Literature DB >> 31873754

Epidemiological profile and north-south gradient driving baseline systemic involvement of primary Sjögren's syndrome.

Pilar Brito-Zerón1,2, Nihan Acar-Denizli3, Wan-Fai Ng4, Ildiko Fanny Horváth5, Astrid Rasmussen6, Raphaele Seror7, Xiaomei Li8, Chiara Baldini9, Jacques-Eric Gottenberg10, Debashish Danda11, Luca Quartuccio12, Roberta Priori13, Gabriela Hernandez-Molina14, Berkan Armagan15, Aike A Kruize16, Seung-Ki Kwok17, Marika Kvarnstrom18, Sonja Praprotnik19, Damien Sene20, Roberto Gerli21, Roser Solans22, Maureen Rischmueller23, Thomas Mandl24, Yasunori Suzuki25, David Isenberg26, Valeria Valim27, Piotr Wiland28, Gunnel Nordmark29, Guadalupe Fraile30, Hendrika Bootsma31, Hideki Nakamura32, Roberto Giacomelli33, Valerie Devauchelle-Pensec34, Benedikt Hofauer35, Michele Bombardieri36, Virginia Fernandes Moça Trevisani37, Daniel Hammenfors38,39, Sandra G Pasoto40, Soledad Retamozo41,42, Tamer A Gheita43, Fabiola Atzeni44,45, Jacques Morel46, Cristina Vollenweider47, Margit Zeher5, Kathy Sivils6, Bei Xu8, Stefano Bombardieri9, Pulukool Sandhya11, Salvatore De Vita12, Antonina Minniti13, Jorge Sánchez-Guerrero14, Levent Kilic15, Eefje van der Heijden16, Sung-Hwan Park17, Marie Wahren-Herlenius18, Xavier Mariette7, Manuel Ramos-Casals2.   

Abstract

OBJECTIVE: To characterize the systemic phenotype of primary Sjögren's syndrome at diagnosis by analysing the EULAR-SS disease activity index (ESSDAI) scores.
METHODS: The Sjögren Big Data Consortium is an international, multicentre registry based on worldwide data-sharing cooperative merging of pre-existing databases from leading centres in clinical research in Sjögren's syndrome from the five continents.
RESULTS: The cohort included 10 007 patients (9352 female, mean 53 years) with recorded ESSDAI scores available. At diagnosis, the mean total ESSDAI score was 6.1; 81.8% of patients had systemic activity (ESSDAI score ≥1). Males had a higher mean ESSDAI (8.1 vs 6.0, P < 0.001) compared with females, as did patients diagnosed at <35 years (6.7 vs 5.6 in patients diagnosed at >65 years, P < 0.001). The highest global ESSDAI score was reported in Black/African Americans, followed by White, Asian and Hispanic patients (6.7, 6.5, 5.4 and 4.8, respectively; P < 0.001). The frequency of involvement of each systemic organ also differed between ethnic groups, with Black/African American patients showing the highest frequencies in the lymphadenopathy, articular, peripheral nervous system, CNS and biological domains, White patients in the glandular, cutaneous and muscular domains, Asian patients in the pulmonary, renal and haematological domains and Hispanic patients in the constitutional domain. Systemic activity measured by the ESSDAI, clinical ESSDAI (clinESSDAI) and disease activity states was higher in patients from southern countries (P < 0.001).
CONCLUSION: The systemic phenotype of primary Sjögren's syndrome is strongly influenced by personal determinants such as age, gender, ethnicity and place of residence, which are key geoepidemiological players in driving the expression of systemic disease at diagnosis.
© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  ethnicity; gender; geoepidemiology; phenotype; primary Sjögren’s syndrome

Year:  2020        PMID: 31873754     DOI: 10.1093/rheumatology/kez578

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  14 in total

1.  Prevalence and clinical presentation of lymphoproliferative disorder in patients with primary Sjögren's syndrome.

Authors:  Agata Sebastian; Marta Madej; Maciej Sebastian; Aleksandra Butrym; Patryk Woytala; Agnieszka Hałoń; Piotr Wiland
Journal:  Rheumatol Int       Date:  2020-02-01       Impact factor: 2.631

2.  Recommendations for evaluation and diagnosis of extra-glandular manifestations of primary sjogren syndrome: results of an epidemiologic systematic review/meta-analysis and a consensus guideline from the Brazilian Society of Rheumatology (articular, pulmonary and renal).

Authors:  Virginia Fernandes Moça Trevisani; Alisson Pugliesi; Sandra Gofinet Pasoto; Maria Lucia Lemos Lopes; Lissiane Karine Noronha Guedes; Samira Tatiyama Miyamoto; Marilena Leal Mesquita Silvestre Fernandes; Sonia Cristina de Magalhães Souza Fialho; Aysa César Pinheiro; Laura Caldas Dos Santos; Simone Appenzeller; Tania Fidelix; Sandra Lúcia Euzébio Ribeiro; Danielle Christinne Soares Egypto de Brito; Tatiana Nayara Libório-Kimura; Maria Carmen Lopes Ferreira Silva Santos; Diego Ustárroz Cantali; Juliana D'Agostino Gennari; Vinicius Tassoni Civile; Ana Carolina Pereira Nunes Pinto; César Ramos Rocha-Filho; Fabiola Reis Oliveira; Aline Pereira da Rocha; Valeria Valim
Journal:  Adv Rheumatol       Date:  2022-06-01

Review 3.  Unique Aspects of Pediatric Sjögren Disease.

Authors:  Rachel L Randell; Scott M Lieberman
Journal:  Rheum Dis Clin North Am       Date:  2021-08-27       Impact factor: 2.670

4.  Fatigue in Saudi Patients with Primary Sjögren's Syndrome and Its Correlation with Disease Characteristics and Outcome Measures: A Cross-Sectional Study.

Authors:  Fahidah AlEnzi; Bashaer Alqahtani; Esam H Alhamad; Maha Daghestani; Yusra Tashkandy; Nashwa Othman; Khalid Alshahrani; Muthurajan P Paramasivam; Rabih Halwani; Mohammed A Omair
Journal:  Open Access Rheumatol       Date:  2020-12-02

5.  Hypocomplementemia in Primary Sjogren's Syndrome: A Retrospective Study of 120 Treatment-Naive Chinese Patients.

Authors:  Meiju Zhou; Fang Yuan
Journal:  Int J Gen Med       Date:  2022-01-08

6.  Bioinformatics Analysis for Identification of Key Genes in Salivary Gland and the Potential of a Combination of Biomarkers for the Diagnosis of SS.

Authors:  Liying Chen; Dingqi Lu; Kai Yu; Shiya He; Liu Liu; Xvfeng Zhang; Bo Feng; Xinchang Wang
Journal:  J Inflamm Res       Date:  2021-08-25

7.  Disease phenotype and diagnostic delay in Saudi patients with primary Sjögren's syndrome: An exploratory cross-sectional study.

Authors:  Mohammed A Omair; Bashaer S AlQahtani; Esam H AlHamad; Yusra A Tashkandy; Nashwa S Othman; Khalid A AlShahrani; Muthurajan P Paramasivam; Fahidah AlEnzi; Rabih Halwani; Maha H Daghestani
Journal:  Saudi Med J       Date:  2021-04       Impact factor: 1.484

8.  Elevated Serum Human Epididymis Protein 4 Is Associated With Disease Activity and Systemic Involvements in Primary Sjögren's Syndrome.

Authors:  Jiali Chen; Feng Sun; Huizhang Bao; Liu Liang; Minghua Zhan; Haihong Yao; Jing He; Yudong Liu
Journal:  Front Immunol       Date:  2021-06-23       Impact factor: 7.561

Review 9.  Biomarkers and Diagnostic Testing for Renal Disease in Sjogren's Syndrome.

Authors:  Giacomo Ramponi; Marco Folci; Salvatore Badalamenti; Claudio Angelini; Enrico Brunetta
Journal:  Front Immunol       Date:  2020-09-17       Impact factor: 7.561

10.  Burden of illness among subgroups of patients with primary Sjögren's syndrome and systemic involvement.

Authors:  Kerry Gairy; Claudia Knight; Papa Anthony; Ben Hoskin
Journal:  Rheumatology (Oxford)       Date:  2021-04-06       Impact factor: 7.580

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