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. 2014 Apr 27;2014:315179. doi: 10.1155/2014/315179

Table 2.

Anti-nuclear antibodies (ANA) in different ANA associated autoimmune rheumatic diseases and healthy individuals.

Antibody AARD
SLE SSc SjS IIM MCTD HI
dsDNA 40–70% <3% <3% <3% <3% <3%
Chromatin 40–70% <3% <3% <3% 5–18% <3%
RNP 10–40% 5–15% <3% 5–15% 100%5 <3%
Sm 5–20% <2% <1% <1% <2%2 <1%
SS-A/Ro60 40–70% 3–10% 60–90% <3% <3% <3%
Ro52/
TRIM21
40–70% 15–30% 70–90% 25–50% <3% <3%
SS-B/La 15–30% 1–5% 60–80% 5–15% <3% <3%
Scl-70 (topo I) 0–5% 20–40%4 <3% <3% <3% <1%
Jo-1 1–3% 1–3% <2% 15–30% <2% <1%
Centromere 2–5% 20–40%4 5–10% 1–3% 2–5% <3%
RNA Pol III <1% 5–25%4 <1% <1% <1% <1%
Ribosomal P 10–30% <2% <2% <2% <2% <1%
PM/Scl 1–3% 5–10% <2% 5–10% <2% <3%
Mi-2 <1% 3–8% <1% 5–15%1 <1% <3%
Ku 5–20% 3–8% <3% 3–10%3 <3% <3%
PCNA <5% <1% <1% <1% <1% <3%
Th/To <1% 3–10% <1% <1% <1% <1%

1Rare in PM, higher prevalence in DM; mild form of disease; early during development.

2Prevalence depends if antigen contains SmBB′ (cross-reactive with RNP).

3Very high titer in PM.

4Anti-Scl-70, anti-centromere, anti-RNA Pol III antibodies tend to be mutually exclusive.

5Part of the classification criteria, therefore should be 100%; however, depending on assay used, some patients might be negative.

Note: Prevalence values were established based on literature and consensus of authors.

Abbreviations: DM: dermatomyositis; IIM: idiopathic inflammatory myopathy (polymyositis/dermatomyositis); MCTD: mixed connective tissue disease; PCNA: proliferating cell nuclear antigen; PM: polymyositis; RA: rheumatoid arthritis; RNA pol III: RNA polymerase III; RNP: ribonucleoprotein; Sm: Smith antigens (U2-U6 RNP); SjS: Sjögren's syndrome; SLE: systemic lupus erythematosus; SPA: Solid phase assay; SSc: systemic sclerosis; TRIM: tripartite motif.