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Reviews

Early diagnosis of primary Sjögren’s syndrome: EULAR-SS task force clinical recommendations

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Pages 137-156 | Received 05 Aug 2015, Accepted 14 Oct 2015, Published online: 22 Dec 2015

References

  • Reference annotations
  • * Of interest
  • ** Of considerable interest
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* Key reference of the proposal of the first internationally-consensuated systemic activity index for SjS.

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* One of the largest series of patients with primary SjS (1115 Italian patients) that analyses the impact on survival of the immunological profile.

  • Fisher BA, Brown RM, Bowman SJ, et al. A review of salivary gland histopathology in primary Sjögren’s syndrome with a focus on its potential as a clinical trials biomarker. Ann Rheum Dis. 2015 Sep;74(9):1645–1650.

* A timely review about the role of histopathology as a biomarker for stratification and response to therapy in patients with primary SjS.

  • Caporali R, Bonacci E, Epis O, et al. Safety and usefulness of minor salivary gland biopsy: retrospective analysis of 502 procedures performed at a single center. Arthritis Rheum. 2008;59:714–720.
  • Brito-Zeron P, Retamozo S, Bové A, et al. Minimally-invasive technique for the biopsy of minor salivary glands: searching for systemic infiltrative diseases in patients presenting with sicca symptoms. Ann Rheum Dis. 2014;73(Suppl2):664.
  • Costa S, Quintin-Roué I, Lesourd A, et al.. Reliability of histopathological salivary gland biopsy assessment in Sjögren’s syndrome: a multicentre cohort study. Rheumatology (Oxford). 2015;54(6):1056–1064.

* Well-designed study that analyses the intraobserver and interobserver reliability of minor salivary gland biopsy in primary SjS.

  • Jonsson R, Theander E, Sjöström B, et al. Autoantibodies present before symptom onset in primary Sjögren syndrome. Jama. 2013;310:1854–1855.
  • Theander E, Jonsson R, Sjöström B, et al. Prediction of Sjögren’s Syndrome years before diagnosis and identification of patients with early onset and severe disease course by autoantibody profiling. Arthritis Rheumatol. 2015 Sep;67(9):2427–2436.

* Very innovative study that demonstrates that SjS-related autoantibodies are present up to 20 years before of the diagnosis of the disease.

