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Unique prefrontal GABA and glutamate disturbances in co-occurring bipolar disorder and alcohol dependence

机译:并发双相情感障碍和酒精依赖中独特的前额叶GABA和谷氨酸紊乱

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摘要

Bipolar disorder (BD) and alcohol dependence (AD) frequently co-occur, and co-occurring BD and AD are associated with devastating public health costs. Minimal neurobiological research exists to guide the development of effective treatments for this treatment-resistant population. We believe the present study represents the first investigation of prefrontal gamma-aminobutyric acid (GABA) and glutamate levels in co-occurring BD and current AD. The participants were 78 individuals who met DSM-IV criteria for BD I/II and current AD (n=20), BD I/II alone (n=19), current AD alone (n=20) or no diagnosis (n=19). The participants completed a baseline diagnostic visit, then returned approximately 4 days later for a two-dimensional J-resolved proton magnetic resonance spectroscopy (1H-MRS) acquisition in dorsal anterior cingulate cortex (dACC). All participants were required to demonstrate ⩾1 week of abstinence from alcohol/drugs via serial biomarker testing before 1H-MRS. A 2 × 2 factorial analysis of variance of cerebrospinal fluid (CSF)-corrected GABA/water concentrations demonstrated a significant BD × AD interaction (F=2.91, P<0.05), signifying uniquely low levels of GABA in BD+AD; this effect doubled when the sample was restricted to individuals who consumed alcohol within 2 weeks of 1H-MRS. There were no overall effects of BD/AD on CSF-corrected glutamate/water levels. However, the BD × AD interaction, signifying uniquely low levels of glutamate in BD+AD, approached statistical significance (F=3.83, P=0.06) in individuals who consumed alcohol within 2 weeks of 1H-MRS. The dACC GABA levels were significantly, negatively associated with Barratt Impulsiveness Scale (r=−0.28, P=0.02) and Obsessive Compulsive Drinking Scale (r=−0.35, P<0.01) scores. If replicated, these results may suggest that future treatment studies should preferentially evaluate therapeutics in BD+AD known to increase prefrontal GABA and glutamate levels.
机译:躁郁症(BD)和酒精依赖(AD)经常同时发生,而BD和AD并发会导致毁灭性的公共卫生成本。已有最小的神经生物学研究来指导对这种耐药人群的有效治疗方法的开发。我们认为,本研究代表了同时发生的BD和当前AD中前额叶γ-氨基丁酸(GABA)和谷氨酸水平的首次调查。参与者为78位符合BD I / II和当前AD(n = 20),仅BD I / II(n = 19),仅当前AD(n = 20)或无诊断(n = 19)。参与者完成了基线诊断访问,然后约4天后返回,在背扣带回皮层(dACC)中进行二维J分辨质子磁共振波谱( 1 H-MRS)采集。在 1 H-MRS之前,要求所有参与者通过系列生物标志物测试证明禁酒1周以戒酒。对脑脊液(CSF)校正的GABA /水浓度的方差进行的2×2因子分析表明,BD×AD相互作用显着(F = 2.91,P <0.05),表明BD + AD中GABA的含量非常低。当样品仅限于在 1 H-MRS的两周内饮酒的人时,这种效果增加了一倍。 BD / AD对CSF校正的谷氨酸/水水平没有总体影响。然而,BD×AD交互作用表明BD + AD中谷氨酸的含量极低,在 1 H-的两周内饮酒的个体具有统计学意义(F = 3.83,P = 0.06)。太太。 dACC GABA水平与Barratt冲动量表(r = -0.28,P = 0.02)和强迫性饮酒量表(r = -0.35,P <0.01)得分显着负相关。如果重复,这些结果可能表明,未来的治疗研究应优先评估已知会增加额叶前GABA和谷氨酸水平的BD + AD中的治疗药物。

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