Evidence map›Paper›PMID 31389840›Full record

ArticleCritical care medicine2019

Old Mice Demonstrate Organ Dysfunction as well as Prolonged Inflammation, Immunosuppression, and Weight Loss in a Modified Surgical Sepsis Model.

Julie A Stortz, McKenzie K Hollen, Dina C Nacionales, Hiroyuki Horiguchi, Ricardo Ungaro, Marvin L Dirain, Zhongkai Wang, Quran Wu, Kevin K Wu, Ashok Kumar and 12 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Critical care medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Innate immune training in the neonatal response to sepsis.Molecular medicine (Cambridge, Mass.) · 2025
    Article
  12. Review
  13. Article
  14. Advancements in Immunity and Dementia Research: Highlights from the 2023 AAIC Advancements: Immunity Conference.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Review
  15. Article
  16. Observational
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 2 institutions in 1 country.

Julie A StortzDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
McKenzie K HollenDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Dina C NacionalesDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Hiroyuki HoriguchiDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Ricardo UngaroDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Marvin L DirainDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Zhongkai WangDepartment of Biostatistics, University of Florida College of Medicine, Gainesville, FL.
Quran WuDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Kevin K WuDepartment of Aging and Geriatric Research, University of Florida College of Medicine, Gainesville, FL.
Ashok KumarDepartment of Neuroscience, University of Florida College of Medicine, Gainesville, FL.
Thomas C FosterDepartment of Neuroscience, University of Florida College of Medicine, Gainesville, FL.
Brian D StewartDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida College of Medicine, Gainesville, FL.
Julia A RossDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida College of Medicine, Gainesville, FL.
Marc SegalDepartment of Medicine, University of Florida College of Medicine, Gainesville, FL.
Azra BihoracDepartment of Medicine, University of Florida College of Medicine, Gainesville, FL.
Scott BrakenridgeDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Frederick A MooreDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Stephanie E WohlgemuthDepartment of Aging and Geriatric Research, University of Florida College of Medicine, Gainesville, FL.
Christiaan LeeuwenburghDepartment of Aging and Geriatric Research, University of Florida College of Medicine, Gainesville, FL.
Alicia M MohrDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Lyle L MoldawerDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
Philip A EfronDepartment of Surgery, University of Florida College of Medicine, Gainesville, FL.
University of Florida · USFlorida College · US

Funding

University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI Peihua Qiu · 2007 to 2026
$22.8M
PICS: A New Horizon for Surgical Critical CareP50GM111152 · NIGMS · UNIVERSITY OF FLORIDA · PI MOORE, FREDERICK A · 2014 to 2018
$10.7M
Integrating data, algorithms and clinical reasoning for surgical risk assessmentR01GM110240 · NIGMS · UNIVERSITY OF FLORIDA · PI BIHORAC, AZRA, RASHIDI, PARISA · 2016 to 2025
$5.1M
Molecular Biology in Burns and TraumaT32GM008721 · NIGMS · UNIVERSITY OF FLORIDA · PI Philip A Efron · 1999 to 2026
$5.0M
Chronic Stress and Anemia Recovery following Major TraumaR01GM105893 · NIGMS · UNIVERSITY OF FLORIDA · PI MOHR, ALICIA M · 2013 to 2021
$3.5M
REGULATION ON MONOKINE PRODUCTION IN TRAUMA AND SURGERYR01GM040586 · NIGMS · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI MOLDAWER, LYLE L · 1988 to 2016
$2.6M
Use of viral-vectors for studying effects of chronic inflammation on executive functionR01AG052258 · NIA · UNIVERSITY OF FLORIDA · PI FOSTER, THOMAS C · 2016 to 2020
$1.9M
Validation of a Genomics Based Prognostic in Severe TraumaR01GM104481 · NIGMS · UNIVERSITY OF FLORIDA · PI MOLDAWER, LYLE L · 2013 to 2016
$1.8M
Hematopoietic Stem Cell Dysfunction in the Elderly after Severe InjuryR01GM113945 · NIGMS · UNIVERSITY OF FLORIDA · PI EFRON, PHILIP A · 2015 to 2019
$1.6M
Systemic inflammation in regulating the onset and progression of brain agingR01AG049711 · NIA · UNIVERSITY OF FLORIDA · PI FOSTER, THOMAS C · 2015 to 2019
$1.5M
NIA NIH HHS P30 AG028740NIA NIH HHS R01 AG049711NIA NIH HHS R01 AG052258NIGMS NIH HHS P50 GM111152NIGMS NIH HHS R01 GM040586NIGMS NIH HHS R01 GM104481NIGMS NIH HHS R01 GM105893NIGMS NIH HHS R01 GM110240NIGMS NIH HHS R01 GM113945NIGMS NIH HHS T32 GM008721
6 · The paper itself

Abstract

objectivesOur goal was to "reverse translate" the human response to surgical sepsis into the mouse by modifying a widely adopted murine intra-abdominal sepsis model to engender a phenotype that conforms to current sepsis definitions and follows the most recent expert recommendations for animal preclinical sepsis research. Furthermore, we aimed to create a model that allows the study of aging on the long-term host response to sepsis.

designExperimental study.

settingResearch laboratory. SUBJECTS: Young (3-5 mo) and old (18-22 mo) C57BL/6j mice.

interventionsMice received no intervention or were subjected to polymicrobial sepsis with cecal ligation and puncture followed by fluid resuscitation, analgesia, and antibiotics. Subsets of mice received daily chronic stress after cecal ligation and puncture for 14 days. Additionally, modifications were made to ensure that "Minimum Quality Threshold in Pre-Clinical Sepsis Studies" recommendations were followed. MEASUREMENTS AND MAIN

resultsOld mice exhibited increased mortality following both cecal ligation and puncture and cecal ligation and puncture + daily chronic stress when compared with young mice. Old mice developed marked hepatic and/or renal dysfunction, supported by elevations in plasma aspartate aminotransferase, blood urea nitrogen, and creatinine, 8 and 24 hours following cecal ligation and puncture. Similar to human sepsis, old mice demonstrated low-grade systemic inflammation 14 days after cecal ligation and puncture + daily chronic stress and evidence of immunosuppression, as determined by increased serum concentrations of multiple pro- and anti-inflammatory cytokines and chemokines when compared with young septic mice. In addition, old mice demonstrated expansion of myeloid-derived suppressor cell populations and sustained weight loss following cecal ligation and puncture + daily chronic stress, again similar to the human condition.

conclusionsThe results indicate that this murine cecal ligation and puncture + daily chronic stress model of surgical sepsis in old mice adhered to current Minimum Quality Threshold in Pre-Clinical Sepsis Studies guidelines and met Sepsis-3 criteria. In addition, it effectively created a state of persistent inflammation, immunosuppression, and weight loss, thought to be a key aspect of chronic sepsis pathobiology and increasingly more prevalent after human sepsis.

Indexed as

Age FactorsAnimalsCecumChemokinesCytokinesDisease Models, AnimalFemaleHumansImmune ToleranceInflammationKaplan-Meier EstimateLigationMaleMiceMice, Inbred C57BLMultiple Organ FailureChemokinesCytokines

Identifiers

PMID31389840
PMCPMC6848973
OpenAlexW2968234569

What OpenQuestion holds

Textmetadata
LicenceTDM
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.