6 research outputs found

    Additional file 1: of The association between high-sensitivity C-reactive protein and metabolic risk factors in black and white South African women: a cross-sectional study

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    Table S1. Adjusted associations between insulin resistance (HOMA-IR) and hsCRP in black and white South African women. Data represents β-coefficients [95% confidence interval] and adjusted-R2. Model 1: hsCRP + age + race/ethnicity + (hsCRP x race/ethnicity interaction); Model 2: (Model 1) + SES + lifestyle factors; Model 3: (Model 2) + WC. hsCRP, C-reactive protein; hsCRP x race/ethnicity, interaction between hsCRP and race/ethnicity; WC, waist circumference; SES, socio-economic status; ln(HOMA-IR), natural log of homeostatic model assessment. *p < 0.05 and **p < 0.001 (PDF 1343 kb

    Additional file 2: of The association between high-sensitivity C-reactive protein and metabolic risk factors in black and white South African women: a cross-sectional study

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    Table S2. Adjusted associations between triglycerides and hsCRP in black and white South African women. Data represents β-coefficients [95% confidence interval] and adjusted-R2. Model 1: hsCRP + age + race/ethnicity + (hsCRP x race/ethnicity interaction); Model 2: (Model 1) + SES + lifestyle factors; Model 3: (Model 2) + WC. hsCRP, C-reactive protein; hsCRP x race/ethnicity, interaction between hsCRP and race/ethnicity; WC, waist circumference; SES, socio-economic status; ln(TG), natural log of triglycerides. *p < 0.05 and **p < 0.001 (PDF 545 kb

    Additional file 4: of The association between high-sensitivity C-reactive protein and metabolic risk factors in black and white South African women: a cross-sectional study

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    Table S4. Adjusted associations between HDL-C and hsCRP in black and white South African women. Data represents β-coefficients [95% confidence interval] and adjusted-R2. Model 1: hsCRP + age + race/ethnicity + (hsCRP x race/ethnicity interaction); Model 2: (Model 1) + SES + lifestyle factors; Model 3: (Model 2) + WC. hsCRP, C-reactive protein; hsCRP x race/ethnicity, interaction between hsCRP and race/ethnicity; WC, waist circumference; SES, socio-economic status; ln(HDL-C), natural log of high-density lipoprotein cholesterol. *p < 0.05 and **p < 0.001 (PDF 549 kb

    Additional file 3: of The association between high-sensitivity C-reactive protein and metabolic risk factors in black and white South African women: a cross-sectional study

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    Table S3. Adjusted associations between total cholesterol and hsCRP in black and white South African women. Data represents β-coefficients [95% confidence interval] and adjusted-R2. Model 1: hsCRP + age + race/ethnicity + (hsCRP x race/ethnicity interaction); Model 2: (Model 1) + SES + lifestyle factors; Model 3: (Model 2) + WC. hsCRP, C-reactive protein; hsCRP x race/ethnicity, interaction between hsCRP and race/ethnicity; WC, waist circumference; SES, socio-economic status; ln(TC), natural log of total cholesterol. *p < 0.05 and **p < 0.001 (PDF 542 kb

    Additional file 5: of The association between high-sensitivity C-reactive protein and metabolic risk factors in black and white South African women: a cross-sectional study

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    Table S5. Adjusted associations between LDL-C and hsCRP in black and white South African women. Data represents β-coefficients [95% confidence interval] and adjusted-R2. Model 1: hsCRP + age + race/ethnicity + (hsCRP x race/ethnicity interaction); Model 2: (Model 1) + SES + lifestyle factors; Model 3: (Model 2) + WC. hsCRP, C-reactive protein; hsCRP x race/ethnicity, interaction between hsCRP and race/ethnicity; WC, waist circumference; SES, socio-economic status; ln(LDL-C), natural log of low-density lipoprotein cholesterol. *p < 0.05 and **p < 0.001. (PDF 565 kb

    Additional file 1: Figure S1. of Association between ethnicity and obesity with high-density lipoprotein (HDL) function and subclass distribution

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    Paraoxonase protein expression in white and black women. Isolated HDL (a–c) and serum (d–f) from each participant was randomly loaded and run on reducing 12.5 % SDS-PAGE gels and transferred to nitrocellulose membrane. Ponceau S staining was used to confirm equal loading. Blots were probed with mouse anti-PON-1 antibody. WN = White normal-weight. WO = White obese. BN = Black normal weight. BO = Black obese. Figure S2. PAF-AH protein expression in white and black women. Isolated HDL (a–c) and serum (d–f) from each participant was randomly loaded and run on reducing 12.5 % SDS-PAGE gels and transferred to nitrocellulose membrane. Ponceau S staining was used to confirm equal loading. Blots were probed with rabbit anti-PAF-AH antibody. WN = White normal-weight. WO = White obese. BN = Black normal weight. BO = Black obese. Figure S3. Vascular Cell Adhesion Molecule (VCAM) expression in endothelial cells treated with HDL. HUVEC cells were treated overnight with 10 μg/ml subject HDL. Cells were exposed to 20 ng/ml tumour necrosis factor (TNF) for 8 h. Cell lysates were harvested and stored in RNAprotect reagent prior to RNA extraction, followed by cDNA synthesis and quantitative real time PCR. Results are presented relative to a no-HDL treatment control. Results are means of 3 independent experiments ± SEM. Figure S4. Antioxidant capacity of isolated HDL. Isolated subject HDL was diluted in phosphate buffer and measured using the Oxygen Radical Absorbance Capacity (ORAC) assay. (PDF 403 kb
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