Evidence map›Paper›PMID 37674990›Full record

ArticleFrontiers in nephrology2022

Levels of Soluble NKG2D Ligands and Cancer History in Patients Starting Hemodialysis.

Kei Nagai, Takashi Tawara, Joichi Usui, Itaru Ebihara, Takashi Ishizu, Masaki Kobayashi, Yoshitaka Maeda, Hiroaki Kobayashi, Kunihiro Yamagata

Open access · diamondAbstract read
In one paragraph

Article in Frontiers in nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

9 authors at 6 institutions in 1 country.

Kei NagaiDepartment of Nephrology, Hitachi General Hospital, Hitachi, Japan.
Takashi TawaraDepartment of Nephrology, Mito Kyodo General Hospital, Mito, Japan.
Joichi UsuiDepartment of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Itaru EbiharaDepartment of Nephrology, Mito Saiseikai General Hospital, Mito, Japan.
Takashi IshizuDepartment of Nephrology, Ushiku Aiwa Hospital, Ushiku, Japan.
Masaki KobayashiDepartment of Nephrology, Tokyo Medical University Kasumigaura Hospital, Ami, Japan.
Yoshitaka MaedaDepartment of Nephrology, JA Toride Medical Center, Toride, Japan.
Hiroaki KobayashiDepartment of Nephrology, Ibaraki Prefectural Central Hospital, Kasama, Japan.
Kunihiro YamagataDepartment of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
University of Tsukuba · JPIbaraki Prefectural Central Hospital · JPJA Toride Medical Center · JPKasumigaura Medical Center · JPMito Saiseikai General Hospital · JPNational Hospital Organization Mito Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune dysfunction in hemodialysis patients is partially due to NK cell impairment. Ligands for NK activating receptors such as NKG2D expressed on cancer cells are involved in NK cell dysfunction and can lead to cancer development. Methods: A cohort with 370 patients who started hemodialysis (HD) was investigated. Serum levels of soluble NKG2D ligands were measured. Cancer history was defined as any cancer diagnosis at induction and hospitalization and death due to cancer during 2-year follow-up. Results: Sixty-two patients with and 308 patients without a cancer history showed mostly comparable biochemical parameters and uremic status at HD induction. Soluble MICB, ULBP-1, and ULBP-2 were detected in sera from most patients starting HD rather than MICA, the most representative NKG2D ligand. Measured NKG2D ligands, except for ULBP-1, were strongly correlated with each other. Correlations between NKG2D ligands and renal function were significant but modest in patients starting HD. Cancer history did not have any impact on levels of soluble NKG2D ligands. Discussion: Even though this investigation lacked a control cohort and serial measurement of parameters, expression patterns of NKG2D ligands were comprehensively described, and the significance of cancer in patients starting HD was elucidated for the first time. Elevated levels of soluble NKG2D ligands occurred potentially due to complex mechanisms of oxidative stress, with insufficient metabolism and excretion in a uremic milieu, but they might mask the significance of elevations in serum levels of soluble NKG2DLs in patients with a cancer history.

Indexed as

cancerend-stage kidney disease (ESKD)MHC class I chain-related genes A (MICA)MHC class I chain-related genes B (MICB)natural killer cell (NK cells)natural killer cell receptor G2D (NKG2D)UL-16-binding protein (ULBP) family

Identifiers

PMID37674990
PMCPMC10479672
OpenAlexW4220662306

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Registered trials

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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.