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Osteopontin promoter polymorphism is associated with increased carotid intima-media thickness.


ABSTRACT: Osteopontin (OPN)-transgenic mice exhibit increased carotid artery intima-media thickness (CIMT), smooth muscle cell proliferation, and atheroma formation.An association of the human T-66G promoter variant with CIMT was examined in Caucasian adults grouped according to metabolic syndrome criteria: present (+MetS; n = 70) or absent (-MetS; n = 70).The G-allele frequency was 22%. For the entire cohort, the G group (TG and GG) was associated with significantly lower age-adjusted and gender-adjusted CIMT compared with the TT group (P = .008); similar analysis by metabolic syndrome group found a significant difference only in the -MetS group (P = .018). Stepwise multivariate regression showed that after age and waist circumference, the T-66G variant was the next most predictive of CIMT (P = .007). These data suggest that in a normoglycemic environment, human vascular OPN gene expression contributes to arterial structure, an effect diminished in dysmetabolic states.Humans with the OPN -66 TT genotype, particularly those without metabolic syndrome, exhibit thicker CIMT.

SUBMITTER: de las Fuentes L 

PROVIDER: S-EPMC2536614 | biostudies-literature | 2008 Aug

REPOSITORIES: biostudies-literature

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Osteopontin promoter polymorphism is associated with increased carotid intima-media thickness.

de las Fuentes Lisa L   Gu C Charles CC   Mathews Santhosh J SJ   Reagan Joann L JL   Ruthmann Nicholas P NP   Waggoner Alan D AD   Lai Chung-Fang CF   Towler Dwight A DA   Dávila-Román Víctor G VG  

Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography 20080411 8


<h4>Background</h4>Osteopontin (OPN)-transgenic mice exhibit increased carotid artery intima-media thickness (CIMT), smooth muscle cell proliferation, and atheroma formation.<h4>Methods</h4>An association of the human T-66G promoter variant with CIMT was examined in Caucasian adults grouped according to metabolic syndrome criteria: present (+MetS; n = 70) or absent (-MetS; n = 70).<h4>Results</h4>The G-allele frequency was 22%. For the entire cohort, the G group (TG and GG) was associated with s  ...[more]

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