Laboratory Medicine ›› 2019, Vol. 34 ›› Issue (11): 1021-1025.DOI: 10.3969/j.issn.1673-8640.2019.11.014

• Orginal Article • Previous Articles     Next Articles

Role of anti-chromatin antibody determined by automatic multiplex bead immunoassay in the diagnosis of connective tissue diseases

WANG Juan1, SHEN Qingying1, WANG Kaiwen2, ZHAO Jiangfeng2   

  1. 1.Department of Clinical Laboratory,Shanghai General Hospital,Shanghai Jiaotong University,Shanghai 200080,China
    2.Department of Rheumatology,South Campus,Renji Hospital,Shanghai Jiaotong University School of Medicine,Shanghai 201112,China
  • Received:2019-06-05 Online:2019-11-30 Published:2019-12-05

Abstract:

Objective To investigate the role of anti-chromatin antibody determined by automatic multiplex bead immunoassay in the diagnosis of connective tissue diseases. Methods The expressions of anti-chromatin antibody in 384 patients with connective tissue diseases [243 cases of systemic lupus erythematosus(SLE),39 cases of polymyositis(PM),15 cases of mixed connective tissue disease(MCTD),51 cases of Sjögen's syndrome(SS),7 cases of systemic sclerosis(SSc) and 29 cases of rheumatoid arthritis(RA)],200 non-rheumatic disease patients(disease control group) and 200 healthy subjects(healthy control group) were determined. Anti-double-stranded DNA(dsDNA) antibodies,anti-histone antibodies and anti-nucleosome antibodies were determined by enzyme-linked immunosorbent assay(ELISA). Anti-nuclear antibodies(ANA) were determined by indirect immunofluorescence. The correlation between systemic lupus erythematosus disease activity index(SLEDAI) score and anti-chromatin antibody was evaluated. Receiver operating characteristic(ROC) curve was used to analyze the roles of these indicators for the diagnosis of SLE. Results The positive rates of anti-chromatin antibodies in healthy control,disease control,SLE,MCTD,PM,SS,SSc and RA groups were 0.00%,1.00%,70.78%,73.33%,23.08%,17.65%,28.57% and 10.34%,respectively. The positive rate of anti-chromatin antibodies increased with the increase of ANA titer. MCTD,PM,SS,SSc and RA groups were merged into non-SLE group. Serum anti-chromatin antibody level in SLE group was higher than that in non-SLE group(P<0.000 1). For anti-chromatin antibody,anti-dsDNA antibody,anti-nucleosome antibody and anti-histone antibody in SLE group,the rates of single-antibody positive and the other 3-antibody negative was 45.39%,32.34%,13.42% and 7.37%,respectively. There were some cross-positive rates among the 4 antibodies. The areas under curves(AUC) of anti-nucleosome antibody,anti-chromatin antibody,anti-dsDNA antibody and anti-histone antibody for the diagnosis of SLE were 0.813,0.779,0.777 and 0.613,respectively. There was no correlation between anti-chromatin antibodies and SLEDAI score (r= 0.124 6,P=0.177 0). There was no statistical significance in serum anti-chromatin antibodies between SLE patients without nephritis and those with nephritis(P>0.05). Conclusions Automatic multiplex bead immunoassay for the determination of anti-chromatin antibody plays a role in the diagnosis of connective tissue diseases.

Key words: Anti-chromatin antibody, Automatic multiplex bead immunoassay, Connective tissue disease

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