Evidence map›Paper›PMID 31197971›Full record

ArticleMolecular genetics & genomic medicine2019

Is polycystic kidney disease associated with malignancy in children?

Brian D Friend, Kami Wolfe Schneider, Timothy Garrington, Laurel Truscott, Julian A Martinez-Agosto, Robert S Venick, Eileen Tsai Chambers, Patricia Weng, Douglas G Farmer, Vivian Y Chang and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Brian D FriendDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.ORCID 0000-0001-8652-4400
Kami Wolfe SchneiderSection of Hematology, Oncology, and Bone Marrow Transplantation, University of Colorado Anschutz Medical Campus, Children's Hospital Colorado, Aurora, Colorado.
Timothy GarringtonSection of Hematology, Oncology, and Bone Marrow Transplantation, University of Colorado Anschutz Medical Campus, Children's Hospital Colorado, Aurora, Colorado.
Laurel TruscottDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.
Julian A Martinez-AgostoDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.ORCID 0000-0001-6776-6949
Robert S VenickDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.
Eileen Tsai ChambersDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.
Patricia WengDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.
Douglas G FarmerDepartment of Surgery, UCLA David Geffen School of Medicine, Los Angeles, California.
Vivian Y ChangDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.
Noah FedermanDepartment of Pediatrics, UCLA Mattel Children's Hospital, Los Angeles, California.
Mattel Children's Hospital · USUniversity of California, Los Angeles · USChildren's Hospital Colorado · USDuke University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolycystic kidney disease (PKD) is an inherited condition characterized by progressive development of end-stage renal disease, hypertension, hepatic fibrosis, and cysts in the kidney, liver, pancreas, spleen, thyroid, and epididymis. While malignancies have been reported in association with PKD in adults, the incidence of malignancies in children with PKD is not currently known.

methodsWe report on five patients with a known history of PKD who developed a malignancy as children at the University of California, Los Angeles and the University of Colorado Anschutz Medical Campus. Patients were included from 2012 to 2017.

resultsWe present five patients with a history of PKD diagnosed with a malignancy during childhood without any additional known mutations to suggest a genetic predisposition to develop cancer. This includes the first reported case of hepatocellular carcinoma in a patient with autosomal recessive polycystic kidney disease.

conclusionOur report illustrates the potential that PKD may be associated with an increased risk for developing cancer, even in children. Further research is necessary to better understand this relationship.

Indexed as

Genetic Predisposition to DiseaseAdolescentChildFemaleHumansInfantMaleNeoplasmsPolycystic Kidney DiseasesReceptors, Cell SurfaceTRPP Cation ChannelsPKHD1 protein, humanReceptors, Cell SurfaceTRPP Cation Channelsgenetic predispositiongenetic sequencingmalignancypolycystic kidney disease

Identifiers

PMID31197971
PMCPMC6625336
OpenAlexW2952912656

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.