Patterns of altered regional brain glucose metabolism in borderline personality disorder and bipolar II disorder

被引:20
作者
Boen, E. [1 ,2 ,3 ]
Hjornevik, T. [4 ]
Hummelen, B. [5 ,6 ]
Elvsashagen, T. [3 ,7 ,8 ]
Moberget, T. [3 ,7 ]
Holtedahl, J. E. [4 ]
Babovic, A. [9 ]
Hol, P. K. [10 ]
Karterud, S. [3 ]
Malt, U. F. [3 ]
机构
[1] Oslo Univ Hosp, Psychosomat & CL Psychiat, Div Mental Hlth & Addict, Oslo, Norway
[2] Diakonhjemmet Hosp, Dept Psychiat, Oslo, Norway
[3] Univ Oslo, Inst Clin Med, Oslo, Norway
[4] KG Jebsen Ctr Psychosis Res, Dept Diagnost Phys, Oslo, Norway
[5] KG Jebsen Ctr Psychosis Res, Dept Personal Psychiat, Oslo, Norway
[6] KG Jebsen Ctr Psychosis Res, Dept Res & Dev, Oslo, Norway
[7] KG Jebsen Ctr Psychosis Res, Norwegian Ctr Mental Disorders Res NORMENT, Oslo, Norway
[8] Oslo Univ Hosp, Dept Neurol, Oslo, Norway
[9] Oslo Univ Hosp, Dept Nucl Med, Oslo, Norway
[10] Oslo Univ Hosp, Intervent Ctr, Oslo, Norway
关键词
bipolar disorder; borderline personality disorder; neuroimaging; WHITE-MATTER ALTERATIONS; RESTING STATE; FEMALE-PATIENTS; VALIDATION; CONNECTIVITY; METAANALYSIS; DEPRESSION; RESPONSES; COGNITION; INSULA;
D O I
10.1111/acps.12997
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective The relationship between borderline personality disorder (BPD) and bipolar II disorder (BIP-II) is disputed but understudied. Here, we investigated brain glucose metabolism in these patient groups and healthy control subjects (HCs). Methods Sixty-five subjects, 22 BPD (19 females), 22 BIP-II (17 females), and 21 HC (14 females), were examined using 2-deoxy-2[18F]-fluoro-d-glucose positron-emission tomography (PET) scanning. Only patients without reciprocal comorbidity were recruited; BPD participants without bipolar spectrum pathology; BIP-II participants without cluster A/B personality pathology. Groups were compared pairwise. Associations with mood state and childhood trauma were analyzed. Results Both patient groups exhibited hypometabolism compared with HCs in insula, brainstem, and frontal white matter. Additionally, BPD patients showed hypometabolism in hypothalamus, midbrain, and striatum; BIP-II patients in cerebellum. Uncorrected analyses showed cortical areas of higher metabolism in BIP-II than BPD, and associations with clinical variables differed between the groups. Conclusion Reduced metabolism in the insula regions was shown in both disorders, suggesting shared pathophysiological mechanisms. The observed patterns of altered metabolism specific to each patient group, as well as the uncorrected results, may also suggest differential pathophysiology. However, these latter findings must be interpreted cautiously given the non-significant corrected results in the direct comparison between the disorders.
引用
收藏
页码:256 / 268
页数:13
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