Evidence map›Paper›PMID 42639025›Full record

ArticleFrontiers in immunology2026

NeuroPORTRESS: prevalence, clinical spectrum, and factors associated with neurological involvement in Sjögren's disease.

Roberto Pereira da Costa, Matilde Bandeira, Manuel Silvério-António, Ana R Lopes, Filipe Cunha-Santos, Paulo J Pereira, Diana Belchior Raimundo, Anita Cunha, Cláudia Pinto Oliveira, Ana C Duarte and 15 more

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Roberto Pereira da Costa *Serviço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
Matilde Bandeira *Serviço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
Manuel Silvério-AntónioServiço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
Ana R LopesServiço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
Filipe Cunha-SantosServiço de Reumatologia, Unidade Local de Saúde da Guarda, Guarda, Portugal.
Paulo J PereiraServiço de Reumatologia, Unidade Local de Saúde de Braga, Braga, Portugal.
Diana Belchior RaimundoServiço de Reumatologia, Unidade Local de Saúde de Loures-Odivelas, Loures, Portugal.
Anita CunhaServiço de Reumatologia, Unidade Local de Saúde do Alto Minho, Ponte de Lima, Portugal.
Cláudia Pinto OliveiraServiço de Reumatologia, Unidade Local de Saúde da Região de Aveiro, Aveiro, Portugal.
Ana C DuarteServiço de Reumatologia, Unidade Local de Saúde Almada-Seixal, Almada, Portugal.
João Madruga DiasServiço de Reumatologia, Unidade Local de Saúde do Médio Tejo, Tomar, Portugal.
Mariana Emília SantosServiço de Reumatologia, Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal.
Maria J GonçalvesServiço de Reumatologia, Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal.
Ana C MonizServiço de Reumatologia, Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal.
Ana I MaduroServiço de Reumatologia, Unidade Local de Saúde de Coimbra, Coimbra, Portugal.
Mariana LuísServiço de Reumatologia, Unidade Local de Saúde de Coimbra, Coimbra, Portugal.
Ana ValidoServiço de Reumatologia, Unidade Local de Saúde do Litoral Alentejano, Santiago do Cacém, Portugal.
Margarida OliveiraServiço de Reumatologia, Unidade Local de Saúde da Cova da Beira, Covilhã, Portugal.
Luísa BritesServiço de Reumatologia, Unidade Local de Saúde da Região de Leiria, Leiria, Portugal.
Catarina TenazinhaServiço de Reumatologia, Unidade Local de Saúde do Algarve, Faro, Portugal.
Nikita KhmelinskiiServiço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
Filipe BarcelosServiço de Reumatologia, Hospital CUF Descobertas, Lisboa, Portugal.
João E FonsecaServiço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
Vasco C RomãoServiço de Reumatologia, Unidade Local de Saúde Santa Maria, Centro Académico de Medicina de Lisboa (CAML), Lisboa, Portugal.
PORTRESS Reuma.pt Task Force

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Neurological involvement is a heterogeneous complication of Sjögren's disease (SjD). We aimed to describe its prevalence and spectrum, and identify factors associated with peripheral (PNS) and central nervous system (CNS) involvement. Methods: We conducted a cross-sectional, multicentre study based on PORTRESS, the Portuguese SjD registry. Demographic and clinical data were compared between groups. Independent associations of overall neurological, PNS, and CNS involvement were identified through logistic regression models using complete-case analysis. Results: Among 1234 patients, 62 (5.0%) had neurological involvement: 46 (3.7%) PNS, 17 (1.4%) CNS, with one patient having both. Patients with neurological manifestations had higher ESSDAI, more cryoglobulinaemia, purpura/cutaneous vasculitis and monoclonal gammopathy, and higher mortality. Cryoglobulinaemia and higher baseline ESSDAI (excluding neurological domains) were independently associated with neurological involvement. PNS involvement was associated with older age at symptom onset, cryoglobulinaemia, lymphopenia and higher ESSDAI. A sensitivity analysis revealed low C4, persistent salivary gland swelling and purpura/cutaneous vasculitis also as independently associated with PNS involvement. CNS involvement was associated with male sex and younger age at diagnosis. Conclusion: Neurological involvement in SjD was infrequent. PNS involvement clustered with vasculitic and B-cell-driven features and worse outcomes, whereas CNS manifestations appeared to show a distinct demographic profile, characterised by younger age and male sex. These findings support separate evaluation of PNS and CNS involvement and may help identify patients requiring neurological surveillance. Given the limited number of cases, particularly of CNS involvement, these findings remain exploratory and require confirmation in larger cohorts.

Indexed as

Central Nervous System DiseasesPeripheral Nervous System DiseasesSjogren's SyndromeAdultAgedCross-Sectional StudiesCryoglobulinemiaFemaleHumansMaleMiddle AgedPortugalPrevalenceRegistriescentral nervous systemindependent associationsneurological involvementperipheral nervous systemSjogren’s disease

Identifiers

PMID42639025
PMCPMC13500490

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.