Prevalence of Oral and Maxillofacial Disorders in Patients with Systemic Scleroderma-A Systematic Review

被引:13
作者
Benz, Korbinian [1 ]
Baulig, Christine [2 ]
Knippschild, Stephanie [2 ]
Strietzel, Frank Peter [3 ]
Hunzelmann, Nicolas [4 ]
Jackowski, Jochen [1 ]
机构
[1] Witten Herdecke Univ, Fac Hlth, Dept Oral Surg & Policlin Ambulance, Alfred Herrhausen Str 45, D-58448 Witten, Germany
[2] Witten Herdecke Univ, Inst Med Biometry & Epidemiol, Fac Hlth, Alfred Herrhausen Str 50, D-58448 Witten, Germany
[3] Charite, Dept Periodontol Oral Med & Oral Surg, Charite Ctr Dent, Assmannshauser Str 4-6, D-14197 Berlin, Germany
[4] Univ Cologne, Dept Dermatol & Venerol, Kerpener Str 62, D-50937 Cologne, Germany
关键词
systemic scleroderma; orofacial manifestations; mucosal changes; skin fibrosis; rare disease; pooled effect estimates; QUALITY-OF-LIFE; OROFACIAL MANIFESTATIONS; SJOGRENS-SYNDROME; SICCA SYMPTOMS; SCLEROSIS; HEALTH; INVOLVEMENT; CLASSIFICATION; FREQUENCY; CRITERIA;
D O I
10.3390/ijerph18105238
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: Systematic scleroderma is a rare chronic autoimmune disease of unknown aetiology. The aim of this study was to identify the prevalence of orofacial pathognomonic conditions in patients with systemic scleroderma using only randomised prospective studies that investigated the treatment of oral and maxillofacial changes, highlighted associations between the disease and Sjogren's syndrome, and/or analysed the effect of oral hygiene. Methods: The literature was systematically reviewed based on Cochrane Library, EMBASE, PubMed, Scopus, and Web of Science articles published up to March 2020. The primary endpoint of this analysis was defined as an estimation of the prevalence of oral mucosal changes in different areas of the oral cavity (oral mucosa, tongue, lip, periodontal status, bones, and other regions) in patients suffering from scleroderma. Therefore, a systematic literature search (Cochrane Library, EMBASE, PubMed, Scopus, and Web of Science) was conducted and limited by the publication date (1950-03/2020) and the publication language (English). Extracted frequencies were pooled using methods for meta-analysis. In order to obtain the highest level of evidence, only prospective study reports were considered to be eligible. Results: After full-text screening, 14 (766 patients) out of 193 publications were eligible for the final analysis. Twelve studies produced reliable results in the final data sets. Calculation of the pooled effect estimate (random effects model) revealed a prevalence of 57.6% (95% CI: 40.8-72.9%) for the main area "lip". For the area "oral mucosa", a prevalence of 35.5% (95% CI: 15.7-62.0%) was calculated. The prevalence for "other regions" was only based on studies with salivary changes and was calculated to be 25.4% (95% CI: 14.2-41.3%). Conclusion: The most pathognomonic conditions in the orofacial region in patients with systemic scleroderma affect the lips, oral mucosa, and salivary glands.
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页数:16
相关论文
共 60 条
[1]   Intraoral reconstruction with "thinned" peroneal artery perforator flaps: An alternative to classic donor areas in comorbid patients [J].
Acartuerk, Tahsin Oguz ;
Maldonado, Andres A. ;
Ereso, Alex .
MICROSURGERY, 2015, 35 (05) :399-402
[2]   Recommendations for the Care of Oral Involvement in Patients With Systemic Sclerosis [J].
Alantar, Alp ;
Cabane, Jean ;
Hachulla, Eric ;
Princ, Guy ;
Ginisty, Danielle ;
Hassin, Michel ;
Sorel, Marc ;
Maman, Louis ;
Pilat, Aurelie ;
Mouthon, Luc .
ARTHRITIS CARE & RESEARCH, 2011, 63 (08) :1126-1133
[3]   SJOGRENS SYNDROME IN PROGRESSIVE SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
ALARCONS.D ;
IBANEZ, G ;
HERNANDE.J ;
VELAZQUE.F ;
GONZALEZ.Y .
AMERICAN JOURNAL OF MEDICINE, 1974, 57 (01) :78-85
[4]  
Albilia JB, 2007, J CAN DENT ASSOC, V73, P831
[5]   Systemic sclerosis [J].
Allanore, Yannick ;
Simms, Robert ;
Distler, Oliver ;
Trojanowska, Maria ;
Pope, Janet ;
Denton, Christopher P. ;
Varga, John .
NATURE REVIEWS DISEASE PRIMERS, 2015, 1
[6]  
[Anonymous], 2006, German Federal Ministry of the Interior
[7]   Systemic sclerosis-associated Sjogren's syndrome and relationship to the limited cutaneous subtype - Results of a prospective study of Sicca syndrome in 133 consecutive patients [J].
Avouac, J. ;
Sordet, C. ;
Depinay, C. ;
Ardizonne, M. ;
Vacher-Lavenu, M. C. ;
Sibilia, J. ;
Kahan, A. ;
Allanore, Y. .
ARTHRITIS AND RHEUMATISM, 2006, 54 (07) :2243-2249
[8]   Associated Autoimmune Diseases in Systemic Sclerosis Define a Subset of Patients with Milder Disease: Results from 2 Large Cohorts of European Caucasian Patients [J].
Avouac, Jerome ;
Airo, Paolo ;
Dieude, Philippe ;
Caramaschi, Paola ;
Tiev, Kiet ;
Diot, Elisabeth ;
Sibilia, Jean ;
Cappelli, Susanna ;
Granel, Brigitte ;
Vacca, Alessandra ;
Wipff, Julien ;
Meyer, Olivier ;
Kahan, Andre ;
Matucci-Cerinic, Marco ;
Allanore, Yannick .
JOURNAL OF RHEUMATOLOGY, 2010, 37 (03) :608-614
[9]   Epidemiology of systemic sclerosis: incidence, prevalence, survival, risk factors, malignancy, and environmental triggers [J].
Barnes, Jammie ;
Mayes, Maureen D. .
CURRENT OPINION IN RHEUMATOLOGY, 2012, 24 (02) :165-170
[10]   Relationship Between Disease Characteristics and Orofacial Manifestations in Systemic Sclerosis: Canadian Systemic Sclerosis Oral Health Study III [J].
Baron, Murray ;
Hudson, Marie ;
Tatibouet, Solene ;
Steele, Russell ;
Lo, Ernest ;
Gravel, Sabrina ;
Gyger, Genevieve ;
El Sayegh, Tarek ;
Pope, Janet ;
Fontaine, Audrey ;
Masetto, Ariel ;
Matthews, Debora ;
Sutton, Evelyn ;
Thie, Norman ;
Jones, Niall ;
Copete, Maria ;
Kolbinson, Dean ;
Markland, Janet ;
Nogueira, Getulio ;
Robinson, David ;
Fritzler, Marvin ;
Gornitsky, Mervyn .
ARTHRITIS CARE & RESEARCH, 2015, 67 (05) :681-690