Why the study?
Does the distribution of achieved systolic blood pressure response explain the discordant clinical outcomes between intensive and standard blood pressure treatment in the SPRINT and ACCORD trials?
Does the distribution of achieved systolic blood pressure response explain the discordant clinical outcomes between intensive and standard blood pressure treatment in the SPRINT and ACCORD trials?
The discordant clinical results between the SPRINT and ACCORD trials may be partially explained by a greater between-group overlap in achieved systolic blood pressure in ACCORD.
May explain SPRINT-ACCORD outcome discordance; leaves open whether achieved SBP overlap affects intensive BP control efficacy.
Background SPRINT (Systolic Blood Pressure Intervention Trial) and the ACCORD (Action to Control Cardiovascular Risk in Diabetes) blood pressure trial used similar interventions but produced discordant results. We investigated whether differences in systolic blood pressure ( SBP ) response contributed to the discordant trial results. Methods and Results We evaluated the distributions of SBP response during the first year for the intensive and standard treatment groups of SPRINT and ACCORD using growth mixture models. We assessed whether significant differences existed between trials in the distributions of SBP achieved at 1 year and the treatment‐independent relationships of achieved SBP with risks of primary outcomes defined in each trial, heart failure, stroke, and all‐cause death. We examined whether visit‐to‐visit variability was associated with heterogeneous treatment effects. Among the included 9027 SPRINT and 4575 ACCORD participants, the difference in mean SBP achieved between treatment groups was 15.7 mm Hg in SPRINT and 14.2 mm Hg in ACCORD , but SPRINT had significantly less between‐group overlap in the achieved SBP (standard deviations of intensive and standard groups, respectively: 6.7 and 5.9 mm Hg in SPRINT versus 8.8 and 8.2 mm Hg in ACCORD ; P <0.001). The relationship between achieved SBP and outcomes was consistent across trials except for stroke and all‐cause death. Higher visit‐to‐visit variability was more common in SPRINT but without treatment‐effect heterogeneity. Conclusions SPRINT and ACCORD had different degrees of separation in achieved SBP between treatment groups, even as they had similar mean differences. The greater between‐group overlap of achieved SBP may have contributed to the discordant trial results.
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Huang et al. (2017) studied this question.
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