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前瞻性神经化学特征分析父母患有双相情感障碍的儿童后代。

Prospective neurochemical characterization of child offspring of parents with bipolar disorder.

机构信息

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, 401 Quarry Road, Stanford, CA 94305, USA.

出版信息

Psychiatry Res. 2013 Nov 30;214(2):153-60. doi: 10.1016/j.pscychresns.2013.05.005. Epub 2013 Sep 9.

Abstract

We wished to determine whether decreases in N-acetyl aspartate (NAA) and increases in myoinositol (mI) concentrations as a ratio of creatine (Cr) occurred in the dorsolateral prefrontal cortex (DLPFC) of pediatric offspring of parents with bipolar disorder (BD) and a healthy comparison group (HC) over a 5-year period using proton magnetic resonance spectroscopy ((1)H-MRS). Paticipants comprised 64 offspring (9-18 years old) of parents with BD (36 with established BD, and 28 offspring with symptoms subsyndromal to mania) and 28 HCs, who were examined for group differences in NAA/Cr and mI/Cr in the DLPFC at baseline and follow-up at either 8, 10, 12, 52, 104, 156, 208, or 260 weeks. No significant group differences were found in metabolite concentrations at baseline or over time. At baseline, BD offspring had trends for higher mI/Cr concentrations in the right DLPFC than the HC group. mI/Cr concentrations increased with age, but no statistically significant group differences were found between groups on follow-up. It may be the case that with intervention youth at risk for BD are normalizing otherwise potentially aberrant neurochemical trajectories in the DLPFC. A longer period of follow-up may be required before observing any group differences.

摘要

我们希望通过质子磁共振波谱(1H-MRS)来确定在 5 年内,父母患有双相情感障碍(BD)和健康对照组(HC)的儿科后代的背外侧前额叶皮质(DLPFC)中是否会出现 N-乙酰天冬氨酸(NAA)减少和肌醇(mI)浓度增加,并且以肌酸(Cr)的比值表示。参与者包括 64 名父母患有 BD 的后代(9-18 岁)(36 名患有确诊 BD,28 名患有亚综合征躁狂的后代)和 28 名 HC,他们在基线和随访时分别在 8、10、12、52、104、156、208 或 260 周时检查了 DLPFC 中 NAA/Cr 和 mI/Cr 的组间差异。在基线或随时间的代谢物浓度没有显著的组间差异。在基线时,BD 后代的右侧 DLPFC 中 mI/Cr 浓度比 HC 组有升高的趋势。mI/Cr 浓度随年龄增长而增加,但在随访时两组之间没有统计学上的显著差异。对于患有 BD 风险的年轻人,用干预措施使 DLPFC 中原本可能异常的神经化学轨迹正常化,这可能是事实。在观察到任何组间差异之前,可能需要更长的随访时间。

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