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. 2019 Jun 24;40(33):2813–2824. doi: 10.1093/eurheartj/ehz402

Figure 1.

Figure 1

Risk of all-cause, cardiovascular, dementia-associated, and cancer mortality as a function of APOE genotype. Cox regression models were adjusted for age (time scale), body mass index, smoking, hypertension, diabetes, lipid-lowering therapy, alcohol consumption, physical inactivity, education, postmenopausal status, hormonal replacement therapy, LDL cholesterol, HDL cholesterol, and plasma triglycerides. APOE, APOE ɛ2/ɛ3/ɛ4 genotype; CI, confidence interval.