Bipolar Disorder Program and Molecular Psychiatry Unit, Hospital de Clínicas, UFRGS, INCT Translational Medicine, Porto Alegre, Brazil.
Prog Neuropsychopharmacol Biol Psychiatry. 2009 Nov 13;33(8):1366-71. doi: 10.1016/j.pnpbp.2009.07.027. Epub 2009 Aug 8.
Recent data show that biomarkers differ in early and late-stage bipolar disorder (BD). Here we propose a model of staging for bipolar disorder that emphasizes the potential use of biomarkers for differentiating early and late-stage BD patients in the inter-episodic period. The proposed model includes a Latent phase: patients at "ultra-high-risk" for developing BD, characterized by a family history of BD, temperament traits, mood, and anxiety symptoms as well as genetic vulnerability for developing the disorder; Stage I: patients who return to their baseline level of functioning when mood episodes resolve; Stage II: biomarkers and functioning impairment are related to comorbidities or rapid-cycling presentations; Stage III: persistent cognitive and functioning impairment in the inter-episode period as well as changes in biomarkers; and Stage IV: same findings as in Stage III associated with extreme cognitive and functioning impairment, to the point that patients are unable to live autonomously. Empirical testing will determine the ability of the present model to inform patients and clinicians about both prognosis and response to treatment.
最近的数据表明,生物标志物在双相情感障碍(BD)的早期和晚期存在差异。在这里,我们提出了一种双相情感障碍分期模型,强调了生物标志物在区分间歇期的早期和晚期双相情感障碍患者方面的潜在应用。所提出的模型包括一个潜伏期:处于发展为 BD 的“超高风险”的患者,其特征是双相情感障碍家族史、气质特征、情绪和焦虑症状以及易患该疾病的遗传易感性;第一阶段:当情绪发作缓解时,患者恢复到基线功能水平;第二阶段:生物标志物和功能障碍与共病或快速循环表现有关;第三阶段:在间歇期持续存在认知和功能障碍以及生物标志物的变化;第四阶段:与第三阶段相同的发现与极端认知和功能障碍有关,以至于患者无法独立生活。实证检验将确定本模型在告知患者和临床医生预后以及对治疗的反应方面的能力。