Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort

Background ― A number of studies confirmed a crucial role of type 1 interferon in pathophysiology of connective tissue diseases. Interferon regulatory factors (IRF) coordinate an expression of type 1 interferon, while interferon regulatory factor 5 (IRF5) gene was recently identified as causing pred...

Full description

Bibliographic Details
Main Authors: Mikhail Yu. Krylov, Lidia P. Ananieva, Irina A. Guseva
Format: Article
Language:English
Published: Limited liability company «Science and Innovations» (Saratov) 2020-12-01
Series:Russian Open Medical Journal
Subjects:
Online Access:http://www.romj.org/node/344
id doaj-16acd699edf5413881236a360049c11d
record_format Article
spelling doaj-16acd699edf5413881236a360049c11d2021-10-06T12:15:47ZengLimited liability company «Science and Innovations» (Saratov)Russian Open Medical Journal2304-34152020-12-0194e041010.15275/rusomj.2020.0410Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohortMikhail Yu. KrylovLidia P. AnanievaIrina A. GusevaBackground ― A number of studies confirmed a crucial role of type 1 interferon in pathophysiology of connective tissue diseases. Interferon regulatory factors (IRF) coordinate an expression of type 1 interferon, while interferon regulatory factor 5 (IRF5) gene was recently identified as causing predisposition to systemic lupus erythematosus and Sjögren syndrome. The objective of our study was to identify possible association of IRF5 rs2004640 (G/T) single nucleotide polymorphism with systemic sclerosis (SSc). Material and Methods―The study involved 236 individuals, including 105 patients with SSc diagnosis and 131 control individuals from Moscow region. The latter were healthy, unrelated to each other, their genders and ages were matched to those of SSc patients. Allele-specific real-time polymerase chain reaction (PCR) was used to study IFR5 rs2004640 polymorphism. Results ― We detected significantly higher percentage of IRF5 T-allele carriers in all patients (59.5%), those with diffuse cutaneous SSc (67.3%), patients with interstitial lung lesions (62.3%), and those with positive titers of anti-topoisomerase I antibodies (66.3%), compared with control group (46.2%). The odds ratios (OR) were: 1.71 (р=0.00), 2.40 (р=0.0004), 1.93 (р=0.002), and 2.30 (р=0.0008), correspondingly. Conclusion ― The replacement of nucleotide G by T in the IRF5 rs2004640 gene polymorphism was associated with a predisposition to SSc. Our data implied an existence of a novel SSc pathogenetic pathway associated with important role of type 1 interferon in pathophysiology of connective tissue diseases.http://www.romj.org/node/344interferonirf5 gene polymorphismsystemic sclerosisinterstitial lung disease
collection DOAJ
language English
format Article
sources DOAJ
author Mikhail Yu. Krylov
Lidia P. Ananieva
Irina A. Guseva
spellingShingle Mikhail Yu. Krylov
Lidia P. Ananieva
Irina A. Guseva
Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort
Russian Open Medical Journal
interferon
irf5 gene polymorphism
systemic sclerosis
interstitial lung disease
author_facet Mikhail Yu. Krylov
Lidia P. Ananieva
Irina A. Guseva
author_sort Mikhail Yu. Krylov
title Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort
title_short Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort
title_full Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort
title_fullStr Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort
title_full_unstemmed Relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: Russian Federation cohort
title_sort relating interferon regulatory factor 5 rs2004640 gene polymorphism to increased risk of systemic sclerosis in the patients: russian federation cohort
publisher Limited liability company «Science and Innovations» (Saratov)
series Russian Open Medical Journal
issn 2304-3415
publishDate 2020-12-01
description Background ― A number of studies confirmed a crucial role of type 1 interferon in pathophysiology of connective tissue diseases. Interferon regulatory factors (IRF) coordinate an expression of type 1 interferon, while interferon regulatory factor 5 (IRF5) gene was recently identified as causing predisposition to systemic lupus erythematosus and Sjögren syndrome. The objective of our study was to identify possible association of IRF5 rs2004640 (G/T) single nucleotide polymorphism with systemic sclerosis (SSc). Material and Methods―The study involved 236 individuals, including 105 patients with SSc diagnosis and 131 control individuals from Moscow region. The latter were healthy, unrelated to each other, their genders and ages were matched to those of SSc patients. Allele-specific real-time polymerase chain reaction (PCR) was used to study IFR5 rs2004640 polymorphism. Results ― We detected significantly higher percentage of IRF5 T-allele carriers in all patients (59.5%), those with diffuse cutaneous SSc (67.3%), patients with interstitial lung lesions (62.3%), and those with positive titers of anti-topoisomerase I antibodies (66.3%), compared with control group (46.2%). The odds ratios (OR) were: 1.71 (р=0.00), 2.40 (р=0.0004), 1.93 (р=0.002), and 2.30 (р=0.0008), correspondingly. Conclusion ― The replacement of nucleotide G by T in the IRF5 rs2004640 gene polymorphism was associated with a predisposition to SSc. Our data implied an existence of a novel SSc pathogenetic pathway associated with important role of type 1 interferon in pathophysiology of connective tissue diseases.
topic interferon
irf5 gene polymorphism
systemic sclerosis
interstitial lung disease
url http://www.romj.org/node/344
work_keys_str_mv AT mikhailyukrylov relatinginterferonregulatoryfactor5rs2004640genepolymorphismtoincreasedriskofsystemicsclerosisinthepatientsrussianfederationcohort
AT lidiapananieva relatinginterferonregulatoryfactor5rs2004640genepolymorphismtoincreasedriskofsystemicsclerosisinthepatientsrussianfederationcohort
AT irinaaguseva relatinginterferonregulatoryfactor5rs2004640genepolymorphismtoincreasedriskofsystemicsclerosisinthepatientsrussianfederationcohort
_version_ 1716840822020767744