Abstract

Sjögren's syndrome (SS) is a chronic and progressive multisystem autoimmune disease typically managed by rheumatologists. Diagnostic delays are common, due in large part to the non-specific and variable nature of SS symptoms and the slow progression of disease. The hallmark characteristics of SS are dry eye and dry mouth, but there are a broad range of other possible symptoms such as joint and muscle pain, skin rashes, chronic dry cough, vaginal dryness, extremity numbness or tingling, and disabling fatigue. Given that dry eye and dry mouth are typically the earliest presenting complaints, eye care clinicians and dental professionals are often the first point of medical contact and can provide critical collaboration with rheumatologists to facilitate both timely diagnosis and ongoing care of patients with SS. Current diagnostic criteria advocated by the American College of Rheumatology are predicated on the presence of signs/symptoms suggestive of SS along with at least two objective factors such as traditional biomarker positivity, salivary gland biopsy findings, and/or presence of keratoconjunctivitis sicca. Traditional biomarkers for SS include the autoantibodies anti-Sjögren's syndrome-related antigen A (SS-A/Ro), anti-Sjögren's syndrome-related antigen B (SS-B/La), antinuclear antibody (ANA) titers, and rheumatoid factor (RF). While diagnostically useful, these biomarkers have low specificity for SS and are not always positive, especially in early cases of SS. Several newly-identified biomarkers for SS include autoantibodies to proteins specific to the salivary and lacrimal glands [SP-1 (salivary gland protein-1), PSP (parotid secretory protein), CA-6 (carbonic anhydrase VI)]. Data suggest that these novel biomarkers may appear earlier in the course of disease and are often identified in cases that test negative to traditional biomarkers. The Sjö® test is a commercially available diagnostic panel that incorporates testing for traditional SS biomarkers (anti-SS-A/Ro, anti-SS-B/La, ANA, and RF), as well as three novel, proprietary early biomarkers (antibodies to SP-1, PSP, and CA-6) which provide greater sensitivity and specificity than traditional biomarker testing alone. Timely diagnosis of SS requires appropriate clinical vigilance for potential SS symptoms, referral and collaborative communication among rheumatology, ophthalmology, and oral care professions, and proactive differential work-up that includes both physical and laboratory evaluations.

Highlights

  • Sjogren’s syndrome (SS) is a chronic, progressive, multisystem autoimmune disease that involves primarily the lacrimal and salivary glands [1, 2]

  • Compared to patients who did not have SS, the SS patients had significantly worse symptoms, conjunctival and corneal staining, and Schirmer’s test results [3]. These findings suggest that all patients with clinically significant aqueous-deficient dry eye (ADDE) should be assessed for SS

  • A recent study in 37 patients with long-standing SS and high anti-SS-A/Ro titer found anti-CA-6 antibodies in 38% of patients but low positivity for antibodies to salivary protein-1 (SP-1) or parotid secretory protein (PSP) [62]. These findings suggest that the novel biomarkers, anti-SP-1 and anti-PSP, are less likely to be detected in advanced primary SS

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Summary

Introduction

Sjogren’s syndrome (SS) is a chronic, progressive, multisystem autoimmune disease that involves primarily the lacrimal and salivary glands [1, 2]. Current diagnostic criteria advocated by the American College of Rheumatology are predicated on the presence of signs/ symptoms suggestive of SS along with at least two objective factors such as traditional biomarker positivity, salivary gland biopsy findings, and/or presence of keratoconjunctivitis sicca.

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