Evidence map›Paper›PMID 37817878›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering

Computational Integration of Renal Histology and Urinary Proteomics using Neural Networks.

Nicholas Lucarelli, Donghwan Yun, Dohyun Han, Brandon Ginley, Kyung Chul Moon, Avi Rosenberg, John Tomaszewski, Seung Seok Han, Pinaki Sarder

Open access · greenAbstract read
In one paragraph

Article in Proceedings of SPIE--the International Society for Optical Engineering. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 2 countries.

Nicholas LucarelliDepartment of Pathology and Anatomical Sciences, University at Buffalo - The State University of New York, Buffalo, New York.
Donghwan YunDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Dohyun HanProteomics Core Facility, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea.
Brandon GinleyDepartment of Pathology and Anatomical Sciences, University at Buffalo - The State University of New York, Buffalo, New York.
Kyung Chul MoonDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Avi RosenbergDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
John TomaszewskiDepartment of Pathology and Anatomical Sciences, University at Buffalo - The State University of New York, Buffalo, New York.
Seung Seok HanDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Pinaki SarderDepartment of Pathology and Anatomical Sciences, University at Buffalo - The State University of New York, Buffalo, New York.
Seoul National University · KRUniversity at Buffalo, State University of New York · USJohns Hopkins Medicine · US

Funding

Computational Imaging of Renal Structures for Diagnosing DiabeticNephropathyR01DK114485 · NIDDK · UNIVERSITY OF FLORIDA · PI Michael Thomas Eadon, Avi Z Rosenberg · 2018 to 2026
$4.7M
NIDDK NIH HHS R01 DK114485
6 · The paper itself

Abstract

Histological image data and molecular profiles provide context into renal condition. Often, a biopsy is drawn to diagnose or monitor a suspected kidney problem. However, molecular profiles can go beyond a pathologist's ability to see and diagnose. Using AI, we computationally incorporated urinary proteomic profiles with microstructural morphology from renal biopsy to investigate new and existing molecular links to image phenotypes. We studied whole slide images of periodic acid-Schiff stained renal biopsies from 56 DN patients matched with 2,038 proteins measured from each patient's urine. Using Seurat, we identified differentially expressed proteins in patients that developed end-stage renal disease within 2 years of biopsy. Glomeruli, globally sclerotic glomeruli, and tubules were segmented from WSI using our previously published HAIL pipeline. For each glomerulus, 315 handcrafted digital image features were measured, and for tubules, 207 features. We trained fully connected networks to predict urinary protein measurements that were differentially expressed between patients who did/ did not progress to ESRD within 2 years of biopsy. The input to this network was either glomerular or tubular histomorphological features in biopsy. Trained network weights were used as a proxy to rank which morphological features correlated most highly with specific urinary proteins. We identified significant image feature-protein pairs by ranking network weights by magnitude. We also looked at which features on average were most significant in predicting proteins. For both glomeruli and tubules, RGB color values and variance in PAS

Indexed as

Artificial Intelligence (AI)Diabetic Nephropathy (DN)Digital PathologyUrinary Proteomics

Identifiers

PMID37817878
PMCPMC10563119
OpenAlexW4226332633

What OpenQuestion holds

Textmetadata
LicenceTDM
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.