ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2022 and some content may be unavailable. To unlock all content for 2022, please visit the archives.

Abstract: FR-PO737

Influence of Baseline Diastolic Blood Pressure (DBP) on the Effects of BP Lowering on All-Cause Mortality: A Meta-Analysis of NIH BP Trials

Session Information

Category: Hypertension and CVD

  • 1502 Hypertension and CVD: Clinical‚ Outcomes‚ and Trials

Authors

  • Sarwal, Amara, University of Utah Health, Salt Lake City, Utah, United States
  • Boucher, Robert E., University of Utah Health, Salt Lake City, Utah, United States
  • Hartsell, Sydney Elizabeth, University of Utah Health, Salt Lake City, Utah, United States
  • Wei, Guo, University of Utah Health, Salt Lake City, Utah, United States
  • Ye, Xiangyang, University of Utah Health, Salt Lake City, Utah, United States
  • Shen, Jincheng, University of Utah Health, Salt Lake City, Utah, United States
  • Chertow, Glenn, Stanford University School of Medicine, Stanford, California, United States
  • Whelton, Paul K., Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States
  • Cheung, Alfred K., University of Utah Health, Salt Lake City, Utah, United States
  • Greene, Tom, University of Utah Health, Salt Lake City, Utah, United States
  • Beddhu, Srinivasan, University of Utah Health, Salt Lake City, Utah, United States
Background

Lowering systolic BP (SBP) in persons with low DBP might affect tissue perfusion and thereby, increase risk for mortality.

Methods

We conducted a meta-analysis of 5 large NIH BP trials that examined the effects of BP goals on ACM outcomes; SPRINT (N = 9264, SBP goal < 120 vs. < 140 mmHg), ACCORD BP standard glycemia arm (N = 2361, SBP goal < 120 vs. < 140 mmHg), SSPS3 ( N= 3008, SBP goal < 130 vs. < 140 mmHg), MDRD (N=838, SBP goal ≤125 with MAP ≤92 vs SBP ≤ 140 with MAP≤ 107 mmHg) and AASK (N =1094, goal MAP < 92 mmHg vs. 102-107 mmHg). We used DerSimonian-Laird random-effects model in Stata 15.1 version to conduct meta-analyses of the interaction between baseline DBP and the BP intervention on mortality outcomes.

Results

Mean baseline DBP in SPRINT, ACCORD BP, SPS-3, MDRD and AASK were 78 ± 12, 76 ± 10, 78 ± 11, 82 ± 11, and 96 ± 14 mmHg, respectively with evidence of heterogeneity. In the 16,565 participants included in the analysis, there were a total of 989 mortality events over 65,656 total years of follow-up. Intensive BP control resulted in overall lower hazard ratio of ACM events, (HR 0.86, CI 0.75, 0.99) (Table). Lower baseline DBP was associated with increased risk of mortality events (HR 1.19, CI 1.09, 1.30) (Table). The interaction term of baseline DBP and the BP intervention on ACM was non-significant in each of the studies and overall (Figure).

Conclusion

In this meta-analysis of large, multicenter NIH funded trials, BP intervention was beneficial for improving ACM rates, but there was no evidence that these beneficial effects were modified by baseline DBP.

Effects of BP intervention on and the associations of baseline DBP with ACM
 Intensive vs Standard BP (HR, CI)HR per 10 mmHg ↓ in baseline DBP (HR, CI)
SPRINT0.81 (0.68, 0.96)1.24 (1.14, 1.34)
ACCORD-BP0.83 (0.60, 1.16)1.39 (1.18,1.64)
SPS31.02 (0.77, 1.33)1.11 (0.97, 1.27)
MDRD1.40(0.70, 2.78)1.25 (0.92, 1.71)
AASK0.74 (0.50,1.10)1.07 (0.93, 1.23)
Overall0.86 (0.75,0.99)1.19 (1.09, 1.30)

Funding

  • NIDDK Support