RORA polymorphisms are associated with ischemic stroke

RAR Related Orphan Receptor A ( RORA ) encodes a nuclear hormone receptor that participates in the pathoetiology of several disorders. We aimed to evaluate association between two RORA variants (rs11639084 and rs4774388) and risk of ischemic stroke among Iranians. These polymorphisms were genotyped using 4P-ARMS-PCR method. The rs11639084 polymorphism was associated with risk of stroke in all assumed inheritance models. T allele of this polymorphism was identified as the risk allele increasing the risk of ischemic stroke with OR (95 % CI) of 18.64 (13.58–25.57), P < 0.0001 and AIC = 29.4. Notably, the TT genotype was found to increase risk of this condition compared with CC genotype (OR (95 % CI) = 309.6 (142.2–683.2)) and CC + TC genotypes (OR (95 % CI) = 62.37 (30.06–129.4)). Since AIC estimates the quality of each model relative to other models, allelic model seems to be the best model for appraisal of the association between rs11639084 and risk of ischemic stroke. The rs4774388 polymorphism was associated with risk of stroke in all assumed inheritance models, except for over-dominant model. C allele of this polymorphism was reported to be the risk allele increasing the risk of ischemic stroke with OR (95 % CI) of 8.56 (6.4–11.43), P < 0.0001 and AIC = 29.6. Accordingly, the CC genotype increased susceptibility to ischemic stroke compared with TT genotype (OR (95 % CI) = 22.4 (14.6–42.5)), as well as combination of the other two genotypes (OR (95 % CI) = 12.92 (8.18–20.4)). Similar to the other polymorphism, the highest AIC value belonged to the allelic model. In brief, we showed associations between two RORA polymorphisms and susceptibility to ischemic stroke in Iranian population. RORA might be the functional link between abnormality in circadian rhythm and risk of ischemic stroke. Moreover, this gene might explain the shared genetic background between obesity and stroke. • RORA variants rs11639084 and rs4774388 were linked to ischemic stroke risk. • T allele of rs11639084 and C allele of rs4774388 increased stroke susceptibility. • RORA may link circadian rhythm disruption and shared genetics of stroke, obesity.

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Publication Details

Journal
Gene Reports
Published
2025-03-05
DOI
https://doi.org/10.1016/j.genrep.2025.102191
Primary Topic
Regulation of Appetite and Obesity
Type
article
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article

RORA polymorphisms are associated with ischemic stroke

Arash Safarzadeh, Mohammad Samadian, Soudeh Ghafouri‐Fard, Arezou Sayad et al.
Gene Reports
Regulation of Appetite and Obesity
article

RORA polymorphisms are associated with ischemic stroke

Arash Safarzadeh, Mohammad Samadian, Soudeh Ghafouri‐Fard, Arezou Sayad, Fatemeh Sadat Feghahati, Maryam Sheikhvand
article en

Abstract

RAR Related Orphan Receptor A ( RORA ) encodes a nuclear hormone receptor that participates in the pathoetiology of several disorders. We aimed to evaluate association between two RORA variants (rs11639084 and rs4774388) and risk of ischemic stroke among Iranians. These polymorphisms were genotyped using 4P-ARMS-PCR method. The rs11639084 polymorphism was associated with risk of stroke in all assumed inheritance models. T allele of this polymorphism was identified as the risk allele increasing the risk of ischemic stroke with OR (95 % CI) of 18.64 (13.58–25.57), P < 0.0001 and AIC = 29.4. Notably, the TT genotype was found to increase risk of this condition compared with CC genotype (OR (95 % CI) = 309.6 (142.2–683.2)) and CC + TC genotypes (OR (95 % CI) = 62.37 (30.06–129.4)). Since AIC estimates the quality of each model relative to other models, allelic model seems to be the best model for appraisal of the association between rs11639084 and risk of ischemic stroke. The rs4774388 polymorphism was associated with risk of stroke in all assumed inheritance models, except for over-dominant model. C allele of this polymorphism was reported to be the risk allele increasing the risk of ischemic stroke with OR (95 % CI) of 8.56 (6.4–11.43), P < 0.0001 and AIC = 29.6. Accordingly, the CC genotype increased susceptibility to ischemic stroke compared with TT genotype (OR (95 % CI) = 22.4 (14.6–42.5)), as well as combination of the other two genotypes (OR (95 % CI) = 12.92 (8.18–20.4)). Similar to the other polymorphism, the highest AIC value belonged to the allelic model. In brief, we showed associations between two RORA polymorphisms and susceptibility to ischemic stroke in Iranian population. RORA might be the functional link between abnormality in circadian rhythm and risk of ischemic stroke. Moreover, this gene might explain the shared genetic background between obesity and stroke. • RORA variants rs11639084 and rs4774388 were linked to ischemic stroke risk. • T allele of rs11639084 and C allele of rs4774388 increased stroke susceptibility. • RORA may link circadian rhythm disruption and shared genetics of stroke, obesity.

Gene ReportsVol. 39
Islamic Azad University, Science and Research Branch (IR), Shahid Beheshti University of Medical Sciences (IR)
Zero hunger
Openalex Percentile: Top 96%
Regulation of Appetite and Obesity
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