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血清诊断线免疫印迹法在特发性炎性肌病中的适用性:肌肉活检并非全部。

Applicability of a serodiagnostic line blot for idiopathic inflammatory myopathy: the muscle biopsy is not all.

作者信息

Fontana Pedro Nogueira, da Silva Vinícius Gomes, Corazzini Roseli, Athayde Natália Merten, Ferreira da Silva Ana Marina Dutra, Brockhausen Igor, Correia Carolina da Cunha, Sobreira Cláudia Ferreira da Rosa, Tomaselli Pedro, Petean Flávio, de Oliveira Rodrigo, Feitoza Pablo Vinícius, Moraes Soane Michel, Saraiva Natália, Hidalgo Rafaela, Fideles Cláudia, Feder David, Carvalho Alzira Alves de Siqueira

机构信息

Neurosciences and Clinical Department, Centro Universitário ABC, Santo André, Brazil.

Faculty of Medical Sciences, Universidade de Pernambuco, Recife, Brazil.

出版信息

Front Neurol. 2025 Jan 6;15:1504260. doi: 10.3389/fneur.2024.1504260. eCollection 2024.

Abstract

INTRODUCTION

Differential diagnosis of rare idiopathic inflammatory myopathies (IIM) is mainly based on clinical aspects, muscle biopsy analysis, and auxiliary assays that determine myositis-specific and associated autoantibodies (MSA and MAA). While MSAs are considered specific for their respective IIM subclass, MAAs can be present in more than one subclass and in other conditions. This study compares results of a multispecific line blot assay with the final diagnosis of IIM patients based on clinical features and muscle biopsy to draw conclusions for the test's applicability in the diagnostic workflow.

METHODS

Samples from patients ( = 50) diagnosed with various forms of IIM, including patients ( = 5) with other myopathies, were analyzed using the EUROLINE Autoimmune Inflammatory Myopathies 16 Ag (IgG), an anti-HMGCR (IgG) line blot, and the Anti-cN-1A ELISA (IgG, all EUROIMMUN).

RESULTS

MSA and MAA were detected in 74.0% (37/50) of sera and were concordant with the final diagnosis in 64.8% (24/37), discordant in 16.2% (6/37) and not evaluable in 18.9% (7/37) of cases. In 100% (5/5) of patients with other myopathies, no MSA was found. MSA/MAA-co-positivity was observed in 18.0% (9/50) of patients. In 30.0% (15/50) of cases, the muscle biopsy analysis was essential to establish the final diagnosis.

CONCLUSION

The agreement between serodiagnostic results and final diagnosis highlights the applicability of the EUROIMMUN myositis-related diagnostic test as first line diagnostic tool in the IIM diagnosis workflow and suggests morphological analysis in cases of inconclusive or negative serology. However, results of diagnostic assays shall always be interpreted in combination with clinical features.

摘要

引言

罕见特发性炎性肌病(IIM)的鉴别诊断主要基于临床症状、肌肉活检分析以及用于确定肌炎特异性和相关自身抗体(MSA和MAA)的辅助检测。虽然MSA被认为对各自的IIM亚类具有特异性,但MAA可存在于多个亚类以及其他病症中。本研究将多特异性线性印迹检测结果与基于临床特征和肌肉活检的IIM患者最终诊断结果进行比较,以得出该检测在诊断流程中的适用性结论。

方法

使用EUROLINE自身免疫性炎性肌病16抗原(IgG)、抗HMGCR(IgG)线性印迹以及抗cN - 1A ELISA(IgG,均为EUROIMMUN产品)对诊断为各种形式IIM的患者(n = 50)的样本进行分析,其中包括患有其他肌病的患者(n = 5)。

结果

在74.0%(37/50)的血清中检测到MSA和MAA,其中64.8%(24/37)与最终诊断一致,16.2%(6/37)不一致,18.9%(7/37)的病例无法评估。在100%(5/5)患有其他肌病的患者中未发现MSA。18.0%(9/50)的患者观察到MSA/MAA共同阳性。在30.0%(15/50)的病例中,肌肉活检分析对确定最终诊断至关重要。

结论

血清学诊断结果与最终诊断之间的一致性突出了EUROIMMUN肌炎相关诊断检测作为IIM诊断流程中一线诊断工具的适用性,并建议在血清学结果不确定或为阴性的情况下进行形态学分析。然而,诊断检测结果应始终结合临床特征进行解读。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/154d/11743459/9b45f96efc12/fneur-15-1504260-g0001.jpg

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