Gulseren Seref, Gurcan Mustafa, Gulseren Leyla, Gelal Fazil, Erol Almila
Department of Psychiatry, Ataturk Training and Research Hospital, Izmir, Turkey.
Arch Med Res. 2006 Jan;37(1):79-85. doi: 10.1016/j.arcmed.2005.04.009.
This study investigates the frequency of hyperintensities, which are common in bipolar disorder, in sufferers' siblings who are free of bipolar disorder and to ascertain whether these lesions reflect any familial characteristics. It offers an assessment of the relationship between these lesions and clinical characteristics.
The study group consisted of 12 patients with bipolar disorder, their siblings who had no history of mental disorder, and a matched control group. All three groups were assessed using SCID-I (Structured Clinical Interview for DSM-IV Axis I Disorders) for diagnosis, and MRI (magnetic resonance imaging) for signal hyperintensity.
No periventricular white matter lesions were encountered in any groups. It was found that in the patients and siblings, the location was in the right cerebral hemisphere in the deep white matter, whereas it was in the left cerebral hemisphere for the control group. Only in the patient group were lesions detected in subcortical white matter in the right cerebral hemisphere. The lesions were localized in the fronto-parietal area. Considering the brain as a whole, more hyperintensities were detected in the patient group compared to the other two groups. The onset of the disorder with a manic episode was increasing probably in the presence of hyperintensities.
Despite being alike in terms of age, more hyperintensities were detected in the patient group than in the siblings and control groups. Contrary to the control group, however, hyperintensities were localized in the right cerebral hemisphere in both the patients and the siblings groups. Hyperintensities seen in the left cerebral hemisphere yield a nonspecific impression. Siblings who have hyperintensities in the right cerebral hemisphere should be followed up and investigated with regard to bipolar disorder.
本研究调查了双相情感障碍患者中常见的高信号在无双相情感障碍的患者亲属中的出现频率,并确定这些病变是否反映了任何家族特征。本研究还评估了这些病变与临床特征之间的关系。
研究组包括12名双相情感障碍患者、他们无精神障碍病史的亲属以及一个匹配的对照组。所有三组均使用SCID-I(《精神疾病诊断与统计手册》第四版轴I障碍结构化临床访谈)进行诊断,并使用MRI(磁共振成像)检测信号高信号。
所有组均未发现脑室周围白质病变。研究发现,患者及其亲属组的病变位于右侧大脑半球深部白质,而对照组的病变位于左侧大脑半球。仅在患者组中,右侧大脑半球的皮质下白质检测到病变。病变位于额顶叶区域。从整个大脑来看,与其他两组相比,患者组检测到更多的高信号。躁狂发作起病的患者可能更易出现高信号。
尽管患者组与亲属组和对照组年龄相仿,但患者组检测到的高信号多于亲属组和对照组。然而,与对照组不同的是,患者组和亲属组的高信号均位于右侧大脑半球。左侧大脑半球出现的高信号提示非特异性表现。右侧大脑半球出现高信号的亲属应针对双相情感障碍进行随访和调查。