Slyepchenko Anastasiya, Minuzzi Luciano, Frey Benicio N
Women's Health Concerns Clinic and Mood Disorders Treatment and Research Centre, St Joseph's Healthcare Hamilton, Hamilton, ON, Canada.
Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.
Front Psychiatry. 2021 Aug 25;12:719241. doi: 10.3389/fpsyt.2021.719241. eCollection 2021.
Bipolar disorder (BD) differs in its clinical presentation in females compared to males. A number of clinical characteristics have been associated with BD in females: more rapid cycling and mixed features; higher number of depressive episodes; and a higher prevalence of BD type II. There is a strong link between BD and risk for postpartum mood episodes, and a substantial percentage of females with BD experience premenstrual mood worsening of varying degrees of severity. Females with premenstrual dysphoric disorder (PMDD)-the most severe form of premenstrual disturbances-comorbid with BD appear to have a more complex course of illness, including increased psychiatric comorbidities, earlier onset of BD, and greater number of mood episodes. Importantly, there may be a link between puberty and the onset of BD in females with comorbid PMDD and BD, marked by a shortened gap between the onset of BD and menarche. In terms of neurobiology, comorbid BD and PMDD may have unique structural and functional neural correlates. Treatment of BD comorbid with PMDD poses challenges, as the first line treatment of PMDD in the general population is selective serotonin reuptake inhibitors, which produce risk of treatment-emergent manic symptoms. Here, we review current literature concerning the clinical presentation, illness burden, and unique neurobiology of BD comorbid with PMDD. We additionally discuss obstacles faced in symptom tracking, and management of these comorbid disorders.
双相情感障碍(BD)在女性中的临床表现与男性不同。一些临床特征与女性BD相关:循环发作更迅速且有混合特征;抑郁发作次数更多;II型双相情感障碍患病率更高。BD与产后情绪发作风险之间存在紧密联系,相当比例的BD女性会经历不同严重程度的经前情绪恶化。患有经前烦躁障碍(PMDD,经前紊乱最严重的形式)且合并BD的女性似乎有更复杂的病程,包括精神共病增加、BD发病更早以及情绪发作次数更多。重要的是,在患有PMDD和BD共病的女性中,青春期与BD发病之间可能存在联系,其特征是BD发病与初潮之间的间隔缩短。在神经生物学方面,BD与PMDD共病可能具有独特的结构和功能神经关联。BD与PMDD共病的治疗带来挑战,因为一般人群中PMDD的一线治疗是选择性5-羟色胺再摄取抑制剂,这会产生治疗引发的躁狂症状风险。在此,我们综述了关于BD与PMDD共病的临床表现、疾病负担及独特神经生物学的当前文献。我们还讨论了症状追踪以及这些共病障碍管理中面临的障碍。