Evidence map›Paper›PMID 33006015›Full record

Trial reportMolecular biology reports2020

Investigation of telomere related gene mutations in idiopathic pulmonary fibrosis.

Halime Yildirim, Pinar Yildiz, Ender Coskunpinar

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 81% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Multi-omics insights into the mechanisms and prognosis of IPF.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2026
    Review
  2. Article
  3. 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

3 authors at 1 institution in 2 countries.

Halime YildirimSchool of Medicine, Department of Medical Biology, University of Health Sciences Turkey, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-9008-7909
Pinar YildizChest Diseases, Yedikule Chest Diseases and Thoracic Surgery Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-6650-1495
Ender CoskunpinarSchool of Medicine, Department of Medical Biology, University of Health Sciences Turkey, Istanbul, Turkey. ecoskunpinar@gmail.com.ORCID http://orcid.org/0000-0002-1003-5544
Sağlık Bilimleri Üniversitesi · TR

Funding

University of Health Sciences, Scientific Research Project Unit 2018/039
6 · The paper itself

Abstract

Idiopathic Pulmonary Fibrosis (IPF) is the most common type of Idiopathic Interstitial Pneumonias (IIP). The aim of this study is to determine the mutation of variants in four telomere-related genes and to determine the possible relationship between these mutations and telomere shortening in order to contribute to the understanding of the pathophysiology of IPF. For this study, 34 individuals with IPF, 32 individuals with non-IPF ILD (Interstitial Lung Disease), and 31 healthy controls between the ages of 40 and 85 were included. The mutation analysis and telomere measurements were examined for the volunteers. According to the mutation screening results, no significant difference was found between the patients with IPF, non-IPF ILD groups and healthy individuals in terms of genotyping analysis. However, in terms of the allele distribution for two genes, statistically significant difference was found in IPF and non-IPF ILD patients (TERT; p = 0.002 and TERC; p = 0.001). According to the telomere length measurement, the telomeres of the patients were shorter than of the control group (p = 0.0001). In compliance with the results of our analysis, it is thought that genes that have allelic significance from the point of gene mutations as well as telomere shortening may be risk factors for the disease.

Indexed as

MutationAdultAgedAged, 80 and overFemaleHumansIdiopathic Pulmonary FibrosisMaleMiddle AgedRNATelomeraseTelomereTelomere HomeostasisRNATelomerasetelomerase RNATERT protein, humanGeneticsIdiopathic pulmonary fibrosisMutationTelomere shortening

Identifiers

PMID33006015
OpenAlexW3090618937

What OpenQuestion holds

Textmetadata
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.