Prisciandaro James J, Schacht Joseph P, Prescot Andrew P, Brenner Helena M, Renshaw Perry F, Brown Truman R, Anton Raymond F
Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Department of Radiology, University of Utah, Salt Lake City, UT, USA.
Addict Biol. 2020 Nov;25(6):e12810. doi: 10.1111/adb.12810. Epub 2019 Aug 1.
Proton magnetic resonance spectroscopy ( H-MRS) studies have demonstrated abnormal levels of a variety of neurometabolites in treatment-seeking individuals with moderate-severe alcohol use disorder (AUD) following acute withdrawal. In contrast, few studies have investigated neurochemical changes across early abstinence in less severe, treatment-naïve AUD. The present study, which represents the primary report of a research grant from ABMRF/The Alcohol Research Fund, measured dorsal anterior cingulate cortex (dACC) GABA, glutamate, and glutamine levels in treatment-naïve AUD (n = 23) via three H-MRS scans spaced across a planned week of abstinence from alcohol. In addition to AUD participants, 12 light drinkers completed two scans, separated by 48 hours, to ensure that results in AUD were not produced by between-scan differences other than abstinence from alcohol. H-MRS spectra were acquired in dACC at each scan using 2D J-resolved point-resolved spectroscopy. Linear mixed modeling results demonstrated a significant increase in GABA, but not glutamate or glutamine (Ps = .237-.626), levels between scans 1 and 2 (+8.88%, .041), with no difference between scans 2 and 3 (+1.00%, .836), in AUD but not LD (F = 1.24, .290) participants. Exploratory regression analyses tentatively revealed a number of significant prospective associations between changes in glutamine levels and heavy drinking, craving, and withdrawal symptoms. Most notably, the present study demonstrated return from abnormally low to normal GABA levels in treatment-naïve AUD within 3 days of their last drink; the pattern of results was consistent with glutamate and glutamine disturbances being exclusive to relatively more severe AUD.
质子磁共振波谱(¹H-MRS)研究表明,在急性戒断后,患有中度至重度酒精使用障碍(AUD)且寻求治疗的个体中,多种神经代谢物水平异常。相比之下,很少有研究调查轻度、未接受过治疗的AUD患者在早期戒酒过程中的神经化学变化。本研究是ABMRF/酒精研究基金一项研究资助的主要报告,通过在计划戒酒一周内进行的三次¹H-MRS扫描,测量了未接受过治疗的AUD患者(n = 23)背侧前扣带回皮质(dACC)中的γ-氨基丁酸(GABA)、谷氨酸和谷氨酰胺水平。除了AUD参与者外,12名轻度饮酒者在间隔48小时的情况下完成了两次扫描,以确保AUD患者的结果不是由除戒酒之外的扫描间差异产生的。每次扫描时,使用二维J分辨点分辨波谱在dACC采集¹H-MRS波谱。线性混合模型结果显示,在AUD患者而非轻度饮酒(LD)参与者中,扫描1和扫描2之间GABA水平显著升高,但谷氨酸或谷氨酰胺水平未升高(P值为0.237 - 0.626)(升高8.88%,P = 0.041),扫描2和扫描3之间无差异(升高1.00%,P = 0.836)(F = 1.24,P = 0.290)。探索性回归分析初步揭示了谷氨酰胺水平变化与大量饮酒、渴望和戒断症状之间的一些显著前瞻性关联。最值得注意的是,本研究表明,未接受过治疗的AUD患者在最后一次饮酒后3天内,GABA水平从异常低恢复到正常;结果模式与谷氨酸和谷氨酰胺紊乱仅存在于相对更严重的AUD中一致。