Literature DB >> 32934136

National Sjögren's Foundation Survey: Burden of Oral and Systemic Involvement on Quality of Life.

Sara S McCoy1, Christie M Bartels2, Ian J Saldanha3, Vatinee Y Bunya4, Esen K Akpek5, Matthew A Makara6, Alan N Baer7.   

Abstract

OBJECTIVE: To define the association between oral and systemic manifestations of Sjögren syndrome (SS) and quality of life (QOL).
METHODS: We analyzed a cross-sectional survey conducted by the Sjögren's Foundation in 2016, with 2961 eligible responses. We defined oral symptom and sign exposures as parotid gland swelling, dry mouth, mouth ulcers/sores, oral candidiasis, trouble speaking, choking or dysphagia, sialolithiasis or gland infection, and dental caries. Systemic exposures included interstitial lung disease, purpura/petechiae/cryoglobulinemia, vasculitis, neuropathy, leukopenia, interstitial nephritis, renal tubular acidosis, autoimmune hepatitis, primary biliary cholangitis, or lymphoma. Outcomes included SS-specific QOL questions generated by SS experts and patients.
RESULTS: Using multivariable regression models adjusted for age, sex, race, and employment, we observed that mouth ulcers or sores, trouble speaking, and dysphagia were associated with poor quality of life. The following oral aspects had the greatest effect on the following QOL areas: (1) mouth ulcers/sores on the challenge and burden of living with SS (OR 4.26, 95% CI 2.89-6.28); (2) trouble speaking on memory and concentration (OR 4.24, 95% CI 3.28-5.48); and (3) dysphagia on functional interference (OR 4.25, 95% CI 3.13-5.79). In contrast, systemic manifestations were associated with QOL to a lesser extent or not at all.
CONCLUSION: Oral manifestations of SS, particularly mouth ulcers or sores, trouble speaking, and dysphagia, were strongly associated with worse QOL. Further study and targeted treatment of these oral manifestations provides the opportunity to improve quality of life in patients with SS.
Copyright © 2021 by the Journal of Rheumatology.

Entities:  

Keywords:  Sjögren syndrome; oral health; quality of life

Mesh:

Year:  2020        PMID: 32934136      PMCID: PMC7956920          DOI: 10.3899/jrheum.200733

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   5.346


  28 in total

1.  Oral involvement in primary Sjögren syndrome.

Authors:  Philip C Fox; Simon J Bowman; Barbara Segal; Frederick B Vivino; Nandita Murukutla; Karen Choueiri; Sarika Ogale; Lachy McLean
Journal:  J Am Dent Assoc       Date:  2008-12       Impact factor: 3.634

2.  The Quality of Life Burden Associated With Voice Disorders in Sjögren's Syndrome.

Authors:  Kristine Tanner; Jenny L Pierce; Ray M Merrill; Karla L Miller; Katherine A Kendall; Nelson Roy
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-04-03       Impact factor: 1.547

3.  Evaluation of Swallowing Functions in Patients with Sjögren's Syndrome.

Authors:  Sibel Eyigör; Baha Sezgin; Gonca Karabulut; Kerem Öztürk; Sercan Göde; Tayfun Kirazlı
Journal:  Dysphagia       Date:  2016-11-12       Impact factor: 3.438

4.  Preserved salivary output and xerostomia-related quality of life in head and neck cancer patients receiving parotid-sparing radiotherapy.

Authors:  B S Henson; M R Inglehart; A Eisbruch; J A Ship
Journal:  Oral Oncol       Date:  2001-01       Impact factor: 5.337

5.  Comparing nebulized water versus saline after laryngeal desiccation challenge in Sjögren's Syndrome.

Authors:  Kristine Tanner; Nelson Roy; Ray M Merrill; Katherine Kendall; Karla L Miller; Daniel O Clegg; Amanda Heller; Daniel R Houtz; Mark Elstad
Journal:  Laryngoscope       Date:  2013-05-14       Impact factor: 3.325

6.  Impact of primary Sjogren's syndrome on smell and taste: effect on quality of life.

Authors:  Usama F Kamel; Peter Maddison; Rhiannon Whitaker
Journal:  Rheumatology (Oxford)       Date:  2009-09-14       Impact factor: 7.580

7.  Quality of life in patients with Sjögren's syndrome and sicca complex.

Authors:  P López-Jornet; F Camacho-Alonso
Journal:  J Oral Rehabil       Date:  2008-10-13       Impact factor: 3.837

8.  Cognition, depression, fatigue, and quality of life in primary Sjögren's syndrome: correlations.

Authors:  Belgin Koçer; Mehmet Engin Tezcan; Hale Zeynep Batur; Şeminur Haznedaroğlu; Berna Göker; Ceyla İrkeç; Rümeysa Çetinkaya
Journal:  Brain Behav       Date:  2016-10-13       Impact factor: 2.708

9.  An Innovative Online Qualitative Study to Explore the Symptom Experience of Patients with Primary Sjögren's Syndrome.

Authors:  Kerry Gairy; Keith Ruark; Susan M Sinclair; Helen Brandwood; Linda Nelsen
Journal:  Rheumatol Ther       Date:  2020-07-28

10.  Peripheral neuropathy and health-related quality of life in patients with primary Sjögren's syndrome: a preliminary report.

Authors:  Marta Jaskólska; Magdalena Chylińska; Anna Masiak; Katarzyna Nowicka-Sauer; Mariusz Siemiński; Marcin Ziętkiewicz; Zenobia Czuszyńska; Zbigniew Zdrojewski
Journal:  Rheumatol Int       Date:  2020-03-14       Impact factor: 2.631

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  2 in total

1.  Symptom-Based Cluster Analysis Categorizes Sjögren's Disease Subtypes: An International Cohort Study Highlighting Disease Severity and Treatment Discordance.

Authors:  Sara S McCoy; Miguel Woodham; Christie M Bartels; Ian J Saldanha; Vatinee Y Bunya; Noah Maerz; Esen K Akpek; Matthew A Makara; Alan N Baer
Journal:  Arthritis Rheumatol       Date:  2022-08-03       Impact factor: 15.483

Review 2.  State of the art and future directions in assessing the quality of life in rare and complex connective tissue and musculoskeletal diseases.

Authors:  Leopoldo Trieste; Sara Cannizzo; Ilaria Palla; Isotta Triulzi; Giuseppe Turchetti
Journal:  Front Med (Lausanne)       Date:  2022-09-23
  2 in total

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