Evidence map›Paper›PMID 39757253›Full record

ArticleCommunications medicine2025

Deep learning-based histopathological assessment of tubulo-interstitial injury in chronic kidney diseases.

Nonoka Suzuki, Kaname Kojima, Silvia Malvica, Kenshi Yamasaki, Yoichiro Chikamatsu, Yuji Oe, Tasuku Nagasawa, Ekyu Kondo, Satoru Sanada, Setsuya Aiba and 10 more

Abstract read
In one paragraph

Article in Communications medicine, 2025. 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
–field-weighted citation impact
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.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Normalized Raman Imaging for Studies of Tissue Physiology of the Kidney.bioRxiv : the preprint server for biology · 2025
    Article
  6. 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

20 authors.

Nonoka Suzuki *Division of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Kaname Kojima *Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan. kojima@megabank.tohoku.ac.jp.ORCID http://orcid.org/0000-0001-5713-2483
Silvia MalvicaJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Kenshi YamasakiDepartment of Dermatology, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0002-5495-4956
Yoichiro ChikamatsuDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Yuji OeDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Tasuku NagasawaDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0002-2012-1171
Ekyu KondoGraduate School of Information Sciences, Tohoku University, Sendai, Japan.
Satoru SanadaDepartment of Nephrology, Japan Community Health Care Organization Sendai Hospital, Sendai, Japan.
Setsuya AibaDepartment of Dermatology, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0003-0632-2388
Hiroshi SatoJR Sendai Hospital, Sendai, Japan.
Mariko MiyazakiDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Sadayoshi ItoDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0002-5092-3626
Mitsuhiro SatoDepartment of Nephrology, Japan Community Health Care Organization Sendai Hospital, Sendai, Japan.
Tetsuhiro TanakaDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0002-2238-4215
Kengo KinoshitaTohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0003-3453-2171
Yoshihide AsanoDepartment of Dermatology, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0001-5560-9778
Avi Z RosenbergJohns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0003-2356-950X
Koji OkamotoDivision of Nephrology, Endocrinology and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan. okamoto5-tky@umin.ac.jp.ORCID http://orcid.org/0000-0002-7601-6557
Kosuke ShidoDepartment of Dermatology, Graduate School of Medicine, Tohoku University, Sendai, Japan.ORCID http://orcid.org/0000-0002-7764-9196

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP23K11314
6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) causes progressive and irreversible damage to the kidneys. Renal biopsies are essential for diagnosing the etiology and prognosis of CKD, while accurate quantification of tubulo-interstitial injuries from whole slide images (WSIs) of renal biopsy specimens is challenging with visual inspection alone.

methodsWe develop a deep learning-based method named DLRS to quantify interstitial fibrosis and inflammatory cell infiltration as tubulo-interstitial injury scores, from WSIs of renal biopsy specimens. DLRS segments WSIs into non-tissue areas, glomeruli, tubules, interstitium, and arteries, and detects interstitial nuclei. It then quantifies these tubulo-interstitial injury scores using the segmented tissues and detected nuclei.

resultsApplied to WSIs from 71 Japanese CKD patients with diabetic nephropathy or benign nephrosclerosis, DLRS-derived scores show concordance with nephrologists' evaluations. Notably, the DLRS-derived fibrosis score has a higher correlation with the estimated glomerular filtration rate (eGFR) at biopsy than scores from nephrologists' evaluations. Validated on WSIs from 28 Japanese tubulointerstitial nephritis patients and 49 European-ancestry patients with nephrosclerosis, DLRS-derived scores show a significant correlation with eGFR. In an expanded analysis of 238 Japanese CKD patients, including 167 from another hospital, deviations in eGFR from expected values based on DLRS-derived scores correlate with annual eGFR decline after biopsy. Inclusion of these deviations and DLRS-derived fibrosis scores improve predictions of the annual eGFR decline.

conclusionsDLRS-derived tubulo-interstitial injury scores are concordant with nephrologists' evaluations and correlated with eGFR across different populations and institutions. The effectiveness of DLRS-derived scores for predicting annual eGFR decline highlights the potential of DLRS as a predictor of renal prognosis.

Identifiers

PMID39757253
PMCPMC11701080

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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.