High blood pressure (BP) is prevalent in patients with type 2 diabetes (T2D). This post hoc analysis evaluated major adverse cardiovascular (CV) events (MACE) and renal events in patients from LEADER and SUSTAIN 6 (CV outcome trials) with T2D and high CV risk who received liraglutide or semaglutide (vs placebo) according to BP categories: normal ( < 120/80 mmHg), elevated (systolic 120-129 mmHg and diastolic < 80 mmHg), stage 1 hypertension (systolic 130-139 mmHg or diastolic 80-89 mmHg), and stage 2 hypertension (systolic 140 mmHg or diastolic 90 mmHg). LEADER and SUSTAIN 6 were global randomized CV outcome trials of liraglutide and semaglutide, vs placebo, in 9340 and 3297 patients, respectively, with T2D and high CV risk. Primary outcome was MACE (CV death, non-fatal myocardial infarction, or non-fatal stroke), with secondary outcomes including nephropathy. We evaluated the cardiorenal effect of liraglutide and semaglutide on the primary and secondary renal endpoints by baseline BP categories using Cox proportional hazards, with treatment and risk group as factors, adjusted for baseline characteristics related to cardiorenal risk. In LEADER, 15%, 14%, 30%, and 41% of patients had normal BP, elevated BP, stage 1 or stage 2 hypertension, respectively; proportions for SUSTAIN 6 were 13%, 13%, 31%, and 43%, respectively. Within each BP category, baseline demographics were generally well balanced across trial groups. The effects of liraglutide and semaglutide on MACE and secondary nephropathy endpoints across BP categories are shown in the Figure. Liraglutide and semaglutide demonstrated consistent improvements in CV and renal outcomes across most baseline BP categories.
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