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Abstract Number: 360

88% of Recent Onset Polyarthritis Patients Are Positive for 14-3-3η Markers and 14-3-3η Auto-Antibodies Inform a Favourable Prognosis

Gilles Boire1, Nathalie Carrier2, Artur Jose de Brum-Fernandes3, Patrick Liang4, Ariel Masetto5, Yuan Gui6, Mairead Murphy6, Walter P. Maksymowych7 and Anthony Marotta8, 1Rheumatology Division, Centre Hospitalier Universitaire de Sherbrooke, Université de Sherbrooke, Sherbrooke, QC, Canada, 2Rheumatology, Universite de Sherbrooke, Sherbrooke, QC, Canada, 3Department of Medicine, Universite de Sherbrooke, Sherbrooke, QC, Canada, 4Rheumatology Division, CHUS, Sherbrooke, QC, Canada, 5Rheumatology, CHUS, Fleurimont, QC, Canada, 6Augurex Life Sciences Corp., North Vancouver, BC, Canada, 7Department of Medicine, University of Alberta, Edmonton, AB, Canada, 81423 Dempsey Road, Augurex Life Sciences Corp., North Vancouver, BC, Canada

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: ACPA, autoantibodies and prognostic factors, Early Rheumatoid Arthritis, Rheumatoid Factor

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Session Information

Title: Rheumatoid Arthritis - Clinical Aspects: Novel Biomarkers and Other Measurements of Disease Activity

Session Type: Abstract Submissions (ACR)

Background/Purpose The 14-3-3η protein has been described as a mechanistic marker that is detectable in serum during the very early stages of RA development. A specific anti-14-3-3η autoantibody response is present in RA serum  and is postulated to be protective when it effectively clears systemic 14-3-3η. This study examined the baseline expression of 14-3-3η markers (protein and pan-autoantibodies) in a recent onset polyarthritis cohort and their association with the progression of joint damage.

Methods 335 subjects were evaluated; 40 DMARD-naïve patients from the Sherbrooke EUPA cohort and 295 controls. Median age was 50 yrs, 2 months median disease duration, 75% were female and 60% were positive for RF and 55% for ACPA. Controls included 106 healthy and 189 disease controls consisting of connective tissue disease, OA, AS or autoimmune disorders. 14-3-3η protein levels were previously tested in this cohort using the Augurex 14-3-3η ELISA (cut-off ≥0.19 ng/ml) and 50% of the recent onset polyarthritis patients were positive. 14-3-3η AAb levels were measured on the MSD ECL platform using an established positive cut-off ≥380 U/ml. The group that was 14-3-3η AAb-only positive, in whom the 14-3-3η protein would have been cleared, was compared to the remainder of the cohort in terms of differences in radiographic progression over 30 months using the Mann-Whitney U-test. The Fisher Exact test was used to determine the association between marker positivity and radiographic progression (SHS≥3 at 30 months).

Results Median (IQR) 14-3-3η AAb values were significantly higher in early RA 617 U/ml (473-742) vs all controls 264 U/ml (200-348), p<0.0001 delivering a ROC AUC of 0.89 (95%CI:0.85-0.94). When compared to healthy subjects, the ROC AUC was 0.95 (95%CI:0.92-0.99), p<0.0001 delivering 93% specificity and 85% sensitivity with a likelihood ratio (LR) of 11.3. Thirty-four patients (85%) were 14-3-3η AAb positive, 88% were positive for either of the 14-3-3η markers and a Pearson correlation between the two 14-3-3η markers of r < 0.01 highlighted their complementary nature. Of the 40 patients, 15 (38%) were only positive for the 14-3-3η AAbs and had significantly less joint damage progression at 30 months, median (IQR) ΔSHS 0 (0-3.5) vs the rest of the cohort, 5 (-0.3–11.5), p<0.03. The Fisher exact test revealed that 14-3-3η AAb positivity (in the absence of the 14-3-3η protein) is associated with less radiographic progression at 30 months yielding an Odds Ratio of 5.3 (95%CI 1.2-23.9). p=0.03. 

Conclusion 14-3-3η and anti-14-3-3η biomarkers identify 88% of recent onset polyarthritis patients and those who are only positive for 14-3-3η AAbs have a more favorable radiographic prognosis. This is potentially due to the more effective clearance of deleterious 14-3-3η protein by anti-14-3-3η antibodies in these patients.


Disclosure:

G. Boire,

Augurex Life Sciences Corp,

5;

N. Carrier,
None;

A. J. de Brum-Fernandes,
None;

P. Liang,
None;

A. Masetto,
None;

Y. Gui,

Augurex Life Sciences Corp,

3;

M. Murphy,

Augurex Life Sciences Corp,

3;

W. P. Maksymowych,

Augurex Life Sciences Corp,

5;

A. Marotta,

Augurex Life Sciences Corp.,

3.

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ACR Meeting Abstracts - https://acrabstracts.org/abstract/88-of-recent-onset-polyarthritis-patients-are-positive-for-14-3-3%ce%b7-markers-and-14-3-3%ce%b7-auto-antibodies-inform-a-favourable-prognosis/

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