Digestive involvement in primary Sjögren's syndrome: analysis from the Sjögrenser registry.


Por: Melchor, S, Sanchez-Piedra, C, Castro, M, Andreu, J, Taboada, V, Olive, A, Rosas, J, Menor, R, Garcia-Aparicio, A, Longo, F, Manrique-Arija, S, Vadillo, J, Lopez-Gonzalez, R, Narvaez, J, Galisteo, C, Martin, J, Naranjo, A, Illera, O, Moreira, B, Raya, E, Lopez, M, Judez, E, Moriano, C, Torrente-Segarra, V, Magallon, B, Astete, C, Castellvi, I, Bohorquez, C, Loricera, J, Belzunegui, J, Carreira, P and Spanish Soc Rheumatology Systemic

Publicada: 1 oct 2020 Ahead of Print: 1 oct 2020
Resumen:
OBJECTIVES: Digestive involvement (DI) has been reported in 10-30% of primary Sjögren's syndrome (pSS) patients, and few studies have systematically analysed the prevalence of DI in pSS patients. The aim of this study was to describe DI prevalence in pSS patients from the Sjögrenser Study, and to analyse its clinical associations. METHODS: All patients included in the Sjögrenser study, a Spanish multicentre randomised cohort, containing demographic, clinical and histologic data, have been analysed retrospectively. Patients were classified according to the presence of DI (oesophageal, gastric, intestinal, hepatic and pancreatic), and we have performed DI clinical associations, descriptive statistics, Student t or ?2 test, and uni and multivariate logistic regression. RESULTS: From 437 included patients, 95% were women, with a median age of 58 years, 71 (16.2%) presented DI: 21 (29.5%) chronic atrophic gastritis, 12 (16.9%) oesophageal motility dysfunction, 3 (4.2%) lymphocytic colitis, 18 (25.3%) primary biliary cholangitis, 15 (21.1%) autoimmune hepatitis, 7 (9.8%) pancreatic involvement and 5 (7%) coeliac disease. Half of them developed DI at the same time or after pSS diagnosis. Patients with DI were significantly older at pSS diagnosis (p=0.032), more frequently women (p=0.009), presented more autoimmune hypothyroidism and C3 hypocomplementaemia (p=0.040), and were treated more frequently with glucocorticoids, immunosuppressant and biologic therapies. Patients with pancreatic involvement presented more central nervous system and renal involvement, Raynaud's phenomenon, lymphoma and C3/C4 hypocomplementaemia. CONCLUSIONS: DI is frequent in Sjögrenser patients, mainly in the form of autoimmune disorders, and seem to be associated with a more severe phenotype. Our results suggest that DI should be evaluated in pSS patients, especially those with more severe disease.

Filiaciones:
Melchor, S:
 Hosp Univ Doce Octubre, Rheumatol Dept, Madrid, Spain

Sanchez-Piedra, C:
 SER, Unidad Invest, Madrid, Spain

Castro, M:
 Hosp Univ Puerta Hierro Majadahonda, Madrid, Spain

Andreu, J:
 Hosp Univ Puerta Hierro Majadahonda, Madrid, Spain

Taboada, V:
 Univ Cantabria, Fac Med, Hosp Univ Marques Valdecilla, Santander, Spain

Olive, A:
 Hosp Badalona Germans Trias & Pujol, Barcelona, Spain

:
 Hosp Marina Baixa, Alicante, Spain

Menor, R:
 Hosp Gen Jerez de la Frontera, Cadiz, Spain

Garcia-Aparicio, A:
 Hosp Virgen de la Salud, Toledo, Spain

Longo, F:
 Hosp Univ Gregorio Maranon, Madrid, Spain

Manrique-Arija, S:
 Hosp Univ Carlos Haya, Malaga, Spain

Vadillo, J:
 Hosp Univ Princesa, Madrid, Spain

Lopez-Gonzalez, R:
 Hosp Virgen de la Concha, Zamora, Spain

Narvaez, J:
 Hosp Univ Bellvitge, Barcelona, Spain

Galisteo, C:
 Hosp Univ Parc Tauli, Barcelona, Spain

Martin, J:
 Hosp Univ Madrid Norte Sanchinarro, Madrid, Spain

Naranjo, A:
 Hosp Univ Doctor Negrin, Las Palmas Gran Canaria, Spain

Illera, O:
 Hosp Univ Infanta Sofia, Madrid, Spain

Moreira, B:
 Complejo Hosp Pontevedra, Pontevedra, Spain

Raya, E:
 Hosp Clin Univ San Cecilio, Granada, Spain

Lopez, M:
 Hosp Meixoeiro, Vigo, Spain

Judez, E:
 Hosp Univ Albacete, Albacete, Spain

Moriano, C:
 Hosp Univ Leon, Leon, Spain

Torrente-Segarra, V:
 Hosp Gen Hosp, Barcelona, Spain

Magallon, B:
 Hosp Univ Miguel Servet, Zaragoza, Spain

Astete, C:
 Hosp Univ Ramon & Cajal, Madrid, Spain

Castellvi, I:
 Hosp Univ Santa Creu & St Pau, Barcelona, Spain

Bohorquez, C:
 Hosp Univ Principe Asturias, Madrid, Spain

Loricera, J:
 Univ Cantabria, Fac Med, Hosp Univ Marques Valdecilla, Santander, Spain

Belzunegui, J:
 Hosp Univ Donostia, Guipuzcoa, Spain

Carreira, P:
 Hosp Univ Doce Octubre, Rheumatol Dept, Madrid, Spain
ISSN: 0392856X





CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
Editorial
Pacini Editore SpA, VIA SANTA MARIA 31, 56126 PISA, ITALY, Italia
Tipo de documento: Article
Volumen: 38 Suppl 126 Número: 4
Páginas: 110-115
WOS Id: 000581183900017
ID de PubMed: 33025900
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