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血清铁蛋白作为川崎病静脉注射免疫球蛋白抵抗和冠状动脉病变诊断及预后的关键生物标志物:一项系统评价和荟萃分析

Serum ferritin as a crucial biomarker in the diagnosis and prognosis of intravenous immunoglobulin resistance and coronary artery lesions in Kawasaki disease: A systematic review and meta-analysis.

作者信息

Wen Huai, Hun Marady, Zhao Mingyi, Han Phanna, He Qingnan

机构信息

Department of Pediatrics, The Third Xiangya Hospital, Central South University, Changsha, China.

Department of Ophthalmology, The Second Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Med (Lausanne). 2022 Aug 10;9:941739. doi: 10.3389/fmed.2022.941739. eCollection 2022.

Abstract

BACKGROUND

Early identification and treatment are paramount for intravenous immunoglobulin (IVIG) resistance and coronary artery lesions (CALs) in patients with Kawasaki disease (KD). Unfortunately, there is no single crucial biomarker to identify these patients in a timely manner, which makes KD the most common cause of acquired heart disease in children in developed countries. Recently, many studies have focused on the association between serum ferritin (SF), IVIG resistance, and CALs in KD. We thus performed a systematic review and meta-analysis to ascertain the diagnostic and prognostic values of SF in predicting IVIG resistance and CALs in KD in the acute phase.

METHODS

The pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), and area under the receiver operating characteristic curve (AUC) were extracted from the data to evaluate the SF levels in KD. The hazard ratios (HRs) of related risk factors and their corresponding 95% confidence intervals (CIs) were applied to compute the pooled assessments of the outcomes.

RESULTS

A total of 11 eligible articles were included in this meta-analysis, including twenty studies for diagnosis and five studies for prognosis. In terms of diagnostic values, SF could identify KD patients in the overall studies with a relatively high pooled sensitivity, specificity, PLR, NLR, DOR, and AUC of 0.76 (95% CI: 0.69-0.82), 0.82 (95% CI: 0.76-0.88), 4.33 (95% CI: 3.07-6.11), 0.29 (95% CI: 0.22-0.38), 15.0 (95% CI: 9.00-25.00), and 0.86 (95% CI: 0.83-0.89), respectively. In studies comparing KD patients and controls, there were a relatively high pooled sensitivity, specificity, PLR, NLR, DOR, and AUC of 0.79 (95% CI: 0.72-0.84), 0.84 (95% CI: 0.79-0.91), 4.61 (95% CI: 3.27-6.51), 0.26 (95% CI: 0.20-0.34), 20.82 (95% CI: 11.83-36.64), and 0.89 (95% CI: 0.86-0.91), respectively. For the prognostic values, we found poor survival outcomes based on KD patients (HR = 1.31, 95% CI: 1.07-1.59, = 0.008).

CONCLUSION

Our meta-analysis suggests that SF may be used as a workable and critical biomarker for the diagnosis and prognosis of IVIG resistance and CALs in patients with KD. We also propose that maintaining the dynamic balance between iron, SF, and ferroptosis will be an important therapeutic strategy to reduce the morbidity of CALs.

SYSTEMATIC REVIEW REGISTRATION

[https://www.crd.york.ac.uk/prospero/], identifier [CRD42022279157].

摘要

背景

对于川崎病(KD)患者的静脉注射免疫球蛋白(IVIG)抵抗和冠状动脉病变(CALs),早期识别和治疗至关重要。不幸的是,目前尚无单一关键生物标志物能够及时识别这些患者,这使得KD成为发达国家儿童后天性心脏病的最常见病因。最近,许多研究聚焦于血清铁蛋白(SF)、IVIG抵抗和KD中CALs之间的关联。因此,我们进行了一项系统评价和荟萃分析,以确定急性期SF在预测KD中IVIG抵抗和CALs方面的诊断和预后价值。

方法

从数据中提取合并敏感度、特异度、阳性似然比(PLR)、阴性似然比(NLR)、诊断比值比(DOR)和受试者工作特征曲线下面积(AUC),以评估KD中的SF水平。应用相关危险因素的风险比(HRs)及其相应的95%置信区间(CIs)来计算结局的合并评估。

结果

本荟萃分析共纳入11篇符合条件的文章,包括20项诊断研究和5项预后研究。在诊断价值方面,SF在总体研究中能够识别KD患者,其合并敏感度、特异度、PLR、NLR、DOR和AUC相对较高,分别为0.76(95%CI:0.69 - 0.82)、0.82(95%CI:0.76 - 0.88)、4.33(95%CI:3.07 - 6.11)、0.29(95%CI:0.22 - 0.38)、15.0(95%CI:9.00 - 25.00)和0.86(95%CI:0.83 - 0.89)。在比较KD患者和对照组的研究中,合并敏感度、特异度、PLR、NLR、DOR和AUC相对较高,分别为0.79(95%CI:0.72 - 0.84)、0.84(95%CI:0.79 - 0.91)、4.61(95%CI:3.27 - 6.51)、0.26(95%CI:0.20 - 0.34)、20.82(95%CI:11.83 - 36.64)和0.89(95%CI:0.86 - 0.91)。对于预后价值,我们发现基于KD患者的生存结局较差(HR = 1.31,95%CI:1.07 - 1.59,P = 0.008)。

结论

我们的荟萃分析表明,SF可作为KD患者IVIG抵抗和CALs诊断及预后的可行且关键的生物标志物。我们还提出,维持铁、SF和铁死亡之间的动态平衡将是降低CALs发病率的重要治疗策略。

系统评价注册

[https://www.crd.york.ac.uk/prospero/],标识符[CRD42022279157]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ab7/9399505/a86b38dfc02f/fmed-09-941739-g001.jpg

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