Evidence map›Paper›PMID 38735283›Full record

Trial reportAmerican journal of nephrology2024

The Role of Angiopoietins in Cardiovascular Outcomes of Kidney Transplant Recipients: An Ancillary Study from the FAVORIT.

Natalie Gendy, Liam Brown, Mary Kate Staunton, Kanika Garg, Nora Hernandez Garcilazo, Long Qian, Yu Yamamoto, Ugochukwu Ugwuowo, Wassim Obeid, Lama Al-Qusairi and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Natalie GendyClinical and Translational Research Accelerator, New Haven, Connecticut, USA, natalie.gendy01@gmail.com.
Liam BrownClinical and Translational Research Accelerator, New Haven, Connecticut, USA.
Mary Kate StauntonClinical and Translational Research Accelerator, New Haven, Connecticut, USA.
Kanika GargClinical and Translational Research Accelerator, New Haven, Connecticut, USA.
Nora Hernandez GarcilazoSection of Nephrology, Yale New Haven Hospital, New Haven, Connecticut, USA.
Long QianSection of Nephrology, Yale New Haven Hospital, New Haven, Connecticut, USA.
Yu YamamotoClinical and Translational Research Accelerator, New Haven, Connecticut, USA.
Ugochukwu UgwuowoClinical and Translational Research Accelerator, New Haven, Connecticut, USA.
Wassim ObeidJohns Hopkins University, Baltimore, Maryland, USA.
Lama Al-QusairiJohns Hopkins University, Baltimore, Maryland, USA.
Andrew BostomDepartment of Family Medicine, Brown University, Providence, Rhode Island, USA.
Sherry G MansourClinical and Translational Research Accelerator, New Haven, Connecticut, USA.

Funding

Evaluation of Angiopoietins as Prognostic Markers of Kidney Allograft Structure and FunctionK23DK127154 · NIDDK · YALE UNIVERSITY · PI MANSOUR, SHERRY GEORGE · 2021 to 2025
$1.0M
NIDDK NIH HHS K23 DK127154
6 · The paper itself

Abstract

introductionKidney 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.

methodsThis 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.

resultsParticipants' 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.

conclusionAngpt-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.

Indexed as

Angiopoietin-1Angiopoietin-2BiomarkersCardiovascular DiseasesKidney TransplantationAdultFemaleHumansKidney Failure, ChronicMaleMiddle AgedTransplant RecipientsAngiopoietin-1Angiopoietin-2ANGPT1 protein, humanANGPT2 protein, humanBiomarkersAngiopoietin-1Angiopoietin-2Cardiovascular diseaseDeceased donor kidney transplantGraft failureMortality

Identifiers

PMID38735283
PMCPMC11444892

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.