Evidence map›Paper›PMID 40637963›Full record

ArticleNeuroinformatics2025

Prediction of Cerebrospinal Fluid (CSF) Pressure with Generative Adversarial Network Synthetic Plasma-CSF Biomarker Pairing.

Phani Paladugu, Rahul Kumar, Jahnavi Yelamanchi, Ethan Waisberg, Joshua Ong, Mouayad Masalkhi, Chirag Gowda, Ryung Lee, Dylan Amiri, Ram Jagadeesan and 3 more

Abstract read
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Article in Neuroinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Phani PaladuguSidney Kimmel Medical College, Philadelphia, PA, USA.
Rahul KumarUniversity of Massachusetts T.H. Chan School of Medicine, Worcester, MA, USA.
Jahnavi YelamanchiTandon School of Engineering, New York University, New York, NY, USA.
Ethan WaisbergDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Joshua OngDepartment of Ophthalmology and Visual Sciences, University of Michigan Kellogg Eye Center, Ann Arbor, MI, USA.
Mouayad MasalkhiUniversity College Dublin School of Medicine, Belfield, Dublin, Ireland.
Chirag GowdaUniversity of Miami Miller School of Medicine, 160 NW 10 Ave, Miami, FL, 33136, USA. gowdachirag24@gmail.com.ORCID http://orcid.org/0009-0002-8177-2784
Ryung LeeTouro College of Osteopathic Medicine, New York, NY, USA.
Dylan AmiriDepartment of Biology, University of Miami, Coral Gables, Florida, USA.
Ram JagadeesanDepartment of Computer Science, Johns Hopkins University Whiting School of Engineering, Baltimore, MD, USA.
Nasif ZamanHuman-Machine Perception Laboratory, Department of Computer Science and Engineering, University of Nevada, Reno, Reno, NV, USA.
Alireza TavakkoliHuman-Machine Perception Laboratory, Department of Computer Science and Engineering, University of Nevada, Reno, Reno, NV, USA.
Andrew G LeeCenter for Space Medicine, Baylor College of Medicine, Houston, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-invasive intracranial pressure (ICP) monitoring can help clinicians safely and efficiently monitor spaceflight-associated neuro-ocular syndrome (SANS), idiopathic intracranial hypertension, and traumatic brain injury in astronauts. Current invasive ICP measurement techniques are unsuitable for austere environments like spaceflight. In this study, we explore the potential of plasma-derived cell-free RNA (cfRNA) biomarkers as non-invasive alternatives to cerebrospinal fluid (CSF) markers for ICP assessment. We conducted a secondary analysis of NASA's Open Science Data Repository datasets 363-364, focusing on plasma and CSF biomarkers related to ICP and neurovascular health. An ensemble model combining Support Vector Machine, Gradient Boosting Regressor, and Ridge Regression was developed to capture plasma-CSF biomarker relationships. To address limited sample size, we employed a Generative Adversarial Network (GAN) to generate synthetic plasma-CSF biomarker pairs, expanding the dataset from 29 to 279 samples. The model's performance was evaluated using Mean Squared Error (MSE) and validated against real biomarker data. The GAN-augmented ensemble model achieved high predictive accuracy with an MSE of 0.0044. Synthetic plasma-CSF pairs closely aligned with actual biomarker distributions, demonstrating their effectiveness in reducing overfitting and enhancing model robustness. Strong correlations between plasma-derived RNA biomarkers and corresponding CSF indicators support their potential as non-invasive proxies for ICP assessment. This study establishes a novel framework for non-invasive ICP monitoring using plasma cfRNA profiles enriched with GAN-generated synthetic data. The approach shows promise for both spaceflight and clinical applications, potentially broadening diagnostic capabilities for ICP-related conditions. However, further validation across diverse populations is necessary, along with careful consideration of bioethical and data security issues associated with synthetic data use in clinical diagnostics.

Indexed as

Cerebrospinal Fluid PressureNeural Networks, ComputerBiomarkersCell-Free Nucleic AcidsGenerative Adversarial NetworksHumansBiomarkersCell-Free Nucleic AcidsBiomarker PredictionGenerative Adversarial NetworksIntracranial PressureMachine Learning in MedicineNon-invasive Diagnostics

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Registered trials

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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.