Stoops William W, Shellenberg Thomas P, Regnier Sean D, Cox David H, Adatorwovor Reuben, Hays Lon R, Anderson Danielle M, Lile Joshua A, Schmitz Joy M, Havens Jennifer R, Sexton Travis R, Fisher Mary B
Department of Behavioral Science, University of Kentucky College of Medicine, 1100 Veterans Drive, Medical Behavioral Science Building, Lexington, KY 40536-0086, USA; Department of Psychiatry, University of Kentucky College of Medicine, 245 Fountain Court, Lexington, KY 40509-1810, USA; Department of Psychology, University of Kentucky College of Arts and Sciences, 171 Funkhouser Drive, Lexington, KY 40506-0044, USA; Center on Drug and Alcohol Research, University of Kentucky College of Medicine, 845 Angliana Ave, Lexington, KY 40508, USA.
Department of Behavioral Science, University of Kentucky College of Medicine, 1100 Veterans Drive, Medical Behavioral Science Building, Lexington, KY 40536-0086, USA; Department of Psychology, University of Kentucky College of Arts and Sciences, 171 Funkhouser Drive, Lexington, KY 40506-0044, USA.
Drug Alcohol Depend. 2025 Jun 1;271:112642. doi: 10.1016/j.drugalcdep.2025.112642. Epub 2025 Mar 7.
Limited prospective research has evaluated the health benefits associated with changing levels of drug use, aside from complete abstinence. This study determined whether lower levels of cocaine use impacted physiological indices (e.g., mean arterial pressure) and biomarkers (e.g., stromal cell derived factor-1a [SDF-1a], soluble intercellular adhesion molecule-1 [ICAM-1], neutrophil activating peptide-2 [CXCL7]) of cardiovascular health.
Treatment seeking participants enrolled in a 12-week single-blind, randomized, controlled cocaine contingency management trial. Participants were randomly assigned to High Value Reinforcers for cocaine abstinence (n = 41), Low Value Reinforcers for cocaine abstinence (n = 33) or a non-contingent Control group (n = 33). Physiological indices were collected at each clinic visit and averaged over each week of treatment. Biomarkers were assayed at 6-week intervals. Percent benzoylecgonine negative urines matching measurement timeframes were used to predict changes in outcomes using generalized linear models.
Reductions in mean arterial pressure were observed in the High Value group, particularly during follow-up (χ= 6.6, p < .05). Regardless of group, less cocaine use was associated with decreased SDF-1a and increased ICAM-1 and CXCL7 levels (all χ> 4.7; p values < 0.05).
Improved blood pressure was observed in the High Value treatment group, who provided the greatest percent of cocaine negative urine samples but did not achieve total abstinence. Less cocaine use was also associated with changes in cardiac biomarkers that may indicate tissue repair. These results indicate that less cocaine use, even without complete abstinence, can improve blood pressure, and potentially heal cardiovascular insult, in individuals with Cocaine Use Disorder.
除了完全戒断外,有限的前瞻性研究评估了与药物使用水平变化相关的健康益处。本研究确定较低水平的可卡因使用是否会影响心血管健康的生理指标(例如平均动脉压)和生物标志物(例如基质细胞衍生因子-1a [SDF-1a]、可溶性细胞间粘附分子-1 [ICAM-1]、中性粒细胞激活肽-2 [CXCL7])。
寻求治疗的参与者参加了一项为期12周的单盲、随机、对照可卡因应急管理试验。参与者被随机分配到高价值强化物促进可卡因戒断组(n = 41)、低价值强化物促进可卡因戒断组(n = 33)或非应急对照组(n = 33)。在每次门诊就诊时收集生理指标,并在治疗的每一周进行平均。生物标志物每隔6周检测一次。使用广义线性模型,将与测量时间框架匹配的苯甲酰芽子碱阴性尿液百分比用于预测结果变化。
高价值组观察到平均动脉压降低,尤其是在随访期间(χ = 6.6,p <.05)。无论组别如何,较少的可卡因使用与SDF-1a降低以及ICAM-1和CXCL7水平升高相关(所有χ > 4.7;p值 < 0.05)。
在高价值治疗组中观察到血压改善,该组提供了最大比例的可卡因阴性尿液样本,但未实现完全戒断。较少的可卡因使用也与心脏生物标志物的变化相关,这可能表明组织修复。这些结果表明,即使没有完全戒断,较少的可卡因使用也可以改善可卡因使用障碍患者的血压,并可能治愈心血管损伤。