Evidence map›Paper›PMID 40682608›Full record

ArticleRheumatology international2025

Normal inflammatory markers in giant cell arteritis: a diagnostic blind spot.

Cara E Currier, A M Bays, J L Thomason

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Article in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

3 authors.

Cara E CurrierElson S Floyd College of Medicine, Washington State University, Spokane, WA, USA.
A M BaysDepartment of Medicine, Division of Rheumatology, University of Washington, Seattle, WA, USA. alisonmb@uw.edu.ORCID 0000-0002-7193-6303
J L ThomasonDepartment of Medicine, Division of Rheumatology, University of Washington, Seattle, WA, USA.ORCID 0000-0002-3942-8982

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGiant cell arteritis (GCA) is a vasculitis requiring urgent diagnosis. Although Erythrocyte Sedimentation Rate (ESR) and C-Reactive Protein (CRP) are important for making the diagnosis, some GCA patients have normal inflammatory markers. We retrospectively analyzed GCA patients with normal versus elevated inflammatory markers to evaluate for differences in clinical presentation and vascular ultrasound to aid in the diagnosis of GCA patients with normal ESR and CRP.

methodsWe conducted a retrospective study with patients diagnosed with GCA through a Fast Track Clinic (FTC). Clinical presentation and ultrasound results were compared in 23 GCA patients with normal ESR and CRP to 107 GCA patients with elevated ESR and/or CRP. We incorporated an additional 159 patients without GCA to calculate the sensitivity and specificity of ESR and CRP for detecting GCA. Data were analyzed using Pearson Chi-square, Fisher's exact test and ROC curves.

resultsCRP is 74% sensitive and 49% specific (AUC = 0.675) compared to ESR with 48% sensitivity and 72% specificity (AUC = 0.644) for detecting GCA. Patients with a longer period between onset of symptoms and measurement of markers (mean of 35 versus 20 days) were more likely to have normal markers (p = 0.03).

conclusionGCA patients present similarly regardless of inflammatory markers. Patients with normal inflammatory markers had a significantly longer time between symptom onset and inflammatory marker measurement. ESR and CRP have some diagnostic accuracy, low inflammatory markers should not preclude a GCA work-up.

Indexed as

C-Reactive ProteinGiant Cell ArteritisInflammation MediatorsAgedAged, 80 and overBiomarkersBlood SedimentationFemaleHumansMaleMiddle AgedPredictive Value of TestsRetrospective StudiesROC CurveSensitivity and SpecificityUltrasonographyBiomarkersC-Reactive ProteinInflammation MediatorsBlood sedimentationC-Reactive proteinGiant cell arteritisVasculitis

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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.