Evidence map›Paper›PMID 27096761›Full record

ArticlePloS one2016

Prospective Evaluation of Procalcitonin, Soluble Triggering Receptor Expressed on Myeloid Cells-1 and C-Reactive Protein in Febrile Patients with Autoimmune Diseases.

Chou-Han Lin, Song-Chou Hsieh, Li-Ta Keng, Ho-Sheng Lee, Hou-Tai Chang, Wei-Yu Liao, Chao-Chi Ho, Chong-Jen Yu

Abstract read
In one paragraph

Article in PloS one, 2016. 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

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Chou-Han LinDepartment of Internal Medicine, Far Eastern Memorial Hospital, New Taipei city, Taiwan.
Song-Chou HsiehDepartment of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Li-Ta KengDepartment of Internal Medicine, National Taiwan University Hospital, Hsin-Chu Branch, Hsin-Chu, Taiwan.
Ho-Sheng LeeDepartment of Internal Medicine, E-Da hospital, Kaoshiung, Taiwan.
Hou-Tai ChangDepartment of Internal Medicine, Far Eastern Memorial Hospital, New Taipei city, Taiwan.
Wei-Yu LiaoDepartment of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Chao-Chi HoDepartment of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Chong-Jen YuDepartment of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBoth procalcitonin (PCT) and soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) have been investigated separately as indicators of infection in patients with autoimmune diseases. Our study simultaneously evaluated both PCT and sTREM-1 along with C-reactive protein (CRP) in febrile patients with autoimmune diseases.

methodsFifty-nine patients were enrolled in the study. The patients were categorized into the infection group (n=24) or the disease flare group (n=35). sTREM-1, PCT and CRP concentrations at fever onset were compared between the two groups of patients.

resultssTREM-1 and CRP did not differ between the two groups. PCT [median (range), ng/ml] was higher in the infection group than in the disease flare group [0.53 (0.02-12.85) vs. 0.12 (0.02-19.23), p=0.001]. The area under the receiver-operating characteristic (ROC) for diagnosis of infection was 0.75 for PCT (p=0.001), 0.63 for CRP (p=0.09) and 0.52 for sTREM-1 (p=0.79). Using 0.2 ng/ml as the cutoff value for PCT, sensitivity was 0.75 and specificity was 0.77. Negative predictive values for PCT were 92%, 87% and 82% for a prevalence of infection of 20%, 30%, and 40%, respectively. Neither immunosuppressants nor biomodulators affected the level of the three biomarkers. However, in patients treated with corticosteroids, the levels of sTREM-1 and CRP were significantly decreased compared with the untreated patients.

conclusionsSetting PCT at a lower cutoff value could provide useful information on excluding infection in febrile patients with autoimmune diseases. The possible effect of corticosteroids on the level of sTREM-1 as an infection marker deserves further study.

Indexed as

Adrenal Cortex HormonesAdultAgedAutoimmune DiseasesCalcitoninCalcitonin Gene-Related PeptideC-Reactive ProteinFemaleFeverHumansImmunosuppressive AgentsMaleMembrane GlycoproteinsMiddle AgedProspective StudiesProtein PrecursorsAdrenal Cortex HormonesCALCA protein, humanCalcitoninCalcitonin Gene-Related PeptideC-Reactive ProteinImmunosuppressive AgentsMembrane GlycoproteinsProtein PrecursorsReceptors, ImmunologicTREM1 protein, humanTriggering Receptor Expressed on Myeloid Cells-1

Identifiers

PMID27096761
PMCPMC4838219

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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.