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RACE/ETHNICITY DETERMINES THE RELATIONSHIPS BETWEEN OXIDATIVE STRESS MARKERS AND BLOOD PRESSURE IN INDIVIDUALS WITH HIGH CARDIOVASCULAR DISEASE RISK
Oxidative stress (OS) and cardiovascular (CV) reactivity are related to CV morbidity and mortality. However, little is known about the relationships between these CV risk factors and their confounders. We hypothesize that higher OS is linked to higher blood pressure (BP) reactivity to acute laborato...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5143227/ https://www.ncbi.nlm.nih.gov/pubmed/27306086 http://dx.doi.org/10.1038/jhh.2016.39 |
Sumario: | Oxidative stress (OS) and cardiovascular (CV) reactivity are related to CV morbidity and mortality. However, little is known about the relationships between these CV risk factors and their confounders. We hypothesize that higher OS is linked to higher blood pressure (BP) reactivity to acute laboratory stressors and in the natural setting. We studied 137 subjects with a family history of hypertension and early myocardial infarction. There were 63 European Americans (EA’s) (38 males) and 74 African Americans (AA’s) (35 males), aged 19 to 36(27.6+/−3.1). The protocol included a competitive video game, cold stressor, and ambulatory BP recording. Blood samples were drawn 6 times for OS markers (8-OHdG and 8-Isoprostane) assay. Repeated measures analyses of covariance were used to test for mean differences and Pearson correlations were used to test OS and BP associations. There were no significant race/ethnicity differences in BP reactivity to either stressor (both p’s>0.48). 8-OHdG levels were significantly lower across all time points for AA’s than for EA’s (p<0.05) while levels of 8-isoprostane did not differ significantly (p>.10). Averaged 8-OHdG levels significantly correlated with SBP reactivity (r=0.45, <0.01) and 24-hour, daytime, and nighttime SBP (r range=0.37 to 0.42, all p’s<0.02) for EA’s but not for AA’s, whereas 8-isoprostane levels were significantly correlated with reactive SBP and nighttime DBP (both r’s=0.38, p<0.01) for AA’s but not for EA’s. These findings suggest a link between OS and BP changes in subjects at high risk for CV disease. Further, race/ethnicity determines which OS marker will impact BP variation implying race/ethnicity differences in OS related mechanisms of CVD. |
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