Evidence map›Paper›PMID 39095577›Full record

ArticlePediatric research2025

Distinct mitochondrial respiration profiles in pediatric patients with febrile illness versus sepsis.

Laura F Sartori, Elena Tsemberis, Tyne Hernandez, Katherine Luchette, Donglan Zhang, Sumera Farooqi, Jenny Bush, John C McCann, Fran Balamuth, Scott L Weiss

Abstract read
In one paragraph

Article in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

3 citing papers in PubMed.

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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

10 authors.

Laura F SartoriDepartment of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA. sartoril@chop.edu.
Elena TsemberisDepartment of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Tyne HernandezDepartment of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Katherine LuchetteUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Donglan ZhangDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Sumera FarooqiNemours Children's Health, Wilmington, DE, USA.
Jenny BushDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
John C McCannDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Fran BalamuthDepartment of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Scott L WeissNemours Children's Health, Wilmington, DE, USA.

Funding

Institutional Clinical and Translational Science AwardKL2TR001879 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$13.7M
Effect of Mitochondrial Quality Control on Systemic Inflammation and Organ Dysfunction in Pediatric SepsisR01HD102396 · NICHD · NEMOURS CHILDREN'S HOSPITAL, DELAWARE · PI WEISS, SCOTT L · 2020 to 2024
$2.3M
NCATS NIH HHS KL2 TR001879NICHD NIH HHS R01 HD102396
6 · The paper itself

Abstract

objectiveMitochondrial dysfunction, linked to sepsis-related organ failure, is unknown in febrile illness.

methodsProspective study of children in an Emergency Department (ED) with febrile illness or without infection (ED controls); secondary analysis of ICU patients with sepsis or without infection (ICU controls). Mitochondrial oxygen consumption measured in peripheral blood mononuclear cells using respirometry, with primary outcome of spare respiratory capacity (SRC). Mitochondrial content measured as citrate synthase (CS: febrile illness and ED controls) and mitochondrial to nuclear DNA ratio (mtDNA:nDNA: all groups).

resultsSRC was lower in febrile illness (6.7 ± 3.0 pmol/sec/10

conclusionMitochondrial SRC was reduced in both febrile illness and sepsis, but due to distinct mitochondrial profiles and impacted by demographics. Further work is needed to determine if mitochondrial profiles could differentiate febrile illness from early sepsis. IMPACT STATEMENT: Mitochondrial dysfunction has been linked to organ failure in sepsis, but whether mitochondrial alterations are evident in febrile illness without sepsis is unknown. In our study, while mitochondrial spare respiratory capacity (SRC), an index of cellular bioenergetic reserve under stress, was reduced in children with both febrile illness and sepsis compared to children without infections, low SRC was driven by increased basal respiration in febrile illness compared with decreased maximal uncoupled respiration in sepsis. Additional research is needed to understand if distinct mitochondrial profiles could be used to differentiate febrile illness from early sepsis in children.

Indexed as

FeverMitochondriaSepsisAdolescentCase-Control StudiesChildChild, PreschoolCitrate (si)-SynthaseDNA, MitochondrialEmergency Service, HospitalFemaleHumansInfantLeukocytes, MononuclearMaleOxygen ConsumptionCitrate (si)-SynthaseDNA, Mitochondrial

Identifiers

PMID39095577
PMCPMC12055561

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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.