躁郁症患者的色觉障碍:系统回顾

Jason Tran , Arnav Gupta , Nicholas Fabiano , Vinita Dhir , Katherine Larose , Iris Lasker , Stanley Wong , Ibrahim Y.Z. Mohammad , Steven Le , Jess G. Fiedorowicz , Risa Shorr , Andrea Zampieri , Alessio Bellato , Samuele Cortese , Marco Solmi
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引用次数: 0

摘要

双相情感障碍(BD)患者普遍存在视觉障碍,其神经病理生理学可能会对色觉产生潜在影响。本系统综述旨在评估躁郁症患者色觉障碍的现有数据,包括色辨别力和色盲。从开始到 2023 年 2 月 28 日,我们在 Medline、Embase 和 Google Scholar 上进行了符合 PRISMA 2020 的全面文献检索。我们的纳入标准是(1) 根据 DSM、ICD 或临床诊断确诊为双相情感障碍 I 或 II 的患者;(2) 调查色觉(即包括色盲和色弱)的研究;(3) 不限制对比组的条件。研究质量评估采用美国国立卫生研究院研究质量评估工具进行。共纳入了来自巴西、荷兰和美国的五项研究,共 338 名患者。三项横断面研究评估了 BD 患者的色辨别能力,两项病例系列研究评估了 BD 患者的色盲情况。三项横断面研究证实,与健康参照者相比,BD 患者在轻度至中度躁狂症期间的色辨别能力有所下降。后两篇文章提出的证据较少,证明 BD 存在 X 连锁遗传。我们的综述显示,有证据表明轻度至中度躁狂症患者的色辨别能力降低。然而,鉴于目前的局限性,还需要进一步的研究来验证这些发现,并扩展到 BD 的其他情绪状态。未来的研究将受益于更多的多机构数据、更大的样本量、适当的盲法、生物标志物的使用以及对混杂因素的统计调整,以充分阐明色觉辨别力在 BD 中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Colour vision impairments in bipolar disorder: A systematic review

Visual impairments are common in patients with bipolar disorder (BD), and the neuropathophysiology may suggest a potential influence on colour vision. This systematic review aimed to assess existing data of colour vision impairment, including chromatic discrimination and colour blindness in patients with BD. Comprehensive literature search compliant with PRISMA 2020 was conducted in Medline, Embase, and Google Scholar from inception to February 28th, 2023. Our inclusion criteria were: (1) patients with a diagnosis of bipolar I or II disorder based on DSM, ICD, or clinical diagnosis, and (2) study investigating colour vision (i.e., including colour blindness and discrimination), with (3) no restrictions on the condition of the comparator group. Study quality appraisal was performed using the NIH Study Quality Assessment Tool. Five studies from Brazil, Netherlands, and USA, with 338 patients were included. Three cross-sectional studies assessed chromatic discrimination and two case-series assessed colour blindness in patients with BD. The three cross-sectional studies support reduced chromatic discrimination during mild to moderate mania in BD when compared to healthy comparators. The latter two articles presented low evidence of an X-linked inheritance of BD. Our review indicates evidence of reduced chromatic discrimination in mild to moderate mania. However, further research is needed to validate these findings and to extend to other mood states in BD given current limitations. Future studies can benefit from further multi-institutional data, larger sample sizes, appropriate blinding, the use of biomarkers, and statistical adjustment to confounders to fully elucidate the role of chromatic discrimination in BD.

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