Evidence map›Paper›PMID 35314666›Full record

ArticleAnnals of transplantation2022

Pre-Transplant Peripheral Lymphocyte Subsets Predict Pneumonia After Renal Transplantation.

Quan Zhuang, Min Yang, Shu Liu, Meng Yu, Jie Jiang, Bo Peng, Yingzi Ming

Open access · hybridAbstract read
In one paragraph

Article in Annals of transplantation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

7 authors at 2 institutions in 1 country.

Quan ZhuangTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).
Min YangTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).
Shu LiuTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).
Meng YuTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).
Jie JiangTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).
Bo PengTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).ORCID 0000-0003-4482-2885
Yingzi MingTransplantation Center, The 3rd Xiangya Hospital of Central South Univeristy, Changsha, Hunan, China (mainland).
Central South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Kidney transplantation (KTx) has been considered as the most effective therapeutic method for end-stage renal disease. Immune monitoring of peripheral lymphocyte subsets (PLS) reflects the real immune status and has been used for diagnosis of pneumonia after KTx. We aimed to investigate the association between pre-transplant PLS and pneumonia in renal allograft recipients. MATERIAL AND METHODS A total of 152 patients receive donation after citizen's death (DCD) kidney allografts in our center between January 2018 and December 2019. Among them, 114 patients were enrolled in our study based on inclusion and exclusion criteria. During the first-year follow-up after KTx, 32 recipients developed pneumonia, and the other 82 recipients did not (stable group). The pre-clinical information and PLS (including the percentages and absolute numbers (Ab No.) of peripheral T, B, and NK cells, as well as CD4/CD8 ratio) results in these 2 groups were calculated by the Mann-Whitney test and receiver operating curve (ROC) analysis. Univariate and multivariate logistic regression analyses were employed to identify risk factors. RESULTS Compared to the stable group, the Ab No. of CD3+, CD8+, and CD4+ T cells, as well as B cells and NK cells, were notably reduced in the pneumonia patients. The area under the curve (AUC) of CD3+ T cell Ab No. was 0.7022. Multivariate analysis demonstrated that pre-transplant B cell Ab No. was the independent risk factor for pneumonia progression after KTx (OR=0.353, P=0.037). CONCLUSIONS Pre-transplant Ab No. of PLS were closely related to pneumonia after KTx. Monitoring pre-transplant PLS could provide more timely and effective prevention and therapy for post-operative pneumonia after KTx.

Indexed as

Kidney Failure, ChronicKidney TransplantationPneumoniaHumansLymphocyte CountLymphocyte Subsets

Identifiers

PMID35314666
PMCPMC8957644
OpenAlexW4212937183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.