Evidence map›Paper›PMID 35958326›Full record

ArticleTranslational lung cancer research2022

Peripheral blood leukocyte mitochondrial DNA content and risk of lung cancer.

Gregory T Kennedy, Nandita Mitra, Trevor M Penning, Alexander S Whitehead, Anil Vachani

Open access · diamondAbstract read
In one paragraph

Article in Translational lung cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Gregory T KennedyPulmonary, Allergy, & Critical Care Division, University of Pennsylvania, Philadelphia, PA, USA.
Nandita MitraDepartment of Biostatics & Epidemiology, University of Pennsylvania, Philadelphia, PA, USA.
Trevor M PenningCenter of Excellence in Environmental Toxicology, University of Pennsylvania, Philadelphia, PA, USA.
Alexander S WhiteheadCenter of Excellence in Environmental Toxicology, University of Pennsylvania, Philadelphia, PA, USA.
Anil VachaniPulmonary, Allergy, & Critical Care Division, University of Pennsylvania, Philadelphia, PA, USA.
Translational Therapeutics (United States) · USUniversity of Pennsylvania · USPhiladelphia VA Medical Center · US

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Metabolic activation of nitroarenes and Nrf2-Keap1R01ES029294 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2019 to 2026
$3.6M
Intraoperative Molecular Imaging of Pulmonary Squamous Cell CarcinomaF32CA254210 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KENNEDY, GREGORY T · 2020 to 2021
$143k
NCI NIH HHS F32 CA254210NIEHS NIH HHS P30 ES013508NIEHS NIH HHS R01 ES029294
6 · The paper itself

Abstract

Background: Previous studies of peripheral blood leukocyte mitochondrial DNA (mtDNA) content and risk of lung cancer have yielded inconsistent results, and no studies have evaluated the association between mtDNA content and post-resection lung cancer outcomes. Methods: Using a case-control study design, we evaluated the association between mtDNA content and risk of lung cancer in 465 cases and 378 controls. We also evaluated the association between mtDNA content and survival in 189 cases with surgically resected non-small cell lung cancer (NSCLC). Relative mtDNA content was measured using a quantitative real-time polymerase chain reaction (PCR) assay in peripheral blood genomic DNA. We calculated odds ratios (ORs) and 95% confidence intervals (CIs) using multivariable logistic regression, adjusting for age, gender, race, and smoking history. Results: mtDNA content was lower in cases compared to controls, with medians of 1.26 [interquartile range (IQR), 0.98-1.70)] and 1.79 (IQR, 1.34-2.10; P<0.001), respectively. Compared to the quartile of subjects with the highest mtDNA content, there was significantly higher likelihood of lung cancer in the second lowest quartile (OR 3.44; 95% CI: 2.06-5.75) and the lowest quartile (OR 6.36; 95% CI: 3.86-10.47). In patients with resected NSCLC, there was no association between lower mtDNA content and recurrence-free survival (RFS) [hazard ratio (HR) 0.89; 95% CI: 0.47-1.66] or overall survival (OS) (HR 0.71; 95% CI: 0.35-1.46). Conclusions: Thus, our results counter previous studies and find that lower mtDNA content is associated with lung cancer risk. Our results suggest that mtDNA content could potentially serve as a risk biomarker, but is not associated with survival outcomes in NSCLC.

Indexed as

Lung cancermitochondrial DNA (mtDNA)risk biomarker

Identifiers

PMID35958326
PMCPMC9359958
OpenAlexW4285549283

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.