Evidence map›Paper›PMID 31793435›Full record

ArticleeLife2019

Chronic muscle weakness and mitochondrial dysfunction in the absence of sustained atrophy in a preclinical sepsis model.

Allison M Owen, Samir P Patel, Jeffrey D Smith, Beverly K Balasuriya, Stephanie F Mori, Gregory S Hawk, Arnold J Stromberg, Naohide Kuriyama, Masao Kaneki, Alexander G Rabchevsky and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 116 citations in OpenAlex.

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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Allison M OwenAging and Critical Care Research Laboratory, University of Kentucky, Lexington, United States.ORCID 0000-0001-5623-4891
Samir P PatelDepartment of Physiology, University of Kentucky, Lexington, United States.
Jeffrey D SmithDepartment of Biosystems and Agricultural Engineering, University of Kentucky, Lexington, United States.
Beverly K BalasuriyaAging and Critical Care Research Laboratory, University of Kentucky, Lexington, United States.
Stephanie F MoriAging and Critical Care Research Laboratory, University of Kentucky, Lexington, United States.
Gregory S HawkDepartment of Statistics, University of Kentucky, Lexington, United States.
Arnold J StrombergDepartment of Statistics, University of Kentucky, Lexington, United States.
Naohide KuriyamaDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Shriners Hospitals for Children, Harvard Medical School, Charlestown, United States.
Masao KanekiDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Shriners Hospitals for Children, Harvard Medical School, Charlestown, United States.
Alexander G RabchevskyDepartment of Physiology, University of Kentucky, Lexington, United States.
Timothy A ButterfieldDepartment of Physiology, University of Kentucky, Lexington, United States.
Karyn A EsserDepartment of Physiology, University of Kentucky, Lexington, United States.ORCID 0000-0002-5791-1441
Charlotte A PetersonDepartment of Physiology, University of Kentucky, Lexington, United States.
Marlene E StarrAging and Critical Care Research Laboratory, University of Kentucky, Lexington, United States.ORCID 0000-0003-0304-348X
Hiroshi SaitoAging and Critical Care Research Laboratory, University of Kentucky, Lexington, United States.ORCID 0000-0002-5845-5177
University of Kentucky · USShriners Hospitals for Children - Erie · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
University of Kentucky Alzheimer's Disease Core Center - Biomarker CoreP30AG028383 · NIA · UNIVERSITY OF KENTUCKY · PI SCHMITT, FREDERICK · 2006 to 2020
$23.3M
University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTIAAN LEEUWENBURGH · 2007 to 2026
$22.8M
The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI FINLIN, BRIAN S · 2012 to 2017
$13.7M
Pilot Projects ProgramP30GM127211 · NIGMS · UNIVERSITY OF KENTUCKY · PI CASSIS, LISA A · 2018 to 2022
$5.7M
Muscle clock disruption accelerates the onset and progression of neurodegenerationR01AR066082 · NIAMS · UNIVERSITY OF KENTUCKY · PI ESSER, KARYN A · 2014 to 2018
$2.0M
Visceral fat gamma delta T cells in sepsis pathogenesisR01GM129532 · NIGMS · UNIVERSITY OF KENTUCKY · PI STARR, MARLENE ELENA · 2018 to 2022
$1.6M
Mechanisms mediating severity of acute pancreatitis in the agedR01AG055359 · NIA · UNIVERSITY OF KENTUCKY · PI SAITO, HIROSHI · 2017 to 2021
$1.6M
The Role of Adipose Tissue in Age-dependent Sensitivity to Critical IllnessR01AG039732 · NIA · UNIVERSITY OF KENTUCKY · PI SAITO, HIROSHI · 2011 to 2015
$1.5M
Targeting Warburg Effect to Reverse Stress-Induced Insulin Resistance in BurnsR01GM115552 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KANEKI, MASAO · 2016 to 2019
$1.3M
Impairment of Directional Neutrophil Migration and Farnesylation in SepsisR01GM117298 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KANEKI, MASAO · 2016 to 2019
$1.3M
NCATS NIH HHS UL1 TR001998NCI NIH HHS P30 CA177558NIAMS NIH HHS R01 AR066082NIA NIH HHS P30 AG028383NIA NIH HHS P30 AG028740NIA NIH HHS R01 AG039732NIA NIH HHS R01 AG055359NIA NIH HHS R01 AG390732NIGMS NIH HHS F31 GM117868NIGMS NIH HHS P20 GM103527NIGMS NIH HHS P30 GM127211NIGMS NIH HHS R01 GM115552NIGMS NIH HHS R01 GM117298NIGMS NIH HHS R01 GM126181NIGMS NIH HHS R01 GM129532
6 · The paper itself

Abstract

Chronic critical illness is a global clinical issue affecting millions of sepsis survivors annually. Survivors report chronic skeletal muscle weakness and development of new functional limitations that persist for years. To delineate mechanisms of sepsis-induced chronic weakness, we first surpassed a critical barrier by establishing a murine model of sepsis with ICU-like interventions that allows for the study of survivors. We show that sepsis survivors have profound weakness for at least 1 month, even after recovery of muscle mass. Abnormal mitochondrial ultrastructure, impaired respiration and electron transport chain activities, and persistent protein oxidative damage were evident in the muscle of survivors. Our data suggest that sustained mitochondrial dysfunction, rather than atrophy alone, underlies chronic sepsis-induced muscle weakness. This study emphasizes that conventional efforts that aim to recover muscle quantity will likely remain ineffective for regaining strength and improving quality of life after sepsis until deficiencies in muscle quality are addressed.

Indexed as

AnimalsAtrophyDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred C57BLMiddle AgedMitochondrial DiseasesMitochondria, MuscleMuscle, SkeletalMuscle WeaknessQuality of LifeSepsischronic critical illnesscritical illness myopathyhuman biologyimmunologyinflammationmedicinemitochondriamousemusclepost-intensive care syndromesepsis

Identifiers

PMID31793435
PMCPMC6890461
OpenAlexW2993005194

What OpenQuestion holds

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LicenceCC BY
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.