{"title":"Re-evaluating the association between alcohol use and in-hospital survival: the role of collider bias","authors":"Tomoko Yasuda, Taisuke Shibata, Atsushi Shiraishi","doi":"10.1186/s13054-025-05442-3","DOIUrl":null,"url":null,"abstract":"<p>Recent studies have reported paradoxical associations between alcohol use and trauma outcomes, sparking debate in public health, trauma surgery, and emergency medicine [1,2,3]. In a recent paper published in Critical Care, Kazuma Sasaki et al. [4] explored the relationship between pre-injury alcohol consumption and traumatic brain injury (TBI) outcomes of hospitalized patients in Japan, reporting a potential direct protective effect of alcohol in conferring survival advantage. While the authors acknowledge the observational nature of their findings, we draw attention to an important methodological issue—namely, collider bias—which may have distorted the reported associations in terms of causal inference. In this Matters Arising, we demonstrate how collider bias can arise in such analyses and discuss the need for caution in the causal interpretation of non-randomized observational studies of this nature.</p><p>Collider bias arises when two exposure variables both influence a third collider variable <i>W</i>, and the analysis conditions on <i>W</i>. This causal relationship can be illustrated using a directed acyclic graph (DAG), where <i>W</i> is located at the collision point of the two arrowheads from two independent variables <i>Z</i>1 and <i>Z</i>2 (Fig. 1A). In this structure, adjusting for <i>W</i>, or selecting or stratifying the sample population based on <i>W</i>, can introduce a collider bias [5]. Such paths with colliders can be a source of selection bias, introducing a methodological flaw to observational research and misleading conclusions when unidentified in study design.</p><figure><figcaption><b data-test=\"figure-caption-text\">Fig. 1</b></figcaption><picture><source srcset=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13054-025-05442-3/MediaObjects/13054_2025_5442_Fig1_HTML.png?as=webp\" type=\"image/webp\"/><img alt=\"figure 1\" aria-describedby=\"Fig1\" height=\"693\" loading=\"lazy\" src=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13054-025-05442-3/MediaObjects/13054_2025_5442_Fig1_HTML.png\" width=\"685\"/></picture><p><b>A</b> DAG illustrating <i>W</i> as a collider variable in the path <i>Z</i>1 → <i>W</i> ← <i>Z</i>2. Before conditioning on <i>W</i>, the relationship between <i>X</i> and <i>Y</i> may be confounded by the path <i>X</i>-<i>Z</i>1-<i>W</i>-<i>Y</i>. However, conditioning on <i>W</i> opens an otherwise closed non-causal pathway <i>X</i>-<i>Z</i>1-<i>W</i>-<i>Z</i>2-<i>Y</i>, creating an apparent association between <i>X</i> and <i>Y</i> [5]. <b>B</b> In the analytic model of this study by Sasaki et al., conditioning on hospitalization with TBI may introduce a non-causal association between alcohol use and in-hospital survival via covariates <i>Z</i>1 and <i>Z</i>2</p><span>Full size image</span><svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-chevron-right-small\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></figure><p>In this study by Sasaki et al., a simplified DAG can be constructed with alcohol use as <i>X</i>, hospitalization with TBI as <i>W</i>, and in-hospital survival as <i>Y</i> (Fig. 1B). Patient demographics may be a factor (<i>Z</i>1) that influences both alcohol use (<i>X</i>) and the likelihood of being hospitalized with TBI (<i>W</i>). Injury severity (<i>Z</i>2) would affect both the likelihood of hospitalization (<i>W</i>) and survival (<i>Y</i>). By making hospitalization with TBI (<i>W</i>) a necessary condition for inclusion in the study, <i>W</i> acts as a collider and can inadvertently open non-causal paths between <i>X</i> and <i>Y</i>. As a result, alcohol use may appear spuriously associated with improved in-hospital survival, even if no true protective effect or causal relationship exists. For example, this could occur if alcohol use (<i>X</i>) is associated with both reduced trauma severity and impaired consciousness, as noted by the authors [4]. This bias arises not from failure to adjust, but rather from conditioning on a variable that sits at the intersection of multiple causes.