4.8 Article

DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjogren's Syndrome

期刊

FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.702037

关键词

primary Sjogren's syndrome; interferon; DNA methylation; autoimmunity; interferonopathies; precision medicine

资金

  1. Knut and Alice Wallenberg Foundation [KAW 2011.0073]
  2. Swedish Research Council for Medicine and Health [VR-MH Dnr 5212014-2263, Dnr 2018-02399, Dnr 2016-01982]
  3. Swedish Rheumatism Association
  4. King Gustaf V's 80-year Foundation
  5. Swedish Society of Medicine
  6. Selander Foundation
  7. Marcus Borgstrom Foundation
  8. Western Norway Regional Health Authority
  9. Science for Life Laboratory, Uppsala University
  10. Swedish Research Council (VR-RFI)
  11. Knut and Alice Wallenberg Foundation

向作者/读者索取更多资源

The study introduced a DNA methylation-based IFN score to identify patients with activation of the IFN system in primary Sjogren's syndrome (pSS). High DNAm IFN scores were associated with younger age at symptom onset and diagnosis, positive SSA and SSB antibodies, hypergammaglobulinemia, low C4, and lymphoma in pSS patients. The DNAm IFN score could be a promising tool for patient stratification, treatment decisions, monitoring, and inclusion in clinical trials.
Primary Sjogren's syndrome (pSS) is an autoimmune inflammatory disease with profound clinical heterogeneity, where excessive activation of the type I interferon (IFN) system is considered one of the key mechanisms in disease pathogenesis. Here we present a DNA methylation-based IFN system activation score (DNAm IFN score) and investigate its potential associations with sub-phenotypes of pSS. The study comprised 100 Swedish patients with pSS and 587 Swedish controls. For replication, 48 patients with pSS from Stavanger, Norway, were included. IFN scores were calculated from DNA methylation levels at the IFN-induced genes RSAD2, IFIT1 and IFI44L. A high DNAm IFN score, defined as > mean(controls) +2SD(controls) (IFN score > 4.4), was observed in 59% of pSS patients and in 4% of controls (p=1.3x10(-35)). Patients with a high DNAm IFN score were on average seven years younger at symptom onset (p=0.017) and at diagnosis (p=3x10(-3)). The DNAm IFN score levels were significantly higher in pSS positive for both SSA and SSB antibodies compared to SSA/SSB negative patients (p(discovery)=1.9x10(-8), p(replication)=7.8x10(-4)). In patients positive for both SSA subtypes Ro52 and Ro60, an increased score was identified compared to single positive patients (p=0.022). Analyzing the discovery and replication cohorts together, elevated DNAm IFN scores were observed in pSS with hypergammaglobulinemia (p=2x10(-8)) and low C4 (p=1.5x10(-3)) compared to patients without these manifestations. Patients < 70 years with ongoing lymphoma at DNA sampling or lymphoma at follow-up (n=7), presented an increased DNAm IFN score compared to pSS without lymphoma (p=0.025). In conclusion, the DNAm-based IFN score is a promising alternative to mRNA-based scores for identification of patients with activation of the IFN system and may be applied for patient stratification guiding treatment decisions, monitoring and inclusion in clinical trials.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据