Evidence mapPaperPMID 39982115Full record

ReviewPhysiological reviews2025

The flux of energy in critical illness and the obesity paradox.

Ariel Jaitovich, Jesse B Hall

Abstract readReview
In one paragraph

Review in Physiological reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
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  11. Chronic succinate exposure does not cause liver injury.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  12. 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

2 authors.

Ariel JaitovichDivision of Pulmonary and Critical Care Medicine, Albany Medical College, Albany, New York, United States.ORCID 0000-0003-4714-2260
Jesse B HallSection of Pulmonary and Critical Care Medicine, The University of Chicago, Chicago, Illinois, United States.

Funding

Metabolic regulation of hypercapnic chronic obstructive pulmonary disease (COPD)-driven skeletal muscle dysfunctionR01HL160661 · NHLBI · ALBANY MEDICAL COLLEGE · 2022 to 2025
$2.2M
Blood DNA Methylation Biomarkers of Post Acute Sequelae of SARS CoV 2 Infection (PASC)R01AI173035 · ALBANY MEDICAL COLLEGE · 2025 to 2025
$775k
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) 160661HHS | NIH | NIAID | Division of Intramural Research (DIR, NIAID) AI173035NHLBI NIH HHS R01 HL160661NIAID NIH HHS R01 AI173035
6 · The paper itself

Abstract

During critical illness, systemic inflammation causes organ-specific metabolic changes. In the immune and inflammatory compartments, predominantly anabolic reprogramming supports cellular replication and inflammatory response execution. Pari passu, catabolism of adipose tissue and skeletal muscle supplies carbon skeletons and enthalpy for inflammatory and immune cell anabolism. The liver plays a key role during these metabolic shifts in enabling adequate supply of glucose and ketone bodies to the circulation. Although often perceived as passive surrogates of prehospitalization frailty, body mass constituents are active parties of an overarching metabolic trade-off that is key for survival after acute insults. Muscle and adipose tissue remodel in response to critical illness and thus profoundly influence the systemic metabolic landscape during and after hospitalization. Whether obesity's effect on patient systemic metabolism and survival is paradoxically beneficial or not remains controversial. Substrate-induced epigenetic changes lead to abnormal transcriptional programs that in turn regulate metabolic pathways critical to patient survival. We present a summary of major mechanisms involved in the flux of energy in critical illness from body mass into immune response execution and suggest future research avenues focused on perturbed immune-metabolic and epigenetic programs that could lead to improved understanding of these processes, and eventually to better outcomes for the critically ill.

Indexed as

Critical IllnessEnergy MetabolismObesityAdipose TissueAnimalsEpigenesis, GeneticHumansInflammationObesity Paradoxbody masscritical illnessimmune reprogrammingobesity paradoxskeletal muscle

Identifiers

PMID39982115
PMCPMC12107714

What Socratic 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 Socratic graph.