</p><p>While the authors use regression and propensity score methods to account for confounding, these methods may not address and potentially even magnify the structural issue of conditioning on a collider. Notably, performing mediation analysis on a population already conditioned on the collider variable (<i>W</i>), as done in this paper, does not address the collider bias introduced initially. We do not dispute the possibility that alcohol interacts with pathophysiological processes in trauma, but the present study design does not allow for drawing causal conclusions. More robust causal inference techniques, such as target trial emulation or structural causal models, are necessary to address these complexities. Moreover, suggestions of direct protective effects of alcohol must be interpreted with caution, given the well-documented harms of alcohol and the potential for public misinterpretation [6, 7].</p><p>In conclusion, this study by Sasaki et al. contributes important data to the ongoing exploration of alcohol and trauma outcomes. However, its causal interpretations are limited by collider bias introduced through selection on hospitalization with TBI. Recognizing and accounting for such structural biases is crucial for valid inference in observational research.</p><p>No datasets were generated or analysed during the current study.</p><dl><dt style=\"min-width:50px;\"><dfn>TBI:</dfn></dt><dd>\n<p>Traumatic brain injury</p>\n</dd><dt style=\"min-width:50px;\"><dfn>DAG:</dfn></dt><dd>\n<p>Directed acyclic graph</p>\n</dd></dl><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Lau G, Gabbe BJ, Mitra B, Dietze PM, Reeder S, Cameron P, et al. Association between acute pre-injury alcohol use and 12-month health outcomes for survivors of major trauma: A registry-based study. Injury. 2024;55:111782. https://doi.org/10.1016/j.injury.2024.111782.</p><p>Article PubMed Google Scholar </p></li><li data-counter=\"2.\"><p>Ng C, Fleury M, Hakmi H, Bronson B, Vosswinkel JA, Huang EC, et al. The impact of alcohol use and withdrawal on trauma outcomes: A case control study. 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Hypertension. 2024;81:1701–15. https://doi.org/10.1161/HYPERTENSIONAHA.124.22703.</p><p>Article CAS PubMed Google Scholar </p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><p>Not applicable.</p><p>Not applicable.</p><h3>Authors and Affiliations</h3><ol><li><p>Department of Emergency and Trauma Medicine, Kameda Medical Center, 929 Higashi-cho, Kamogawa, Chiba, 296-8602, Japan</p><p>Tomoko Yasuda, Taisuke Shibata & Atsushi Shiraishi</p></li></ol><span>Authors</span><ol><li><span>Tomoko Yasuda</span>View author publications<p><span>You can also search for this author in</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Taisuke Shibata</span>View author publications<p><span>You can also search for this author in</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Atsushi Shiraishi</span>View author publications<p><span>You can also search for this author in</span><span>PubMed<span> </span>Google Scholar</span></p></li></ol><h3>Contributions</h3><p>T.Y. wrote the main manuscript text and prepared the figure. All authors have made substancial contributions to the conception and revision of the manuscript.</p><h3>Corresponding author</h3><p>Correspondence to Atsushi Shiraishi.</p><h3>Conflict of interest</h3>\n<p>The authors declare no competing interests.</p>\n<h3>Consent to participate</h3>\n<p>Not applicable.</p>\n<h3>Consent for publication</h3>\n<p>Not applicable.