Evidence map›Paper›PMID 41874566›Full record

ArticleKidney3602026

Quantitative Assessment of Kidney Interstitial Fibrosis Using Optical Spectroscopy Mediated through a Fine Needle Probe.

Saran Lotfollahzadeh, Parth Jalihal, Ousama A'amar, Ji Young Chung, Meghan Howard, Emily Oros, Eladio Rodriguez-Diaz, Mostafa Belghasem, Aman Kumar, Sayeed Malik and 3 more

Abstract read
In one paragraph

Article in Kidney360, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Saran LotfollahzadehDepartment of Medicine, Renal Section, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0001-5560-2912
Parth JalihalDepartment of Medicine, Renal Section, Boston University School of Medicine, Boston, Massachusetts.ORCID 0009-0000-1411-6643
Ousama A'amarDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, Massachusetts.ORCID 0009-0004-7909-4587
Ji Young ChungDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, Massachusetts.
Meghan HowardDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, Massachusetts.ORCID 0009-0009-9445-5340
Emily OrosDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, Massachusetts.
Eladio Rodriguez-DiazDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, Massachusetts.
Mostafa BelghasemDepartment of Medicine, Renal Section, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0002-2097-6882
Aman KumarBoston Veterans Administration Healthcare System, Boston, Massachusetts.ORCID 0000-0002-2568-423
Sayeed MalikBoston Veterans Administration Healthcare System, Boston, Massachusetts.ORCID 0009-0009-4967-7905
Jean FrancisDepartment of Medicine, Renal Section, Boston University School of Medicine, Boston, Massachusetts.
Vipul C ChitaliaDepartment of Medicine, Renal Section, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0002-6663-6058
Irving J BigioDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, Massachusetts.ORCID 0000-0003-4168-1466

Funding

Multidisciplinary Training Program in Cardiovascular EpidemiologyT32HL125232 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Matthew G. Nayor, Vanessa Xanthakis · 2016 to 2026
$5.0M
Disease-specific risk factors for thrombosis following vascular interventionsR01HL166608 · NHLBI · BOSTON MEDICAL CENTER · PI Vipul C Chitalia, KATYA RAVID · 2023 to 2026
$2.7M
Boston University Chobanian and Avedisian School of Medicine Fibrosis Affinity Research CollaborativeNHLBI Division of Intramural Research R01HL166608NHLBI Division of Intramural Research T32HL125232NHLBI NIH HHS R01 HL166608NHLBI NIH HHS T32 HL125232
6 · The paper itself

Abstract

key pointsIntrarenal elastic-scattering spectroscopy at multiple sites accurately quantifies kidney fibrosis in a CKD rat model. Machine learning analysis predicted the histologic fibrosis grades with >98% accuracy. This method provided a rapid, objective tool for kidney evaluation at the point of care without increasing bleeding complications.

backgroundQuantitative assessment of renal fibrosis on biopsy remains a time-consuming step and is subject to interobserver variability, staining inconsistencies, and sampling errors, given the heterogeneous nature of renal fibrosis. An objective, rapid, and point-of-care evaluation method at multiple locations in the kidney is particularly needed for preimplantation donor kidney assessment, where such limitations can lead to the erroneous nonuse of approximately 20% of grafts. We investigated the accuracy of an orthogonal technique-elastic scattering spectroscopy (ESS)-and compared it against the conventional interstitial fibrosis and tubular atrophy (IFTA) scale.

methodsCKD was induced in rats via an adenine-enriched diet. A customized fine-needle ESS probe was used to acquire spectral data at predetermined intrarenal depths, followed by standard histopathologic scoring. Linear regression was initially used to correlate ESS-derived spectral features with expert-reported IFTA scores. Subsequently, both continuous and categorical random forests (RFs) were implemented to predict fibrosis severity.

resultsRF regression applied to the 300-500 nm spectral range yielded R2 values of 0.925, 0.917, and 0.838 at depths of 1.5, 3 mm (renal cortex), and 5 mm (corticomedullary junction and medulla) depths, respectively. Averaging across depths increased the R2 to 0.961. Corresponding categorical RF accuracies were 98.14%, 96.74%, and 93.49%, with an averaged overall accuracy of 98.61% following five-fold cross-validation.

conclusionsIntrarenal ESS provides a robust, depth-resolved, and quantitative estimation of fibrosis that closely parallels histologic IFTA scoring. Multidepth sampling improves predictive accuracy by minimizing local variability. ESS thus represents a promising, objective, rapid, and scalable adjunct for point-of-care kidney tissue evaluation at multiple points within the kidney without increasing risk of bleeding.

Indexed as

KidneyRenal Insufficiency, ChronicSpectrum AnalysisAnimalsDisease Models, AnimalFibrosisMachine LearningMaleRatsRats, Sprague-Dawleyfibrosisrenal fibrosis

Identifiers

PMID41874566
PMCPMC13450960

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.