Evidence map›Paper›PMID 37780586›Full record

ArticleThe journal of allergy and clinical immunology. Global2022

Moderate-to-severe lower respiratory tract infection in early life is associated with increased risk of polysensitization and atopic dermatitis: Findings from the CHILD Study.

Maria Medeleanu, Julia E M Upton, Myrtha E Reyna Vargas, Ruixue Dai, Piushkumar J Mandhane, Elinor Simons, Stuart E Turvey, Padmaja Subbarao, Theo J Moraes

Open access · goldAbstract read
In one paragraph

Article in The journal of allergy and clinical immunology. Global, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. From Fetus to Eight: the CHILD Cohort Study.American journal of epidemiology · 2024
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  4. Article
  5. Article
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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

9 authors at 4 institutions in 1 country.

Maria MedeleanuTranslational Medicine Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Julia E M UptonDivision of Immunology and Allergy, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Myrtha E Reyna VargasTranslational Medicine Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Ruixue DaiTranslational Medicine Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Piushkumar J MandhaneDivision of Pediatric Respirology, Pulmonary and Asthma, University of Alberta, Edmonton, Alberta, Canada.
Elinor SimonsSection of Allergy and Immunology, Department of Pediatrics and Child Health, University of Manitoba and Children's Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada.
Stuart E TurveyDepartment of Pediatrics, British Columbia Children's Hospital, The University of British Columbia, Vancouver, British Columbia, Canada.
Padmaja SubbaraoTranslational Medicine Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Theo J MoraesTranslational Medicine Program, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
University of Toronto · CAChildren's Hospital Research Institute of Manitoba · CAUniversity of Alberta · CAUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Respiratory infections in infancy are associated with the development of allergic asthma and atopy. Delineating whether symptomatic infections are a marker of atopic predisposition or contribute to atopic development is important for preventive strategies. We hypothesized that early, severe lower respiratory tract infections (LRTIs) may be a risk factor for the development of atopic disease. Objective: Our aim was to determine whether clinically defined, moderate-to-severe LRTIs in infancy are associated with the development of atopic dermatitis and allergic sensitization at preschool age. Methods: LRTI timing and severity in the first 18 months of life was defined by using the Canadian Healthy Infant Longitudinal Development study questionnaires. Polysensitization and atopic dermatitis were determined by standardized skin prick testing and structured clinical assessments. Longitudinal associations between LRTI severity and clinical outcomes at ages 3 years and 5 years were determined by adjusted repeated measures generalized estimation equations. Results: Moderate-to-severe LRTIs were associated with increased odds of polysensitization (odds ratio = 1.91 [95% CI = 1.16-3.15]; Conclusions: These results highlight severe infant LRTI as an important risk factor for allergic and atopic disease (ie, polysensitization and atopic dermatitis), and they suggest that this risk is independent of maternal

Indexed as

allergyatopic dermatitisatopyfood allergypediatricsRespiratory infection

Identifiers

PMID37780586
PMCPMC10509933
OpenAlexW4205909979

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.