</p>\n<h3>Ethical approval</h3>\n<p>Not applicable.</p><h3>Publisher's Note</h3><p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p><p><b>Open Access</b> This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. 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0-.92-.08-1.33-.25-.41-.16-.77-.4-1.08-.7-.3-.31-.54-.69-.72-1.13-.17-.44-.26-.95-.26-1.52zm4.61-.62c0-.55-.11-.98-.34-1.28-.23-.31-.58-.47-1.06-.47-.41 0-.77.15-1.08.45-.31.29-.5.73-.57 1.3zm3.01 2.23c.31.24.61.43.92.57.3.13.63.2.98.2.38 0 .65-.08.83-.23s.27-.35.27-.6c0-.14-.05-.26-.13-.37-.08-.1-.2-.2-.34-.28-.14-.09-.29-.16-.47-.23l-.53-.22c-.23-.09-.46-.18-.69-.3-.23-.11-.44-.24-.62-.4s-.33-.35-.45-.55c-.12-.21-.18-.46-.18-.75 0-.61.23-1.1.68-1.49.44-.38 1.06-.57 1.83-.57.48 0 .91.08 1.29.25s.71.36.99.57l-.74.98c-.24-.17-.49-.32-.73-.42-.25-.11-.51-.16-.78-.16-.35 0-.6.07-.76.21-.17.15-.25.33-.25.54 0 .14.04.26.12.36s.18.18.31.26c.14.07.29.14.46.21l.54.19c.23.09.47.18.7.29s.44.24.64.4c.19.16.34.35.46.58.11.23.17.5.17.82 0 .3-.06.58-.17.83-.12.26-.29.48-.51.68-.23.19-.51.34-.84.45-.34.11-.72.17-1.15.17-.48 0-.95-.09-1.41-.27-.46-.19-.86-.41-1.2-.68z" fill="#535353"/></g></svg>\" width=\"57\"/><h3>Cite this article</h3><p>Yasuda, T., Shibata, T. & Shiraishi, A. Re-evaluating the association between alcohol use and in-hospital survival: the role of collider bias. <i>Crit Care</i> <b>29</b>, 203 (2025). https://doi.org/10.1186/s13054-025-05442-3</p><p>Download citation<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><ul data-test=\"publication-history\"><li><p>Received<span>: </span><span><time datetime=\"2025-04-27\">27 April 2025</time></span></p></li><li><p>Accepted<span>: </span><span><time datetime=\"2025-05-04\">04 May 2025</time></span></p></li><li><p>Published<span>: </span><span><time datetime=\"2025-05-20\">20 May 2025</time></span></p></li><li><p>DOI</abbr><span>: </span><span>https://doi.org/10.1186/s13054-025-05442-3</span></p></li></ul><h3>Share this article</h3><p>Anyone you share the following link with will be able to read this content:</p><button data-track=\"click\" data-track-action=\"get shareable link\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Get shareable link</button><p>Sorry, a shareable link is not currently available for this article.</p><p data-track=\"click\" data-track-action=\"select share url\" data-track-label=\"button\"></p><button data-track=\"click\" data-track-action=\"copy share url\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Copy to clipboard</button><p> Provided by the Springer Nature SharedIt content-sharing initiative </p>","PeriodicalId":10811,"journal":{"name":"Critical Care","volume":"14 1","pages":""},"PeriodicalIF":8.8000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical Care","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13054-025-05442-3","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CRITICAL CARE MEDICINE","Score":null,"Total":0}
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Abstract
Recent studies have reported paradoxical associations between alcohol use and trauma outcomes, sparking debate in public health, trauma surgery, and emergency medicine [1,2,3]. In a recent paper published in Critical Care, Kazuma Sasaki et al. [4] explored the relationship between pre-injury alcohol consumption and traumatic brain injury (TBI) outcomes of hospitalized patients in Japan, reporting a potential direct protective effect of alcohol in conferring survival advantage. While the authors acknowledge the observational nature of their findings, we draw attention to an important methodological issue—namely, collider bias—which may have distorted the reported associations in terms of causal inference. In this Matters Arising, we demonstrate how collider bias can arise in such analyses and discuss the need for caution in the causal interpretation of non-randomized observational studies of this nature.
