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1.
J Am Heart Assoc ; 7(24): e009117, 2018 12 18.
Article in English | MEDLINE | ID: mdl-30561265

ABSTRACT

Background Exposure to green vegetation has been linked to positive health, but the pathophysiological processes affected by exposure to vegetation remain unclear. To study the relationship between greenness and cardiovascular disease, we examined the association between residential greenness and biomarkers of cardiovascular injury and disease risk in susceptible individuals. Methods and Results In this cross-sectional study of 408 individuals recruited from a preventive cardiology clinic, we measured biomarkers of cardiovascular injury and risk in participant blood and urine. We estimated greenness from satellite-derived normalized difference vegetation index ( NDVI ) in zones with radii of 250 m and 1 km surrounding the participants' residences. We used generalized estimating equations to examine associations between greenness and cardiovascular disease biomarkers. We adjusted for residential clustering, demographic, clinical, and environmental variables. In fully adjusted models, contemporaneous NDVI within 250 m of participant residence was inversely associated with urinary levels of epinephrine (-6.9%; 95% confidence interval, -11.5, -2.0/0.1 NDVI ) and F2-isoprostane (-9.0%; 95% confidence interval, -15.1, -2.5/0.1 NDVI ). We found stronger associations between NDVI and urinary epinephrine in women, those not on ß-blockers, and those who had not previously experienced a myocardial infarction. Of the 15 subtypes of circulating angiogenic cells examined, 11 were inversely associated (8.0-15.6% decrease/0.1 NDVI ), whereas 2 were positively associated (37.6-45.8% increase/0.1 NDVI ) with contemporaneous NDVI . Conclusions Independent of age, sex, race, smoking status, neighborhood deprivation, statin use, and roadway exposure, residential greenness is associated with lower levels of sympathetic activation, reduced oxidative stress, and higher angiogenic capacity.


Subject(s)
Cardiovascular Diseases/prevention & control , Plants , Residence Characteristics , Urbanization , Adult , Biomarkers/blood , Biomarkers/urine , Built Environment , Cardiovascular Diseases/metabolism , Cardiovascular Diseases/pathology , Cardiovascular Diseases/physiopathology , Cross-Sectional Studies , Endothelial Progenitor Cells/pathology , Epinephrine/urine , F2-Isoprostanes/urine , Female , Humans , Kentucky , Male , Middle Aged , Oxidative Stress , Protective Factors , Risk Assessment , Risk Factors , Sympathetic Nervous System/metabolism , Sympathetic Nervous System/physiopathology
2.
PLoS One ; 13(10): e0205851, 2018.
Article in English | MEDLINE | ID: mdl-30321232

ABSTRACT

Circulating angiogenic cells (CACs) of various described phenotypes participate in the regeneration of the damaged endothelium, but the abundance of these cells is highly influenced by external cues including diabetes. It is not entirely clear which CAC populations are most reflective of endothelial function nor which are impacted by diabetes. To answer these questions, we enrolled a human cohort with variable CVD risk and determined relationships between stratified levels of CACs and indices of diabetes and vascular function. We also determined associations between CAC functional markers and diabetes and identified pro-angiogenic molecules which are impacted by diabetes. We found that subjects with low levels of CD34+/AC133+/CD31+/CD45dim cells (CAC-3) had a significantly higher incidence of diabetes (p = 0.004), higher HbA1c levels (p = 0.049) and higher CVD risk scores. Furthermore, there was an association between low CAC-3 levels and impaired vascular function (p = 0.023). These cells from diabetics had reduced levels of CXCR4 and VEGFR2, while diabetics had higher levels of certain cytokines and pro-angiogenic molecules. These results suggest that quantitative and functional defects of CD34+/AC133+/CD31+/CD45dim cells are associated with diabetes and vascular impairment and that this cell type may be a prognostic indicator of CVD and vascular dysfunction.


