Levenson Jessica C, Axelson David A, Merranko John, Angulo Melina, Goldstein Tina R, Mullin Benjamin C, Goldstein Benjamin I, Brent David A, Diler Rasim, Hickey Mary Beth, Monk Kelly, Sakolsky Dara, Kupfer David J, Birmaher Boris
Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Nationwide Children's Hospital Research Institute and The Ohio State University College of Medicine, Columbus, OH, USA.
Bipolar Disord. 2015 Dec;17(8):836-48. doi: 10.1111/bdi.12345. Epub 2015 Nov 7.
Disruptions in sleep and dysregulation in circadian functioning may represent core abnormalities in the pathophysiology of bipolar disorder (BP). However, it is not clear whether these dysfunctions are state or trait markers of BP. This report compared sleep and circadian phenotypes among three groups: offspring of parents with BP diagnosed with BP at intake (BP/OB; n = 47), offspring of parents with BP without BP at intake (non-BP/OB; n = 386), and offspring of matched control parents who did not have BP (controls; n = 301). We also examined the association of baseline sleep parameters with subsequent development of BP among the non-BP/OB group.
Pittsburgh Bipolar Offspring Study youth (ages 6-18 years) and their parents completed assessments every two years pertaining to the child's sleep and circadian phenotypes and current psychopathology. Mixed-effects models examined differences in baseline sleep and circadian variables among the three groups.
BP/OB offspring who were in a mood episode differed significantly on sleep parameters from the non-BP/OB and the offspring of controls, such as having inadequate sleep. Mixed logistic regression procedures showed that baseline sleep and circadian variables, such as frequent waking during the night, significantly predicted the development of BP among non-BP/OB over longitudinal follow-up.
While lifetime diagnostic status accounted for differences among the groups in sleep and circadian disturbances, psychopathology explained the differences even further. Additionally, sleep disturbance may be a prognostic indicator of the development of BP in high-risk youth. Future studies are required to further disentangle whether sleep and circadian disruption are state or trait features of BP.
睡眠中断和昼夜节律功能失调可能是双相情感障碍(BP)病理生理学的核心异常表现。然而,尚不清楚这些功能障碍是BP的状态标记还是特质标记。本报告比较了三组人群的睡眠和昼夜节律表型:摄入期被诊断为BP的双相情感障碍患者的后代(BP/OB;n = 47)、摄入期未患BP的双相情感障碍患者的后代(非BP/OB;n = 386)以及未患BP的匹配对照父母的后代(对照组;n = 301)。我们还研究了非BP/OB组中基线睡眠参数与BP后续发展之间的关联。
匹兹堡双相情感障碍后代研究中的青少年(6 - 18岁)及其父母每两年完成一次关于孩子睡眠和昼夜节律表型以及当前精神病理学的评估。混合效应模型检验了三组之间基线睡眠和昼夜节律变量的差异。
处于情绪发作期的BP/OB后代在睡眠参数方面与非BP/OB后代和对照组后代有显著差异,比如睡眠不足。混合逻辑回归分析显示,基线睡眠和昼夜节律变量,如夜间频繁醒来,在纵向随访中能显著预测非BP/OB组中BP的发展。
虽然终生诊断状态解释了各组在睡眠和昼夜节律紊乱方面的差异,但精神病理学进一步解释了这些差异。此外,睡眠障碍可能是高危青少年发生BP的一个预后指标。未来需要进一步研究以厘清睡眠和昼夜节律紊乱是BP的状态特征还是特质特征。