دانلود مقاله ISI انگلیسی شماره 73046
ترجمه فارسی عنوان مقاله

چه ویژگی های بالینی قبل از شروع اختلال دو قطبی؟

عنوان انگلیسی
What clinical features precede the onset of bipolar disorder?
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
73046 2015 7 صفحه PDF
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Journal of Psychiatric Research, Volume 62, March 2015, Pages 71–77

ترجمه کلمات کلیدی
اختلال دو قطبی، ژنتیک، روانپزشکی، نوجوانان در خطر، ریسک بالا
کلمات کلیدی انگلیسی
Bipolar disorder; Genetic; Psychopathology; Adolescent; At risk; High risk

چکیده انگلیسی

Despite a growing number of reports, there is still limited knowledge of the clinical features that precede the onset of bipolar disorder (BD). To explore this, we investigated baseline data from a prospectively evaluated longitudinal cohort of subjects aged 12–30 years to compare: first, lifetime rates of clinical features between a) subjects at increased genetic risk for developing BD (‘AR’), b) participants from families without mental illness (‘controls’), and c) those with established BD; and, second, prior clinical features that predict the later onset of affective disorders in these same three groups. This is the first study to report such comparisons between these three groups (though certainly not the first to compare AR and control samples). 118 AR participants with a parent or sibling with BD (including 102 with a BD parent), 110 controls, and 44 BD subjects were assessed using semi-structured interviews. AR subjects had significantly increased lifetime risks for depressive, anxiety and behavioural disorders compared to controls. Unlike prior reports, preceding anxiety and behavioural disorders were not found to increase risk for later onset of affective disorders in the AR sample, perhaps due to limited sample size. However, preceding behavioural disorders did predict later onset of affective disorders in the BD sample. The findings that i) AR subjects had higher rates of depressive, anxiety and behavioural disorders compared to controls, and ii) prior behavioural disorders increased the risk to later development of affective disorders in the BD group, suggest the possibility of therapeutic targeting for these disorders in those at high genetic risk for BD.