Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Department of Psychology, Georgia State University, Atlanta, GA, USA.
Neuropsychopharmacology. 2024 Feb;49(3):593-599. doi: 10.1038/s41386-023-01737-7. Epub 2023 Sep 26.
Prior research has shown that racial discrimination (RD) impacts activation in threat network regions, including the ventromedial prefrontal cortex (vmPFC) and middle occipital cortex during attention to threat-relevant stimuli. However, little is known about the biological mechanisms that may modulate these effects; inflammation may be a pathway linking RD and threat network activation. As such, the current study aimed to explore whether systemic inflammation, measured by C-reactive protein (CRP) levels, may moderate the relationship between RD and activation in the vmPFC and middle occipital cortex during attention to threat. Blood samples for inflammatory marker (CRP) assays were obtained from forty Black American women (mean [SD] age, 39.93 [9.97] years; range, 22-58 years) recruited from an ongoing trauma study; participants also viewed threat-relevant stimuli as part of an attention task during fMRI. We found that CRP moderated the relationship between RD and vmPFC activation during attention to threat, such that participants with relatively higher concentrations of CRP ( ≥ 23.97 mg/L) demonstrated significant positive associations between RD and vmPFC activation [β = 0.18, CI (0.04, 0.32), t = 2.65, p = 0.01]. No significant associations were observed for participants who showed moderate (10.89 mg/L) or low (0.20 mg/L) CRP concentrations. CRP did not moderate the relationship between RD and middle occipital cortex activation. Our data present a mechanism through which RD may influence immune system activation and, in turn, threat network activation. Inflammation may contribute to brain health vulnerabilities in Black Americans via its effects on threat circuits; this merits further investigation in large-scale studies.
先前的研究表明,种族歧视(RD)会影响威胁网络区域的激活,包括腹内侧前额叶皮层(vmPFC)和中枕叶皮层,而当注意到与威胁相关的刺激时更是如此。然而,对于可能调节这些影响的生物学机制知之甚少;炎症可能是将 RD 与威胁网络激活联系起来的途径。因此,本研究旨在探讨全身炎症是否可以调节 C 反应蛋白(CRP)水平,以调节 RD 与威胁相关注意期间 vmPFC 和中枕叶皮层激活之间的关系。从正在进行的创伤研究中招募了 40 名美国黑人女性(平均[SD]年龄,39.93[9.97]岁;范围,22-58 岁)的血液样本进行炎症标志物(CRP)检测;参与者还在 fMRI 期间进行了与威胁相关的刺激的注意任务。我们发现 CRP 调节了 RD 与威胁相关注意期间 vmPFC 激活之间的关系,以至于 CRP 浓度较高的参与者(≥23.97mg/L)在 RD 与 vmPFC 激活之间存在显著的正相关关系[β=0.18,CI(0.04,0.32),t=2.65,p=0.01]。在 CRP 浓度适中(10.89mg/L)或较低(0.20mg/L)的参与者中,没有观察到显著的相关性。CRP 没有调节 RD 与中枕叶皮层激活之间的关系。我们的数据提出了一种机制,通过该机制,RD 可能会影响免疫系统的激活,进而影响威胁网络的激活。炎症可能会通过对威胁回路的影响而导致黑人群体的大脑健康脆弱性;这需要在大型研究中进一步调查。