Evidence map›Paper›PMID 41282786›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Serum mtDNA DAMP abundance, fragmentation and heteroplasmic variants associate with Acute Respiratory Failure outcome: A secondary analysis of study NCT00976833.

Grant T Daly, Emily M Hartsell, Viktor M Pastukh, Justin T Roberts, Adeyeye I Haastrup, Lina D Purcell, Madhuri S Mulekar, D Clark Files, Peter E Morris, Mark N Gillespie and 1 more

Registry-linked trialAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00976833 (Standardized Rehabilitation for ICU Patients With Acute Respiratory Failure), which is not on this map. Not yet cited in PubMed.

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

NCT00976833 nacompletednot on this map

Standardized Rehabilitation for ICU Patients With Acute Respiratory Failure

TypeinterventionalSponsorWake Forest UniversityRan2009 to 2015Enrolled300ConditionsAcute Respiratory FailureArmsStandardized Rehabilitation, Usual Care
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Grant T DalyDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.ORCID 0000-0002-4109-0546
Emily M HartsellDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.ORCID 0000-0003-0268-9916
Viktor M PastukhDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.
Justin T RobertsDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.ORCID 0000-0003-4433-1234
Adeyeye I HaastrupDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.
Lina D PurcellWake Forest Baptist Medical Center, Winston-Salem, NC, USA.
Madhuri S MulekarDept. of Mathematics and Statistics, University of South Alabama College of Arts and Sciences, Mobile, AL, USA.ORCID 0000-0001-8659-728X
D Clark FilesWake Forest Baptist Medical Center, Winston-Salem, NC, USA.ORCID 0000-0002-1595-4080
Peter E MorrisDivision of Pulmonary, Allergy and Critical Care Medicine, Dept. of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Mark N GillespieDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.ORCID 0009-0000-1278-1666
Raymond J LangleyDept. of Pharmacology, University of South Alabama Whiddon College of Medicine, Mobile, AL, USA.ORCID 0000-0001-8849-9325

Funding

CTSA UM1 at the University of Alabama at BirminghamUM1TR004771 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PATRICE DELAFONTAINE, Orlando M Gutierrez · 2024 to 2026
$29.2M
NCATS NIH HHS UM1 TR004771
6 · The paper itself

Abstract

Background: Serum mitochondrial DNA (mtDNA) fragments act as proinflammatory damage-associated molecular patterns (DAMPs), and have been linked to outcomes in critical illness. However, their prognostic value remains uncertain, possibly due to confounding nuclear mitochondrial insertions (NUMTs) which obscure both quantitation and variant detection. Methods: Using a targeted deep sequencing and bioinformatics workflow, we created filtering strategies to minimize NUMT-related artifacts. To evaluate the method, we performed a secondary analysis of serum samples collected from NCT00976833, a study of acute respiratory failure patients. By modeling DNA insert size distributions, we excluded likely NUMT-derived DNA fragments based on their size, improving the accuracy of mtDNA DAMP fragmentomic analysis. To improve variant detection, we introduced a novel "read mismatch percentage" metric to identify NUMT-induced chimeric read pairs, enabling identification of mtDNA variants. Results: Mean NUMT-depleted, but not raw, mtDNA insert size was lower in non-survivors. Short DNA inserts (<150 bp) displayed little NUMT contamination, and their abundance and size correlated with mortality more strongly than total mtDNA abundance. Sequence variants were called and some associated with survival and post-acute quality of life. Variant m.1,719G>A, found in small humanin-like 3 ( Conclusions: Our results addressed limitations of standard qPCR-based methods for the study of mtDNA DAMPs. Beyond addressing confounding NUMT, the method identified fragmentomic and variant associations overlooked by qPCR. Cell-free DNA fragmentomic and variant information are well-established biomarkers for cancer, and this method could facilitate similar patient-specific biomarkers in the context of critical illness. The method is composed of commercially available reagents and open source software, which could additionally promote adoption and reproducibility.

Indexed as

acute respiratory failurecell-free DNADAMPsheteroplasmymitochondrial DNA

Identifiers

PMID41282786
PMCPMC12637733

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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.