Subject(s)
Diabetes Mellitus, Type 2/blood , Endothelial Cells/cytology , Endothelium, Vascular/physiopathology , Stem Cells/cytology , Adult , Aged , Cardiovascular Diseases/diagnosis , Cytokines/metabolism , Diabetes Mellitus, Type 2/complications , Endothelium, Vascular/metabolism , Female , Glycated Hemoglobin/metabolism , Humans , Hyperglycemia/metabolism , Male , Middle Aged , Neovascularization, Pathologic , Obesity/complications , Obesity/pathology , Phenotype , Receptors, CXCR4/metabolism , Risk Factors , Vascular Endothelial Growth Factor Receptor-2/metabolism , Young Adult
3.
Arterioscler Thromb Vasc Biol ; 35(11): 2468-77, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26293462

ABSTRACT

OBJECTIVES: Previous studies have shown that residential proximity to a roadway is associated with increased cardiovascular disease risk. Yet, the nature of this association remains unclear, and its effect on individual cardiovascular disease risk factors has not been assessed. The objective of this study was to determine whether residential proximity to roadways influences systemic inflammation and the levels of circulating angiogenic cells. APPROACH AND RESULTS: In a cross-sectional study, cardiovascular disease risk factors, blood levels of C-reactive protein, and 15 antigenically defined circulating angiogenic cell populations were measured in participants (n=316) with moderate-to-high cardiovascular disease risk. Attributes of roadways surrounding residential locations were assessed using geographic information systems. Associations between road proximity and cardiovascular indices were analyzed using generalized linear models. Close proximity (<50 m) to a major roadway was associated with lower income and higher rates of smoking but not C-reactive protein levels. After adjustment for potential confounders, the levels of circulating angiogenic cells in peripheral blood were significantly elevated in people living in close proximity to a major roadway (CD31(+)/AC133(+), AC133(+), CD34(+)/AC133(+), and CD34(+)/45(dim)/AC133(+) cells) and positively associated with road segment distance (CD31(+)/AC133(+), AC133(+), and CD34(+)/AC133(+) cells), traffic intensity (CD31(+)/AC133(+) and AC133(+) cells), and distance-weighted traffic intensity (CD31(+)/34(+)/45(+)/AC133(+) cells). CONCLUSIONS: Living close to a major roadway is associated with elevated levels of circulating cells positive for the early stem marker AC133(+). This may reflect an increased need for vascular repair. Levels of these cells in peripheral blood may be a sensitive index of cardiovascular injury because of residential proximity to roadways.


Subject(s)
Antigens, CD/blood , Automobiles , Endothelial Progenitor Cells/drug effects , Environmental Exposure/adverse effects , Environmental Pollutants/adverse effects , Glycoproteins/blood , Inflammation Mediators/blood , Peptides/blood , Residence Characteristics , Vehicle Emissions , AC133 Antigen , Adult , Biomarkers/blood , Cell Count , Cross-Sectional Studies , Endothelial Progenitor Cells/immunology , Endothelial Progenitor Cells/metabolism , Female , Humans , Kentucky , Male , Middle Aged , Up-Regulation
4.
Endocr Pract ; 18(5): 668-75, 2012.
Article in English | MEDLINE | ID: mdl-22548950

ABSTRACT

OBJECTIVE: To determine whether the plasma level of sex hormone-binding globulin (SHBG) identifies South Asian Indian children at risk for metabolic syndrome. METHODS: Adults and their children aged 5 to 9 years were recruited at the annual health fair at the Hindu temple serving the South Asian Indian community in Louisville, Kentucky. Anthropometric data were collected in adults and children, and blood pressure, lipid, and glucose levels were measured in adults. SHBG levels were measured in children using a fingerstick blood sample. In adults, metabolic syndrome was diagnosed according to the International Diabetes Federation criteria. Twelve months later, follow-up anthropometric data were obtained for a portion of the children. RESULTS: The study included 30 sets of parents and 30 children. The prevalence of metabolic syndrome among 310 adults attending the health fair was 42% in men and 39% in women. Children with 1 parent with metabolic syndrome had 24% lower SHBG levels that increased to 55% if both parents had metabolic syndrome. SHBG levels were inversely related to waist circumference and to body mass index percentile. Both SHBG and waist circumference predicted weight gain over 1 year in children. CONCLUSIONS Low SHBG levels were found in South Asian Indian children whose parents had attributes of metabolic syndrome. The dose dependency of SHBG is consistent with inheritance of a genetic trait, and if the results are applicable to other racial/ethnic groups, SHBG may be a useful marker to identify at-risk children for early intervention.


Subject(s)
Metabolic Syndrome/metabolism , Sex Hormone-Binding Globulin/metabolism , Adult , Child , Child, Preschool , Female , Humans , Male , Risk Factors , Young Adult
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