Chiu, Yen-Ling Shu, Kai-Hsiang Yang, Feng-Jung Chou, Tzu-Ying Chen, Ping-Min Lay, Fang-Yun Pan, Szu-Yu Lin, Cheng-Jui Litjens, Nicolle Betjes, Michiel Bermudez, Selma Kao, Kung-Chi Chia, Jean-San Wang, George Peng, Yu-Sen Chuang, Yi-Fang Additional file 1: of A comprehensive characterization of aggravated aging-related changes in T lymphocytes and monocytes in end-stage renal disease: the iESRD study Table S1. Relationships between dialysis vintage and immune cell subsets using tertiles of dialysis vintage, least squares regression and robust regression. Table S2. Numbers of age-related immune cells correlate with cardiovascular risk factors and systemic inflammation in ESRD patients. Table S3. Comparisons of circulatory T cell and monocyte subset cell numbers between ESRD patients with and without diabetes. Table S4. End-stage renal disease patients with concurrent coronary artery disease or cardiovascular disease display more immunosenescence. Table S5. Logistic regression model for coronary artery disease and cardiovascular disease using subset percentage to characterize the combinatorial immunophenotype. Figure S1. Representative staining of lymphocytes and monocytes. Figure S2. Correlogram of immune cell subsets among healthy donors and ESRD patients. (DOCX 1447 kb) Immunosenescence;Aging;CVD;Inflammation;ESRD 2018-11-08
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