Baseline Diastolic Blood Pressure and Cardiovascular Outcomes in SPRINT Participants with Chronic Kidney Disease

被引:5
作者
Chang, Tara, I [1 ]
Wei, Guo [2 ,3 ,4 ]
Boucher, Robert [2 ]
Kramer, Holly [5 ,6 ]
Chertow, Glenn M. [1 ]
Cheung, Alfred K. [2 ,7 ]
Greene, Tom [3 ,4 ]
Whelton, Paul K. [8 ]
Beddhu, Srinivasan [2 ,7 ]
机构
[1] Stanford Univ, Div Nephrol, Palo Alto, CA 94304 USA
[2] Univ Utah, Div Nephrol & Hypertens, Sch Med, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Populat Hlth Sci, Div Biostat, Sch Med, Salt Lake City, UT 84112 USA
[4] Univ Utah, Dept Internal Med, Div Biostat, Sch Med, Salt Lake City, UT 84112 USA
[5] Loyola Univ Chicago, Dept Publ Hlth Sci, Stritch Sch Med, Maywood, IL USA
[6] Hines Vet Affairs Med Ctr, Med Serv, Hines, IL USA
[7] Vet Affairs Salt Lake City Hlth Care Syst, Med Serv, Salt Lake City, UT USA
[8] Tulane Univ, Dept Epidemiol, Sch Publ Hlth & Trop Med, New Orleans, LA 70118 USA
来源
KIDNEY360 | 2020年 / 1卷 / 05期
基金
美国国家卫生研究院;
关键词
Hypertension; Blood Pressure; Cause of Death; Randomized Controlled Trials; Renal Insufficiency; Chronic; SPRINT; HYPERTENSIVE PATIENTS; TRIAL;
D O I
10.34067/KID.0000982019
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background We sought to determine whether intensive systolic BP (SBP) lowering was harmful in Systolic Blood Pressure Intervention Trial (SPRINT) participants with CKD (eGFR,60 ml/min per 1.73 m(2)) and lower baseline diastolic BP (DBP). Methods We related baseline DBP with the SPRINT primary composite end point (myocardial infarction, acute coronary syndrome, stroke, acute decompensated heart failure, or cardiovascular death) and all-cause death. We examined the effect of intensive SBP lowering on these outcomes across the range of baseline DBPs using Cox regression with treatment by baseline DBP interaction terms. Results Among 2646 SPRINT participants with CKD, lower baseline DBP was associated with a higher adjusted hazard of the primary composite end point and all-cause death. For example, participants with baseline DBP of 61 mm Hg (mean baseline DBP in the lowest tertile) experienced a 37% (95% CI, 7% to 75%) higher hazard of the primary outcome relative to participants with baseline DBP of 75 mm Hg (mean baseline DBP for overall). The benefit of intensive SBP lowering was consistent across a range of baseline DBPs on rates of the primary composite end point (linear interaction P value =0.56) and all-cause death (linear interaction P value = 0.20). Conclusions Among SPRINT participants with baseline CKD, lower DBP was associated with higher rates of the primary composite end point and all-cause death. However, DBP did not seem to modify the benefit of intensive SBP lowering on the primary composite end point or all-cause death. Our results suggest that lower DBP should not necessarily impede more intensive SBP lowering in patients with mild to moderate CKD.
引用
收藏
页码:368 / 375
页数:8
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