Research ArticleHeavy daily alcohol intake at the population level predicts the weight of alcohol in cirrhosis burden worldwide
Graphical abstract
Introduction
Excessive use of alcohol is a main cause of global mortality, contributing to deaths through cancers, toxic organ damage, and accidents and injuries [1]. Detailed data on the burden of alcohol-associated mortality were released in the 2014 World Health Organization (WHO) Global Status Report on Alcohol and Health, which is the most detailed and comprehensive report of this kind [2]. This publication emphasizes the significant contribution alcohol use makes to the global cirrhosis burden, with approximately half of global cirrhosis deaths attributed to alcohol use. Attention should be placed on detrimental patterns and levels of alcohol use that lead to cirrhosis in order to reduce associated mortality.
Previous studies have demonstrated a dose-response relationship between alcohol intake and an individual’s risk for developing cirrhosis [3], [4], [5], [6]. There is also substantial support for a threshold effect, wherein the risk for developing cirrhosis is constant over time if a threshold of intake is surpassed [7], [8], [9]. For a given level of total consumption, the pattern of drinking may confer higher risk for cirrhosis; for example, drinking on a daily basis has been shown to be associated with higher risk [6], [7], [9]. Some studies have investigated the potential influences of factors including binge drinking [10], [11], duration of consumption over lifetime [7], [9], and alcohol type [6], [12], [13]. Cofactors that have been shown to increase risk of alcoholic cirrhosis include cigarette smoking [14], [15], excess weight [16], and viral hepatitis [17]. Consumption of certain substances, such as coffee and tea, may provide a protective effect against the development of liver disease [18], [19]. For all variables discussed, the potential for significant geographical variation exists, due to cultural and socioeconomic differences in exposure to risk or protective factors. The economics and policies of alcohol sale can also be expected to vary considerably across the globe and to influence the way it is consumed [20].
On a population level, an association between alcohol consumption and cirrhosis mortality has been well documented, reflecting the risk relationship demonstrated on the individual level [21], [22], [23], [24]. Most population level studies have assessed the effect of per capita drinking on the death rate from cirrhosis, primarily in Europe and the U.S. One study compared the effect of per capita consumption on cirrhosis mortality in European countries that predominantly consume spirits as opposed to wine and beer [21]. Moreover, it has been hypothesized that differences in population drinking patterns (e.g., heavy episodic vs. daily drinking) shape the relationship between alcohol consumption and cirrhosis mortality [22]. However, to our knowledge, there are no studies assessing the influence of daily drinking patterns on cirrhosis mortality at the population level, or on the burden of alcoholic cirrhosis specifically. In this study, we aimed to identify the main determinants of cirrhosis mortality and the weight of alcohol in the global cirrhosis burden. We used recent data reported in the WHO 2014 Global Status Report on Alcohol and Health to evaluate associations between population drinking, cirrhosis cofactors, and economic indicators and the burden of alcoholic cirrhosis.
Section snippets
Database development
We obtained detailed data on 193 countries from the WHO Global Information System on Alcohol and Health, accessed July, 2014 (http://apps.who.int/gho/data/node.main.GISAH?lang=en). From this data repository, we abstracted country-specific data on levels of alcohol consumption, drinking patterns, and our main outcome variables: the fraction of cirrhosis attributable to alcohol use (alcohol-attributable fraction, AAF), and the age-standardized death rate from cirrhosis (ASDR). The WHO collected
Geographical variation in alcohol consumption, cirrhosis mortality and contribution from alcohol
We first analyzed the geographical patterns of alcohol consumption and cirrhosis mortality. The characteristics of the global cirrhosis burden and its potential determinants are described in Table 1. On a per capita basis, the highest alcohol consumption was observed in Europe with 10 liters/year (3677 standard drinks/year). In contrast, the rate was 1.1 liters/year (79 standard drinks/year) in the Eastern Mediterranean. There, an average of 6.5% of the population reported drinking, in contrast
Discussion
This study presented the geographical patterns of the cirrhosis burden worldwide and the contribution by alcohol to that burden (alcohol-attributable fraction of cirrhosis, AAF). We investigated potential relationships between population parameters of alcohol intake, drinking patterns, and predisposing factors for cirrhosis, and the outcome variable of AAF. The results support the conclusion that daily drinking and overall per capita consumption independently influence the contribution of
Financial support
This work was supported by the National Institute on Alcohol Abuse and Alcoholism (NIAAA) (1U01AA021908-01) and P30 DK34987. JA wishes to express his gratitude to the Mexican National Council of Science and Technology (CONACYT, Mexico City, Mexico) for partially supporting his predoctoral stay at IDIBAPS.
Conflict of interest
The authors who have taken part in this study declared that they do not have anything to disclose regarding funding or conflict of interest with respect to this manuscript.
Author contribution
ES participated in the conception and design of this study, interpretation, and manuscript writing. JA, MCL and JGA performed the statistical analysis and DC contributed to the interpretation of the results. ES, NN, JA, MCL, RB, and JGA participated in the collection, analysis and interpretation of the data and revision of the final version of the manuscript. RB was involved in the conception, design and supervision of this paper, analysis and interpretation of the data and participated in
Acknowledgements
We would like to thank Anne Green for her numerous contributions to the study effort, as well as Gemma Odena, Jiegen Chen, Veronica Massey, and Jaeyoun Cheong for their constant support and help.
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These authors contributed equally as joint first authors.