  • Goules AV, Tzioufas AG. Imaging: diagnostic value of ultrasonography in Sjögren’s syndrome. Nat Rev Rheumatol. 2014;10:450–452.
  • Theander E, Mandl T. Primary Sjögren’s syndrome: diagnostic and prognostic value of salivary gland ultrasonography using a simplified scoring system. Arthritis Care Res (Hoboken). 2014;66:1102–1107.
  • Cornec D, Jousse-Joulin S, Pers JO, et al. Contribution of salivary gland ultrasonography to the diagnosis of Sjögren’s syndrome: toward new diagnostic criteria?. Arthritis Rheum. 2013;65(1):216–225.
  • Salaffi F, Carotti M, Iagnocco A, et al. Ultrasonography of salivary glands in primary Sjögren’s syndrome: a comparison with contrast sialography and scintigraphy. Rheumatology (Oxford). 2008;47(8):1244–1249.
  • Cornec D, Jousse-Joulin S, Saraux A, et al. Salivary gland ultrasound to diagnose Sjögren’s syndrome: a claim to standardize the procedure. Rheumatology (Oxford). 2015;54:199–200.
  • Baldini C, Luciano N, Tarantini G, et al. Salivary gland ultrasonography: a highly specific tool for the early diagnosis of primary Sjögren’s syndrome. Arthritis Res Ther. 2015;17:146.
  • Hammenfors DS, Brun JG, Jonsson R, et al. Diagnostic utility of major salivary gland ultrasonography in primary Sjögren’s syndrome. Clin Exp Rheumatol. 2015;33:56–62.
  • Cornec D, Jousse-Joulin S, Marhadour T, et al. Salivary gland ultrasonography improves the diagnostic performance of the 2012 American College of Rheumatology classification criteria for Sjögren’s syndrome. Rheumatology (Oxford). 2014;53:1604–1607.
  • Ren YD, Li XR, Zhang J, et al. Conventional MRI techniques combined with MR sialography on T2-3D-DRIVE in Sjögren syndrome. Int J Clin Exp Med. 2015;8:3974–3982.
  • Ziakas PD, Poulou LS, Thanos L. Towards integrating positron emission tomography for work-up of patients with Sjögren’s syndrome and associated lymphomas. Autoimmun Rev. 2014;13:327–329.
  • Cohen C, Mekinian A, Uzunhan Y, et al. 18F-fluorodeoxyglucose positrón emission tomography/computer tomography as an objective tool for assessingdisease activity in Sjögren’s syndrome. Autoimmun Rev. 2013;12:1109–1114.
  • Baldini C, Gallo A, Perez P, et al. Saliva as an ideal milieu for emerging diagnostic approaches in primary Sjögren’s syndrome. Clin Exp Rheumatol. 2012;30:785–790.
  • Tzioufas AG, Kapsogeorgou EK. Biomarkers. Saliva proteomics is a promising tool to study Sjögren syndrome. Nat Rev Rheumatol. 2015;11:202–203.
  • Delaleu N, Mydel P, Kwee I, et al. High fidelity between saliva proteomics and the biologic state of salivary glands defines biomarker signatures for primary Sjögren’s syndrome. Arthritis Rheumatol. 2015;67:1084–1095.
  • Deutsch O, Krief G, Konttinen YT, et al. Identification of Sjögren’s syndrome oral fluid biomarker candidates following high-abundance protein depletion. Rheumatology (Oxford). 2015;54:884–890.
  • Von Thun Und Hohenstein-Blaul N, Funke S, Grus FH. Tears as a source of biomarkers for ocular and systemic diseases. Exp Eye Res. 2013;117:126–137.
  • Arbuckle MR, McClain MT, Rubertone MV, et al. Development of autoantibodies before the clinical onset of systemic lupus erythematosus. N Engl J Med. 2003;349:1526–1533.
  • Retamozo S, Akasbi M, Brito-Zerón P, et al. Anti-Ro52 antibody testing influences the classification and clinical characterisation of primary Sjögren’s syndrome. Clin Exp Rheumatol. 2012;30:686–692.
  • Mekinian A, Nicaise-Roland P, Chollet-Martin S, et al. Anti-SSA Ro52/Ro60 antibody testing by immunodot could help the diagnosis of Sjogren’s syndrome in the absence of anti-SSA/SSB antibodies by ELISA. Rheumatology (Oxford). 2013;52:2223–2228.
  • Gordon P, Khamashta MA, Rosenthal E, et al. Anti-52 kDa Ro, anti-60 kDa Ro, and anti-La antibody profiles in neonatal lupus. J Rheumatol. 2004;31:2480–2487.
  • Shiboski SC, Shiboski CH, Criswell L, et al.; Sjögren’s International Collaborative Clinical Alliance (SICCA) Research Groups. American College of Rheumatology classification criteria for Sjögren’s syndrome: a data-driven, expert consensus approach in the Sjögren’s International Collaborative Clinical Alliance cohort. Arthritis Care Res (Hoboken). 2012;64:475–487.
  • Vitali C, Bootsma H, Bowman SJ, et al. Classification criteria for Sjogren’s syndrome: we actually need to definitively resolve the long debate on the issue. Ann Rheum Dis. 2013;72:476–478.

* A critical review of the current classification criteria, signed by the members of the EULAR Study Group on Disease Activity Criteria for Sjögren’s syndrome.

  • Cornec D, Saraux A, Cochener B, et al. Level of agreement between 2002 American-European Consensus Group and 2012 American College of Rheumatology classification criteria for Sjögren’s syndrome and reasons for discrepancies. Arthritis Res Ther. 2014;16:R74.
  • Rasmussen A, Ice JA, Li H, et al. Comparison of the American-European Consensus Group Sjogren’s syndrome classification criteria to newly proposed American College of Rheumatology criteria in a large, carefully characterised sicca cohort. Ann Rheum Dis. 2014;73:31–38.

