Evidence map›Paper›PMID 38126504›Full record

ArticleSarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG2023

Can TERT rs2853669 polymorphysm indicate fibrosis in sarcoidosis?

Sümeyye Kement, Eda Turgut Ugurtay, Aslı Tanrıvermis Sayıt, Pınar Tascı, Meftun Unsal

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Article in Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 33% of its field
1 · What the graph read from it

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sümeyye KementDepartment of Chest Diseases, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey. sumeyyeekement@gmail.com.
Eda Turgut UgurtayBlack Sea Advanced Technology Research and Application Center, Biotechnology Unit, Ondokuz Mayıs University, Samsun, Turkey. edaturgut@gmail.com.
Aslı Tanrıvermis SayıtDepartment of Radiology, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey. asli.tanrivermissayit@omu.edu.tr.
Pınar TascıDepartment of Chest Diseases, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey. pnr.tsc.19@gmail.com.
Meftun UnsalDepartment of Chest Diseases, Ondokuz Mayıs University Faculty of Medicine, Samsun, Turkey. meftununsal@gmail.com.
Ondokuz Mayıs University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimSarcoidosis is a systemic inflammatory disease of unknown cause, characterized by the presence of non-caseating granulomas, which can affect all organs in the body, especially the lung. The fibrotic stage 4 of sarcoidosis usually does not respond adequately to treatment and may cause respiratory distress in the patient. Some telomerase gene polymorphisms have been significantly associated with lung cancer and idiopathic pulmonary fibrosis. In our study, we aimed to investigate the relationship between telomerase mutation and progression to fibrosis in patients with sarcoidosis.

methodsA total of 93 patients, including 18 males and 73 females, who were clinically and histopathologically diagnosed with sarcoidosis were included in the study. The 78 patients included in the study were classified as non-fibrotic and 15 as fibrotic sarcoidosis. In telomerase rs2853669 single nucleotide polymorphism, three genotypes, homozygous TT, homozygous CC and heterozygous TC, were determined as the genotypes of the patients.

resultsWhen non-fibrotic and fibrotic sarcoidosis groups were compared, no significant difference was found in terms of genotypes (p=0.76).  The FEV1 (forced expiratory volume in the first second) % of the CC genotype was lower than that of the other genotypes (p=0.01).

conclusionsIn sarcoidosis patients, telomerase rs2853669 polymorphism does not indicate progression to fibrosis, but since FEV1% was found to be lower in individuals with homozygous CC polymorphism, it is thought that it may predict loss of respiratory function. Further studies are needed to evaluate the association of telomerase polymorphisms with fibrosis in sarcoidosis.

Identifiers

PMID38126504
PMCPMC10965005
OpenAlexW4390069587

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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.