Alterations of the cerebellum and basal ganglia in bipolar disorder mood states detected by quantitative T1ρ mapping.
Alterations of the cerebellum and basal ganglia in bipolar disorder mood states detected by quantitative T1ρ mapping.
复制标题
躁郁症情绪状态中小脑和基底神经节的改变,通过定量T1ρ映射检测到。
DOI:
10.1111/bdi.12581
复制
发表时间:
2018-06
影响因子:
5.4
通讯作者:
Wemmie JA
中科院分区:
文献类型:
--
作者:
Johnson CP;Christensen GE;Fiedorowicz JG;Mani M;Shaffer JJ Jr;Magnotta VA;Wemmie JA
Quantitative T1ρ mapping is a magnetic resonance imaging technique sensitive to pH and other cellular and microstructural factors and is a potentially valuable tool for identifying brain alterations in bipolar disorder. Recently, this technique identified differences in the cerebellum and cerebral white matter of euthymic patients versus healthy controls consistent with reduced pH in these regions, suggesting an underlying metabolic abnormality. The current study builds upon this prior work to investigate brain T1ρ differences across euthymic, depressed, and manic mood states of bipolar disorder. Forty participants with bipolar I disorder and 29 healthy control participants balanced for age and gender were enrolled. Participants with bipolar disorder were imaged in one or more mood states, yielding 27, 12, and 13 imaging sessions in euthymic, depressed, and manic mood states, respectively. Three-dimensional, whole-brain anatomical images and T1ρ maps were acquired for all participants, enabling voxel-wise evaluation of T1ρ differences between bipolar mood state and healthy control groups. All three mood state groups had increased T1ρ relaxation times in the cerebellum compared to the healthy control group. Additionally, the depressed and manic groups had reduced T1ρ relaxation times in and around the basal ganglia compared to the control and euthymic groups. This study implicates the cerebellum and basal ganglia in the pathophysiology of bipolar disorder and its mood states, the roles of which are relatively unexplored. These findings motivate further investigation of the underlying cause of the abnormalities, and the potential role of altered metabolic activity in these regions.
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影响因子:
6.8
作者:
Fatemi SH;Folsom TD;Rooney RJ;Thuras PD
通讯作者:
Thuras PD
影响因子:
3.3
作者:
Heng, Serene;Song, Allen W.;Sim, Kang
通讯作者:
Sim, Kang
影响因子:
3.7
作者:
Bolbecker AR;Hong SL;Kent JS;Klaunig MJ;O'Donnell BF;Hetrick WP
通讯作者:
Hetrick WP
影响因子:
5.7
作者:
Avants BB;Tustison NJ;Song G;Cook PA;Klein A;Gee JC
通讯作者:
Gee JC
DOI:
10.1089/104454603322724931
发表时间:
2003-12-01
影响因子:
1.9
作者:
Cecil, KM;DelBello, MP;Strakowski, SM
通讯作者:
Strakowski, SM