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The Role of Angiopoietins in Cardiovascular Outcomes of Kidney Transplant Recipients: An Ancillary Study from the FAVORIT.
Gendy, Natalie; Brown, Liam; Staunton, Mary Kate; Garg, Kanika; Hernandez Garcilazo, Nora; Qian, Long; Yamamoto, Yu; Ugwuowo, Ugochukwu; Obeid, Wassim; Al-Qusairi, Lama; Bostom, Andrew; Mansour, Sherry G.
Afiliação
  • Gendy N; Clinical and Translational Research Accelerator, New Haven, Connecticut, USA, natalie.gendy01@gmail.com.
  • Brown L; Schulich School of Medicine, Western University, London, Ontario, Canada, natalie.gendy01@gmail.com.
  • Staunton MK; Clinical and Translational Research Accelerator, New Haven, Connecticut, USA.
  • Garg K; Clinical and Translational Research Accelerator, New Haven, Connecticut, USA.
  • Hernandez Garcilazo N; Clinical and Translational Research Accelerator, New Haven, Connecticut, USA.
  • Qian L; Section of Nephrology, Yale New Haven Hospital, New Haven, Connecticut, USA.
  • Yamamoto Y; Section of Nephrology, Yale New Haven Hospital, New Haven, Connecticut, USA.
  • Ugwuowo U; Clinical and Translational Research Accelerator, New Haven, Connecticut, USA.
  • Obeid W; Clinical and Translational Research Accelerator, New Haven, Connecticut, USA.
  • Al-Qusairi L; Johns Hopkins University, Baltimore, Maryland, USA.
  • Bostom A; Johns Hopkins University, Baltimore, Maryland, USA.
  • Mansour SG; Department of Family Medicine, Brown University, Providence, Rhode Island, USA.
Am J Nephrol ; : 1-10, 2024 Jul 17.
Article em En | MEDLINE | ID: mdl-38735283
ABSTRACT

INTRODUCTION:

Kidney transplant recipients (KTRs) have increased risk of cardiovascular disease (CVD) mortality. We investigated vascular biomarkers, angiopoietin-1, and angiopoietin-2 (angpt-1, -2), in CVD development in KTRs.

METHODS:

This ancillary study from the FAVORIT evaluates the associations of baseline plasma angpt-1, -2 levels in CVD development (primary outcome) and graft failure (GF) and death (secondary outcomes) in 2000 deceased donor KTRs. We used Cox regression to analyze the association of biomarker quartiles with outcomes. We adjusted for demographic; CVD- and transplant-related variables; medications; urine albumin-to-creatinine ratio; and randomization status. We calculated areas under the curves (AUCs) to predict CVD or death, and GF or death by incorporating biomarkers alongside clinical variables.

RESULTS:

Participants' median age was 52 IQR [45, 59] years with 37% women and 73% identifying as white. Median time from transplantation was 3.99 IQR [1.58, 7.93] years and to CVD development was 2.54 IQR [1.11-3.80] years. Quartiles of angpt-1 were not associated with outcomes. Whereas higher levels of angpt-2 (quartile 4) were associated with about 2 times the risk of CVD, GF, and death (aHR 1.85 [1.25-2.73], p < 0.01; 2.24 [1.36-3.70)], p < 0.01; 2.30 [1.48-3.58], p < 0.01, respectively) as compared to quartile 1. Adding angiopoietins to preexisting clinical variables improved prediction of CVD or death (AUC improved from 0.70 to 0.72, p = 0.005) and GF or death (AUC improved from 0.68 to 0.70, p = 0.005). Angpt-2 may partially explain the increased risk of future CVD in KTRs. Further research is needed to assess the utility of using angiopoietins in the clinical care of KTRs.

CONCLUSION:

Angpt-2 may be a useful prognostic tool for future CVD in KTRs. Combining angiopoietins with clinical markers may tailor follow-up to mitigate CVD risk.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article