Paediatric Rheumatology
SAMHD1 associates with inflammation and vasculitis in paediatric-onset systemic lupus erythematosus
X. Zhao1, C. Li2, S. Li3, J. Zhang4, W. Kuang5, J. Deng6, X. Tan7, C. Li8, J. Wang9
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China. licaifeng123@yeah.net
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
- Department of Rheumatology, National Centre for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, China.
CER15569
2022 Vol.40, N°9
PI 1801, PF 1807
Paediatric Rheumatology
PMID: 35579088 [PubMed]
Received: 09/02/2022
Accepted : 16/04/2022
In Press: 10/05/2022
Published: 20/09/2022
Abstract
OBJECTIVES:
In this study, we aimed to explore the expression of the Aicardi-Goutières syndrome (AGS) mutant gene SAMHD1 in paediatric-onset systemic lupus erythematosus (pSLE), its correlations with clinical and laboratory parameters, and the relationship between its expression and the type 1 interferon (IFN) signalling pathway.
METHODS:
Peripheral blood from 98 pSLE patients and 44 gender and age-matched healthy individuals were examined. Gene expression levels of SAMDH1 and interferon-stimulated genes (ISGs; MxA, IRF3 and IRF7) were evaluated using real-time RT-PCR assays.
RESULTS:
SAMHD1 levels in pSLE patients were significantly increased compared to those in healthy donors (p<0.001). SAMHD1 was associated with serum ferritin (r=0.221, p=0.042) in pSLE patients. SAMHD1 levels were significantly increased (p<0.05) in pSLE patients with butterfly erythema, alopecia, and photosensitivity. SAMHD1 was positively correlated with MxA, IRF3 and IRF7 levels, indicating that SAMHD1 was associated with the type 1 IFN signalling pathway.
CONCLUSIONS:
SAMHD1 was significantly increased and correlated with MxA, IRF3 and IRF7 in pSLE patients.