Collider bias arises when two exposure variables both influence a third collider variable W, and the analysis conditions on W. This causal relationship can be illustrated using a directed acyclic graph (DAG), where W is located at the collision point of the two arrowheads from two independent variables Z1 and Z2 (Fig. 1A). In this structure, adjusting for W, or selecting or stratifying the sample population based on W, can introduce a collider bias [5]. Such paths with colliders can be a source of selection bias, introducing a methodological flaw to observational research and misleading conclusions when unidentified in study design.
Fig. 1
A DAG illustrating W as a collider variable in the path Z1 → W ← Z2. Before conditioning on W, the relationship between X and Y may be confounded by the path X-Z1-W-Y. However, conditioning on W opens an otherwise closed non-causal pathway X-Z1-W-Z2-Y, creating an apparent association between X and Y [5]. B In the analytic model of this study by Sasaki et al., conditioning on hospitalization with TBI may introduce a non-causal association between alcohol use and in-hospital survival via covariates Z1 and Z2
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In this study by Sasaki et al., a simplified DAG can be constructed with alcohol use as X, hospitalization with TBI as W, and in-hospital survival as Y (Fig. 1B). Patient demographics may be a factor (Z1) that influences both alcohol use (X) and the likelihood of being hospitalized with TBI (W). Injury severity (Z2) would affect both the likelihood of hospitalization (W) and survival (Y). By making hospitalization with TBI (W) a necessary condition for inclusion in the study, W acts as a collider and can inadvertently open non-causal paths between X and Y. As a result, alcohol use may appear spuriously associated with improved in-hospital survival, even if no true protective effect or causal relationship exists. For example, this could occur if alcohol use (X) is associated with both reduced trauma severity and impaired consciousness, as noted by the authors [4]. This bias arises not from failure to adjust, but rather from conditioning on a variable that sits at the intersection of multiple causes.
While the authors use regression and propensity score methods to account for confounding, these methods may not address and potentially even magnify the structural issue of conditioning on a collider. Notably, performing mediation analysis on a population already conditioned on the collider variable (W), as done in this paper, does not address the collider bias introduced initially. We do not dispute the possibility that alcohol interacts with pathophysiological processes in trauma, but the present study design does not allow for drawing causal conclusions. More robust causal inference techniques, such as target trial emulation or structural causal models, are necessary to address these complexities. Moreover, suggestions of direct protective effects of alcohol must be interpreted with caution, given the well-documented harms of alcohol and the potential for public misinterpretation [6, 7].
In conclusion, this study by Sasaki et al. contributes important data to the ongoing exploration of alcohol and trauma outcomes. However, its causal interpretations are limited by collider bias introduced through selection on hospitalization with TBI. Recognizing and accounting for such structural biases is crucial for valid inference in observational research.
No datasets were generated or analysed during the current study.
TBI:
Traumatic brain injury
DAG:
Directed acyclic graph
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Authors and Affiliations
Department of Emergency and Trauma Medicine, Kameda Medical Center, 929 Higashi-cho, Kamogawa, Chiba, 296-8602, Japan
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Taisuke ShibataView author publications
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Atsushi ShiraishiView author publications
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T.Y. wrote the main manuscript text and prepared the figure. All authors have made substancial contributions to the conception and revision of the manuscript.
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Correspondence to Atsushi Shiraishi.
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Yasuda, T., Shibata, T. & Shiraishi, A. Re-evaluating the association between alcohol use and in-hospital survival: the role of collider bias. Crit Care29, 203 (2025). https://doi.org/10.1186/s13054-025-05442-3
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DOI: https://doi.org/10.1186/s13054-025-05442-3
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期刊介绍:
Critical Care is an esteemed international medical journal that undergoes a rigorous peer-review process to maintain its high quality standards. Its primary objective is to enhance the healthcare services offered to critically ill patients. To achieve this, the journal focuses on gathering, exchanging, disseminating, and endorsing evidence-based information that is highly relevant to intensivists. By doing so, Critical Care seeks to provide a thorough and inclusive examination of the intensive care field.