Evidence map›Paper›PMID 28146340›Full record

ArticleJournal of clinical laboratory analysis2017

Serum Clara cell protein and atopic phenotype in children up to 2 years of age.

Nevenka Ilic, Natasa Mihailovic

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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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

1 citing paper in PubMed.

  1. Article
4 · The record

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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

2 authors.

Nevenka IlicDepartment of Allergology and Immunology, Public Health Institute, Kragujevac, Serbia.ORCID http://orcid.org/0000-0003-2938-942X
Natasa MihailovicDepartment of Biostatistics, Public Health Institute, Kragujevac, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLow value of serum Clara cell protein (CC16) is associated with bronchial hyperreactivity in children.

objectiveTo evaluate the serum CC16 in relation to atopy and previously manifested LRTD.

methodsIn the population of 163 healthy 5- to 24-month-old children, atopy was determined by Phadiatop-infant (serum-specific IgE≥0.35 kUA/L), serum CC16 by ELISA, while data on previously manifested low respiratory tract diseases (LRTD) were collected from the Health Care Center database.

resultsIn atopic children, serum CC16 negatively correlated with age (r -.281, P=.041, n=53), while in nonatopic children, this correlation was positive (r .200, P=.036, n=110). Atopic ≥8-month-old children with previously manifested LRTD had lower level of CC16 (3.07 ng/mL) in relation to atopic children without LRTD at the same age (6.51 ng/mL), P=.029 (value of serum CC16≥4.8 ng/mL indicates atopic phenotype without LRTD 75% sensitivity, 87.5% specificity). In 8- to 24-month-old children with previously manifested pneumonia, serum CC16 was lower in atopic (2.9 ng/mL) in relation to nonatopic children (3.7 ng/mL), P=.029 (serum CC16 ≤3.4 ng/mL indicating atopy in the group of children with pneumonia, sensitivity 100%, and specificity 77%). Atopic 8- to 24-month-old children with previously manifested pneumonia had lower CC16 in relation to other atopic children in this age (P=.021) (for cutoff CC16≤3.4 ng/mL sensitivity 100%, specificity 77%), and also often chronic wheezing (atopic with pneumonia 83.3%, n=5/6 vs atopic without pneumonia 21.4%, n=3/14), P=.018.

conclusionLow serum CC16 is associated with previously expressed pneumonia and chronic wheezing in atopic children.

Indexed as

AsthmaPneumoniaBiomarkersCase-Control StudiesChild, PreschoolHumansHypersensitivityInfantPhenotypeRespiratory SoundsUteroglobinBiomarkersSCGB1A1 protein, humanUteroglobinallergyasthmabiomarkersClara cell protein

Identifiers

PMID28146340
PMCPMC6817215

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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.