Evidence map›Paper›PMID 40114276›Full record

ArticleArthritis research & therapy2025

The impact of disease activity and interferon-α on the nervous system in systemic lupus erythematosus.

Kristoffer A Zervides, Elsa Grenmyr, Shorena Janelidze, Petrus Linge, Jessika Nystedt, Petra C Nilsson, Pia C Sundgren, Oskar Hansson, Anders A Bengtsson, Andreas Jönsen

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
–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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  7. HAPI Cells are SIM-A9-related Mouse Microglial Cells Useful forbioRxiv : the preprint server for biology · 2026
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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

10 authors.

Kristoffer A ZervidesDepartment of Clinical Sciences, Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden. kristoffer.zervides@med.lu.se.ORCID 0000-0003-4311-1635
Elsa GrenmyrDepartment of Clinical Sciences, Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden.
Shorena JanelidzeClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Petrus LingeDepartment of Clinical Sciences, Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden.
Jessika NystedtDepartment of Clinical Sciences, Neurology, Lund University, Skåne University Hospital, Lund, Sweden.
Petra C NilssonDepartment of Clinical Sciences, Neurology, Lund University, Skåne University Hospital, Lund, Sweden.
Pia C SundgrenDepartment of Clinical Sciences, Diagnostic Radiology, Lund University, Skåne University Hospital, Lund, Sweden.
Oskar HanssonClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Anders A Bengtsson *Department of Clinical Sciences, Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden.
Andreas Jönsen *Department of Clinical Sciences, Rheumatology, Lund University, Skåne University Hospital, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) patients, with or without neuropsychiatric SLE (NPSLE), exhibit greater neuronal impairment compared to healthy individuals in terms of neuronal damage, magnet resonance imaging (MRI) changes and cognitive dysfunction. Interferon (IFN)-α is a key immunopathogenic driver of SLE, being persistently overexpressed in the majority of patients. This longitudinal study aimed to investigate whether disease activity and serum IFN-α levels over time were associated with objective findings of neuronal impairment regarding (i) higher plasma neurofilament light (NfL) concentrations, (ii) structural alterations on MRI, and (iii) cognitive dysfunction upon testing.

methodsSixty-six consecutive female SLE outpatients were enrolled in a cross-sectional study. Retrospectively, prior visits with concomitant blood samples (n = 199) were selected from the Lund Lupus Cohort database and biobank. Serum IFN-α concentrations were measured using an electrochemiluminescence immunoassay. IFN-α lupus phenotypes were defined as high (n = 24) or low (n = 33) by considering persistent elevations in serum IFN-α concentrations despite low SLE Disease Activity Index-2000 (SLEDAI-2 K) scores. SLEDAI-2 K lupus phenotypes were defined as moderate-high (n = 31) or low (n = 35) based on SLEDAI-2 K scores from all 576 available visits prior to the study. Ongoing neuronal damage was assessed by plasma NfL concentration measurements using Simoa at the 199 visits. Structural MRI alterations and cognitive dysfunction according to the CNS-Vital Signs test battery were the additional outcomes. Multivariate linear mixed-effect, linear regression, and logistic regression models were used for the statistical analyses.

resultsVisits with higher disease activity were associated with higher plasma NfL concentrations (e.g. SLEDAI-2 K total: p = 1.5*10

conclusionsThe study suggests that disease activity and IFN-α may drive neuronal affliction in SLE, also in the absence of overt neuropsychiatric symptoms, and that controlling disease activity could improve the cerebral outcome.

Indexed as

Interferon-alphaLupus Erythematosus, SystemicLupus Vasculitis, Central Nervous SystemAdultCognitive DysfunctionCross-Sectional StudiesFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMiddle AgedNeurofilament ProteinsRetrospective StudiesInterferon-alphaneurofilament protein LNeurofilament ProteinsCognitive dysfunctionDisease activityInterferonMRINeurofilamentSystemic lupus erythematosus

Identifiers

PMID40114276
PMCPMC11924660

What OpenQuestion holds

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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.