肌炎特异性自身抗体在特发性炎性肌病诊断和肿瘤风险预测中的价值。

IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Journal of International Medical Research Pub Date : 2025-08-01 Epub Date: 2025-08-04 DOI:10.1177/03000605251362969
Lili Shi, Rong Min, Yanyan Wu, Jiahui Liu, Xia Liu, Peichang Wang
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引用次数: 0

摘要

目的探讨肌炎特异性自身抗体在临床怀疑为特发性炎性肌病患者的诊断及肿瘤风险预测中的价值。方法回顾性分析357例临床疑似特发性炎性肌病患者的肌炎特异性自身抗体及临床特点。统计分析评估肌炎特异性自身抗体与临床症状之间的关系。结果357例疑似特发性炎性肌病患者中,抗合成酶与抗ro52共出现率为52.63%。单因素分析显示,抗合成酶和抗ro52阳性患者的特发性炎性肌病诊断率明显高于血清阴性患者。抗信号识别颗粒检测阳性的患者与检测阴性的患者相比,表现出不同的血清学特征和诊断结果。肌炎特异性自身抗体与肿瘤生物标志物之间存在显著相关性。多因素logistic回归分析发现血清肌酐和抗合成酶抗体阳性是特发性炎性肌病的独立诊断预测因子。抗合成酶抗体与特发性炎性肌病独立相关。抗合成酶和抗ro52同时阳性与特发性炎性肌病的诊断密切相关。肌炎抗体与肿瘤生物标志物显著相关,突出了它们在早期癌症筛查中的潜在效用。血清肌酐升高也与特发性炎性肌病独立相关,具有诊断意义。结论肌炎特异性自身抗体对特发性炎性肌病的早期肿瘤筛查和诊断具有潜在的临床价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The value of myositis-specific autoantibodies in the diagnosis of idiopathic inflammatory myopathy and tumor risk prediction.

The value of myositis-specific autoantibodies in the diagnosis of idiopathic inflammatory myopathy and tumor risk prediction.

The value of myositis-specific autoantibodies in the diagnosis of idiopathic inflammatory myopathy and tumor risk prediction.

The value of myositis-specific autoantibodies in the diagnosis of idiopathic inflammatory myopathy and tumor risk prediction.

ObjectiveTo investigate the value of myositis-specific autoantibodies in the diagnosis of idiopathic inflammatory myopathy and tumor risk prediction in patients with clinically suspected idiopathic inflammatory myopathy.MethodsThis retrospective study analyzed the myositis-specific autoantibodies and clinical characteristics of 357 patients with clinically suspected idiopathic inflammatory myopathy. Statistical analyses were conducted to assess the associations between myositis-specific autoantibodies and clinical symptoms.ResultsAmong the 357 patients with suspected idiopathic inflammatory myopathy, the co-occurrence rate of anti-synthetase and anti-Ro52 was 52.63%. Univariate analysis demonstrated significantly higher diagnostic rates of idiopathic inflammatory myopathy in patients positive for anti-synthetase and anti-Ro52 than in those who were seronegative. Patients who tested positive for anti-signal recognition particle exhibited distinct serological profiles and diagnostic outcomes compared with those who tested negative. Significant associations were observed between myositis-specific autoantibodies and tumor biomarkers. Multivariate logistic regression analysis identified serum creatinine and anti-synthetase antibody positivity as independent diagnostic predictors of idiopathic inflammatory myopathy.DiscussionAnti-synthetase antibodies were independently associated with idiopathic inflammatory myopathy. Co-positivity for anti-synthetase and anti-Ro52 was closely related to the diagnosis of idiopathic inflammatory myopathy. Myositis antibodies were significantly correlated with tumor biomarkers, highlighting their potential utility in early cancer screening. Elevated serum creatinine was also independently associated with idiopathic inflammatory myopathy, exhibiting diagnostic significance.ConclusionMyositis-specific autoantibodies have potential clinical value for early tumor screening and the diagnosis of idiopathic inflammatory myopathy.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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