Department of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, MN, United States.
Department of Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, United States; Department of Psychiatry, Harvard Medical School, Boston, MA, United States; Division of Translational Neuroscience, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Schizophr Res. 2023 May;255:69-78. doi: 10.1016/j.schres.2023.03.030. Epub 2023 Mar 23.
Elevated markers of peripheral inflammation are common in psychosis spectrum disorders and have been associated with brain anatomy, pathology, and physiology as well as clinical outcomes. Preliminary evidence suggests a link between inflammatory cytokines and C-reactive protein (CRP) with generalized cognitive impairments in a subgroup of individuals with psychosis. Whether these patients with elevated peripheral inflammation demonstrate deficits in specific cognitive domains remains unclear. To examine this, seventeen neuropsychological and sensorimotor tasks and thirteen peripheral inflammatory and microvascular markers were quantified in a subset of B-SNIP consortium participants (129 psychosis, 55 healthy controls). Principal component analysis was conducted across the inflammatory markers, resulting in five inflammation factors. Three discrete latent cognitive domains (Visual Sensorimotor, General Cognitive Ability, and Inhibitory Behavioral Control) were characterized based on the neurobehavioral battery and examined in association with inflammation factors. Hierarchical clustering analysis identified cognition-sensitive high/low inflammation subgroups. Among persons with psychotic disorders but not healthy controls, higher inflammation scores had significant associations with impairments of Inhibitory Control (R = 0.100, p-value = 2.69e, q-value = 0.004) and suggestive associations with Visual Sensorimotor function (R = 0.039, p-value = 0.024, q-value = 0.180), but not with General Cognitive Ability (R = 0.015, p-value = 0.162). Greater deficits in Inhibitory Control were observed in the high inflammation patient subgroup, which represented 30.2 % of persons with psychotic disorders, as compared to the low inflammation psychosis subgroup. These findings indicate that inflammation dysregulation may differentially impact specific neurobehavioral domains across psychotic disorders, particularly performance on tasks requiring ongoing behavioral monitoring and control.
外周炎症标志物升高在精神疾病谱系障碍中很常见,并且与大脑解剖结构、病理学和生理学以及临床结果有关。初步证据表明,在精神疾病患者亚组中,炎症细胞因子和 C 反应蛋白(CRP)与广泛的认知障碍之间存在关联。这些外周炎症升高的患者是否在特定认知领域存在缺陷尚不清楚。为了研究这一点,B-SNIP 联盟参与者的一部分(129 名精神病患者,55 名健康对照者)中定量检测了 17 项神经心理学和感觉运动任务以及 13 项外周炎症和微血管标志物。对炎症标志物进行了主成分分析,得出了 5 个炎症因子。根据神经行为测试,将三个离散的潜在认知域(视觉感觉运动、一般认知能力和抑制行为控制)特征化,并与炎症因子进行了关联研究。层次聚类分析确定了对认知敏感的高低炎症亚组。在精神障碍患者中(而非健康对照组中),较高的炎症评分与抑制控制障碍显著相关(R=0.100,p 值=2.69e,q 值=0.004),与视觉感觉运动功能呈提示性关联(R=0.039,p 值=0.024,q 值=0.180),但与一般认知能力无关(R=0.015,p 值=0.162)。与低炎症精神病亚组相比,在高炎症患者亚组中观察到抑制控制能力的更大缺陷,该亚组占精神障碍患者的 30.2%。这些发现表明,炎症失调可能会在精神疾病中以不同的方式影响特定的神经行为域,特别是需要持续行为监测和控制的任务。