17 research outputs found

    Characteristics of the three samples of European-Americans and two samples of African-Americans.

    No full text
    <p>*TG units: ARIC—mmol/L; FRAM—Meq/L; MESA—mg/dL</p><p>**HDL units: ARIC—mmol/L; FRAM & MESA—mg/dL</p><p>Characteristics of the three samples of European-Americans and two samples of African-Americans.</p

    List of 31 triglyceride (TG)-associated SNPs with their respective genomic position, risk allele (TG increasing), TG effect size (weight used in GRS), association with T2D incidence, and interaction with TG phenotype in European- and African-Americans (EA, AA).

    No full text
    <p>Covariates include age, sex, BMI, TG, and HDL.</p><p>List of 31 triglyceride (TG)-associated SNPs with their respective genomic position, risk allele (TG increasing), TG effect size (weight used in GRS), association with T2D incidence, and interaction with TG phenotype in European- and African-Americans (EA, AA).</p

    Classification trees identifying profiles of participants who gained ≥3% weight between baseline and the third annual visit in participants, stratified by race (African American women versus white women).

    No full text
    <p>(* indicates that due to small sample size, odds ratio and 95% confidence interval could not be converted; CI, confidence interval; OR, odds ratio) <b><i>A</i></b>: African American women. <b><i>B</i></b>: White women.</p

    Stepwise logistic regression odds ratios of 3% or more weight gain, stratified by race (African Americans vs. whites) in participants enrolled in an ancillary study of the Women’s Health Initiative Observational Study at Baylor College of Medicine and Wake Forest School of Medicine between February 1995 and July 1998.

    No full text
    <p>CI, confidence interval; BMI, body mass index.</p><p>* In the analysis for African American women, due to scanty sample size, a lifetime partner variable was excluded.</p><p><sup>†</sup> Weight-change was assessed at the third annual visit.</p><p>** Intentional weight loss of more than 10 pounds was examined within the past 20 years, when participants were not pregnant or sick.</p><p>Stepwise logistic regression odds ratios of 3% or more weight gain, stratified by race (African Americans vs. whites) in participants enrolled in an ancillary study of the Women’s Health Initiative Observational Study at Baylor College of Medicine and Wake Forest School of Medicine between February 1995 and July 1998.</p

    N, mean age (standard deviation) and percentage of males and ApoE ε3 carriers, in the GOLDN study population by LRP-1 genotype group.

    No full text
    †<p>a = minor allele; A = major allele.</p>‡<p><i>P</i>-values were derived from tests of null hypothesis that no group is different, using a 1-way ANOVA for continuous traits or the χ<sup>2</sup> test for categorical variables.</p

    Parameter estimates from linear regression models looking at the effects of <i>LRP-1</i> I10701 SNP and <i>ApoE</i> isoforms on BMI in the GOLDN study population.

    No full text
    a<p><i>P</i>-values were derived from mixed linear models, specifying a Kenward Rogers correction on the estimator, with <i>LRP-1</i> I10701 SNP and <i>ApoE</i> genotype frequency, an interaction between ApoE and LRP-1 genotype frequency, age and age<sup>2</sup>, sex, smoking, total alcohol and center of data collection as predictors, and BMI (logarithmically transformed) as the outcome.</p
    corecore