Key result
A genotype variant (rs4986938) translating reduced expression of the beta estrogen receptor gene was directly associated with increased intima-media thickness at the carotid wall (P=0.001) and sinus (P=0.002).
Why the study?
There is debate on the role of estrogens in modulating atherosclerosis risk in women, and the influence of estrogen receptor SNPs on carotid intima-media thickness has not been investigated.
Are genetic variants translating reduced expression of the beta estrogen receptor gene associated with increased carotid intima-media thickness in healthy late postmenopausal women?
Cross-Sectional (n=91)
No
Are genetic variants translating reduced expression of the beta estrogen receptor gene associated with increased carotid intima-media thickness in healthy late postmenopausal women?
Reduced estrogenic function at the tissue level, as indicated by the ERβ rs4986938 TT genotype, is independently associated with increased subclinical atherosclerosis (carotid IMT) in postmenopausal women.
Answers are grounded in this paper and cite their sources.
Supports ERβ variant role in subclinical atherosclerosis; leaves open whether genotyping informs postmenopausal risk assessment.
There is debate on the role of estrogens in modulating the risk for atherosclerosis in women. Our purpose was to investigate whether the size of the estrogenic impact was independently associated with variation of carotid intima-media thickness (IMT) in healthy late postmenopausal women. The levels of circulating estrogens have been used in previous studies but the influence of SNPs of the estrogen receptors (ER) α and β have not been investigated.We performed a crossed-sectional study of 91 women in a university hospital. We used a double approach in which, in addition to the measurement of estradiol levels by ultrasensitive methods, genetic variants (SNPs) associated with differing expression of the ER α and β genes were assessed. Multivariable analysis was used to examine the association of candidate factors with the value of IMT and plaque detection at both the carotid wall and the sinus.A genotype combination translating reduced gene expression of the ERβ was directly associated with IMT at both the carotid wall (P = .001) and the sinus (P = .002). Other predictors of IMT were the levels of glucose, positively associated with IMT at both the carotid wall (P < .001) and the sinus (P = .001), age positively associated with IMT at the sinus (P = .003), and levels of vitamin D, positively associated with IMT at the carotid wall (P = .04).Poorer estrogenic impact, as concordant with a SNP variant imposing reduced expression of the ERβ, was directly associated with IMT at both the carotid wall and the sinus. Glucose level, vitamin D only for the carotid wall, and age only for the sinus, also emerged as independent factors in the IMT variance.
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Cano-Marquina et al. (2021) conducted a cross-sectional in Subclinical atherosclerosis in postmenopausal women (n=91). Genotype TT of the SNP rs4986938 of the ERb gene vs. Other genotypes (CC, CT) was evaluated on Carotid intima-media thickness (IMT) at the carotid wall (Estimate 0.138, p=0.001). A genotype variant (rs4986938) translating reduced expression of the beta estrogen receptor gene was directly associated with increased intima-media thickness at the carotid wall (P=0.001) and sinus (P=0.002).
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