Evidence map›Paper›PMID 30991107›Full record

Observational studyJournal of the American College of Surgeons2019

Persistently Elevated Glucagon-Like Peptide-1 Levels among Critically Ill Surgical Patients after Sepsis and Development of Chronic Critical Illness and Dismal Long-Term Outcomes.

Scott C Brakenridge, Frederick A Moore, Nicole R Mercier, Michael Cox, Quron Wu, Lyle L Moldawer, Alicia M Mohr, Philip A Efron, R Stephen Smith

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Journal of the American College of Surgeons, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.3field-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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  15. Activation of TLRs Triggers GLP-1 Secretion in Mice.International journal of molecular sciences · 2023
    Article
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  20. Dysregulated Immunity and Immunotherapy after Sepsis.Journal of clinical medicine · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Scott C BrakenridgeDepartment of Surgery, University of Florida, Gainesville, FL.
Frederick A MooreDepartment of Surgery, University of Florida, Gainesville, FL.
Nicole R MercierUniversity of Arkansas for Medical Sciences, Little Rock, AR.
Michael CoxDepartment of Surgery, University of Florida, Gainesville, FL.
Quron WuDepartment of Surgery, University of Florida, Gainesville, FL.
Lyle L MoldawerDepartment of Surgery, University of Florida, Gainesville, FL.
Alicia M MohrDepartment of Surgery, University of Florida, Gainesville, FL.
Philip A EfronDepartment of Surgery, University of Florida, Gainesville, FL.
R Stephen SmithDepartment of Surgery, University of Florida, Gainesville, FL. Electronic address: Steve.Smith@surgery.ufl.edu.
University of Florida · USUniversity of Arkansas for Medical Sciences · US

Funding

University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTIAAN LEEUWENBURGH · 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
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
Hematopoietic Stem Cell Dysfunction in the Elderly after Severe InjuryR01GM113945 · NIGMS · UNIVERSITY OF FLORIDA · PI EFRON, PHILIP A · 2015 to 2019
$1.6M
The acute development and persistence of frailty, comorbidity and disability in critically ill elderly patients after severe traumatic injury: ?induced frailty?R03AG056444 · NIA · UNIVERSITY OF FLORIDA · PI BRAKENRIDGE, SCOTT CHARLES · 2017 to 2018
$223k
NIA NIH HHS P30 AG028740NIA NIH HHS R03 AG056444NIGMS NIH HHS P50 GM111152NIGMS NIH HHS R01 GM105893NIGMS NIH HHS R01 GM113945NIGMS NIH HHS T32 GM008721
6 · The paper itself

Abstract

backgroundGlucagon-like peptide-1 (GLP-1) is a gut-derived incretin hormone that stimulates insulin secretion, cellular glucose uptake, and has immune-regulatory functions. Glucagon-like peptide-1 is markedly altered after trauma and sepsis, but the implications remain unclear. STUDY

designWe performed an analysis of a prospective, longitudinal cohort study of critically ill surgical patients with sepsis. Patient characteristics and clinical data were collected, as well as peripheral blood sampling for biomarker analysis, out to 28 days after sepsis onset. We prospectively adjudicated sepsis diagnosis, severity, clinical outcomes, and 6-month follow-up.

resultsThe cohort included 157 septic surgical patients with significant physiologic derangement (Maximum Sequential Organ Failure Assessment [SOFA] score 8, interquartile range [IQR] 4 to 11), a high rate of multiple organ failure (50.3%), and septic shock (24.2%). Despite high disease severity, both early death (<14 days; n = 4, 2.9%) and overall inpatient mortality were low (n = 12, 7.6%). However, post-discharge 6-month mortality was nearly 3-fold higher (19.7%). Both GLP-1 and interleukin [IL]-6 levels were significantly elevated for 21 days (p ≤ 0.01) in patients who developed chronic critical illness (CCI) compared with patients with a rapid recovery. Elevated GLP-1 at 24 hours was a significant independent predictor for the development of CCI after controlling for IL-6 and glucose levels (p = 0.027), and at day 14 for death or severe functional disability at 6 months (WHO/Zubrod score 4-5, p = 0.014).

conclusionsElevated GLP-1 within 24 hours of sepsis is a predictor of early death or persistent organ dysfunction. Among early survivors, persistently elevated GLP-1 levels at day 14 are strongly predictive of death or severe functional disability at 6 months. Persistently elevated GLP-1 levels may be a marker of a nonresolving catabolic state that is associated with muscle wasting and dismal outcomes after sepsis and chronic critical illness.

Indexed as

Critical IllnessAgedBiomarkersChronic DiseaseFemaleFloridaFollow-Up StudiesGlucagon-Like Peptide 1HumansIncidenceIntensive Care UnitsMaleMiddle AgedProspective StudiesSepsisSurgical Wound InfectionBiomarkersGlucagon-Like Peptide 1

Identifiers

PMID30991107
PMCPMC6599553
OpenAlexW2939032636

What OpenQuestion holds

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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.