Visualization and Quantification of the Association Between Breast Cancer and Cholesterol in the All of Us Research Program

被引:3
作者
Feng, Jianglin [1 ]
Astiazaran-Symonds, Esteban [2 ]
Karnes, Jason H. [1 ,3 ,4 ]
机构
[1] Univ Arizona, Coll Pharm, Dept Pharm Practice & Sci, Tucson, AZ USA
[2] Univ Arizona, Coll Med Tucson, Dept Med, Tucson, AZ USA
[3] Vanderbilt Univ, Dept Biomed Informat, Med Ctr, Nashville, TN USA
[4] Univ Arizona, Dept Pharm Practice & Sci, Coll Pharm, 1295 N Martin Ave, Tucson, AZ 85721 USA
基金
美国国家卫生研究院;
关键词
Breast cancer; total cholesterol; low-density lipoprotein cholesterol; high-density lipoprotein cholesterol; triglycerides; antihyperlipidemic treatment; electronic medical records; BODY-MASS INDEX; RISK; BIOMARKERS; LIPIDS;
D O I
10.1177/11769351221144132
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidemiologic evidence for the association of cholesterol and breast cancer is inconsistent. Several factors may contribute to this inconsistency, including limited sample sizes, confounding effects of antihyperlipidemic treatment, age, and body mass index, and the assumption that the association follows a simple linear function. Here, we aimed to address these factors by combining visualization and quantification a large-scale contemporary electronic health record database (the All of Us Research Program). We find clear visual and quantitative evidence that breast cancer is strongly, positively, and near-linearly associated with total cholesterol and low-density lipoprotein cholesterol, but not associated with triglycerides. The association of breast cancer with high-density lipoprotein cholesterol was non-linear and age dependent. Standardized odds ratios were 2.12 (95% confidence interval 1.9-2.48), P = 5.6 x 10(-31) for total cholesterol; 1.99 (1.75-2.26), P = 2.6 x 10(-26) for low-density lipoprotein cholesterol; 1.69 (1.3-2.2), P = 9.0 x 10(-5) for high-density lipoprotein cholesterol at age < 56; and 0.65 (0.55-0.78), P = 1.2 x 10(-6) for high-density lipoprotein cholesterol at age > 56. The inclusion of the lipid levels measured after antihyperlipidemic treatment in the analysis results in erroneous associations. We demonstrate that the use of the logistic regression without inspecting risk variable linearity and accounting for confounding effects may lead to inconsistent results.
引用
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页数:10
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