Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Bipolar Disorder Program, Neurosciences Institute, Favaloro University, Buenos Aires, Argentina.
Bipolar Disord. 2020 Feb;22(1):28-37. doi: 10.1111/bdi.12841. Epub 2019 Oct 2.
Neurocognitive deficits have been widely reported in euthymic Bipolar Disorder (BD) patients and contribute to functional disability. However, the longitudinal trajectory of these deficits remains a subject of debate. Although most research to this date shows that neurocognitive deficits tend to be stable among middle-age BD patients, it remains plausible that deterioration occurs at either early or late stages of this condition.
We conducted a comprehensive meta-analysis of studies that reported longitudinal neurocognitive performance among individuals with BD either within the year of their diagnosis or among late-life BD patients. Pooled effects of standardized mean differences (SMDs) for changes in neuropsychological scores over follow-up were estimated using random effects model. We also examined effect moderators, such as length of follow-up, mood state, or pharmacological load.
Eight studies met inclusion criteria for recent-onset and four studies for late-life BD analysis. No evidence for a deterioration in neurocognitive functioning was observed among recent-onset BD patients (8 studies, 284 patients, SMD: 0.12, 95% CI -0.06 to 0.30, mean follow-up: 17 months) nor for late-life BD patients (4 studies, 153 patients, SMD: -0.35, 95% CI -0.84 to 0.15, mean follow-up: 33 months). None of the moderators were shown to be significant.
These results, when appraised together with the findings in middle-life BD patients and individuals at genetic risk for BD, suggest that neurodevelopmental factors might play a significant role in cognitive deficits in BD and do not support the notion of progressive cognitive decline in most patients with BD.
心境稳定的双相情感障碍(BD)患者存在广泛的神经认知缺陷,这导致了其功能障碍。然而,这些缺陷的纵向轨迹仍然存在争议。尽管迄今为止的大多数研究表明,BD 患者的神经认知缺陷往往在中年时保持稳定,但在这种情况下,无论是早期还是晚期,都有可能出现恶化。
我们对报告了 BD 患者在诊断后一年内或老年期 BD 患者中纵向神经认知表现的研究进行了全面的荟萃分析。使用随机效应模型估计了随访期间神经心理评分变化的标准化均数差(SMD)的汇总效应。我们还检查了效应调节剂,如随访时间长度、情绪状态或药物负荷。
八项研究符合近期发病的纳入标准,四项研究符合老年期 BD 分析的纳入标准。在近期发病的 BD 患者(8 项研究,284 名患者,SMD:0.12,95%CI-0.06 至 0.30,平均随访时间:17 个月)或老年期 BD 患者(4 项研究,153 名患者,SMD:-0.35,95%CI-0.84 至 0.15,平均随访时间:33 个月)中,均未观察到神经认知功能恶化的证据。没有发现任何调节剂有显著意义。
当与中年 BD 患者和具有 BD 遗传风险的个体的研究结果一起评估时,这些结果表明神经发育因素可能在 BD 的认知缺陷中发挥重要作用,并且不支持大多数 BD 患者认知能力逐渐下降的观点。