Evidence map›Paper›PMID 35938682›Full record

ArticlePediatric transplantation2022

Malnutrition and immune cell subsets in children undergoing kidney transplantation.

Brian I Shaw, Hui-Jie Lee, Robert Ettenger, Paul Grimm, Elaine F Reed, Minnie Sarwal, Linda Stempora, Barry Warshaw, Congwen Zhao, Olivia M Martinez and 3 more

Open access · greenAbstract read
In one paragraph

Article in Pediatric transplantation, 2022. 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
0.2field-weighted citation impact, top 48% of its field
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, 1 citations in OpenAlex.

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

13 authors at 6 institutions in 1 country.

Brian I ShawDepartment of Surgery, Duke University, Durham, North Carolina, USA.ORCID 0000-0002-2317-6549
Hui-Jie LeeDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Robert EttengerDepartment of Pediatrics, University of California, Los Angeles, California, USA.ORCID 0000-0002-9973-7349
Paul GrimmDepartment of Pediatrics, Stanford University, Palo Alto, California, USA.
Elaine F ReedDepartment of Pathology, University of California, Los Angeles, California, USA.
Minnie SarwalDepartment of Surgery, University of California, San Francisco, California, USA.
Linda StemporaDepartment of Surgery, Duke University, Durham, North Carolina, USA.
Barry WarshawDepartment of Pediatrics, Children's Healthcare Atlanta, Atlanta, Georgia, USA.
Congwen ZhaoDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Olivia M MartinezDepartment of Surgery, Stanford University School of Medicine, Palo Alto, California, USA.
Nancie J MacIverDepartment of Pediatrics, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
Allan D KirkDepartment of Surgery, Duke University, Durham, North Carolina, USA.
Eileen T ChambersDepartment of Surgery, Duke University, Durham, North Carolina, USA.
Duke University · USPalo Alto University · USUniversity of California, Los Angeles · USChildren's Healthcare of Atlanta · USUniversity of California, San Francisco · USUniversity of North Carolina at Chapel Hill · US

Funding

UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ian Michael Carroll · 1999 to 2026
$31.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
Development of Transplant Strategies Uniquely Responsive to the Needs of ChildrenU01AI077821 · NIAID · EMORY UNIVERSITY · PI KIRK, ALLAN D. · 2008 to 2012
$7.5M
The Impact of Epstein Barr Virus Infection on the Immune Response in Pediatric Transplant RecipientsU01AI135947 · NIAID · STANFORD UNIVERSITY · PI MARTINEZ, OLIVIA M · 2018 to 2021
$3.6M
Leptin as a Regulator of T Cell Metabolism and FunctionK08DK087944 · NIDDK · DUKE UNIVERSITY · PI MACIVER, NANCIE · 2010 to 2014
$678k
Metabolic reprogramming to improve EGFRvIII CAR T cell persistenceR21CA253163 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MACIVER, NANCIE · 2021 to 2022
$402k
NCI NIH HHS K12 CA090625NCI NIH HHS R21 CA253163NIAID NIH HHS U01 AI077821NIAID NIH HHS U01 AI135947NIDDK NIH HHS K08 DK087944NIDDK NIH HHS P30 DK056350NIGMS NIH HHS T32 GM007171
6 · The paper itself

Abstract

backgroundMalnutrition, including obesity and undernutrition, among children is increasing in prevalence and is common among children on renal replacement therapy. The effect of malnutrition on the pre-transplant immune system and how the pediatric immune system responds to the insult of both immunosuppression and allotransplantation is unknown. We examined the relationship of nutritional status with post-transplant outcomes and characterized the peripheral immune cell phenotypes of children from the Immune Development of Pediatric Transplant (IMPACT) study.

methodsNinety-eight patients from the IMPACT study were classified as having obesity, undernutrition, or normal nutrition-based pre-transplant measurements. Incidence of infectious and alloimmune outcomes at 1-year post-transplantation was compared between nutritional groups using Gray's test and Fine-Gray subdistribution hazards model. Event-free survival was estimated by Kaplan-Meier method and compared between groups. Differences in immune cell subsets between nutritional groups over time were determined using generalized estimating equations accounting for the correlation between repeated measurements.

resultsWe did not observe that nutritional status was associated with infectious or alloimmune events or event-free survival post-transplant. We demonstrated that children with obesity had distinct T-and B-cell signatures relative to those with undernutrition and normal nutrition, even when controlling for immunosuppression. Children with obesity had a lower frequency of CD8 Tnaive cells 9-month post-transplant (p < .001), a higher frequency of CD4 CD57 + PD1- T cells, and lower frequencies of CD57-PD1+ CD8 and CD57-PD1- CD8 T cells at 12-month transplant (p < .05 for all).

conclusionsChildren with obesity have distinct immunophenotypes that may influence the tailoring of immunosuppression.

Indexed as

Kidney TransplantationMalnutritionCD8-Positive T-LymphocytesHumansImmunosuppression TherapyObesityimmunosuppressionimmunosuppressive treatmentinductionkidney

Identifiers

PMID35938682
PMCPMC9669171
OpenAlexW4290653867

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.