Articles / Dry eyes, dry mouth and fatigue: When should GPs think Sjögren’s disease?


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Clinical Immunologist, Westmead Hospital and ICPMR; Post-Doctoral Researcher, The Westmead Institute for Medical Research; Clinical Senior Lecturer, Faculty of Medicine and Health, University of Sydney
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Dry eyes and dry mouth are common complaints and most are not caused by Sjögren’s disease, which is part of what makes the condition easy to miss.
Sjögren’s disease is a systemic autoimmune condition that particularly affects the salivary and tear glands. The textbook picture is persistent dry eyes and dry mouth, but patients may also present with fatigue, joint pain, recurrent salivary gland swelling or potentially serious manifestations involving the lungs, kidneys, skin or nervous system. Challengingly, some people have little or no obvious dryness when more systemic features first emerge. Sjögren’s disease usually presents in females around 40s to 50s.
That variability matters. Sjögren’s can significantly affect quality of life and, in a subset of patients, is associated with serious complications including organ involvement and lymphoma. The challenge is not to investigate every patient with dry eyes, but to recognise when the overall pattern deserves a closer look.
Dryness symptoms are common, and careful evaluation to look for underlying causes is key. Dry eyes (xerophthalmia) may be caused by excessive screen time, contact lenses or ageing. Dry mouth (xerostomia) may be caused by diabetes, medications or anxiety. Dry eyes may manifest as gritty or burning eyes, and dry mouth may manifest with difficulty swallowing, or early and severe dental disease. Not every patient will volunteer these symptoms and may need to be asked specifically.
Consider Sjögren’s if the sicca is unexplained after evaluation, particularly when accompanied by the other cardinal signs including fatigue, arthralgias and possibly organ disease.
Sometimes dryness symptoms may appear after organ manifestations, so the absence of dryness does not rule out Sjögren’s disease.
There is no single test to diagnose Sjögren’s disease, and it is important to investigate mimics such as diabetes mellitus, and potential organ involvement, as guided by the clinical evaluation.
Autoimmune serology may be helpful. Antinuclear antibody (ANA) positivity can be seen in around 80% of cases. Likewise, anti-Ro60/TROVE2 and anti-Ro52/TRIM21 serum autoantibodies (previously known as anti-SSA/Ro) may be positive in up to 70-80% of individuals.
Anti-Ro52/TRIM21 and anti-Ro60/TROVE2 antibodies are an important part of the internationally recognised ACR/EULAR classification criteria, while ANA, anti-SSB/La and rheumatoid factor can provide additional information. Rheumatoid factor can be positive in approximately 50% of Sjögren’s patients but lacks diagnostic specificity.
Serology needs to be interpreted in context. A positive autoantibody does not automatically mean a patient has Sjögren’s, and negative serology does not necessarily exclude it. Around a quarter of patients may lack the classic serological markers, so if the index of suspicion for Sjögren’s remains high, they should be further referred for evaluation.
Additional investigations could be considered, including salivary gland imaging (ultrasound) and objective measures of sicca (e.g., Schirmer’s test).
In Australia, and depending on the location, a referral to a rheumatologist or clinical immunologist should be considered after the initial evaluation for the work-up or confirmation of Sjögren’s disease.
Below is a list of referral prompts, although they are by no means an exhaustive or definitive list:
Specialist assessment may involve objective testing of tear or salivary function, further immunological investigation and, in selected patients, a minor salivary gland biopsy.
Some features warrant particular attention. Persistent salivary gland enlargement, lymphadenopathy, unexplained weight loss, and palpable purpura have been associated with a higher risk of lymphoproliferative disease in Sjögren’s and should warrant further and prompt assessment.
For many patients, the burden of Sjögren’s is not captured by test results or an official diagnosis.
Dryness can affect eating, speaking, sleeping, dental health and everyday comfort. Fatigue and pain can also be particularly disabling, and can affect occupation, daily function, and socialisation. Management often involves several disciplines, including primary care, clinical immunology or rheumatology, ophthalmology, oral medicine and dentistry.
Globally, there is currently no approved disease-modifying therapy that treats Sjögren’s as a whole, so much of care remains directed towards relieving dryness, protecting the eyes and teeth, managing pain and fatigue, and treating specific systemic manifestations when they occur. Targeted treatments are advancing through clinical development, however, reflecting a growing understanding of the immune pathways involved in the disease.
Monitoring and follow-up in GP can support effective symptom management, and reduce the risk of complications. This includes:
Although Sjögren’s may be clinically stable for some, it is important to be on the lookout for complications that arise such as lymphoma, which occurs in 5-10% of patients with Sjögren’s.
One reason Sjögren’s remains difficult to diagnose and manage is that it is not the same disease in every patient. Globally, efforts are being made to better understand the pathophysiology and risk factors for the development of this disease. This will lead to the development of new biomarkers for the diagnosis and prognosis in Sjögren’s, as well as targeted therapies.
The aim is to move towards a future where we can better identify which patients are likely to remain relatively stable, which may be at greater risk of systemic complications, and eventually which treatments are most likely to help them. That work is still developing, and emerging biomarkers are not yet substitutes for established clinical assessment. For GPs today, however, earlier recognition remains one of the most useful contributions we can make.
Lee AYS, Rischmueller M. The diagnosis and misdiagnosis of Sjögren disease. Internal Medicine Journal. 2024;54:833-835. doi: 10.1111/imj.16395
Price EJ et al. British Society for Rheumatology guideline on management of adult and juvenile onset Sjögren disease. Rheumatology. 2025;64:409-439. doi: 10.1093/rheumatology/keae152
Shiboski CH et al. 2016 American College of Rheumatology/European League Against Rheumatism Classification Criteria for Primary Sjögren’s Syndrome: A Consensus and Data-Driven Methodology Involving Three International Patient Cohorts. Arthritis Rheumatol. 2017;69:35-45. doi: 10.1002/art.39859
Hoi A, Lee AYS, Marshall G, Kirana C, Rischmueller M. Sjögren’s disease in Australia: why we need to pay attention. MJA InSight+. 2025
Dr Adrian Lee (MBBS BMedSc(Hons) PhD FRACP FRCPA AFRACMA) is a Clinical Immunologist at Westmead Hospital and ICPMR, Post-Doctoral Researcher at The Westmead Institute for Medical Research, and Clinical Senior Lecturer in the Faculty of Medicine and Health at the University of Sydney. His clinical and research foci are in autoimmunity, autoantibodies, B cells and Sjögren’s disease.
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Clinical Immunologist, Westmead Hospital and ICPMR; Post-Doctoral Researcher, The Westmead Institute for Medical Research; Clinical Senior Lecturer, Faculty of Medicine and Health, University of Sydney
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