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一个简化参数集,有助于在噬血细胞性淋巴组织细胞增生症的诊断中尽早做出决策。

A Minimal Parameter Set Facilitating Early Decision-making in the Diagnosis of Hemophagocytic Lymphohistiocytosis.

机构信息

Center of Translational Immunology, University Medical Center Utrecht, Heidelberglaan 100, 3584CX, Utrecht, The Netherlands.

Department of Pediatric Immunology and Infectious Diseases, UMC Utrecht, Utrecht, The Netherlands.

出版信息

J Clin Immunol. 2021 Aug;41(6):1219-1228. doi: 10.1007/s10875-021-01005-7. Epub 2021 Mar 29.

Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening immune dysregulation syndrome characterized by uncontrolled immune cell activation. Timely diagnosis is important, since early treatment can improve survival rates. However, completing all assessments needed to reach ≥5 positive criteria out of the 8 HLH-2004 criteria can be time consuming and may delay timely initiation of treatment. Hence, we applied a data-driven approach to identify a minimal parameter set for early decision-making towards the initiation of HLH-specific treatment. We retrospectively evaluated 165 patients from five Dutch tertiary hospitals with suspected HLH. Sixteen pHLH (median age 0.5 years) and 70 sHLH patients (median age 8.7 years) were identified using the HLH-2004 criteria. Clustering analysis and multi-receiver operator characteristics were used to identify parameters distinctive of HLH. The presence of either increased ferritin, cytopenia in ≥2 lineages, or splenomegaly distinguished HLH from non-HLH cases with a negative predictive value of 100%. A minimal parameter set consisting of 2 major criteria (phagocytosis and splenomegaly) and 3 minor criteria (cytopenia, increased ferritin, and increased triglycerides/low fibrinogen) predicted HLH with 95% (88-99) sensitivity and 94% (86-98) specificity. This finding was replicated in an independent retrospective validation cohort of 109 US patients (n = 109). By dividing a subset of the HLH-2004 criteria into major and minor criteria, this strategy uses the evaluation of less than 5 criteria to quickly identify patients with HLH. When confirmed in a prospective setting, this approach could be of value for timely diagnosis and treatment of HLH.

摘要

噬血细胞性淋巴组织细胞增生症(HLH)是一种危及生命的免疫失调综合征,其特征是免疫细胞失控激活。及时诊断很重要,因为早期治疗可以提高生存率。然而,完成 HLH-2004 标准中的 8 项标准中≥5 项阳性标准的所有评估可能会很耗时,并可能延迟及时开始治疗。因此,我们应用数据驱动的方法来确定一个最小参数集,以便尽早决定开始 HLH 特异性治疗。我们回顾性评估了来自荷兰五家三级医院的 165 例疑似 HLH 患者。使用 HLH-2004 标准,确定了 16 例原发性 HLH(中位年龄 0.5 岁)和 70 例继发性 HLH 患者(中位年龄 8.7 岁)。聚类分析和多接收器操作者特征用于识别 HLH 的特征参数。铁蛋白升高、≥2 系血细胞减少或脾肿大的存在可将 HLH 与非 HLH 病例区分开来,其阴性预测值为 100%。由 2 项主要标准(吞噬作用和脾肿大)和 3 项次要标准(血细胞减少、铁蛋白升高和甘油三酯升高/纤维蛋白原降低)组成的最小参数集预测 HLH 的敏感性为 95%(88-99),特异性为 94%(86-98)。这一发现在美国的一个独立回顾性验证队列中得到了复制(n=109)。通过将 HLH-2004 标准的一部分分为主要标准和次要标准,这种策略使用不到 5 项标准的评估来快速识别患有 HLH 的患者。如果在前瞻性研究中得到证实,这种方法可能有助于 HLH 的及时诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc0/8310853/0d9f7bf12bf3/10875_2021_1005_Fig1_HTML.jpg

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