Abstract

One hundred and fifty RA patients classified into two equal subgroups according to the presence of sicca symptoms, in addition to seventy five healthy controls. All patients were subjected to self-reported questionnaire about sicca symptoms, DAS 28, Unstimulated whole salivary flow rate (UWSFR), Schirmer's test, ESR, CRP, RF, Anti- CCP, Anti-Ro, Anti-La antibodies, serum and salivary CXC ligand 13 (CXCL13), B cell activating factor (BAFF), ultrasonography for major salivary gland and biopsy of minor salivary gland.

Highlights

  • Secondary Sjogren’s syndrome (SS) was occurring in approximately 30% of RA patients [1] where involvement of exocrine lacrimal and salivary glands occurs

  • Secondary SS is manifested by dry eyes ( Keratoconjuntivitis sicca) and dry mouth [2]

  • The study was carried out on one hundred and fifty patients with rheumatoid arthritis diagnosed according to the American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) 2010 criteria for diagnosing of RA [6]

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Summary

Introduction

Secondary Sjogren’s syndrome (SS) was occurring in approximately 30% of RA patients [1] where involvement of exocrine lacrimal and salivary glands occurs. The decrease of salivary and lacrimal functions in RA is assumed to be related to the lymphocytic infiltrate present in the affected glands. Diagnosis of SS has traditionally depended on signs, symptoms, serologic test, and invasive procedures such as minor salivary gland biopsy. Work from several independent groups has shown common, consistent, and characteristic findings on parotid and minor salivary gland ultrasound among patients with SS. Salivary ultrasonography is a new method that holds the possibility of noninvasively providing important diagnostic information about major salivary glands in SS without radiation or surgery [4]

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