* The authors compare the performance of the American-European Consensus Group (AECG) and the newly proposed American College of Rheumatology (ACR) classification criteria for Sjögren’s Syndrome (SS) and found that there is no clear evidence for increased value of the new ACR criteria over the old AECG criteria from the clinical or biological perspective.

  • Quartuccio L, Baldini C, Priori R, et al. The classification criteria for Sjögren syndrome: issues for their improvement from the study of a large Italian cohort of patients. Ann Rheum Dis. 2014;73:e35.
  • Hernández-Molina G, Avila-Casado C, Nuñez-Alvarez C, et al. Utility of the American-European Consensus Group and American College of Rheumatology Classification Criteria for Sjögren’s syndrome in patients with systemic autoimmune diseases in the clinical setting. Rheumatology (Oxford). 2015;54:441–448.

* In Mexican patients with primary SjS, the authors found that the feasibility of the AECG criteria is superior to that of the ACR criteria, although their performance was similar among patients with systemic autoimmune diseases.

  • Seror R, Theander E, Bootsma H, et al. Outcome measures for primary Sjögren’s syndrome: a comprehensive review. J Autoimmun. 2014;51:51–56.
  • Bowman SJ, Fox RI. Classification criteria for Sjogren’s syndrome: nothing ever stands still!. Ann Rheum Dis. 2014 Jan;73(1):1–2.
  • Seror R, Gottenberg JE, Devauchelle-Pensec V, et al. European League Against Rheumatism Sjögren’s Syndrome Disease Activity Index and European League Against Rheumatism Sjögren’s Syndrome Patient-Reported Index: a complete picture of primary Sjögren’s syndrome patients. Arthritis Care Res (Hoboken). 2013;65:1358–1364.
  • Brito-Zerón P, Kostov B, Solans R, et al.; on behalf of the SS Study Group; Autoimmune Diseases Study Group (GEAS); Spanish Society of Internal Medicine (SEMI). Systemic activity and mortality in primary Sjögren syndrome: predicting survival using the EULAR-SS Disease Activity Index (ESSDAI) in 1045 patients. Ann Rheum Dis. 2014 Nov 28. pii: annrheumdis-2014-206418. [Epub ahead of print].

* The first study that shows that patients with primary SS who present at diagnosis with high systemic activity (ESSDAI ≥14) and/or predictive immunological markers (especially those with more than one), are at higher risk of death.

  • Seror R, Ravaud P, Mariette X, et al.; EULAR Sjögren’s Task Force. EULAR Sjogren’s Syndrome Patient Reported Index (ESSPRI): development of a consensus patient index for primary Sjogren’s syndrome. Ann Rheum Dis. 2011 Jun;70(6):968–972.
  • Seror R, Bootsma H, Saraux A, et al.; on behalf of the EULAR Sjögren’s Task Force. Defining disease activity states and clinically meaningful improvement in primary Sjögren’s syndrome with EULAR primary Sjögren’s syndrome disease activity (ESSDAI) and patient-reported indexes (ESSPRI). Ann Rheum Dis. 2014 Dec 5. pii: annrheumdis-2014-206008. [Epub ahead of print].
  • Seror R, Bowman SJ, Brito-Zerón P, et al. EULAR Sjögren’s syndrome disease activity index (ESSDAI): a user guide. RMD Open. 2015;1:e000022. DOI:10.1136/rmdopen-2014-000022.
  • Seror R, Baron G, Vitali C, et al. Development of CLINESSDAI score (Clinical EULAR Sjögren’s Syndrome Disease Activity Index) without biological domain: a tool for biological studies. Ann Rheum Dis. 2015;74(Suppl2):579.
  • Cornec D, Devauchelle-Pensec V, Mariette X, et al. Development of the Sjögren’s Syndrome Responder Index, a data-driven composite endpoint for assessing treatment efficacy. Rheumatology (Oxford). 2015 Sep;54(9):1699–1708.

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