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Acta Psychiatr Scand ; 139(3): 256-268, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30552759

RESUMO

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.


Assuntos
Transtorno Bipolar/metabolismo , Transtorno da Personalidade Borderline/metabolismo , Encéfalo/metabolismo , Adulto , Transtorno Bipolar/diagnóstico por imagem , Transtorno da Personalidade Borderline/diagnóstico por imagem , Encéfalo/diagnóstico por imagem , Feminino , Fluordesoxiglucose F18 , Humanos , Masculino , Neuroimagem , Tomografia por Emissão de Pósitrons , Compostos Radiofarmacêuticos , Adulto Jovem
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