Evidence map›Paper›PMID 29324810›Full record

ArticlePloS one2018

Course of SP-D, YKL-40, CCL18 and CA 15-3 in adult patients hospitalised with community-acquired pneumonia and their association with disease severity and aetiology: A post-hoc analysis.

Simone M C Spoorenberg, Stefan M T Vestjens, G P Voorn, Coline H M van Moorsel, Bob Meek, Pieter Zanen, Ger T Rijkers, Willem Jan W Bos, Jan C Grutters, Ovidius study group

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% of its field
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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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 at 3 institutions in 1 country.

Simone M C SpoorenbergDepartment of Internal Medicine, St Antonius Hospital, Nieuwegein, The Netherlands.ORCID 0000-0001-6113-4916
Stefan M T VestjensDepartment of Internal Medicine, St Antonius Hospital, Nieuwegein, The Netherlands.
G P VoornDepartment of Medical Microbiology and Immunology, St Antonius Hospital, Nieuwegein, The Netherlands.
Coline H M van MoorselDepartment of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.
Bob MeekDepartment of Medical Microbiology and Immunology, St Antonius Hospital, Nieuwegein, The Netherlands.
Pieter ZanenDivision of Heart and Lungs, University Medical Centre Utrecht, Utrecht, The Netherlands.
Ger T RijkersDepartment of Medical Microbiology and Immunology, St Antonius Hospital, Nieuwegein, The Netherlands.
Willem Jan W BosDepartment of Internal Medicine, St Antonius Hospital, Nieuwegein, The Netherlands.
Jan C GruttersDepartment of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.
Ovidius study group
St. Antonius Ziekenhuis · NLUniversity Medical Center Utrecht · NLRoosevelt Institute for American Studies · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimSP-D, YKL-40, CCL18 and CA 15-3 are pulmonary markers that have been extensively investigated in different chronic pulmonary diseases. However, in acute pulmonary diseases, such as community-acquired pneumonia (CAP), little is known about the course of these markers and their relationship with the aetiological agent. The aim of this study was to investigate the course of these four markers in CAP and to study influence of disease severity, aetiology and antibiotic use prior to admission on their course.

methodsWe included 291 adult patients hospitalised with CAP and 20 healthy controls. Measurements were performed in serum of day 0, 2, and 4, and at least 30 days after admission.

resultsOur most important results were: 1) At all time-points, including 30 days after admission, YKL-40 and CCL18 levels were higher in CAP patients compared to healthy controls; and 2) Patients with CAP caused by an intracellular, atypical bacterium had lower YKL-40 and especially CCL18 levels on and during admission in comparison with other or unknown CAP aetiology.

conclusionsOur findings suggest that these pulmonary markers could be useful to assess CAP severity and, especially YKL-40 and CCL18 by helping predict CAP caused by atypical pathogens.

Indexed as

BiomarkersChemokines, CCChitinase-3-Like Protein 1Community-Acquired InfectionsFemaleHumansMaleMiddle AgedMucin-1PneumoniaPulmonary Surfactant-Associated Protein DSeverity of Illness IndexBiomarkersCCL18 protein, humanChemokines, CCCHI3L1 protein, humanChitinase-3-Like Protein 1Mucin-1Pulmonary Surfactant-Associated Protein D

Identifiers

PMID29324810
PMCPMC5764260
OpenAlexW2783604070

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.