Division of Pulmonary and Critical Care Medicine, University of Wisconsin, Madison, Wisconsin.
Clinical Research Office, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois.
Ann Surg. 2022 Dec 1;276(6):e961-e968. doi: 10.1097/SLA.0000000000004770. Epub 2021 Feb 1.
We aimed to examine biomarkers for screening unhealthy alcohol use in the trauma setting.
Self-report tools are the practice standard for screening unhealthy alcohol use; however, their collection suffers from recall bias and incomplete collection by staff.
We performed a multi-center prospective clinical study of 251 adult patients who arrived within 24 hours of injury with external validation in another 60 patients. The Alcohol Use Disorders Identification Test served as the reference standard. The following biomarkers were measured: (1) PEth; (2) ethyl glucuronide; (3) ethyl sulfate; (4) gamma-glutamyl-transpeptidase; (5) carbohydrate deficient transferrin; and (6) blood alcohol concentration (BAC). Candidate single biomarkers and multivariable models were compared by considering discrimination (AUROC). The optimal cutpoint for the final model was identified using a criterion for setting the minimum value for specificity at 80% and maximizing sensitivity. Decision curve analysis was applied to compare to existing screening with BAC.
PEth alone had an AUROC of 0.93 [95% confidence interval (CI): 0.92-0.93] in internal validation with an optimal cutpoint of 25 ng/mL. A 4- variable biomarker model and the addition of any single biomarker to PEth did not improve AUROC over PEth alone ( P > 0.05). Decision curve analysis showed better performance of PEth over BAC across most predicted probability thresholds. In external validation, sensitivity and specificity were 76.0% (95% CI: 53.0%-92.0%) and 73.0% (95% CI: 56.0%-86.0%), respectively.Conclusion and Relevance: PEth alone proved to be the single best biomarker for screening of unhealthy alcohol use and performed better than existing screening systems with BAC. PEth may overcome existing screening barriers.
本研究旨在探讨创伤环境中用于筛查不健康饮酒的生物标志物。
自我报告工具是筛查不健康饮酒的标准方法;然而,由于回忆偏倚和工作人员采集不完整,其应用受到限制。
我们对 251 名在受伤后 24 小时内到达的成年患者进行了多中心前瞻性临床研究,并在另外 60 名患者中进行了外部验证。以酒精使用障碍识别测试为参考标准。测量了以下生物标志物:(1)P-乙基己烯醛;(2)乙基葡萄糖醛酸苷;(3)乙基硫酸盐;(4)γ-谷氨酰转肽酶;(5)碳水化合物缺乏转铁蛋白;和(6)血液酒精浓度(BAC)。通过考虑区分度(AUROC)比较了候选单生物标志物和多变量模型。使用设定特异性最小值为 80%且最大化灵敏度的标准,确定最终模型的最佳截断点。应用决策曲线分析比较了现有的 BAC 筛查方法。
在内部验证中,P-乙基己烯醛单独使用时 AUROC 为 0.93[95%置信区间(CI):0.92-0.93],最佳截断点为 25ng/mL。四变量生物标志物模型和向 P-乙基己烯醛中添加任何单一生物标志物均未提高 AUROC(P>0.05)。决策曲线分析表明,PEth 在大多数预测概率阈值下的表现优于 BAC。在外验证中,敏感性和特异性分别为 76.0%(95%CI:53.0%-92.0%)和 73.0%(95%CI:56.0%-86.0%)。
P-乙基己烯醛单独使用被证明是筛查不健康饮酒的最佳单一生物标志物,其性能优于现有的 BAC 筛查系统。P-乙基己烯醛可能克服了现有的筛查障碍。