Sealock Julia M, Chen Guanhua, Davis Lea K
Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA.
Complex Psychiatry. 2023 Dec;9(1-4):1-10. doi: 10.1159/000528605. Epub 2022 Dec 9.
Antidepressants have documented anti-inflammatory effects on pro-inflammatory biomarkers. However, the long-term effects of antidepressants on inflammatory markers and the effects of different antidepressant classes on pro-inflammatory biomarkers are largely unexplored. Here, we evaluate the short- and long-term effects of all antidepressant classes on a clinical immune marker, white blood cell count (WBC).
Using a retrospective study design, we extracted WBC count and prescription medications from electronic health records at Vanderbilt University Medical Center. We created a longitudinal model to evaluate the short- and long-term effects of these medications on WBC count. We validated our longitudinal model using two known anti-inflammatory medications, biologic immunosuppressants, and chemotherapy, and one medication class without known immunomodulatory properties, contraceptives. We used the longitudinal model to determine the effects of antidepressant use on WBC count stratified by drug class.
Biologic immunosuppressant and chemotherapy use was associated with decreased WBC count, but contraceptive use did not associate with changes in WBC count, validating our longitudinal modeling approach. All antidepressant classes were associated with decreased WBC count in the long-term cohorts. SSRI and atypical use also associated with decreased WBC count in the short-term cohort.
Using electronic health record data, we show all antidepressant classes exhibit anti-inflammatory effects on a clinical immune marker, WBC count. Additionally, our results indicate that in some cases the anti-inflammatory effects of antidepressants persist over at least a 1-year time frame. Our work contributes to the immunomodulatory knowledge of antidepressants and motivates future studies investigating alternative therapeutic routes for antidepressants.
抗抑郁药已被证明对促炎生物标志物具有抗炎作用。然而,抗抑郁药对炎症标志物的长期影响以及不同类别的抗抑郁药对促炎生物标志物的影响在很大程度上尚未得到探索。在此,我们评估了所有类别的抗抑郁药对临床免疫标志物白细胞计数(WBC)的短期和长期影响。
采用回顾性研究设计,我们从范德比尔特大学医学中心的电子健康记录中提取白细胞计数和处方药信息。我们创建了一个纵向模型来评估这些药物对白细胞计数的短期和长期影响。我们使用两种已知的抗炎药物、生物免疫抑制剂和化疗药物,以及一种没有已知免疫调节特性的药物类别(避孕药)来验证我们的纵向模型。我们使用纵向模型来确定按药物类别分层的抗抑郁药使用对白细胞计数的影响。
生物免疫抑制剂和化疗药物的使用与白细胞计数降低有关,但避孕药的使用与白细胞计数变化无关,这验证了我们的纵向建模方法。在长期队列中,所有类别的抗抑郁药都与白细胞计数降低有关。在短期队列中,选择性5-羟色胺再摄取抑制剂(SSRI)和非典型抗抑郁药的使用也与白细胞计数降低有关。
利用电子健康记录数据,我们表明所有类别的抗抑郁药对临床免疫标志物白细胞计数均表现出抗炎作用。此外,我们的结果表明,在某些情况下,抗抑郁药的抗炎作用至少持续1年时间。我们的工作有助于增进对抗抑郁药免疫调节作用的了解,并推动未来研究探索抗抑郁药的替代治疗途径。