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Rhinological manifestations of Sjögren's syndrome: a cohort-matched, prospective, cross-sectional, observational study

Published online by Cambridge University Press:  23 August 2021

U F Kamel*
Affiliation:
Department of Otolaryngology, Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK
P J Maddison
Affiliation:
School of Sport Health and Exercise Science, Bangor University, Wales, UK
*
Author for correspondence: Dr Usama F Kamel, Department of Otolaryngology, Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK E-mail: usama.kamel@nhs.net Fax: +44 151 525 6086

Abstract

Objective

To assess the prevalence of abnormal rhinological findings in a Sjögren's syndrome population.

Methods

A cohort-matched, prospective, cross-sectional, observational study was conducted. Sixty-seven subjects (30 patients and 37 controls) were enrolled. Rhinological assessment including smell threshold was evaluated using a standardised, validated clinical test as part of a larger study.

Results

Smell thresholds were –4.4 and –5.4 in the Sjögren's syndrome and control groups, respectively (p = 0.001). Hyposmia (threshold values of less than −4.5) was demonstrated in the Sjögren's syndrome group (47 per cent). Smell was negatively correlated with age (p = 0.040). Nasal septal perforation was noted in 3 Sjögren's syndrome patients (10 per cent) and nasal mucosal dryness in 10 patients (33 per cent), but none of the control group were affected.

Conclusion

Hyposmia in Sjögren's syndrome was demonstrated using the Smell Threshold Test. Nasal septal perforation and nasal mucosa dryness were also noted in patients with Sjögren's syndrome. A diagnosis of Sjögren's syndrome should be considered and investigated in smell deprivation and/or nasal septal perforation patients.

Type
Main Articles
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

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Footnotes

Dr U F Kamel takes responsibility for the integrity of the content of the paper

References

Fox, RI. Sjogren's syndrome. Lancet 2005;366:321–31CrossRefGoogle ScholarPubMed
Vitali, C, Bombardieri, S, Jonsson, R, Moutsopoulos, HM, Alexander, EL, Carsons, SE et al. Classification criteria for Sjogren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis 2002;61:554–8CrossRefGoogle ScholarPubMed
Rasmussen, N, Brofeldt, S, Manthorpe, R. Smell and nasal findings in patients with primary Sjogren's syndrome. Scand J Rheumatol Suppl 1986;61:142–5Google ScholarPubMed
Midilli, R, Gode, S, Oder, G, Kabasakal, Y, Karci, B. Nasal and paranasal involvement in primary Sjogren's syndrome. Rhinology 2013;51:265–7Google Scholar
Freeman, SR, Sheehan, PZ, Thorpe, MA, Rutka, JA. Ear, nose, and throat manifestations of Sjogren's syndrome: retrospective review of a multidisciplinary clinic. J Otolaryngol 2005;34:20–4CrossRefGoogle ScholarPubMed
Kamel, UF, Maddison, P, Whitaker, R. Impact of primary Sjogren's syndrome on smell and taste: effect on quality of life. Rheumatology (Oxford) 2009;48:1512–14CrossRefGoogle ScholarPubMed
Doty, RL, McKeown, DA, Lee, WW, Shaman, P. A study of the test-retest reliability of ten olfactory tests. Chem Senses 1995;20:645–56CrossRefGoogle ScholarPubMed
Doty, RL, Gregor, TP, Settle, RG. Influence of intertrial interval and sniff-bottle volume on phenyl ethyl alcohol odor detection thresholds. Chem Senses 1986;11:259–64CrossRefGoogle Scholar
Servioli, L, Maciel, G, Nannini, C, Crowson, CS, Matteson, EL, Cornec, D et al. Association of smoking and obesity on the risk of developing primary Sjogren syndrome: a population-based cohort study. J Rheumatol 2019;46:727–30CrossRefGoogle ScholarPubMed
Doig, JA, Whaley, K, Dick, WC, Nuki, G, Williamson, J, Buchanan, WW. Otolaryngological aspects of Sjogren's syndrome. Br Med J 1971;4:460–3CrossRefGoogle ScholarPubMed
Henkin, RI, Talal, N, Larson, AL, Mattern, CF. Abnormalities of taste and smell in Sjogren's syndrome. Ann Intern Med 1972;76:375–83CrossRefGoogle ScholarPubMed
Doty, RL. Olfactory dysfunction and its measurement in the clinic. World J Otorhinolaryngol Head Neck Surg 2015;1:2833CrossRefGoogle ScholarPubMed
Mueller, C, Temmel, AF, Quint, C, Rieger, A, Hummel, T. Olfactory function in HIV-positive subjects. Acta Otolaryngol 2002;122:6771CrossRefGoogle ScholarPubMed
Sijan Gobeljic, M, Milic, V, Pejnovic, N, Damjanov, N. Chemosensory dysfunction, oral disorders and oral health-related quality of life in patients with primary Sjogren's syndrome: comparative cross-sectional study. BMC Oral Health 2020;20:187CrossRefGoogle ScholarPubMed
Weiffenbach, JM, Fox, PC. Odor identification ability among patients with Sjogren's syndrome. Arthritis Rheum 1993;36:1752–4CrossRefGoogle ScholarPubMed
Doty, RL. Epidemiology of smell and taste dysfunction. Handb Clin Neurol 2019;164:313CrossRefGoogle ScholarPubMed
Henkin, RI, Velicu, I. cAMP and cGMP in nasal mucus: relationships to taste and smell dysfunction, gender and age. Clin Invest Med 2008;31:E71–7CrossRefGoogle ScholarPubMed
Cain, WS, Gent, J, Catalanotto, FA, Goodspeed, RB. Clinical evaluation of olfaction. Am J Otolaryngol 1983;4:252–6CrossRefGoogle ScholarPubMed