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急性螯合疗法相关的尿液钆变化、自述 flares 严重程度和钆沉积病中的血清细胞因子。

Acute Chelation Therapy-Associated Changes in Urine Gadolinium, Self-reported Flare Severity, and Serum Cytokines in Gadolinium Deposition Disease.

机构信息

From the Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.

CytoAnalytics, Denver, CO.

出版信息

Invest Radiol. 2021 Jun 1;56(6):374-384. doi: 10.1097/RLI.0000000000000752.

Abstract

OBJECTIVES

The aim of this study was to determine the following in patients who have undergone magnetic resonance imaging with gadolinium-based contrast agents (GBCAs) and meet the proposed diagnostic criteria for gadolinium deposition disease (GDD): (1) the effectiveness of chelation therapy (CT) with intravenous Ca-diethylenetriaminepentaacetic acid in removing retained gadolinium (Gd) and factors affecting the amount removed; (2) the frequency of CT-induced Flare, that is, GDD diagnostic symptom worsening, and factors affecting Flare intensity; (3) whether, as reported in a separate cohort, GDD patients' serum cytokine levels differ significantly from those in healthy normal controls and change significantly in response to CT; and (4) whether urine Gd, Flare reaction, and serum cytokine findings in GDD patients are mimicked in non-ill patients described as having gadolinium storage condition (GSC).

MATERIALS AND METHODS

Twenty-one GDD subjects and 3 GSC subjects underwent CT. Patients provided pre-CT and post-CT 24-hour urine samples for Gd content determination along with pre-CT and 24-hour post-CT serum samples for cytokine analysis. Patients rated potential Flare 24 hours after CT. Pre-CT and post-CT 24-hour urine Gd analyses and Luminex serum cytokine assays were performed blind to patients' GDD and GSC status and all other data except age and sex. Serum cytokine levels in a healthy normal control group of age- and sex-matched subjects drawn from Stanford influenza vaccination studies were measured once, contemporaneously with those of GDD and GSC patients, using the same Luminex assay.

RESULTS

Urine Gd amounts increased post-CT by 4 times or more after 87% of the 30 CT sessions. The most important factors appeared to be the time since the last GBCA dose and the cumulative dose received. Urine Gd amounts for GDD and GSC patients fell in the same ranges. All GDD patients, and no GSC patient, reported a Flare 24 hours post-CT. Linear regression found that Flare intensity was significantly predicted by a model including pre- and post-CT Gd amounts and the number of GBCA-enhanced magnetic resonance imaging. Post-CT, multiple cytokines showed strong positive relationships with GDD patients' Flare intensity in multivariable models. The pre-CT serum levels of 12 cytokines were significantly different in GDD patients compared with healthy flu vaccine controls. The small number of GSC patients precluded analogous statistical testing. Post-CT, GDD patients' serum levels of 20 cytokines were significantly decreased, and 2 cytokines significantly increased. These cytokines did not exhibit the same change pattern in the 3 GSC patients. The small number of GSC patients precluded statistical comparisons of GSC to GDD patients' results.

CONCLUSIONS

In this preliminary study, 24-hour urine Gd content increased markedly and similarly in GDD and GSC patients after Ca-diethylenetriaminepentaacetic acid CT. Post-CT Flare reaction developed only in GDD patients. The current study is the second finding significantly different serum cytokine levels in GDD patients compared with healthy normal controls. These differences and the difference between GDD and GSC patients' Flare and cytokine responses to CT suggest some inflammatory, immunologic, or other physiological differences in patients with GDD. Further research into the treatment and physiological underpinnings of GDD is warranted.

摘要

目的

本研究旨在确定以下接受过基于钆的造影剂(GBCA)磁共振成像并符合 GDD 诊断标准的患者:(1)静脉注射 Ca-二亚乙基三胺五乙酸螯合疗法(CT)去除残留钆(Gd)的效果以及影响去除量的因素;(2)CT 诱导的 Flare(即 GDD 诊断症状恶化)的频率以及影响 Flare 强度的因素;(3)GDD 患者的血清细胞因子水平是否与健康正常对照组有显著差异,并在 CT 治疗后是否发生显著变化,正如另一队列报告的那样;(4)在描述为具有钆储存状态(GSC)的非患病患者中,是否模拟了 GDD 患者的尿 Gd、Flare 反应和血清细胞因子发现。

材料和方法

21 名 GDD 患者和 3 名 GSC 患者接受 CT。患者在 CT 前和 CT 后 24 小时内提供尿液样本,以确定 Gd 含量,同时在 CT 前和 CT 后 24 小时内提供血清样本,以进行细胞因子分析。患者在 CT 后 24 小时内评估潜在的 Flare。在不知道患者 GDD 和 GSC 状态以及年龄和性别等所有其他数据的情况下,对 30 次 CT 治疗中的 21 次进行了盲法的 CT 前后 24 小时尿 Gd 分析和 Luminex 血清细胞因子检测。从斯坦福流感疫苗研究中选取年龄和性别匹配的健康正常对照组的血清细胞因子水平进行了一次测量,与 GDD 和 GSC 患者同时使用相同的 Luminex 检测方法进行测量。

结果

在 87%的 30 次 CT 治疗中,30 次 CT 治疗后,尿液 Gd 量增加了 4 倍或更多。最重要的因素似乎是最后一次 GBCA 剂量的时间和累积剂量。GDD 和 GSC 患者的尿液 Gd 量落在相同范围内。所有 GDD 患者都报告了 CT 后 24 小时的 Flare,而没有 GSC 患者报告了 Flare。线性回归发现,Flare 强度可由包括 CT 前后 Gd 量和 GBCA 增强磁共振成像次数的模型显著预测。CT 后,在多变量模型中,多种细胞因子与 GDD 患者的 Flare 强度呈强烈的正相关关系。与健康流感疫苗对照组相比,GDD 患者的 12 种细胞因子的血清水平在 CT 前显著不同。由于 GSC 患者数量较少,因此无法进行类似的统计检验。CT 后,GDD 患者的 20 种细胞因子血清水平显著降低,2 种细胞因子显著增加。在 3 名 GSC 患者中,这些细胞因子没有表现出相同的变化模式。由于 GSC 患者数量较少,因此无法对 GSC 与 GDD 患者的结果进行统计比较。

结论

在这项初步研究中,在接受 Ca-二亚乙基三胺五乙酸 CT 治疗后,GDD 和 GSC 患者的 24 小时尿液 Gd 含量均显著增加。只有 GDD 患者出现 CT 后 Flare 反应。目前的研究是第二次发现 GDD 患者的血清细胞因子水平与健康正常对照组有显著差异。这些差异以及 GDD 和 GSC 患者对 CT 的 Flare 和细胞因子反应之间的差异表明,GDD 患者在炎症、免疫或其他生理方面存在一些差异。需要进一步研究 GDD 的治疗和生理基础。

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