohol consumption and body mass index on hepatic steatosis in a general population sample of European men and women. Aliment Pharmacol Ther. 2015;41: 467–476. pmid:25588768
- 50. Tsukamoto H, Horne W, Kamimura S, Niemelä O, Parkkila S, Ylä-Herttuala S et al. Experimental liver cirrhosis induced by alcohol and iron. J Clin Invest. 1995;96: 620–630. pmid:7615836
- 51. Liu B, Balkwill A, Reeves G, Beral V, Million Women Study Collaborators. Body mass index and risk of liver cirrhosis in middle aged UK women: prospective study. BMJ. 2010;340: c912. pmid:20223875
- 52. Tsai J, Ford ES, Zhao G, Li C, Greenlund KJ, Croft JB. Co-occurrence of obesity and patterns of alcohol use associated with elevated serum hepatic enzymes in US adults. J Behav Med. 2012;35: 200–210. pmid:21626151
- 53. Fraser A, Harris R, Sattar N, Ebrahim S, Davey Smith G, Lawlor DA. Alanine aminotransferase, gamma-glutamyltransferase, and incident diabetes: the British Women's Heart and Health Study and meta-analysis. Diabetes Care. 2009;32: 741–750. pmid:19131466
- 54. Ghouri N, Preiss D, Sattar N. Liver enzymes, nonalcoholic fatty liver disease, and incident cardiovascular disease: a narrative review and clinical perspective of prospective data. Hepatology. 2010;52: 1156–1161. pmid:20658466
- 55. Kozakova M, Palombo C, Eng MP, Dekker J, Flyvbjerg A, Mitrakou A et al. Fatty liver index, gamma-glutamyltransferase, and early carotid plaques. Hepatology. 2012;55: 1406–1415. pmid:22334565
- 56. Lee DH, Jacobs DR Jr, Gross M, Kiefe CI, Roseman J, Lewis CE et al. Gamma-glutamyltransferase is a predictor of incident diabetes and hypertension: the Coronary Artery Risk Development in Young Adults (CARDIA) Study. Clin Chem. 2003;49: 1358–1366. pmid:12881453
- 57. Lee DH, Silventoinen K, Hu G, Jacobs DR Jr, Jousilahti P, Sundvall J et al. Serum gamma-glutamyltransferase predicts non-fatal myocardial infarction and fatal coronary heart disease among 28,838 middle-aged men and women. Eur Heart J. 2006;27: 2170–2176. pmid:16772340
- 58. Targher G, Bertolini L, Rodella S, Tessari R, Zenari L, Lippi G et al. Nonalcoholic fatty liver disease is independently associated with an increased incidence of cardiovascular events in type 2 diabetic patients. Diabetes Care. 2007;30: 2119–2121. pmid:17519430
- 59. Sundberg CJ. Physical activity: what is already being done and how we can avert 1 million deaths annually in future. Br J Sports Med. 2016;50: 319. pmid:26936163
- 60. Warburton DE, Bredin SS. Reflections on physical activity and health: what should we recommend? Can J Cardiol. 2016;32: 495–504. pmid:26995692
- 61. Kyu HH, Bachman VF, Alexander LT, Mumford JE, Afshin A, Estep K et al. Physical activity and risk of breast cancer, colon cancer, diabetes, ischemic heart disease, and ischemic stroke events: systematic review and dose-response meta-analysis for the Global Burden of Disease Study 2013. BMJ. 2016;354: i3857. pmid:27510511
- 62. Lawlor DA, Sattar N, Smith GD, Ebrahim S. The associations of physical activity and adiposity with alanine aminotransferase and gamma-glutamyltransferase. Am J Epidemiol. 2005;161: 1081–1088. pmid:15901629
- 63. Perreault K, Bauman A, Johnson N, Britton A, Rangul V, Stamatakis E. Does physical activity moderate the association between alcohol drinking and all-cause, cancer and cardiovascular diseases mortality? A pooled analysis of eight British population cohorts. Br J Sports Med. 2017;51: 651–657. pmid:27581162
- 64. Breitling LP, Raum E, Müller H, Rothenbacher D, Brenner H. Synergism between smoking and alcohol consumption with respect to serum gamma-glutamyltransferase. Hepatology. 2009;49: 802–808. pmid:19152425
- 65. Park EY, Lim MK, Oh JK, Cho H, Bae MJ, Yun EH et al. Independent and supra-additive effects of alcohol consumption, cigarette smoking, and metabolic syndrome on the elevation of serum liver enzyme levels. PLoS One. 2013;8: e63439. pmid:23667618
- 66. Danielsson J, Kangastupa P, Laatikainen T, Aalto M, Niemelä O. Dose- and gender-dependent interactions between coffee consumption and serum GGT activity in alcohol consumers. Alcohol Alcohol. 2013;48: 303–307. pmid:23492307
- 67. Xiao Q, Sinha R, Graubard BI, Freedman ND. Inverse associations of total and decaffeinated coffee with liver enzyme levels in National Health and Nutrition Examination Survey 1999–2010. Hepatology. 2014;60: 2091–2098. pmid:25124935
- 68. Goh GB, Chow WC, Wang R, Yuan JM, Koh WP. Coffee, alcohol and other beverages in relation to cirrhosis mortality: the Singapore Chinese Health Study. Hepatology. 2014;60: 661–669. pmid:24753005
- 69. Duffy JC, Alanko T. Self-reported consumption measures in sample surveys: a simulation study of alcohol consumption. J Off Stat. 1992;8: 327–350.
- 70. Fillmore KM, Stockwell T, Chikritzhs T, Bostrom A, Kerr W. Moderate alcohol use and reduced mortality risk: systematic error in prospective studies and new hypotheses. Ann Epidemiol. 2007;17: S16–S23. pmid:17478320