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A meta-analysis of randomized controlled clinical trials for implications of acute treatment effects on glomerular filtration rate for long-term kidney protection.
Heerspink, Hiddo J L; Eddington, Devin; Chaudhari, Juhi; Estacio, Raymond; Imai, Enyu; Goicoechea, Marian; Hannedouche, Thierry; Haynes, Richard; Jafar, Tazeen H; Johnson, David W; van Kruijsdijk, Rob C M; Lewis, Julia B; Li, Philip K T; Neuen, Brendon L; Perrone, Ronald D; Ruggenenti, Piero; Wanner, Christoph; Woodward, Mark; Xie, Di; Greene, Tom; Inker, Lesley A.
Afiliación
  • Heerspink HJL; Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Eddington D; Population Health Sciences, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Chaudhari J; Division of Nephrology, Tufts Medical Center, Boston, Massachusetts, USA.
  • Estacio R; Department of Medicine, University of Colorado, Colorado, USA.
  • Imai E; Nakayamadera Imai Clinic, Takarazuka, Japan.
  • Goicoechea M; Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Hannedouche T; Service de Néphrologie, Hôpitaux Universitaires de Strasbourg, Faculté de Médecine, Strasbourg, France.
  • Haynes R; Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.
  • Jafar TH; Program in Health Services and Systems Research, Duke-NUS Medical School, Singapore.
  • Johnson DW; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • van Kruijsdijk RCM; Department of Nephrology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Lewis JB; Division of Nephrology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Li PKT; Division of Nephrology, Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, Hong Kong.
  • Neuen BL; The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Perrone RD; Division of Nephrology, Tufts Medical Center, Boston, Massachusetts, USA.
  • Ruggenenti P; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy; Unit of Nephrology, Azienda Ospedaliera Ospedale Papa Giovanni XXIII, Bergamo, Italy.
  • Wanner C; Department of Clinical Research and Epidemiology, Renal Research Unit, Comprehensive Heart Failure Center, University of Würzburg, Würzburg, Germany.
  • Woodward M; The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia; The George Institute for Global Health, School of Public Health, Imperial College London, London, UK.
  • Xie D; Division of Nephrology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Greene T; Population Health Sciences, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Inker LA; Division of Nephrology, Tufts Medical Center, Boston, Massachusetts, USA. Electronic address: lesley.inker@tuftsmedicine.org.
Kidney Int ; 2024 Jun 18.
Article en En | MEDLINE | ID: mdl-38901604
ABSTRACT
Pharmacologic interventions to slow chronic kidney disease progression, such as ACE-inhibitors, angiotensin receptor blockers, or sodium glucose co-transporter 2 inhibitors, often produce acute treatment effects on glomerular filtration rate (GFR) that differ from their long-term chronic treatment effects. Observational studies assessing the implications of acute effects cannot distinguish acute effects from GFR changes unrelated to the treatment. Here, we performed meta-regression analysis of multiple trials to isolate acute effects to determine their long-term implications. In 64 randomized controlled trials (RCTs), enrolling 154,045 participants, we estimated acute effects as the mean between-group difference in GFR slope from baseline to three months, effects on chronic GFR slope (starting at three months after randomization), and effects on three composite kidney endpoints defined by kidney failure (GFR 15 ml/min/1.73m2 or less, chronic dialysis, or kidney transplantation) or sustained GFR declines of 30%, 40% or 57% decline, respectively. We used Bayesian meta-regression to relate acute effects with treatment effects on chronic slope and the composite kidney endpoints. Overall, acute effects were not associated with treatment effects on chronic slope. Acute effects were associated with the treatment effects on composite kidney outcomes such that larger negative acute effects were associated with lesser beneficial effects on the composite kidney endpoints. Associations were stronger when the kidney composite endpoints were defined by smaller thresholds of GFR decline (30% or 40%). Results were similar in a subgroup of interventions with supposedly hemodynamic effects that acutely reduce GFR. For studies with GFR 60 mL/min/1.73m2 or under, negative acute effects were associated with larger beneficial effects on chronic GFR slope. Thus, our data from a large and diverse set of RCTs suggests that acute effects of interventions may influence the treatment effect on clinical kidney outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Kidney Int Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Kidney Int Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos