艾司西酞普兰对广泛性焦虑症患者C-C基趋化因子配体5和成纤维细胞生长因子2的免疫调节潜力

IF 1.7 4区 医学 Q3 CLINICAL NEUROLOGY
Swathi Suresh, Rachna Gupta, Shruti Srivastava, Sumita Halder, Seema Garg
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引用次数: 0

摘要

目的:C-C基序趋化因子配体5 (CCL5)和成纤维细胞生长因子2 (FGF2)与神经炎症的关系越来越密切。本研究评估了艾司西酞普兰对广泛性焦虑症(GAD)患者血清CCL5和FGF2水平的影响。方法:30例经DSM-5诊断为广泛性焦虑症的患者(18-50岁)和30例健康对照。所有GAD患者均接受艾司西酞普兰治疗,随访12周。采用ELISA法测定了艾司西酞普兰治疗前后GAD患者血清CCL5和FGF2水平,并测定了健康对照组的基线水平。结果:我们发现与健康对照相比,GAD患者血清CCL5水平显著升高(p = 0.001),治疗后仍保持较高水平,无显著变化。然而,治疗前健康对照组与GAD患者血清FGF2水平具有可比性,无显著差异,治疗后GAD患者血清FGF2水平显著升高(p = 0.011)。结论:使用艾司西酞普兰治疗后,GAD患者血清CCL5水平持续升高,FGF2显著升高。这表明艾司西酞普兰可能对CCL5和FGF2发挥部分免疫调节作用,从而调节GAD的炎症驱动机制。未来的研究需要在更大的人群和更长的随访中进一步检验这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunomodulatory Potential of Escitalopram on C-C Motif Chemokine Ligand 5 and Fibroblast Growth Factor 2 in Patients With Generalised Anxiety Disorder

Objective

C-C motif chemokine ligand 5 (CCL5) and fibroblast growth factor 2 (FGF2) have been increasingly linked to neuroinflammation. This study evaluated the impact of escitalopram on serum CCL5 and FGF2 levels in patients with generalised anxiety disorder (GAD).

Methods

Thirty patients (18–50 years) with GAD diagnosed by DSM-5 criteria, and 30 healthy controls were included. All GAD patients received escitalopram and were followed up for 12 weeks. Serum CCL5 and FGF2 levels were measured before and after escitalopram treatment in GAD patients, with a baseline measurement in healthy controls using ELISA.

Results

We found that serum CCL5 levels were significantly increased (p = 0.001) in GAD patients compared to healthy controls and remained higher after treatment without any significant change. However, serum FGF2 levels were comparable and did not differ significantly between healthy controls and GAD patients before treatment, and increased significantly (p = 0.011) after escitalopram treatment in GAD patients.

Conclusion

In GAD patients, serum levels of CCL5 remained elevated and FGF2 increased significantly post-treatment with escitalopram. This suggests that escitalopram could exert a partial immunomodulatory effect on CCL5 and FGF2, thus modulating inflammation-driven mechanisms of GAD. Future research in larger populations and longer follow-ups is needed to further examine these findings.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal: -All aspects of clinical psychopharmacology- Efficacy and safety studies of novel and standard psychotropic drugs- Studies of the adverse effects of psychotropic drugs- Effects of psychotropic drugs on normal physiological processes- Geriatric and paediatric psychopharmacology- Ethical and psychosocial aspects of drug use and misuse- Psychopharmacological aspects of sleep and chronobiology- Neuroimaging and psychoactive drugs- Phytopharmacology and psychoactive substances- Drug treatment of neurological disorders- Mechanisms of action of psychotropic drugs- Ethnopsychopharmacology- Pharmacogenetic aspects of mental illness and drug response- Psychometrics: psychopharmacological methods and experimental design
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