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Effects of Semaglutide on Albuminuria and Kidney Function in People With Overweight or Obesity With or Without Type 2 Diabetes: Exploratory Analysis From the STEP 1, 2, and 3 Trials.
Heerspink, Hiddo J L; Apperloo, Ellen; Davies, Melanie; Dicker, Dror; Kandler, Kristian; Rosenstock, Julio; Sørrig, Rasmus; Lawson, Jack; Zeuthen, Niels; Cherney, David.
Afiliação
  • Heerspink HJL; Department of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, the Netherlands.
  • Apperloo E; Department of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, the Netherlands.
  • Davies M; Diabetes Research Centre, University of Leicester, Leicester, U.K.
  • Dicker D; Leicester Diabetes Centre, University Hospitals of Leicester NHS Trust, Leicester, U.K.
  • Kandler K; NIHR Leicester Biomedical Research Centre, Leicester, U.K.
  • Rosenstock J; Internal Medicine D, Hasharon Hospital-Rabin Medical Center, Petach-Tikva, Israel.
  • Sørrig R; Sackler School of Medicine, Tel Aviv University, Tel-Aviv, Israel.
  • Lawson J; Medical & Science, Novo Nordisk A/S, Søborg, Denmark.
  • Zeuthen N; Velocity Clinical Research at Medical City, Dallas, TX.
  • Cherney D; Global Medical Affairs, Novo Nordisk A/S, Søborg, Denmark.
Diabetes Care ; 46(4): 801-810, 2023 04 01.
Article em En | MEDLINE | ID: mdl-36801984
ABSTRACT

OBJECTIVE:

These post hoc analyses of the Semaglutide Treatment Effect in People with obesity (STEP) 1-3 trials (NCT03548935, NCT03552757, and NCT03611582) explored the effects of semaglutide (up to 2.4 mg) on kidney function. RESEARCH DESIGN AND

METHODS:

STEP 1-3 included adults with overweight/obesity; STEP 2 patients also had type 2 diabetes. Participants received once-weekly subcutaneous semaglutide 1.0 mg (STEP 2 only), 2.4 mg, or placebo for 68 weeks, plus lifestyle intervention (STEP 1 and 2) or intensive behavioral therapy (STEP 3). Changes in urine albumin-to-creatinine ratio (UACR) and UACR status from baseline to week 68 were assessed for STEP 2. Changes in estimated glomerular filtration rate (eGFR) were assessed from pooled STEP 1-3 data.

RESULTS:

In STEP 2, 1,205 (99.6% total cohort) patients had UACR data; geometric mean baseline UACR was 13.7, 12.5, and 13.2 mg/g with semaglutide 1.0 mg, 2.4 mg, and placebo, respectively. At week 68, UACR changes were -14.8% and -20.6% with semaglutide 1.0 mg and 2.4 mg, respectively, and +18.3% with placebo (between-group differences [95% CI] vs. placebo -28.0% [-37.3, -17.3], P < 0.0001 for semaglutide 1.0 mg; -32.9% [-41.6, -23.0], P = 0.003 for semaglutide 2.4 mg). UACR status improved in greater proportions of patients with semaglutide 1.0 mg and 2.4 mg versus placebo (P = 0.0004 and P = 0.0014, respectively). In the pooled STEP 1-3 analyses, 3,379 participants had eGFR data; there was no difference between semaglutide 2.4 mg and placebo in eGFR trajectories at week 68.

CONCLUSIONS:

Semaglutide improved UACR in adults with overweight/obesity and type 2 diabetes. In participants with normal kidney function, semaglutide did not have an effect on eGFR decline.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article