Anti-protein arginine methyltransferase 5 (PRMT5) antibodies is associated with interstitial lung disease in rheumatoid arthritis
Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagn...
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Published in | Scientific reports Vol. 15; no. 1; pp. 29421 - 7 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
11.08.2025
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Abstract | Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagnosed with SSc, 87 patients with RA, and 31 healthy control subjects. Serum levels of the anti-PRMT5 antibodies were measured using a double-antigen sandwich enzyme-linked immunosorbent assay (ELISA). Patients with SSc exhibited higher serum levels (
p
< 0.001) and seropositivity rates (48.5% vs. 0%,
p
< 0.0001) of anti-PRMT5 antibodies compared to healthy subjects. Notably, serum levels of anti-PRMT5 antibodies were significantly elevated in patients with RA compared to healthy controls (
p
< 0.001), with a corresponding increase in the rate of seropositivity (14.9% vs. 0%,
p
< 0.05). Receiver operating curve analysis for anti-PRMT5 antibody levels yielded area under the curve values of 0.768 for distinguishing RA patients from healthy controls, and 0.903 for distinguishing SSc patients from controls. Furthermore, elevated levels of anti-PRMT5 antibodies were significantly associated with the presence of interstitial lung disease (ILD) (
p
< 0.0001) and antinuclear antibody positivity (
p
< 0.01). This study not only confirms the association of the anti-PRMT5 antibodies with SSc but also, for the first time, demonstrates a significant association between the anti-PRMT5 antibodies and RA, particularly in the context of RA-associated ILD. |
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AbstractList | Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagnosed with SSc, 87 patients with RA, and 31 healthy control subjects. Serum levels of the anti-PRMT5 antibodies were measured using a double-antigen sandwich enzyme-linked immunosorbent assay (ELISA). Patients with SSc exhibited higher serum levels (
p
< 0.001) and seropositivity rates (48.5% vs. 0%,
p
< 0.0001) of anti-PRMT5 antibodies compared to healthy subjects. Notably, serum levels of anti-PRMT5 antibodies were significantly elevated in patients with RA compared to healthy controls (
p
< 0.001), with a corresponding increase in the rate of seropositivity (14.9% vs. 0%,
p
< 0.05). Receiver operating curve analysis for anti-PRMT5 antibody levels yielded area under the curve values of 0.768 for distinguishing RA patients from healthy controls, and 0.903 for distinguishing SSc patients from controls. Furthermore, elevated levels of anti-PRMT5 antibodies were significantly associated with the presence of interstitial lung disease (ILD) (
p
< 0.0001) and antinuclear antibody positivity (
p
< 0.01). This study not only confirms the association of the anti-PRMT5 antibodies with SSc but also, for the first time, demonstrates a significant association between the anti-PRMT5 antibodies and RA, particularly in the context of RA-associated ILD. Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagnosed with SSc, 87 patients with RA, and 31 healthy control subjects. Serum levels of the anti-PRMT5 antibodies were measured using a double-antigen sandwich enzyme-linked immunosorbent assay (ELISA). Patients with SSc exhibited higher serum levels ( p < 0.001) and seropositivity rates (48.5% vs. 0%, p < 0.0001) of anti-PRMT5 antibodies compared to healthy subjects. Notably, serum levels of anti-PRMT5 antibodies were significantly elevated in patients with RA compared to healthy controls ( p < 0.001), with a corresponding increase in the rate of seropositivity (14.9% vs. 0%, p < 0.05). Receiver operating curve analysis for anti-PRMT5 antibody levels yielded area under the curve values of 0.768 for distinguishing RA patients from healthy controls, and 0.903 for distinguishing SSc patients from controls. Furthermore, elevated levels of anti-PRMT5 antibodies were significantly associated with the presence of interstitial lung disease (ILD) ( p < 0.0001) and antinuclear antibody positivity ( p < 0.01). This study not only confirms the association of the anti-PRMT5 antibodies with SSc but also, for the first time, demonstrates a significant association between the anti-PRMT5 antibodies and RA, particularly in the context of RA-associated ILD. Abstract Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagnosed with SSc, 87 patients with RA, and 31 healthy control subjects. Serum levels of the anti-PRMT5 antibodies were measured using a double-antigen sandwich enzyme-linked immunosorbent assay (ELISA). Patients with SSc exhibited higher serum levels (p < 0.001) and seropositivity rates (48.5% vs. 0%, p < 0.0001) of anti-PRMT5 antibodies compared to healthy subjects. Notably, serum levels of anti-PRMT5 antibodies were significantly elevated in patients with RA compared to healthy controls (p < 0.001), with a corresponding increase in the rate of seropositivity (14.9% vs. 0%, p < 0.05). Receiver operating curve analysis for anti-PRMT5 antibody levels yielded area under the curve values of 0.768 for distinguishing RA patients from healthy controls, and 0.903 for distinguishing SSc patients from controls. Furthermore, elevated levels of anti-PRMT5 antibodies were significantly associated with the presence of interstitial lung disease (ILD) (p < 0.0001) and antinuclear antibody positivity (p < 0.01). This study not only confirms the association of the anti-PRMT5 antibodies with SSc but also, for the first time, demonstrates a significant association between the anti-PRMT5 antibodies and RA, particularly in the context of RA-associated ILD. Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagnosed with SSc, 87 patients with RA, and 31 healthy control subjects. Serum levels of the anti-PRMT5 antibodies were measured using a double-antigen sandwich enzyme-linked immunosorbent assay (ELISA). Patients with SSc exhibited higher serum levels (p < 0.001) and seropositivity rates (48.5% vs. 0%, p < 0.0001) of anti-PRMT5 antibodies compared to healthy subjects. Notably, serum levels of anti-PRMT5 antibodies were significantly elevated in patients with RA compared to healthy controls (p < 0.001), with a corresponding increase in the rate of seropositivity (14.9% vs. 0%, p < 0.05). Receiver operating curve analysis for anti-PRMT5 antibody levels yielded area under the curve values of 0.768 for distinguishing RA patients from healthy controls, and 0.903 for distinguishing SSc patients from controls. Furthermore, elevated levels of anti-PRMT5 antibodies were significantly associated with the presence of interstitial lung disease (ILD) (p < 0.0001) and antinuclear antibody positivity (p < 0.01). This study not only confirms the association of the anti-PRMT5 antibodies with SSc but also, for the first time, demonstrates a significant association between the anti-PRMT5 antibodies and RA, particularly in the context of RA-associated ILD.Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed to to explore the association between anti-PRMT5 antibodies and rheumatoid arthritis (RA). The study recruited a cohort of 33 patients diagnosed with SSc, 87 patients with RA, and 31 healthy control subjects. Serum levels of the anti-PRMT5 antibodies were measured using a double-antigen sandwich enzyme-linked immunosorbent assay (ELISA). Patients with SSc exhibited higher serum levels (p < 0.001) and seropositivity rates (48.5% vs. 0%, p < 0.0001) of anti-PRMT5 antibodies compared to healthy subjects. Notably, serum levels of anti-PRMT5 antibodies were significantly elevated in patients with RA compared to healthy controls (p < 0.001), with a corresponding increase in the rate of seropositivity (14.9% vs. 0%, p < 0.05). Receiver operating curve analysis for anti-PRMT5 antibody levels yielded area under the curve values of 0.768 for distinguishing RA patients from healthy controls, and 0.903 for distinguishing SSc patients from controls. Furthermore, elevated levels of anti-PRMT5 antibodies were significantly associated with the presence of interstitial lung disease (ILD) (p < 0.0001) and antinuclear antibody positivity (p < 0.01). This study not only confirms the association of the anti-PRMT5 antibodies with SSc but also, for the first time, demonstrates a significant association between the anti-PRMT5 antibodies and RA, particularly in the context of RA-associated ILD. |
ArticleNumber | 29421 |
Author | Petersen, Frank Ma, Aiping Guo, Jiaxi Zhou, Qiaomiao Yu, Xinhua Lin, Shaowei Huang, Heqing Lin, Yikai Huang, Renliang |
Author_xml | – sequence: 1 givenname: Renliang surname: Huang fullname: Huang, Renliang organization: Department of Genetics and Prenatal Diagnosis, Hainan Women and Children’s Medical Center – sequence: 2 givenname: Jiaxi surname: Guo fullname: Guo, Jiaxi organization: Department of Respiratory and Critical Medicine, School of Medicine, The First Affiliated Hospital of Xiamen University, Xiamen University, Priority Area Chronic Lung Diseases, Research Center Borstel-Leibniz Lung Center, Member of the German Center for Lung Research (DZL) – sequence: 3 givenname: Qiaomiao surname: Zhou fullname: Zhou, Qiaomiao organization: Department of Genetics and Prenatal Diagnosis, Hainan Women and Children’s Medical Center – sequence: 4 givenname: Heqing surname: Huang fullname: Huang, Heqing organization: Department of Rheumatology, School of Medicine, The First Affiliated Hospital of Xiamen University, Xiamen University – sequence: 5 givenname: Shaowei surname: Lin fullname: Lin, Shaowei organization: Department of Nuclear Medicine, School of Medicine, The First Affiliated Hospital of Xiamen University, Xiamen University – sequence: 6 givenname: Yikai surname: Lin fullname: Lin, Yikai organization: Department of Radiology, School of Medicine, The First Affiliated Hospital of Xiamen University, Xiamen University – sequence: 7 givenname: Frank surname: Petersen fullname: Petersen, Frank organization: Priority Area Chronic Lung Diseases, Research Center Borstel-Leibniz Lung Center, Member of the German Center for Lung Research (DZL) – sequence: 8 givenname: Xinhua surname: Yu fullname: Yu, Xinhua email: xinhuayu@fz-borstel.de organization: Department of Genetics and Prenatal Diagnosis, Hainan Women and Children’s Medical Center, Priority Area Chronic Lung Diseases, Research Center Borstel-Leibniz Lung Center, Member of the German Center for Lung Research (DZL) – sequence: 9 givenname: Aiping surname: Ma fullname: Ma, Aiping email: aiping.ma@xmu.edu.cn organization: Department of Respiratory and Critical Medicine, School of Medicine, The First Affiliated Hospital of Xiamen University, Xiamen University |
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Keywords | Anti-PRMT5 antibodies Interstitial lung diseases Rheumatoid arthritis Systemic sclerosis |
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References | T Shao (14741_CR13) 2021; 12 VL Kronzer (14741_CR12) 2023; 5 Y Katanasaka (14741_CR16) 2024; 15 J Chen (14741_CR6) 2015; 67 LC Litzler (14741_CR15) 2019; 10 S Chen (14741_CR8) 2005; 24 14741_CR11 K Didier (14741_CR1) 2018; 9 F van den Hoogen (14741_CR5) 2013; 72 A Ma (14741_CR10) 2025; 16 14741_CR14 14741_CR2 S Mehra (14741_CR3) 2013; 12 D Aletaha (14741_CR4) 2010; 62 F Faul (14741_CR7) 2009; 41 14741_CR9 |
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Snippet | Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present study aimed... Abstract Recently, anti-protein arginine methyltransferase 5 (PRMT5) antibodies has been identified a novel marker for systemic sclerosis (SSc). The present... |
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SubjectTerms | 631/250 692/4023 Adult Aged Anti-PRMT5 antibodies Antibodies Antigens Antinuclear antibodies Arthritis, Rheumatoid - blood Arthritis, Rheumatoid - complications Arthritis, Rheumatoid - immunology Autoantibodies - blood Autoantibodies - immunology Autoimmune diseases Biomarkers Biomarkers - blood Case-Control Studies Enzyme-linked immunosorbent assay Expected values Female Humanities and Social Sciences Humans Interstitial lung diseases Investigations Lung diseases Lung Diseases, Interstitial - blood Lung Diseases, Interstitial - complications Lung Diseases, Interstitial - immunology Male Middle Aged multidisciplinary Protein arginine methyltransferase Protein-Arginine N-Methyltransferases - immunology Proteins Rheumatoid arthritis Rheumatology ROC Curve Science Science (multidisciplinary) Scleroderma Scleroderma, Systemic - blood Scleroderma, Systemic - immunology Serum levels Software Systemic sclerosis Variance analysis |
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Title | Anti-protein arginine methyltransferase 5 (PRMT5) antibodies is associated with interstitial lung disease in rheumatoid arthritis |
URI | https://link.springer.com/article/10.1038/s41598-025-14741-2 https://www.ncbi.nlm.nih.gov/pubmed/40790333 https://www.proquest.com/docview/3238564914 https://www.proquest.com/docview/3238717758 https://pubmed.ncbi.nlm.nih.gov/PMC12340103 https://doaj.org/article/91642a423f864aa9811f733896c47d0f |
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