Evidence map›Paper›PMID 34215756›Full record

ArticleNPJ genomic medicine2021

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

Zhigang Wang, Hongen Xu, Tianchao Xiang, Danhua Liu, Fei Xu, Lixiang Zhao, Yonghua Feng, Linan Xu, Jialu Liu, Ye Fang and 13 more

Open access · goldAbstract read
In one paragraph

Article in NPJ genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Evaluation for genetic disease in kidney transplant candidates: A practice resource.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Review
  4. Review
  5. Article
  6. 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

23 authors at 6 institutions in 2 countries.

Zhigang Wang *Department of Kidney Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Hongen Xu *Precision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.ORCID http://orcid.org/0000-0001-7895-0899
Tianchao Xiang *Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.
Danhua LiuPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Fei XuDepartment of Kidney Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Lixiang ZhaoDepartment of Kidney Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Yonghua FengDepartment of Kidney Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Linan XuDepartment of Nephrology, Children's Hospital of Fudan University, Shanghai, China.
Jialu LiuDepartment of Nephrology, Children's Hospital of Fudan University, Shanghai, China.
Ye FangDepartment of Nephrology, Children's Hospital of Fudan University, Shanghai, China.
Huanfei LiuPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Ruijun LiPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Xinxin HuPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Jingyuan GuanPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Longshan LiuOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Guiwen FengDepartment of Kidney Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Qian ShenDepartment of Nephrology, Children's Hospital of Fudan University, Shanghai, China.
Hong XuDepartment of Nephrology, Children's Hospital of Fudan University, Shanghai, China.
Dmitrij FrishmanDepartment of Bioinformatics, Technische Universität München, Freising, Germany.
Wenxue TangPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Jiancheng GuoPrecision Medicine Center of Zhengzhou University, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China. gjc@zzu.edu.c.ORCID http://orcid.org/0000-0001-8553-4105
Jia RaoDepartment of Nephrology, Children's Hospital of Fudan University, Shanghai, China. jiarao@fudan.edu.cn.ORCID http://orcid.org/0000-0003-2839-3419
Wenjun ShangDepartment of Kidney Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China. fccshangwj@zzu.edu.cn.ORCID http://orcid.org/0000-0002-9234-979X
Zhengzhou University · CNFirst Affiliated Hospital of Zhengzhou University · CNChildren's Hospital of Fudan University · CNShanghai Medical College of Fudan University · CNSun Yat-sen University · CNTechnical University of Munich · DE

Funding

National Natural Science Foundation of China (National Science Foundation of China) NSFC-8182207
6 · The paper itself

Abstract

Determining the etiology of end-stage renal disease (ESRD) constitutes a great challenge in the context of renal transplantation. Evidence is lacking on the genetic findings for adult renal transplant recipients through exome sequencing (ES). Adult patients on kidney transplant waitlist were recruited from 2017 to 2019. Trio-ES was conducted for the families who had multiple affected individuals with nephropathy or clinical suspicion of a genetic kidney disease owing to early onset or extrarenal features. Pathogenic variants were confirmed in 62 from 115 families post sequencing for 421 individuals including 195 health family members as potential living donors. Seventeen distinct genetic disorders were identified confirming the priori diagnosis in 33 (28.7%) families, modified or reclassified the clinical diagnosis in 27 (23.5%) families, and established a diagnosis in two families with ESRD of unknown etiology. In 14.8% of the families, we detected promising variants of uncertain significance in candidate genes associated with renal development or renal disease. Furthermore, we reported the secondary findings of oncogenes in 4.4% of the patients and known single-nucleotide polymorphisms associated with pharmacokinetics in our cohort to predict the drug levels of tacrolimus and mycophenolate. The diagnostic utility of the genetic findings has provided new clinical insight in most families that help with preplanned renal transplantation.

Identifiers

PMID34215756
PMCPMC8253729
OpenAlexW3173433364

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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.