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Effects of Intensive Blood Pressure Control in Patients with and without Albuminuria: Post Hoc Analyses from SPRINT.
Chang, Alex R; Kramer, Holly; Wei, Guo; Boucher, Robert; Grams, Morgan E; Berlowitz, Dan; Bhatt, Udayan; Cohen, Debbie L; Drawz, Paul; Punzi, Henry; Freedman, Barry I; Haley, William; Hawfield, Amret; Horwitz, Edward; McLouth, Christopher; Morisky, Don; Papademetriou, Vasilios; Rocco, Michael V; Wall, Barry; Weiner, Daniel E; Zias, Athena; Beddhu, Srinivasan.
Afiliação
  • Chang AR; Kidney Health Research Institute, Department of Population Health Sciences, Geisinger Health System, Danville, Pennsylvania.
  • Kramer H; Division of Nephrology, Loyola University Medical Center, Maywood, Illinois.
  • Wei G; Division of Nephrology & Hypertension, University of Utah School of Medicine, Salt Lake City, Utah.
  • Boucher R; Division of Nephrology & Hypertension, University of Utah School of Medicine, Salt Lake City, Utah.
  • Grams ME; Division of Nephrology, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Berlowitz D; Department of Public Health, University of Massachusetts-Lowell, Lowell, Massachusetts.
  • Bhatt U; Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio.
  • Cohen DL; Renal Division, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Drawz P; Division of Renal Diseases and Hypertension, University of Minnesota, Minneapolis, Minnesota.
  • Punzi H; Punzi Medical Center, Trinity Hypertension and Metabolic Research Institute, Carollton, Texas.
  • Freedman BI; Section on Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Haley W; Division of Nephrology, Mayo Clinic, Jacksonville, Florida.
  • Hawfield A; Section on Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Horwitz E; Division of Nephrology, MetroHealth Medical Center, Cleveland, Ohio.
  • McLouth C; Division of Public Health Sciences, Department of Biostatistics and Data Science, Wake Forest Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Morisky D; Department of Community Health Sciences, University of California, Los Angeles Fielding School of Public Health, Los Angeles, California.
  • Papademetriou V; Department of Cardiology, Veterans Affairs Medical Center, Georgetown University, Washington, DC.
  • Rocco MV; Section on Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Wall B; Division of Nephrology, Veterans Affairs Medical Center, Memphis, Tennessee.
  • Weiner DE; Division of Nephrology, Tufts Medical Center, Boston, Massachusetts.
  • Zias A; Stony Brook University School of Medicine, Stony Brook, New York.
  • Beddhu S; Division of Nephrology & Hypertension, University of Utah School of Medicine, Salt Lake City, Utah.
Clin J Am Soc Nephrol ; 15(8): 1121-1128, 2020 08 07.
Article em En | MEDLINE | ID: mdl-32669306
ABSTRACT
BACKGROUND AND

OBJECTIVES:

It is unclear whether the presence of albuminuria modifies the effects of intensive systolic BP control on risk of eGFR decline, cardiovascular events, or mortality. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS The Systolic Blood Pressure Intervention Trial randomized nondiabetic adults ≥50 years of age at high cardiovascular risk to a systolic BP target of <120 or <140 mm Hg, measured by automated office BP. We compared the absolute risk differences and hazard ratios of ≥40% eGFR decline, the Systolic Blood Pressure Intervention Trial primary cardiovascular composite outcome, and all-cause death in those with or without baseline albuminuria (urine albumin-creatinine ratio ≥30 mg/g).

RESULTS:

Over a median follow-up of 3.1 years, 69 of 1723 (4%) participants with baseline albuminuria developed ≥40% eGFR decline compared with 61 of 7162 (1%) participants without albuminuria. Incidence rates of ≥40% eGFR decline were higher in participants with albuminuria (intensive, 1.74 per 100 person-years; standard, 1.17 per 100 person-years) than in participants without albuminuria (intensive, 0.48 per 100 person-years; standard, 0.11 per 100 person-years). Although effects of intensive BP lowering on ≥40% eGFR decline varied by albuminuria on the relative scale (hazard ratio, 1.48; 95% confidence interval, 0.91 to 2.39 for albumin-creatinine ratio ≥30 mg/g; hazard ratio, 4.55; 95% confidence interval, 2.37 to 8.75 for albumin-creatinine ratio <30 mg/g; P value for interaction <0.001), the absolute increase in ≥40% eGFR decline did not differ by baseline albuminuria (incidence difference, 0.38 events per 100 person-years for albumin-creatinine ratio ≥30 mg/g; incidence difference, 0.58 events per 100 person-years for albumin-creatinine ratio <30 mg/g; P value for interaction =0.60). Albuminuria did not significantly modify the beneficial effects of intensive systolic BP lowering on cardiovascular events or mortality evaluated on relative or absolute scales.

CONCLUSIONS:

Albuminuria did not modify the absolute benefits and risks of intensive systolic BP lowering.
Assuntos
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pressão Sanguínea / Albuminúria / Taxa de Filtração Glomerular / Hipertensão / Rim / Nefropatias / Anti-Hipertensivos Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pressão Sanguínea / Albuminúria / Taxa de Filtração Glomerular / Hipertensão / Rim / Nefropatias / Anti-Hipertensivos Idioma: En Ano de publicação: 2020 Tipo de documento: Article