Dai Zheng, Abate Marie A, Al-Mamun Mohammad A, Kraner James C, Mock Allen R, Smith Gordon S
Health Affairs Institute, West Virginia University, Morgantown, West Virginia.
School of Pharmacy, West Virginia University, Morgantown, West Virginia.
J Stud Alcohol Drugs. 2025 May;86(3):358-366. doi: 10.15288/jsad.24-00054. Epub 2024 Sep 16.
The purpose of this study was to examine sex differences in overdose (OD) mortality based on substances involved.
We conducted a retrospective database analysis of West Virginia OD decedents (12,666 unintentional OD deaths, 2005-early 2023). Exposures were substances judged to contribute to death. The main outcome measure was determination of male to female death ratios with varying co-intoxicant involvement, particularly related to alcohol and fentanyl. Secondary outcomes included associations of fentanyl concentrations with alcohol concentrations and male sex, including fentanyl and inactive metabolite norfentanyl concentration variability between sexes.
Alcohol co-intoxication in OD deaths was associated with higher male:female death ratios, from 2.0 (alcohol absent) to 3.3 (alcohol present). There was a greater increase over time in alcohol involvement in recent deaths involving females compared with males (relative increases of 52% vs. 6%, respectively). Male:female ratios with alcohol and fentanyl co-involvement ranged from 5.9:1 (only two drugs involved) to 2.4:1 (≥5 substances), with females significantly more likely to have multiple substances contributing to death. Overall, males had statistically significantly larger fentanyl to norfentanyl median concentration ratios compared with females (8.8 vs. 6.9, respectively). Multivariable analyses found that alcohol presence was associated with a statistically significant 22% reduction in predicted fentanyl concentrations.
Male:female ratios in unintentional OD deaths were higher with greater alcohol involvement and lower with fewer co-intoxicants. Fentanyl and norfentanyl concentration differences by sex were observed. It is important to determine possible contributors to sex differences in OD death rates to better target prevention and treatment initiatives.
本研究旨在根据涉及的物质探讨过量用药(OD)死亡率的性别差异。
我们对西弗吉尼亚州的OD死亡者(2005年至2023年初的12,666例非故意OD死亡)进行了回顾性数据库分析。暴露物质为被判定导致死亡的物质。主要结局指标是确定不同合并中毒情况下男性与女性的死亡率,特别是与酒精和芬太尼相关的情况。次要结局包括芬太尼浓度与酒精浓度及男性性别的关联,包括两性之间芬太尼及其无活性代谢产物去甲芬太尼浓度的变异性。
OD死亡中的酒精合并中毒与更高的男性与女性死亡率相关,从2.0(无酒精)到3.3(有酒精)。与男性相比,近期女性死亡中酒精参与度随时间的增加幅度更大(相对增加分别为52%和6%)。酒精和芬太尼合并参与时的男性与女性比例范围为5.9:1(仅涉及两种药物)至2.4:1(≥5种物质),女性更有可能有多种物质导致死亡。总体而言,男性芬太尼与去甲芬太尼的中位数浓度比值在统计学上显著高于女性(分别为8.8和6.9)。多变量分析发现,酒精的存在与预测的芬太尼浓度在统计学上显著降低22%相关。
非故意OD死亡中的男性与女性比例在酒精参与度较高时更高,合并中毒较少时更低。观察到了两性之间芬太尼和去甲芬太尼浓度的差异。确定OD死亡率性别差异的可能影响因素对于更好地针对性开展预防和治疗举措很重要。