Evidence map›Paper›PMID 31256873›Full record

ArticleTransplantation proceedings

Cause of End-Stage Renal Disease Is Not a Risk Factor for Cytomegalovirus Infection After Kidney Transplant.

Tripti Singh, Stephen Peery, Brad C Astor, Sandesh Parajuli, Arjang Djamali, Sarah E Panzer

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Transplantation proceedings. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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

6 authors at 2 institutions in 1 country.

Tripti SinghDepartment of Medicine, Division of Nephrology, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA. Electronic address: tsingh@medicine.wisc.edu.
Stephen PeeryDepartment of Medicine, Division of Nephrology, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA.
Brad C AstorDepartment of Medicine, Division of Nephrology, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA; Department of Population Health Sciences, University of Wisconsin-Madison School of Medicine and Public Health, Madison WI, USA.
Sandesh ParajuliDepartment of Medicine, Division of Nephrology, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA.
Arjang DjamaliDepartment of Medicine, Division of Nephrology, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA; Department of Surgery, Division of Transplantation, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA.
Sarah E PanzerDepartment of Medicine, Division of Nephrology, University of Wisconsin-Madison Hospital and Clinics, Madison WI, USA.
University of Wisconsin–Madison · USUW Health University Hospital · US

Funding

Improving long-term allograft survival in kidney transplantation by targeting B cell survival cytokinesK23DK122136 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI PANZER, SARAH E · 2019 to 2022
$663k
NIDDK NIH HHS K23 DK122136
6 · The paper itself

Abstract

backgroundCytomegalovirus infection (CMV) after kidney transplantation leads to increased morbidity and mortality. Whether the cause of end-stage renal disease (ESRD) influences the risk of CMV infection post-transplant is not known.

methodsWe analyzed data from 2741 adult kidney transplant recipients from January 1993 through December 2014. The causes of ESRD included diabetes mellitus (n = 947), hypertension (n = 442), polycystic kidney disease (n = 549), and glomerulonephritis (GN) (n = 803). The primary outcome was incidence of CMV infection, defined as the first episode of detectable CMV DNA in the blood following transplant.

resultsThree hundred and thirty patients developed a CMV infection over a median follow-up of 4.5 years. Patients with diabetes mellitus (DM) as the cause of ESRD had a higher incidence of CMV infection post-transplant compared to patients with GN (2.37 vs 1.58/100 person-years, P < .005) whereas hypertension (HTN) and autosomal dominant polycystic kidney disease (PKD) were similar (2.17 and 2.07/100 person-years). DM was associated with a 35% higher risk of CMV infection compared to GN in unadjusted analyses [hazard ratio=1.35 [95% confidence interval 1.02-1.78], P = .04). However, after adjustment for age, the risk of CMV infection was similar in all groups (DM: age-adjusted hazard ratio 1.02 [0.78-1.39]; HTN: 0.96 (0.67-1.36); PKD: 1.08 [0.78-1.48]; compared to GN). The risk of CMV infection increased with age (adjusted hazard ratio=1.32 [1.18-1.47] for every decade of life, P < .001).

conclusionsOur study demonstrates that the cause of ESRD is not a significant risk factor for CMV infection in kidney transplant recipients once adjusted for age. Future studies are needed to identify risk factors for CMV infection to define patient-centered monitoring and prevention.

Indexed as

Postoperative ComplicationsAdultAntiviral AgentsCytomegalovirus InfectionsFemaleHumansIncidenceKidney DiseasesKidney Failure, ChronicKidney TransplantationMaleMiddle AgedProportional Hazards ModelsRisk FactorsAntiviral Agents

Identifiers

PMID31256873
PMCPMC7444315
OpenAlexW2954724350

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.