Duffy Anne, Jones Steven, Goodday Sarah, Bentall Richard
Department of Psychiatry, University of Calgary, Calgary, Alberta, Canada (Dr Duffy); Mood Disorders Centre of Ottawa, Ottawa, Ontario, Canada (Dr Duffy); Lancaster University, Division of Health Research, Lancaster, United Kingdom (Dr Jones); Department of Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada (Ms Goodday, Dr Bentall); University of Liverpool, Institute of Psychology Health and Society, Liverpool, United Kingdom (Ms Goodday and Dr Bentall).
Int J Neuropsychopharmacol. 2015 Jun 25;19(1):pyv071. doi: 10.1093/ijnp/pyv071.
Psychiatric illnesses like bipolar disorder are increasingly understood to be neurodevelopmental disorders with clinical, psychological, and biological indicators recognizable long before the emergence of the full-blown syndromes.
This paper is a selective review of findings from studies of high-risk children of affected parents that inform the knowledge of illness risk and development markers of bipolar disorder. We specifically focus on candidate clinical, biological, and psychological risk indicators that could serve as targets for future early intervention and prevention studies.
There is convergent evidence from prospective studies that bipolar disorder typically debuts as depressive episodes after puberty. In some high-risk children, sleep and anxiety disorders precede mood disorders by several years and reflect an increased vulnerability. An association between early exposure to adversity (eg, exposure to parental illness, neglect from mother) and increased risk of psychopathology may be mediated through increased stress reactivity evident at both behavioral and biological levels. Inter-related psychological processes including reward sensitivity, unstable self-esteem, rumination, and positive self-appraisal are risk factors for mood disorders. Disturbances in circadian rhythm and immune dysfunction are associated with mood disorders and may be vulnerability markers influenced by these other risk factors.
There is accruing evidence of a number of measurable and potentially modifiable markers of vulnerability and developing illness in youth at familial risk for bipolar disorder. Longitudinal studies of multiple biological and psychological risk processes in high-risk offspring, both individually and together, will improve our understanding of illness onset and lead to the development of specific early interventions.
双相情感障碍等精神疾病越来越被认为是神经发育障碍,在全面综合征出现之前很久就有可识别的临床、心理和生物学指标。
本文是对来自受影响父母的高危儿童研究结果的选择性综述,这些研究为双相情感障碍的疾病风险和发展标志物知识提供了信息。我们特别关注那些可作为未来早期干预和预防研究目标的候选临床、生物学和心理风险指标。
前瞻性研究有一致的证据表明,双相情感障碍通常在青春期后以抑郁发作首次出现。在一些高危儿童中,睡眠和焦虑障碍比情绪障碍早出现数年,反映出易感性增加。早期暴露于逆境(如父母患病、母亲忽视)与精神病理学风险增加之间的关联可能通过行为和生物学层面明显增加的应激反应性来介导。包括奖励敏感性、不稳定的自尊、沉思和积极的自我评估在内的相互关联的心理过程是情绪障碍的风险因素。昼夜节律紊乱和免疫功能障碍与情绪障碍有关,可能是受这些其他风险因素影响的易感性标志物。
越来越多的证据表明,在有双相情感障碍家族风险的青少年中,存在许多可测量且可能可改变的易感性和疾病发展标志物。对高危后代中多种生物学和心理风险过程进行纵向研究,无论是单独研究还是综合研究,都将提高我们对疾病发作的理解,并导致特定早期干预措施的发展。