ECT & CRP, quo vadis? - A retrospective study of low-grade inflammation in patients with depression undergoing electroconvulsive therapy

Q2 Medicine
Moritz Spangemacher , Sebastian Karl , Suna Su Aksay , Eva Kathrin Lamadé , Jana Plemper , Alexander Sartorius , Bruno Pedraz-Petrozzi
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Abstract

Introduction

Electroconvulsive therapy (ECT) is the most effective treatment for severe depression. Depression has been associated with low-grade inflammation (LGI), as indicated by elevated C-reactive protein (CRP) levels compared to healthy individuals. While the effect of ECT on inflammation markers remains unclear, some evidence suggests that higher baseline CRP levels may predict remission in ECT. Additionally, LGI could influence the seizure threshold and thus the required stimulation dose.

Materials and methods

This retrospective study examined the potential link between LGI and treatment outcomes as well as stimulation doses across multiple ECT sessions, controlling for age and interparticipant variability. The hypothesis of this study was that LGI was associated with ECT remission as well as with ECT dosing in people with depression. Two groups were defined, depending on CRP levels, those with LGI (CRP 3–10 mg/L) and those without (CRP < 3 mg/L). Generalized linear models were used to analyze maximum ECT doses, while linear mixed models were applied to assess changes in ECT doses over time.

Results

After 10 ECT sessions, we found no significant difference in remission rates between patients with (n = 52) and without LGI (n = 143). However, patients with baseline LGI had higher maximum ECT doses. A linear mixed model revealed that the number of sessions and baseline LGI significantly influenced ECT doses, with patients with baseline LGI needing higher doses, particularly at the seventh session. Age also was associated with both maximum doses and dose adjustments throughout the ECT series, but the influence of LGI on ECT dose was independent of age, since no age differences were observed between groups.

Conclusions

Baseline inflammation was not associated with remission rates, but it had a significant association with ECT dosing. Therefore, while CRP may not be a reliable biomarker for predicting ECT response in depression, baseline inflammation could indicate the need for a higher stimulation dose.
导言电休克疗法(ECT)是治疗严重抑郁症最有效的方法。与健康人相比,抑郁症患者的 C 反应蛋白(CRP)水平升高,表明抑郁症与低度炎症(LGI)有关。虽然 ECT 对炎症指标的影响尚不明确,但有证据表明,较高的基线 CRP 水平可能预示着 ECT 的缓解。此外,LGI 可能会影响癫痫发作阈值,从而影响所需的刺激剂量。这项回顾性研究考察了 LGI 与治疗结果以及多次 ECT 治疗的刺激剂量之间的潜在联系,并控制了年龄和参与者之间的差异。本研究的假设是,LGI 与抑郁症患者的 ECT 缓解以及 ECT 剂量有关。根据 CRP 水平将患者分为两组,即 LGI 组(CRP 3-10 mg/L)和非 LGI 组(CRP < 3 mg/L)。我们使用广义线性模型来分析ECT的最大剂量,同时使用线性混合模型来评估ECT剂量随时间的变化。然而,基线LGI患者的最大ECT剂量更高。线性混合模型显示,治疗次数和基线LGI对ECT剂量有显著影响,基线LGI患者需要的剂量更高,尤其是在第七次治疗时。年龄也与整个ECT系列的最大剂量和剂量调整有关,但LGI对ECT剂量的影响与年龄无关,因为各组间未观察到年龄差异。因此,虽然 CRP 可能不是预测抑郁症患者 ECT 反应的可靠生物标志物,但基线炎症可能表明需要更高的刺激剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomarkers in Neuropsychiatry
Biomarkers in Neuropsychiatry Medicine-Psychiatry and Mental Health
CiteScore
4.00
自引率
0.00%
发文量
12
审稿时长
7 weeks
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