Evidence map›Paper›PMID 41429816›Full record

ArticleScientific reports2025

Optimizing intervertebral disc cell metabolic phenotyping with machine learning and artificial neural networks.

Md Entaz Bahar, Rizi Firman Maulidi, Quang Nhat Ngo, Deok Ryong Kim

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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

4 authors.

Md Entaz BaharDepartment of Biochemistry and Convergence Medical Sciences, Institute of Medical Science, Gyeongsang National University College of Medicine, Jinju, Republic of Korea.
Rizi Firman MaulidiDepartment of Biochemistry and Convergence Medical Sciences, Institute of Medical Science, Gyeongsang National University College of Medicine, Jinju, Republic of Korea.
Quang Nhat NgoDepartment of Biochemistry and Convergence Medical Sciences, Institute of Medical Science, Gyeongsang National University College of Medicine, Jinju, Republic of Korea.
Deok Ryong KimDepartment of Biochemistry and Convergence Medical Sciences, Institute of Medical Science, Gyeongsang National University College of Medicine, Jinju, Republic of Korea. drkim@gnu.ac.kr.

Funding

National Research Foundation of Korea,South Korea RS-2023-00219399National Research Foundation of Korea,South Korea RS-2023-00238051
6 · The paper itself

Abstract

Biological phenotyping of cellular metabolism is essential for deciphering health and disease states. The Seahorse XF analyzer enables direct measurement of oxygen consumption rate (OCR) and extracellular acidification rate (ECAR), providing insight into mitochondrial function and glycolytic activity in living cells. Accurate phenotyping requires meticulous preparation, including forming a uniform cell monolayer and carefully titrating critical reagents such as the uncoupler carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP), to ensure precise and reproducible bioenergetic measurements. Artificial neural networks (ANN) and machine learning (ML) algorithms serve as powerful tools for analyzing experimental findings, enhancing the accuracy of result predictions, and reducing the number of experimental treatments and combinations required. This study was designed to optimize seahorse bioenergetics flux analysis using ML and ANN for in vitro metabolic phenotyping attributes. The performance of the ANN and ML models was assessed using root mean square error (RMSE), mean square error (MSE), mean absolute error, and accuracy percentage. We applied supervised ML techniques in the Regression and Classification Learner App to evaluate the predictive capability of various algorithms. Our findings indicated that fine and boosted trees in the regression model, as well as fine and medium trees and linear and quadratic support vector machines (SVM) in the classification model, enhanced data prediction accuracy. Notably, we developed a rigorous biological workflow for bioenergetic phenotyping by integrating unsupervised machine learning with a supervised ANN, which closely aligned with experimental data and minimized discrepancies between predicted and observed values. This approach establishes a robust, unbiased, and data-driven framework for high-resolution metabolic phenotyping. By uniting precise experimental biology with advanced computational analysis, our study highlights a powerful synergy with significant promise for both fundamental research and therapeutic discovery.

Indexed as

Intervertebral DiscMachine LearningNeural Networks, ComputerAlgorithmsAnimalsEnergy MetabolismHumansMitochondriaOxygen ConsumptionPhenotypeArtificial neural networksBioenergetics fluxMachine learningMetabolic phenotypeOxygen consumption rate

Identifiers

PMID41429816
PMCPMC12722773

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.