Evidence map›Paper›PMID 38885291›Full record

ArticleThe Journal of infectious diseases2024

Breath Biomarkers of Pediatric Malaria: Reproducibility and Response to Antimalarial Therapy.

Amalia Z Berna, X Rosalind Wang, Lucy B Bollinger, Josephine Banda, Patricia Mawindo, Tasha Evanoff, Diana L Culbertson, Karl Seydel, Audrey R Odom John

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Breath volatile profiling reveals a diagnostic signature of MASLD in children.medRxiv : the preprint server for health sciences · 2026
    Article
  2. Article
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.

Amalia Z BernaDivision of Infectious Diseases, Department of Pediatrics, Children's Hospital of Philadelphia, Pennsylvania.ORCID 0000-0003-4932-5415
X Rosalind WangDepartment of Data Science, Western Sydney University, Sydney, Australia.ORCID 0000-0001-5454-6197
Lucy B BollingerDepartment of Pediatrics, Northwest Permanente, Portland, Oregon.
Josephine BandaBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.
Patricia MawindoBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.
Tasha EvanoffDepartment of Psychiatry, Harvard University, Boston, Massachusetts.
Diana L CulbertsonDepartment of Pediatrics, Seattle Children's Hospital, Washington.
Karl SeydelBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.ORCID 0000-0001-9859-9549
Audrey R Odom JohnDivision of Infectious Diseases, Department of Pediatrics, Children's Hospital of Philadelphia, Pennsylvania.ORCID 0000-0001-8395-8537

Funding

Breathprinting as a window into gut microbiome chemoecologyR01HD109963 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI Andrew Leon Kau, Audrey Ragan Odom John · 2022 to 2026
$3.4M
Towards noninvasive diagnosis of malariaR21AI144472 · NIAID · WASHINGTON UNIVERSITY · PI ODOM JOHN, AUDREY RAGAN · 2019 to 2020
$485k
Microbial Origin of Breath Volatile MetabolitesR21AI154370 · NIAID · WASHINGTON UNIVERSITY · PI KAU, ANDREW LEON, ODOM JOHN, AUDREY RAGAN · 2020 to 2021
$473k
Burroughs Wellcome FundNational Institute of Allergy and Infectious Diseases R21AI154370NIAID NIH HHS R21 AI144472NIAID NIH HHS R21 AI154370NICHD NIH HHS R01 HD109963NIGMS NIH HHSNIH HHS
6 · The paper itself

Abstract

backgroundMany insect-borne pathogens appear to manipulate the odors of their hosts in ways that influence vector behaviors. In our prior work, we identified characteristic changes in volatile emissions of cultured Plasmodium falciparum parasites in vitro and during natural human falciparum malaria. In the current study, we prospectively evaluate the reproducibility of these findings in an independent cohort of children in Blantyre, Malawi.

methodsWe enrolled febrile children under evaluation for malaria and collected breath from children with and without malaria, as well as healthy controls. Using gas chromatography/mass spectrometry, we characterized breath volatiles associated with malaria. By repeated sampling of children with malaria before and after antimalarial use, we determined how breath profiles respond to treatment. In addition, we investigated the stage-specificity of biomarkers through correlation with asexual and sexual-stage parasitemia.

resultsOur data provide robust evidence that P. falciparum infection leads to specific, reproducible changes in breath compounds. While no individual compound served as an adequate classifier in isolation, selected volatiles together yielded high sensitivity for diagnosis of malaria. Overall, the results of our predictive models suggest the presence of volatile signatures that reproducibly predict malaria infection status and determine response to therapy, even in cases of low parasitemia.

Indexed as

AntimalarialsBiomarkersBreath TestsMalaria, FalciparumPlasmodium falciparumChildChild, PreschoolFemaleGas Chromatography-Mass SpectrometryHumansInfantMalawiMaleParasitemiaProspective StudiesReproducibility of ResultsAntimalarialsBiomarkersVolatile Organic Compoundsbreathdiagnosticsexpiratory airmalariamass spectrometryvolatile organic compounds

Identifiers

PMID38885291
PMCPMC11481311

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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.