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. Author manuscript; available in PMC: 2018 Jun 1.
Published in final edited form as: Semin Arthritis Rheum. 2016 Sep 13;46(6):692–698. doi: 10.1016/j.semarthrit.2016.09.001

Table 2.

Prevalence of ACPA subtypes among 1033 women from the Nurses’ Health Study and Nurses’ Health Study II in a nested case-control study, at the time of blood draw [1989-90 (NHS) or 1996-99 (NHSII)]

ACPA
subtype*
Pre-clinical RA
Cases
(n=255)
Matched
Controls
(n=778)
p value
Biglycan 12 (4.7%) 7 (0.9%) <0.001
Clusterin 26 (10.2%) 13 (1.7%) <0.001
Enolase 6 (2.4%) 4 (0.5%) 0.02
Fibrinogen 45 (17.7%) 34 (4.4%) <0.001
Histone 2A 14 (5.5%) 11 (1.4%) 0.001
Histone 2B 22 (8.6%) 13 (1.7%) <0.001
Vimentin 38 (14.9%) 16 (2.1%) <0.001

≥1 ACPA 59 (23.1%) 59 (7.6%) <0.001
≥2 ACPAs 40 (15.7%) 16 (2.1%) <0.001

P values are from univariable conditional logistic regression models.

*

For each ACPA subtype, antibodies against the following number of epitopes were tested. Subjects testing positive for antibody against one or more epitope were considered positive for that ACPA subtype: biglycan (1), clusterin (2), enolase (1), fibrinogen (5), histone 2A (2), histone 2B (2), vimentin (2)