Evidence map›Paper›PMID 27206492›Full record

ArticleBMC immunology2016

Applied immuno-epidemiological research: an approach for integrating existing knowledge into the statistical analysis of multiple immune markers.

Bernd Genser, Joachim E Fischer, Camila A Figueiredo, Neuza Alcântara-Neves, Mauricio L Barreto, Philip J Cooper, Leila D Amorim, Marcus D Saemann, Thomas Weichhart, Laura C Rodrigues

Abstract readComparative Study
In one paragraph

Article in BMC immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

10 authors.

Bernd GenserInstituto de Saúde Coletiva, Federal University of Bahia, Rua Basílio da Gama, s/n - Canela, Salvador, BA, 40110-040, Brazil. bernd.genser@bgstats.com.
Joachim E FischerMannheim Institute of Public Health, Social and Preventive Medicine, University of Heidelberg, Heidelberg, Germany.
Camila A FigueiredoInstituto de Ciências da Saúde, Federal University of Bahia, Salvador, Brazil.
Neuza Alcântara-NevesInstituto de Ciências da Saúde, Federal University of Bahia, Salvador, Brazil.
Mauricio L BarretoInstituto de Saúde Coletiva, Federal University of Bahia, Rua Basílio da Gama, s/n - Canela, Salvador, BA, 40110-040, Brazil.
Philip J CooperInstitute of Infection and Immunity, St George's University of London, London, UK.
Leila D AmorimInstituto de Saúde Coletiva, Federal University of Bahia, Rua Basílio da Gama, s/n - Canela, Salvador, BA, 40110-040, Brazil.
Marcus D SaemannClinical Division of Nephrology, Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Thomas WeichhartInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Laura C RodriguesLondon School of Hygiene & Tropical Medicine, London, UK.

Funding

Wellcome Trust 088862/Z/09
6 · The paper itself

Abstract

backgroundImmunologists often measure several correlated immunological markers, such as concentrations of different cytokines produced by different immune cells and/or measured under different conditions, to draw insights from complex immunological mechanisms. Although there have been recent methodological efforts to improve the statistical analysis of immunological data, a framework is still needed for the simultaneous analysis of multiple, often correlated, immune markers. This framework would allow the immunologists' hypotheses about the underlying biological mechanisms to be integrated.

resultsWe present an analytical approach for statistical analysis of correlated immune markers, such as those commonly collected in modern immuno-epidemiological studies. We demonstrate i) how to deal with interdependencies among multiple measurements of the same immune marker, ii) how to analyse association patterns among different markers, iii) how to aggregate different measures and/or markers to immunological summary scores, iv) how to model the inter-relationships among these scores, and v) how to use these scores in epidemiological association analyses. We illustrate the application of our approach to multiple cytokine measurements from 818 children enrolled in a large immuno-epidemiological study (SCAALA Salvador), which aimed to quantify the major immunological mechanisms underlying atopic diseases or asthma. We demonstrate how to aggregate systematically the information captured in multiple cytokine measurements to immunological summary scores aimed at reflecting the presumed underlying immunological mechanisms (Th1/Th2 balance and immune regulatory network). We show how these aggregated immune scores can be used as predictors in regression models with outcomes of immunological studies (e.g. specific IgE) and compare the results to those obtained by a traditional multivariate regression approach.

conclusionThe proposed analytical approach may be especially useful to quantify complex immune responses in immuno-epidemiological studies, where investigators examine the relationship among epidemiological patterns, immune response, and disease outcomes.

Indexed as

Allergy and ImmunologyEpidemiologyAsthmaBiomarkersBiomedical ResearchBrazilChildComputer SimulationCytokinesData Interpretation, StatisticalHumansHypersensitivity, ImmediateImmunoglobulin EIntegrated Advanced Information Management SystemsOutcome Assessment, Health CarePredictive Value of TestsBiomarkersCytokinesImmunoglobulin EConceptual frameworksCorrelated immune markersCytokinesImmuno-epidemiologyStatistical analysis

Identifiers

PMID27206492
PMCPMC4875650

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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.