Evidence map›Paper›PMID 39941146›Full record

ArticleInternational journal of molecular sciences2025

Mitochondrial

Li-Na Lee, I-Shiow Jan, Wen-Ru Chou, Wei-Lun Liu, Yen-Liang Kuo, Chih-Yueh Chang, Hsiu-Ching Chang, Jia-Luen Liu, Chia-Lin Hsu, Chia-Nan Lin and 5 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Li-Na LeeDepartment of Laboratory Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei City 24352, Taiwan.ORCID 0000-0002-7654-2450
I-Shiow JanDepartment of Laboratory Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10051, Taiwan.
Wen-Ru ChouDepartment of Internal Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei City 24352, Taiwan.
Wei-Lun LiuSchool of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei City 242062, Taiwan.ORCID 0000-0001-8593-8492
Yen-Liang KuoDepartment of Internal Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei City 24352, Taiwan.ORCID 0000-0001-9687-9352
Chih-Yueh ChangDepartment of Internal Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei City 24352, Taiwan.
Hsiu-Ching ChangDepartment of Laboratory Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10051, Taiwan.
Jia-Luen LiuOne-Star Technology, New Taipei City 11051, Taiwan.
Chia-Lin HsuDepartment of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10051, Taiwan.
Chia-Nan LinDepartment of Medical Imaging, Fu Jen Catholic University Hospital, New Taipei City 24352, Taiwan.ORCID 0000-0002-3026-0917
Ke-Yun ChaoDepartment of Respiratory Therapy, College of Medicine, Fu Jen Catholic University, New Taipei City 24352, Taiwan.
Chi-Wei TsengDepartment of Respiratory Therapy, Fu Jen Catholic University Hospital, New Taipei City 24352, Taiwan.
I-Hsien LeeDepartment of Critical Care Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei City 24352, Taiwan.
Jann-Tay WangDepartment of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10051, Taiwan.
Jann-Yuan WangDepartment of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10051, Taiwan.ORCID 0000-0003-3406-366X

Funding

Fu Jen Catholic University Hospital PL202008003VNational Science Council of Taiwan 110-2635-B-030-001
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) has been associated with mitochondrial dysfunction. We investigated whether mitochondrial DNA variants in peripheral blood leukocytes (PBLs), which affect proteins of the respiratory chain and mitochondrial function, could be associated with an increased risk and poor prognosis of IPF. From 2020 to 2022, we recruited 36 patients (age: 75.3 ± 8.5; female: 19%) with IPF, and 80 control subjects (age: 72.3 ± 9.0; female: 27%). The mitochondrial genome of peripheral blood leukocytes was determined using next-generation sequencing. During a 45-month follow-up, 10 (28%) patients with IPF remained stable and the other 26 (72%) progressed, with 12 (33%) mortalities. IPF patients had more non-synonymous (NS) variants (substitution/deletion/insertion) in mitochondrial

Indexed as

Electron Transport Complex IVIdiopathic Pulmonary FibrosisMitochondriaRNA, TransferAgedAged, 80 and overCase-Control StudiesDNA, MitochondrialFemaleGenetic Predisposition to DiseaseHumansLeukocytesMaleMiddle AgedPrognosisRisk FactorsDNA, MitochondrialElectron Transport Complex IVRNA, Transfercytochrome c oxidase subunit 3 (COX3)idiopathic pulmonary fibrosis (IPF)mitochondrial DNA (mtDNA)nonsynonymous varianttRNA variant

Identifiers

PMID39941146
PMCPMC11818280

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Registered trials

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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.