scholarly journals Is There Hearing Loss In Sjogren's Syndrome? A Cohort Matched Cross-sectional Observational study

2016 ◽  
Vol 130 (S3) ◽  
pp. S184-S185
Author(s):  
Usama Kamel ◽  
Peter Maddison ◽  
Rhiannon Whitaker
1996 ◽  
Vol 75 (10) ◽  
pp. 666-668 ◽  
Author(s):  
Martin S. Trott ◽  
Gordon B. Hughes ◽  
Leonard H. Calabrese ◽  
Barbara P. Barna ◽  
Richard H. Nodar

Immune sensorineural hearing loss is manifested in several systemic immune diseases.1,2 Although hearing loss has been previously documented in patients with Sjögren's syndrome (SS),3 the effect of SS on hearing is unclear. This prospective study was designed to assess the presence of hearing loss in 14 patients with SS and, if sensorineural hearing loss was present, to determine if the hearing loss was immune-mediated. Patients were evaluated with basic audiologic tests as well as for cellular immune inner ear reactivity as measured by the lymphocyte transformation test (LTT).4 Three patients had evidence of sensorineural hearing loss. Two patients had a positive LTT without evidence of sensorineural hearing loss. This preliminary study suggests that SS may not directly cause sensorineural hearing loss, immune-mediated or otherwise.


2016 ◽  
Vol 75 (Suppl 2) ◽  
pp. 309.2-309
Author(s):  
S. Lechtman ◽  
M.-P. Debray ◽  
B. Crestani ◽  
C. Bancal ◽  
M. Hourseau ◽  
...  

2021 ◽  
Vol 80 (Suppl 1) ◽  
pp. 1186.1-1186
Author(s):  
S. Beider ◽  
T. Witte ◽  
D. Ernst

Background:Patients with primary Sjögren´s syndrome (pSS) suffer from pain, oral or ocular dryness and fatigue. Such symptoms can have a detrimental impact on health-related quality of life. The prevalence of mental health disorders in patients with pSS is considerably higher than in the general population [1]. Regular physical activity, such as nordic walking, improves aerobic capacity and may reduce reported fatigue [2]. According to current European League Against Rheumatism (EULAR) recommendations, management of pSS concomitant diseases should be evaluated in patients presenting with fatigue and pain, and severity scored using specific tools [3].Objectives:This study analyses the frequency and severity of depressive symptoms in patients with pSS and their relationship to fatigue and physical activity.Methods:In this monocentric, cross-sectional study, patients with pSS attending our Rheumatology clinic between January 2019 and March 2020 completed standardized questionnaires: Beck´s depression inventory second edition (BDI II) and the international physical activity questionnaire short form (IPAQ-SF). Data were analyzed using SPSS 26 (IBM, Armonk, NY, USA). The tests include bivariate and partial correlations and nonparametric Kruskal-Wallis-Test.Results:In total, 134 patients were included. The majority were female (117/134, 87.3 %), and the patients median age was 57 [21 – 85] years. Median duration of disease-related symptoms at inclusion was 56 months (range 0-388 months). Physical activity was low in 44. 8 % (n = 60), moderate in 32.1 % (n = 43), and high in 23.1 % (n = 31) of patients. Depressive symptoms of varying severity were identified in 76/134 (56.7%) of patients. Severe depression occurred in 10/76 (13.2%) and moderate depression in 14/76 (18.4%) patients. The remaining 52/76 (68.4%) patients had minimal or mild depression. Over two-thirds (67.7%) of patients reporting high physical activity showed no depression and no one with a high level of physical activity had severe depression. There was a clear association between the BDI II depression score and the level of physical activity (p = 0.003) regardless of age and illness duration. However, not all the symptoms assessed by BDI II had the same impact. From 21 items of the BDI II Inventory, symptoms such as loss of energy and fatigue were profoundly relevant, being reported by over 75 % of patients. The main depressive symptoms, which had a strong negative correlation with the level of physical activity were loss of energy (p < 0.001), sadness (p=0.018), inability to make decisions (p=0.007) and loss of pleasure (p=0.004). Somatic symptoms of decreased activation such as fatigue (p=0.026) and concentration difficulty (p=0.013) were also significant. The cognitive, self-negative symptoms were not associated with the level of physical activity.Conclusion:A negative correlation of physical activity with fatigue and depression in patients with pSS has been demonstrated. The somatic symptoms of decreased activation played a profound role in this association, while the cognitive self-negotiation symptoms were not influenced by physical activity in our patients. Such symptoms as fatigue and loss of energy could potentially be reduced by exercises and functional training and consequently decrease the level of depression. An intervention study in this regard would be recommended.References:[1]Cui, Y., et al., Anxiety and depression in primary Sjögren’s syndrome: a cross-sectional study. BMC psychiatry, 2018. 18(1): p. 1-8.[2]Strömbeck, B., E. Theander, and L. Jacobsson, Effects of exercise on aerobic capacity and fatigue in women with primary Sjögren’s syndrome. Rheumatology, 2007. 46(5): p. 868-871.[3]Ramos-Casals, M., et al., EULAR recommendations for the management of Sjögren’s syndrome with topical and systemic therapies. Annals of the rheumatic diseases, 2020. 79(1): p. 3-18.Disclosure of Interests:None declared


2017 ◽  
Vol 84 (3) ◽  
pp. 317-321 ◽  
Author(s):  
Sarah Lechtman ◽  
Marie-Pierre Debray ◽  
Bruno Crestani ◽  
Catherine Bancal ◽  
Muriel Hourseau ◽  
...  

Author(s):  
Z. Assy ◽  
F. J. Bikker ◽  
O. Picauly ◽  
H. S. Brand

Abstract Objective Sjögren’s syndrome patients use different dry-mouth interventions for the relieve of their oral dryness. Recently, it was shown that patients with dry-mouth complaints have regional differences in perceived intra-oral dryness. Therefore, the aim of the present study was to investigate whether the use of dry-mouth interventions is related to the perceived regional oral dryness. Materials and methods A cross-sectional study was performed among Sjögren’s patients. Volunteers could anonymously administer various questionnaires, including the Regional Oral Dryness Inventory (RODI), Xerostomia Inventory (XI), Bother Index (BI) and a list of dry-mouth interventions. Results Sjögren’s syndrome patients use a wide variety for the relieve of oral dryness. “Drinking water’’ and “moistening the lips’’ were used most frequently. Dry-mouth interventions, “drinking water’’, “rinsing of the mouth”, and “drinking small volumes” had significant associations with the RODI-scores of the posterior palate, and anterior and posterior tongue, respectively. On the other hand, “using mouth gel’’ had a significant association with the RODI-scores of the inside cheeks. Conclusion Sjögren’s syndrome patients are more likely to use mouth gels when their inside cheeks were experienced as most dry, while they drank water, rinsed their mouth or drank small volumes if the posterior palate, and anterior and posterior tongue were considered as dry. It can be concluded that intra-oral dryness affects dry-mouth perception and thereby also the use of the various dry-mouth interventions. Clinical relevance The therapeutic choice of dry-mouth interventions by Sjögren’s syndrome patients seems to some extent to be related to dryness at specific intra-oral regions.


2017 ◽  
Vol 63 (1) ◽  
pp. 7-9
Author(s):  
Raquel Sousa Almeida ◽  
◽  
Ana Alves Oliveira ◽  
Petra M. Pego ◽  
Yahia Abuowda ◽  
...  

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