Association of anti-HMGCR antibodies of the IgM isotype with refractory immune-mediated necrotizing myopathy

被引:0
作者
Yang, Hongxia [1 ,2 ]
Sun, Chao [1 ]
Ye, Lifang [1 ]
Xu, Yuetong [1 ]
Lin, Sang [1 ]
Peng, Qinglin [1 ]
Wang, Guochun [1 ]
Lu, Xin [1 ]
机构
[1] China Japan Friendship Hosp, Dept Rheumatol, Key Lab Myositis, 2 Yinhua St, Beijing 100029, Peoples R China
[2] Peking Univ First Hosp, Dept Clin Lab, Beijing, Peoples R China
关键词
Immune-mediated necrotizing myopathy; Anti-HMGCR; Autoantibodies isotypes; Outcome; CYCLIC CITRULLINATED PEPTIDE; ANTI-3-HYDROXY-3-METHYLGLUTARYL-COENZYME; AUTOANTIBODIES; CLASSIFICATION; UPDATE;
D O I
10.1186/s13075-024-03387-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) autoantibodies are one of the myositis-specific antibodies which is associated with immune-mediated necrotizing myopathy (IMNM). However, the relationship between anti-HMGCR isotypes and prognosis has not yet been fully investigated. This study was conducted to gain insight into the association between anti-HMGCR isotypes and clinical, and prognosis in IMNM patients who were positive for anti-HMGCR antibodies. Methods Levels of anti-HMGCR isotypes (IgG, IgA and IgM) were assessed by enzyme-linked immunosorbent assay (ELISA) in 123 consecutive serum samples obtained from 71 patients who were positive for anti-HMGCR IgG at baseline. Disease activity was assessed by manual muscle testing (MMT) 8, Physician's Global Assessment (PGA) visual analog scale (VAS), and muscle VAS. Results Baseline anti-HMGCR IgG levels were correlated with PGA VAS (r = 0.24; p = 0.04), muscle VAS (r = 0.32; p < 0.01), and MMT8(r=-0.24; p = 0.04), and baseline anti-HMGCR IgM levels were positively correlated with PGA VAS (r = 0.27, p = 0.02), muscle VAS (r = 0.24, p = 0.04). Anti-HMGCR IgM positive patients had a lower age of onset [29(25,46) vs. 51(33,65), p = 0.006], and a higher proportion of neck weakness (63.5% vs. 34.6%, p = 0.031) compared with anti-HMGCR IgM negative patients. Longitudinal analysis showed that the changes in anti-HMGCR IgG levels were correlated with the changes in the PGA VAS (beta = 3.830; p < 0.0001), muscle VAS (beta = 2.893; p < 0.0001), MMT8 (beta=-19.368; p < 0.0001), and creatine kinase (CK) levels (beta = 3900.05, p < 0.0001). Anti-HMGCR IgM levels were weakly correlated with anti-HMGCR IgA levels at baseline (r = 0.33, p < 0.01), and the variations in anti-HMGCR IgA levels were correlated with the changes in anti-HMGCR IgM levels during follow-up (beta = 0.885; p < 0.0001). There were more patients with anti-HMGCR IgM who showed a refractory course than those who were with anti-HMGCR IgM negative (polycyclic course: 40% vs. 25%; chronic continuous course: 46.7% vs. 20.5%, p = 0.018). Conclusion In anti-HMGCR IgG-positive IMNM patients, the levels of anti-HMGCR IgG are associated with disease activity, and anti-HMGCR IgM is associated with refractory outcome and poor prognosis.
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