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Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography

OBJECTIVE: Juvenile Sjögren's syndrome (SS) is a rare, poorly defined, and possibly underdiagnosed condition affecting children and adolescents. The aim of this study was to characterize symptoms and clinical findings of juvenile SS and to explore the clinical application of major salivary glan...

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Autores principales: Hammenfors, Daniel S., Valim, Valéria, Bica, Blanca E. R. G., Pasoto, Sandra G., Lilleby, Vibke, Nieto‐González, Juan Carlos, Silva, Clovis A., Mossel, Esther, Pereira, Rosa M. R., Coelho, Aline, Bootsma, Hendrika, Thatayatikom, Akaluck, Brun, Johan G., Jonsson, Malin V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972604/
https://www.ncbi.nlm.nih.gov/pubmed/30697959
http://dx.doi.org/10.1002/acr.23839
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author Hammenfors, Daniel S.
Valim, Valéria
Bica, Blanca E. R. G.
Pasoto, Sandra G.
Lilleby, Vibke
Nieto‐González, Juan Carlos
Silva, Clovis A.
Mossel, Esther
Pereira, Rosa M. R.
Coelho, Aline
Bootsma, Hendrika
Thatayatikom, Akaluck
Brun, Johan G.
Jonsson, Malin V.
author_facet Hammenfors, Daniel S.
Valim, Valéria
Bica, Blanca E. R. G.
Pasoto, Sandra G.
Lilleby, Vibke
Nieto‐González, Juan Carlos
Silva, Clovis A.
Mossel, Esther
Pereira, Rosa M. R.
Coelho, Aline
Bootsma, Hendrika
Thatayatikom, Akaluck
Brun, Johan G.
Jonsson, Malin V.
author_sort Hammenfors, Daniel S.
collection PubMed
description OBJECTIVE: Juvenile Sjögren's syndrome (SS) is a rare, poorly defined, and possibly underdiagnosed condition affecting children and adolescents. The aim of this study was to characterize symptoms and clinical findings of juvenile SS and to explore the clinical application of major salivary gland ultrasonography (SGUS) in patients with juvenile SS. METHODS: A cross‐sectional multicenter study recruited patients with disease onset until age 18 years (n = 67). Disease characteristics were recorded, and unstimulated whole sialometry and SGUS examination of the parotid and submandibular salivary glands were performed. RESULTS: The female:male ratio was 58:9. The mean age at first symptom was 10.2 years and 12.1 years at diagnosis. Ocular and oral symptoms were noted in 42 of 67 patients (63%) and 53 of 66 patients (80%), respectively. The American‐European Consensus Group or American College of Rheumatology/European League Against Rheumatism classification criteria for primary SS were fulfilled by 42 of 67 patients (63%). Pathologic SGUS findings were observed in 41 of 67 patients (61%); 26 of 41 SGUS+ patients (63%) fulfilled primary SS criteria. Salivary gland enlargements/parotitis were noted in 37 of 58 patients and were nonsignificantly associated with SGUS+ status (P = 0.066). The mean levels of saliva were 5.6 ml/15 minutes in SGUS– patients compared to 3.3 ml/15 minutes in the SGUS+ patients (P = 0.049). A total of 36 of 41 SGUS+ patients (88%) were anti‐Ro/La+ compared to 14 of 26 SGUS– patients (54%) (P = 0.001). In addition, 24 of 39 SGUS+ patients (62%) were positive for rheumatoid factor (RF), whereas only 5 of 25 SGUS– patients (20%) were RF+ (P = 0.001). CONCLUSION: Juvenile SS is characterized by a large spectrum of clinical symptoms and findings. Several glandular and extraglandular parameters such as hyposalivation, swollen salivary glands, and autoantibodies are associated with pathologic SGUS findings.
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spelling pubmed-69726042020-01-27 Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography Hammenfors, Daniel S. Valim, Valéria Bica, Blanca E. R. G. Pasoto, Sandra G. Lilleby, Vibke Nieto‐González, Juan Carlos Silva, Clovis A. Mossel, Esther Pereira, Rosa M. R. Coelho, Aline Bootsma, Hendrika Thatayatikom, Akaluck Brun, Johan G. Jonsson, Malin V. Arthritis Care Res (Hoboken) Pediatrics OBJECTIVE: Juvenile Sjögren's syndrome (SS) is a rare, poorly defined, and possibly underdiagnosed condition affecting children and adolescents. The aim of this study was to characterize symptoms and clinical findings of juvenile SS and to explore the clinical application of major salivary gland ultrasonography (SGUS) in patients with juvenile SS. METHODS: A cross‐sectional multicenter study recruited patients with disease onset until age 18 years (n = 67). Disease characteristics were recorded, and unstimulated whole sialometry and SGUS examination of the parotid and submandibular salivary glands were performed. RESULTS: The female:male ratio was 58:9. The mean age at first symptom was 10.2 years and 12.1 years at diagnosis. Ocular and oral symptoms were noted in 42 of 67 patients (63%) and 53 of 66 patients (80%), respectively. The American‐European Consensus Group or American College of Rheumatology/European League Against Rheumatism classification criteria for primary SS were fulfilled by 42 of 67 patients (63%). Pathologic SGUS findings were observed in 41 of 67 patients (61%); 26 of 41 SGUS+ patients (63%) fulfilled primary SS criteria. Salivary gland enlargements/parotitis were noted in 37 of 58 patients and were nonsignificantly associated with SGUS+ status (P = 0.066). The mean levels of saliva were 5.6 ml/15 minutes in SGUS– patients compared to 3.3 ml/15 minutes in the SGUS+ patients (P = 0.049). A total of 36 of 41 SGUS+ patients (88%) were anti‐Ro/La+ compared to 14 of 26 SGUS– patients (54%) (P = 0.001). In addition, 24 of 39 SGUS+ patients (62%) were positive for rheumatoid factor (RF), whereas only 5 of 25 SGUS– patients (20%) were RF+ (P = 0.001). CONCLUSION: Juvenile SS is characterized by a large spectrum of clinical symptoms and findings. Several glandular and extraglandular parameters such as hyposalivation, swollen salivary glands, and autoantibodies are associated with pathologic SGUS findings. John Wiley and Sons Inc. 2019-12-10 2020-01 /pmc/articles/PMC6972604/ /pubmed/30697959 http://dx.doi.org/10.1002/acr.23839 Text en © 2019 The Authors. Arthritis Care & Research published by Wiley Periodicals, Inc. on behalf of American College of Rheumatology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Pediatrics
Hammenfors, Daniel S.
Valim, Valéria
Bica, Blanca E. R. G.
Pasoto, Sandra G.
Lilleby, Vibke
Nieto‐González, Juan Carlos
Silva, Clovis A.
Mossel, Esther
Pereira, Rosa M. R.
Coelho, Aline
Bootsma, Hendrika
Thatayatikom, Akaluck
Brun, Johan G.
Jonsson, Malin V.
Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography
title Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography
title_full Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography
title_fullStr Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography
title_full_unstemmed Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography
title_short Juvenile Sjögren's Syndrome: Clinical Characteristics With Focus on Salivary Gland Ultrasonography
title_sort juvenile sjögren's syndrome: clinical characteristics with focus on salivary gland ultrasonography
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972604/
https://www.ncbi.nlm.nih.gov/pubmed/30697959
http://dx.doi.org/10.1002/acr.23839
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