Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Department of Neurology, Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
J Neurovirol. 2023 Aug;29(4):440-448. doi: 10.1007/s13365-023-01142-2. Epub 2023 Jun 8.
Depression is a common illness in people with HIV (PWH) and is associated with substantial morbidity and mortality. The mechanisms that underpin depression in PWH remain incompletely elucidated, and more research is therefore needed to develop effective treatments. One hypothesis is that neurotransmitter levels may be altered. These levels could be influenced by the chronic inflammation and viral persistence that occurs in PWH. We examined a panel of cerebrospinal fluid (CSF) neurotransmitters in PWH on suppressive antiretroviral therapy (ART), many of whom had a current depression diagnosis. CSF monoamine neurotransmitters and their metabolites were measured from participants in studies at the Emory Center for AIDS Research (CFAR). Only participants on stable ART with suppressed HIV RNA from both plasma and CSF were analyzed. Neurotransmitter levels were measured with high-performance liquid chromatography (HPLC). Neurotransmitters and their metabolites included dopamine (DA), homovanillic acid (HVA, a major metabolite of dopamine), serotonin (5-HT), 5-hydroxyindole-3-acetic acid (5-HIAA, a major metabolite of serotonin), and 4-hydroxy-3-methoxyphenylglycol (MHPG, a major metabolite of norepinephrine). Multivariable logistic regression was used to evaluate factors associated with depression. There were 79 PWH with plasma and CSF HIV RNA levels < 200 copies/mL at the time of the visit, and 25 (31.6%) carried a current diagnosis of depression. Participants with depression were significantly older (median age 53 years versus 47 years, P = 0.014) and were significantly less likely to be African American (48.0% versus 77.8%, P = 0.008). Participants with depression had significantly lower dopamine levels (median 0.49 ng/mL versus 0.62 ng/mL, P = 0.03) and significantly lower 5-HIAA levels (median 12.57 ng/mL versus 15.41 ng/mL, P = 0.015). Dopamine and 5-HIAA were highly correlated. In the multivariable logistic regression models, lower 5-HIAA was significantly associated with the depression diagnosis when accounting for other significant demographic factors. The associations between lower 5-HIAA, lower dopamine, and depression in PWH suggest that altered neurotransmission may contribute to these comorbid conditions. However, the effects of antidepressants on neurotransmitters cannot be ruled out as a factor in the 5-HIAA results.
抑郁症是 HIV 感染者(PWH)中常见的疾病,与大量发病率和死亡率相关。抑郁症在 PWH 中的发病机制仍不完全清楚,因此需要更多的研究来开发有效的治疗方法。一种假设是神经递质水平可能发生改变。这些水平可能会受到 PWH 中慢性炎症和病毒持续存在的影响。我们检查了接受抑制性抗逆转录病毒疗法(ART)的 PWH 中一组脑脊液(CSF)神经递质,其中许多人目前被诊断患有抑郁症。来自埃默里艾滋病研究中心(CFAR)研究的参与者的 CSF 单胺神经递质及其代谢物进行了测量。仅分析了来自同时具有抑制性血浆和 CSF HIV RNA 的稳定 ART 参与者。使用高效液相色谱法(HPLC)测量神经递质水平。神经递质及其代谢物包括多巴胺(DA)、高香草酸(HVA,多巴胺的主要代谢物)、血清素(5-HT)、5-羟吲哚-3-乙酸(5-HIAA,血清素的主要代谢物)和 4-羟基-3-甲氧基苯乙二醇(MHPG,去甲肾上腺素的主要代谢物)。多变量逻辑回归用于评估与抑郁症相关的因素。在就诊时,有 79 名 PWH 的血浆和 CSF HIV RNA 水平<200 拷贝/ml,其中 25 名(31.6%)目前被诊断为抑郁症。患有抑郁症的参与者年龄明显较大(中位数年龄 53 岁与 47 岁,P=0.014),且明显不太可能为非裔美国人(48.0%与 77.8%,P=0.008)。患有抑郁症的参与者多巴胺水平明显较低(中位数 0.49ng/ml 与 0.62ng/ml,P=0.03),5-HIAA 水平明显较低(中位数 12.57ng/ml 与 15.41ng/ml,P=0.015)。多巴胺和 5-HIAA 高度相关。在多变量逻辑回归模型中,当考虑到其他重要的人口统计学因素时,较低的 5-HIAA 与抑郁症诊断显著相关。在 PWH 中,较低的 5-HIAA、较低的多巴胺与抑郁症之间的关联表明,神经递质传递的改变可能导致这些共病。然而,不能排除抗抑郁药对神经递质的影响是 5-HIAA 结果的一个因素。