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Licensed Unlicensed Requires Authentication Published by De Gruyter August 22, 2012

Serum kallikrein-8 correlates with skin activity, but not psoriatic arthritis, in patients with psoriatic disease

  • Azza Eissa , Daniela Cretu , Antoninus Soosaipillai , Arane Thavaneswaran , Fawnda Pellett , Anastasia Diamandis , Ferda Cevikbas , Martin Steinhoff , Eleftherios P. Diamandis , Dafna Gladman and Vinod Chandran EMAIL logo

Abstract

Background: About 30% of cutaneous psoriasis (PsC) patients develop psoriatic arthritis (PsA) in the joint, which is under-recognized by dermatologists. Biomarkers for PsA are needed so that early referral to a rheumatologist is made. Kallikreins (KLKs) are secreted serine proteases implicated in skin desquamation and inflammation. This study examined KLK potential as serum biomarkers of PsA in cutaneous psoriasis patients.

Methods: KLKs were measured by ELISAs in synovial fluids of three PsA patients and three control early osteoarthritis (OA) patients, as well as in a cohort of 152 serum samples collected from age- and sex-matched PsC patients, with (n=76) or without PsA (n=76). KLK expression in psoriatic plaques was examined by immunohistochemistry. Univariate and multivariate logistic regression analyses were conducted to analyze the association between serum KLK levels and disease class (PsC, PsA). Serum KLKs that associated with PsA were correlated with clinical parameters of skin and joint activity.

Results: Among the seven KLKs tested, KLK6 and KLK8 were elevated in both PsA synovial fluids and psoriatic plaques, but only serum KLK8 levels were associated with psoriatic disease (odds ratio=2.56, p=0.03). Although significantly elevated in PsC and PsA sera compared to healthy controls, KLK8 did not discriminate PsA from PsC patients. KLK8 correlated positively with the psoriasis area and severity index (PASI) (r=0.43, p=0.001) independent of age, sex and psoriasis duration (β=1.153, p=0.0003) and exhibited no correlations with tender or swollen joint counts.

Conclusions: Increased KLK8 serum level in PsA patients reflects disease activity in the skin but not in the joints. Serum KLK levels are not useful for screening psoriasis patients for PsA.


Corresponding author: Dr. Vinod Chandran, Division of Rheumatology, University of Toronto, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital, 1E 416, 399 Bathurst Street, Toronto, Ontario, M5T 2S8, Canada, Phone: +1-416-603-5192, Fax: + 1-416-603-9387

Vinod Chandran is supported by a grant from the Canadian Institutes of Health Research through a New Emerging Team grant. The study was supported by grants from The Arthritis Society, Canada and the Krembil Foundation.

Conflict of interest statement

Authors’ conflict of interest disclosure: The authors state that there are no conflicts of interest regarding the publication of this article. Study support played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

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Received: 2012-04-18
Accepted: 2012-07-15
Published Online: 2012-08-22
Published in Print: 2013-02-01

©2013 by Walter de Gruyter Berlin Boston

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