Kessing Lars Vedel, Munkholm Klaus, Faurholt-Jepsen Maria, Miskowiak Kamilla Woznica, Nielsen Lars Bo, Frikke-Schmidt Ruth, Ekstrøm Claus, Winther Ole, Pedersen Bente Klarlund, Poulsen Henrik Enghusen, McIntyre Roger S, Kapczinski Flavio, Gattaz Wagner F, Bardram Jakob, Frost Mads, Mayora Oscar, Knudsen Gitte Moos, Phillips Mary, Vinberg Maj
Department of Psychiatry, Psychiatric Center Copenhagen, Copenhagen, Denmark.
Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
BMJ Open. 2017 Jun 23;7(6):e015462. doi: 10.1136/bmjopen-2016-015462.
Bipolar disorder is an often disabling mental illness with a lifetime prevalence of 1%-2%, a high risk of recurrence of manic and depressive episodes, a lifelong elevated risk of suicide and a substantial heritability. The course of illness is frequently characterised by progressive shortening of interepisode intervals with each recurrence and increasing cognitive dysfunction in a subset of individuals with this condition. Clinically, diagnostic boundaries between bipolar disorder and other psychiatric disorders such as unipolar depression are unclear although pharmacological and psychological treatment strategies differ substantially. Patients with bipolar disorder are often misdiagnosed and the mean delay between onset and diagnosis is 5-10 years. Although the risk of relapse of depression and mania is high it is for most patients impossible to predict and consequently prevent upcoming episodes in an individual tailored way. The identification of objective biomarkers can both inform bipolar disorder diagnosis and provide biological targets for the development of new and personalised treatments. Accurate diagnosis of bipolar disorder in its early stages could help prevent the long-term detrimental effects of the illness.The present Bipolar Illness Onset study aims to identify (1) a composite blood-based biomarker, (2) a composite electronic smartphone-based biomarker and (3) a neurocognitive and neuroimaging-based signature for bipolar disorder.
The study will include 300 patients with newly diagnosed/first-episode bipolar disorder, 200 of their healthy siblings or offspring and 100 healthy individuals without a family history of affective disorder. All participants will be followed longitudinally with repeated blood samples and other biological tissues, self-monitored and automatically generated smartphone data, neuropsychological tests and a subset of the cohort with neuroimaging during a 5 to 10-year study period.
The study has been approved by the Local Ethical Committee (H-7-2014-007) and the data agency, Capital Region of Copenhagen (RHP-2015-023), and the findings will be widely disseminated at international conferences and meetings including conferences for the International Society for Bipolar Disorders and the World Federation of Societies for Biological Psychiatry and in scientific peer-reviewed papers.
NCT02888262.
双相情感障碍是一种常导致残疾的精神疾病,终生患病率为1%-2%,躁狂和抑郁发作复发风险高,终生自杀风险升高且具有显著的遗传度。疾病进程的特征通常是每次复发时发作间期逐渐缩短,部分患者会出现认知功能障碍加重。临床上,双相情感障碍与其他精神疾病(如单相抑郁症)之间的诊断界限并不明确,尽管药物和心理治疗策略存在很大差异。双相情感障碍患者常被误诊,从发病到诊断的平均延迟为5至10年。尽管抑郁和躁狂复发风险很高,但对大多数患者来说,无法预测并因此以个体化方式预防即将到来的发作。识别客观生物标志物既能为双相情感障碍诊断提供依据,也能为开发新的个性化治疗提供生物学靶点。早期准确诊断双相情感障碍有助于预防该疾病的长期有害影响。目前的双相情感障碍发病研究旨在识别:(1)一种基于血液的复合生物标志物;(2)一种基于电子智能手机的数据复合生物标志物;(3)双相情感障碍的神经认知和神经影像学特征。
该研究将纳入300例新诊断/首发双相情感障碍患者、200例其健康的兄弟姐妹或后代以及100例无情感障碍家族史的健康个体。在5至10年的研究期间,所有参与者将接受纵向随访,采集重复的血液样本和其他生物组织样本,进行自我监测并自动生成智能手机数据,接受神经心理学测试,部分队列成员还将接受神经影像学检查。
该研究已获得当地伦理委员会(H-7-2014-007)和哥本哈根首都地区数据机构(RHP-2015-023)的批准,研究结果将在国际会议上广泛传播,包括国际双相情感障碍学会和世界生物精神病学协会联合会的会议,并发表在科学同行评审论文中。
NCT02888262。