Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
Department of Psychology, University of Pittsburgh, Pittsburgh, PA, USA.
Neuropsychopharmacology. 2022 Aug;47(9):1693-1701. doi: 10.1038/s41386-022-01341-1. Epub 2022 May 20.
Depressive symptomology has been linked to low-grade peripheral inflammatory markers (PIMs), specifically C-reactive protein (CRP) and white blood cell count (WBC). However, such associations may be affected by multiple moderators (including race/ethnicity), though few well-powered and racially diverse studies have examined this. We examined 31 moderators of PIM-depression relationships in a large racially diverse cohort (n = 21,570). We also examined if associations between PIM and depression severity were dependent on clinical cutpoints for moderate depressive symptoms and elevated CRP. We found several positive moderators of PIM-depression relationships for both WBC and CRP: ongoing medication use (antidepressant, statin, or any prescription drug), presence of sleep concerns, and poor health status (β's = 0.06-0.21, p's < 0.05). For both WBC and CRP, individuals of non-Hispanic White race/ethnicity were found to have stronger PIM-depression associations overall relative to minoritized groups (B's = 0.14 to 1.01, p's < 0.05). For CRP, stronger PIM-depression relationships existed for individuals with moderate (or greater) depression severity or elevated CRP (B's = 0.27 to 0.49, p's < 0.05). Thus, a wide range of moderators appears to affect PIM-depression associations. These results could help identify participants with strong coupling of PIM-depression severity, to guide future research and personalized treatments for depression and to indicate gaps in the applicability of widely referenced theoretical models among racial/ethnic minoritized groups.
抑郁症状与低水平外周炎症标志物(PIMs)有关,特别是 C 反应蛋白(CRP)和白细胞计数(WBC)。然而,这种关联可能受到多种调节剂(包括种族/民族)的影响,尽管少数强大且种族多样化的研究已经对此进行了研究。我们在一个大型种族多样化的队列(n=21570)中检查了 PIM-抑郁关系的 31 个调节剂。我们还检查了 PIM 与抑郁严重程度之间的关联是否取决于中度抑郁症状和 CRP 升高的临床切点。我们发现白细胞计数和 CRP 与 PIM 抑郁关系存在几个积极的调节剂:持续用药(抗抑郁药、他汀类药物或任何处方药)、存在睡眠问题和健康状况不佳(β=0.06-0.21,p<0.05)。对于白细胞计数和 CRP,与少数族裔群体相比,非西班牙裔白人种族/民族的个体总体上具有更强的 PIM-抑郁关联(B=0.14 至 1.01,p<0.05)。对于 CRP,在中度(或更高)抑郁严重程度或 CRP 升高的个体中,PIM-抑郁关系更强(B=0.27 至 0.49,p<0.05)。因此,许多调节剂似乎会影响 PIM-抑郁关联。这些结果可以帮助确定具有 PIM-抑郁严重程度强耦合的参与者,为未来的抑郁研究和个性化治疗提供指导,并表明广泛参考的理论模型在少数族裔群体中的适用性存在差距。