Late-Life Bipolar Disorder Subtypes According to Age Onset

J. Regala, Pedro Costa, Rafael Costa, João Reis
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Abstract

Abstract: This article characterizes the clinical differences between bipolar disorder (BD) subtypes in 44 early-onset (EOBD), 32 late-onset (LOBD), and 30 very-late-onset (VLOBD) disorders. We considered vascular mania in five LOBD and 17 VLOBD, with an association with right-sided lesions for VLOBD. Other nonvascular-related brain injuries preceded the emergence of mania: traumatic brain injury (one LOBD, two VLOBD), epilepsy/brain tumor (one LOBD), multiple sclerosis (one LOBD), and HIV-encephalopathy/cerebral toxoplasmosis (two VLOBD). No secondary mania was identified in 21.4% of the VLOBD and 64% of the LOBDd, corresponding to presumptive idiopathic/primary BD. A transdiagnostic conversion within the affective disorder spectrum occurred in 50% of the VLOBD, 30.8% of the LOBD, and 20.5% of the EOBD across the lifespan. An interplay between genetics and age-specific processes may underlie the neurobiological underpinnings of late-life-onset idiopathic/primary BD.
根据发病年龄划分的晚年躁郁症亚型
摘要:本文描述了双相情感障碍(BD)亚型在 44 例早发型(EOBD)、32 例晚发型(LOBD)和 30 例极晚发型(VLOBD)中的临床差异。我们考虑了 5 例 LOBD 和 17 例 VLOBD 中的血管性躁狂症,其中 VLOBD 与右侧病变有关。在出现躁狂症之前,还有其他非血管性脑损伤:脑外伤(1 例 LOBD,2 例 VLOBD)、癫痫/脑肿瘤(1 例 LOBD)、多发性硬化(1 例 LOBD)和 HIV 脑病/脑弓形体病(2 例 VLOBD)。在 21.4% 的 VLOBD 和 64% 的 LOBDd 中未发现继发性躁狂症,这与推定的特发性/原发性 BD 相符。在整个生命周期中,50%的VLOBD患者、30.8%的LOBD患者和20.5%的EOBD患者发生了情感障碍谱系内的跨诊断转换。遗传和年龄特异性过程之间的相互作用可能是晚年发病的特发性/原发性BD的神经生物学基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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