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Kidney and heart failure events are bidirectionally associated in patients with type 2 diabetes and cardiovascular disease.
Sharma, Abhinav; Inzucchi, Silvio E; Testani, Jeffrey M; Ofstad, Anne Pernille; Fitchett, David; Mattheus, Michaela; Verma, Subodh; Zannad, Faiez; Wanner, Christoph; Kraus, Bettina J.
Afiliação
  • Sharma A; Division of Cardiology, McGill University Health Centre, Montreal, Quebec, Canada.
  • Inzucchi SE; Yale University School of Medicine, New Haven, CT, USA.
  • Testani JM; Yale University School of Medicine, New Haven, CT, USA.
  • Ofstad AP; Boehringer Ingelheim Norway KS, Asker, Norway.
  • Fitchett D; Oslo Diabetes Research Center, Oslo, Norway.
  • Mattheus M; St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Verma S; Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany.
  • Zannad F; St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Wanner C; Université de Lorraine, INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Nancy, France.
  • Kraus BJ; INSERM 1116, CHRU de Nancy, FCRIN INI-CRCT, Nancy, France.
ESC Heart Fail ; 11(2): 737-747, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38155446
ABSTRACT

AIMS:

This study aimed to evaluate the bidirectional relationship between kidney and cardiovascular (CV) events in trial participants with type 2 diabetes and CV disease. METHODS AND

RESULTS:

Post hoc analyses of EMPA-REG OUTCOME using Cox regression models were performed to assess the association of baseline factors with risk of a kidney event and bidirectional associations of incident kidney events and CV events. Among placebo-treated participants, baseline factors significantly associated with greater kidney event risk included lower baseline estimated glomerular filtration rate, albuminuria, higher uric acid, low-density lipoprotein cholesterol levels, and prior heart failure (HF). Coronary artery disease was not associated with increased risk. In placebo-treated participants, occurrence of an incident non-fatal kidney event increased the subsequent risk of hospitalization for HF (HHF) but not 3-point major adverse CV events (non-fatal stroke, non-fatal myocardial infarction, and CV death). Vice versa, HHF (but not myocardial infarction/stroke) increased the risk of subsequent kidney events. These associations were generally also seen in empagliflozin-treated participants and in the overall population. Interestingly, the risk of kidney events following HHF was not significantly increased in the relatively small number of placebo-treated participants already diagnosed with HF at baseline.

CONCLUSIONS:

These findings demonstrate a bidirectional inter-relationship between HHF and kidney events. Further exploration of this relationship and strategies to optimize the use of therapies to reduce both kidney and HF outcomes is warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Acidente Vascular Cerebral / Diabetes Mellitus Tipo 2 / Insuficiência Cardíaca / Infarto do Miocárdio Limite: Humans Idioma: En Revista: ESC Heart Fail Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Acidente Vascular Cerebral / Diabetes Mellitus Tipo 2 / Insuficiência Cardíaca / Infarto do Miocárdio Limite: Humans Idioma: En Revista: ESC Heart Fail Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá