Epidemiology of neurological manifestations ...
Document type :
Article dans une revue scientifique
PMID :
Permalink :
Title :
Epidemiology of neurological manifestations in Sjögren's syndrome: data from the French ASSESS Cohort.
Author(s) :
Carvajal Alegria, Guillermo [Auteur]
Guellec, Dewi [Auteur]
Mariette, Xavier [Auteur]
Gottenberg, Jacques-Eric [Auteur]
Dernis, Emmanuelle [Auteur]
Dubost, Jean-Jacques [Auteur]
Trouvin, Anne-Priscille [Auteur]
Hachulla, Eric [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Larroche, Claire [Auteur]
Le Guern, Veronique [Auteur]
Cornec, Divi [Auteur]
Devauchelle-Pensec, Valerie [Auteur]
Saraux, Alain [Auteur]
Guellec, Dewi [Auteur]
Mariette, Xavier [Auteur]
Gottenberg, Jacques-Eric [Auteur]
Dernis, Emmanuelle [Auteur]
Dubost, Jean-Jacques [Auteur]
Trouvin, Anne-Priscille [Auteur]
Hachulla, Eric [Auteur]

Lille Inflammation Research International Center - U 995 [LIRIC]
Larroche, Claire [Auteur]
Le Guern, Veronique [Auteur]
Cornec, Divi [Auteur]
Devauchelle-Pensec, Valerie [Auteur]
Saraux, Alain [Auteur]
Journal title :
RMD open
Abbreviated title :
RMD Open
Volume number :
2
Pages :
e000179
Publication date :
2016-01-01
ISSN :
2056-5933
2056-5933
2056-5933
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
OBJECTIVES: Neurological manifestations seem common in primary Sjogren's syndrome (pSS) but their reported prevalences vary. We investigated the prevalence and epidemiology of neurological manifestations in a French ...
Show more >OBJECTIVES: Neurological manifestations seem common in primary Sjogren's syndrome (pSS) but their reported prevalences vary. We investigated the prevalence and epidemiology of neurological manifestations in a French nationwide multicentre prospective cohort of patients with pSS, the Assessment of Systemic Signs and Evolution in Sjogren's syndrome (ASSESS) cohort. METHODS: The ASSESS cohort, established in 2006, includes 395 patients fulfilling American-European Consensus Group criteria for pSS. Demographic and clinical data were compared between patient groups with and without neurological manifestations, and across patient groups with peripheral nervous system (PNS) manifestations, central nervous system (CNS) manifestations and no neurological manifestations. RESULTS: Data at inclusion were available for 392 patients, whose mean age was 58+/-12 years. Mean follow-up was 33.9 months. Neurological manifestations were present in 74/392 (18.9%) patients, including 63 (16%) with PNS manifestations and 14 (3.6%) with CNS manifestations. Prevalences were 9.2% for pure sensory neuropathy, 5.3% for sensorimotor neuropathy, 1.3% for cerebral vasculitis and 1.0% for myelitis. Neurological manifestations were associated with greater pSS activity as assessed using the ESSDAI (9.4+/-6.8 vs 4.3+/-4.8; p<0.001) and proportion of patients taking immunomodulatory/immunosuppressive drugs (32.4% (24/74) versus 13.8% (44/318), p=0003). New neurological symptoms were more common in patients with than without prior neurological manifestations (RR=3.918 (95% CI 1.91 to 8.05); p<0.001). CONCLUSIONS: Prevalences of peripheral and central neurological manifestations in pSS are about 15% and 5%, respectively. Neurological manifestations are associated with greater pSS activity. New neurological manifestations are more common in patients with prior neurological involvement.Show less >
Show more >OBJECTIVES: Neurological manifestations seem common in primary Sjogren's syndrome (pSS) but their reported prevalences vary. We investigated the prevalence and epidemiology of neurological manifestations in a French nationwide multicentre prospective cohort of patients with pSS, the Assessment of Systemic Signs and Evolution in Sjogren's syndrome (ASSESS) cohort. METHODS: The ASSESS cohort, established in 2006, includes 395 patients fulfilling American-European Consensus Group criteria for pSS. Demographic and clinical data were compared between patient groups with and without neurological manifestations, and across patient groups with peripheral nervous system (PNS) manifestations, central nervous system (CNS) manifestations and no neurological manifestations. RESULTS: Data at inclusion were available for 392 patients, whose mean age was 58+/-12 years. Mean follow-up was 33.9 months. Neurological manifestations were present in 74/392 (18.9%) patients, including 63 (16%) with PNS manifestations and 14 (3.6%) with CNS manifestations. Prevalences were 9.2% for pure sensory neuropathy, 5.3% for sensorimotor neuropathy, 1.3% for cerebral vasculitis and 1.0% for myelitis. Neurological manifestations were associated with greater pSS activity as assessed using the ESSDAI (9.4+/-6.8 vs 4.3+/-4.8; p<0.001) and proportion of patients taking immunomodulatory/immunosuppressive drugs (32.4% (24/74) versus 13.8% (44/318), p=0003). New neurological symptoms were more common in patients with than without prior neurological manifestations (RR=3.918 (95% CI 1.91 to 8.05); p<0.001). CONCLUSIONS: Prevalences of peripheral and central neurological manifestations in pSS are about 15% and 5%, respectively. Neurological manifestations are associated with greater pSS activity. New neurological manifestations are more common in patients with prior neurological involvement.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Inserm
Université de Lille
CHU Lille
Université de Lille
CHU Lille
Research team(s) :
Immunity, inflammation and fibrsis in auto and allo-reactivity
Submission date :
2019-03-01T14:10:51Z