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本文引用的文献

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Predicting progression from undifferentiated connective tissue disease to definite connective tissue disease: A systematic review and meta-analysis.预测未分化结缔组织病向明确结缔组织病的进展:系统评价和荟萃分析。
Autoimmun Rev. 2022 Nov;21(11):103184. doi: 10.1016/j.autrev.2022.103184. Epub 2022 Aug 27.
2
The Role of Clinical Features and Serum Biomarkers in Identifying Patients with Incomplete Lupus Erythematosus at Higher Risk of Transitioning to Systemic Lupus Erythematosus: Current Perspectives.临床特征和血清生物标志物在识别不完全性红斑狼疮患者向系统性红斑狼疮转变高风险中的作用:当前观点
J Inflamm Res. 2022 Feb 18;15:1133-1145. doi: 10.2147/JIR.S275043. eCollection 2022.
3
Integrative Analysis Reveals a Molecular Stratification of Systemic Autoimmune Diseases.整合分析揭示了系统性自身免疫性疾病的分子分层。
Arthritis Rheumatol. 2021 Jun;73(6):1073-1085. doi: 10.1002/art.41610. Epub 2021 Apr 26.
4
Clinical and Immunological Profile of Mixed Connective Tissue Disease and a Comparison of Four Diagnostic Criteria.混合性结缔组织病的临床和免疫学特征以及四种诊断标准的比较
Int J Rheumatol. 2020 Jan 29;2020:9692030. doi: 10.1155/2020/9692030. eCollection 2020.
5
"Mixed connective tissue disease": a condition in search of an identity.“混合性结缔组织病”:一种有待明确界定的病症。
Clin Exp Med. 2020 May;20(2):159-166. doi: 10.1007/s10238-020-00606-7. Epub 2020 Mar 4.
6
2019 European League Against Rheumatism/American College of Rheumatology Classification Criteria for Systemic Lupus Erythematosus.2019 年欧洲抗风湿病联盟/美国风湿病学会系统性红斑狼疮分类标准。
Arthritis Rheumatol. 2019 Sep;71(9):1400-1412. doi: 10.1002/art.40930. Epub 2019 Aug 6.
7
Mixed connective tissue disease: state of the art on clinical practice guidelines.混合性结缔组织病:临床实践指南的最新进展
RMD Open. 2018 Oct 18;4(Suppl 1):e000783. doi: 10.1136/rmdopen-2018-000783. eCollection 2018.
8
Mixed Connective Tissue Disease and Epitope Spreading: An Historical Cohort Study.混合性结缔组织病与表位扩展:一项历史性队列研究。
J Clin Rheumatol. 2017 Apr;23(3):155-159. doi: 10.1097/RHU.0000000000000500.
9
Mixed connective tissue disease-enigma variations?混合性结缔组织病——谜团种种?
Rheumatology (Oxford). 2017 Mar 1;56(3):326-333. doi: 10.1093/rheumatology/kew265.
10
Diagnosis and risk stratification in patients with anti-RNP autoimmunity.抗RNP自身免疫患者的诊断与风险分层
Lupus. 2015 Sep;24(10):1057-66. doi: 10.1177/0961203315575586. Epub 2015 Mar 2.

针对Sm/RNP共同基序和U1 RNP的联合自身反应性与混合性结缔组织病及系统性红斑狼疮的关联

Association of Combined Autoreactivity to Sm/RNP Common Motif and U1 RNP With Mixed Connective Tissue Disease and Systemic Lupus Erythematosus.

作者信息

Ni Ruoning, Lenert Aleksander, Lenert Petar

机构信息

The University of Iowa, Iowa City.

出版信息

ACR Open Rheumatol. 2024 Dec;6(12):856-862. doi: 10.1002/acr2.11739. Epub 2024 Sep 13.

DOI:10.1002/acr2.11739
PMID:39270208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11638137/
Abstract

OBJECTIVE

This study aimed to evaluate the clinical features in patients with suspected connective tissue disease who tested positive for anti-Sm/RNP common motif antibody with or without associated anti-RNP antibody.

METHODS

The titers of anti-Sm/RNP and anti-RNP antibodies were measured by the multiplex solid-phase bioassays (Bio-Rad). Clinical manifestations were compared among the three subgroups (RNP only, Sm/RNP only, and double positive for RNP and Sm/RNP). Patients were further evaluated for the diagnosis of mixed connective tissue disease (MCTD) and/or systemic lupus erythematosus (SLE) using accepted classification criteria.

RESULTS

A total of 133 patients were included in this study. The rates of inflammatory arthritis and Raynaud phenomenon were significantly higher in patients testing positive for both anti-RNP and anti-Sm/RNP antibodies compared to anti-RNP only or anti-Sm/RNP only (69.1% vs 28.8% vs 25.0%, P < 0.0001 for arthritis and 59.5% vs 23.3% vs 37.5%, P = 0.0005 for Raynaud phenomenon). Area under the curve (AUC) values were 0.68 (95% confidence interval [CI] 0.59-0.77, P < 0.0001) for anti-Sm/RNP titers and 0.65 (95% CI 0.55-0.74, P = 0.0039) for anti-RNP titers with inflammatory arthritis. AUC values were 0.67 (95% CI 0.58-0.77, P = 0.0002) for anti-Sm/RNP titers and 0.59 (95% CI 0.49-0.69, P = 0.0352) for anti-RNP titers with Raynaud phenomenon. The odds ratios for the diagnosis of MCTD and SLE were significantly higher in patients with double positivity compared to those testing solely positive for anti-RNP antibody.

CONCLUSION

Anti-Sm/RNP common motif autoreactivity when combined with anti-RNP antibody positivity identifies those patients who are closely related with certain clinical manifestations and who are associated with well-defined connective tissue disease such as MCTD or SLE.

摘要

目的

本研究旨在评估抗Sm/RNP共同基序抗体检测呈阳性且伴有或不伴有抗RNP抗体的疑似结缔组织病患者的临床特征。

方法

采用多重固相生物测定法(伯乐公司)检测抗Sm/RNP和抗RNP抗体的滴度。比较三个亚组(仅RNP阳性、仅Sm/RNP阳性以及RNP和Sm/RNP均为阳性)的临床表现。使用公认的分类标准对患者进行进一步评估,以诊断混合性结缔组织病(MCTD)和/或系统性红斑狼疮(SLE)。

结果

本研究共纳入133例患者。与仅抗RNP或仅抗Sm/RNP抗体阳性的患者相比,抗RNP和抗Sm/RNP抗体均呈阳性的患者炎症性关节炎和雷诺现象的发生率显著更高(关节炎:69.1% 对28.8% 对25.0%,P<0.0001;雷诺现象:59.5% 对23.3% 对37.5%,P = 0.0005)。抗Sm/RNP滴度诊断炎症性关节炎的曲线下面积(AUC)值为0.68(95%置信区间[CI] 0.59 - 0.77,P<0.0001),抗RNP滴度的AUC值为0.65(95% CI 0.55 - 0.74,P = 0.0039)。抗Sm/RNP滴度诊断雷诺现象的AUC值为0.67(95% CI 0.58 - 0.77,P = 0.0002),抗RNP滴度的AUC值为0.59(95% CI 0.49 - 0.69,P = 0.0352)。与仅抗RNP抗体呈阳性的患者相比,双阳性患者诊断MCTD和SLE的比值比显著更高。

结论

抗Sm/RNP共同基序自身反应性与抗RNP抗体阳性相结合,可识别出与某些临床表现密切相关且与明确的结缔组织病(如MCTD或SLE)相关的患者。