Evidence map›Paper›PMID 42228316›Full record

ArticleClinical and experimental nephrology2026

Applications of donor-derived cell-free DNA in kidney transplantation healthcare: view from a prospective single-center study.

Phuong Thanh Nguyen, Hirofumi Nakaoka, Shigeki Mitsunaga, Hiromichi Aoyama, Hiroshi Kitamura, Kenichi Saigo, Ituro Inoue

Abstract read
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Article in Clinical and experimental nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Phuong Thanh NguyenDepartment of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Shizuoka, Japan.
Hirofumi NakaokaDepartment of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Shizuoka, Japan. hnakaoka@kufm.kagoshima-u.ac.jp.ORCID http://orcid.org/0000-0002-8454-1159
Shigeki MitsunagaHuman Genetics Laboratory, National Institute of Genetics, Shizuoka, Japan.
Hiromichi AoyamaDepartment of Surgery, National Hospital Organization Chiba-East Hospital, Chiba, Japan.
Hiroshi KitamuraDepartment of Pathology, National Hospital Organization Chiba-East Hospital, Chiba, Japan.
Kenichi SaigoDepartment of Surgery, National Hospital Organization Chiba-East Hospital, Chiba, Japan.
Ituro InoueDepartment of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Shizuoka, Japan.

Funding

AMED 24ek0510040h0002JSPS KAKENHI JP16K10445
6 · The paper itself

Abstract

backgroundNon-invasive biomarkers are essential for monitoring transplant health, particularly for detecting acute rejection. Donor-derived cell-free DNA (dd-cfDNA) has emerged as a promising biomarker in solid organ transplantation, but optimized methodology and comprehensive evaluation in kidney transplantation (KTx), especially in Japan, are currently limited.

methodsWe developed a customized approach for dd-cfDNA quantification and evaluated its utility as a biomarker in KTx. In this prospective longitudinal study, 322 blood samples were collected from 39 KTx recipients, mostly within the first year and up to 5 years post-transplant. Quantification was performed using a modified targeted sequencing protocol using a 1,000-SNP probe panel tailored to East Asian genetic backgrounds. The resulting dd-cfDNA values were correlated with clinical parameters and histological findings.

resultsGeneral longitudinal dynamics of dd-cfDNA in KTx patients were comprehensively described. Elevated dd-cfDNA was consistently associated with acute rejection and graft injuries. In particular, dd-cfDNA significantly distinguished rejection from non-rejection episodes (p = 1.9 × 10

conclusionsOur study demonstrated that dd-cfDNA is a robust, non-invasive biomarker for detecting allograft rejection and injury in KTx and is superior for monitoring patients' immunosuppressive response. We also present a scalable, cost-effective sequencing-based methodology for quantifying dd-cfDNA, suitable for clinical application.

Indexed as

Cell-Free Nucleic AcidsGraft RejectionKidney TransplantationTissue DonorsAdultBiomarkersFemaleHumansImmunosuppressive AgentsJapanLongitudinal StudiesMaleMiddle AgedPredictive Value of TestsProspective StudiesTime FactorsBiomarkersCell-Free Nucleic AcidsImmunosuppressive AgentsAcute rejectionDonor-derived cell-free DNAImmunosuppressantKidney transplantLiquid biopsyTargeted sequencing

Identifiers

PMID42228316
PMCPMC13518428

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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.