Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease

Alzheimer’s disease (AD) is a leading cause of dementia worldwide. As current diagnostic approaches remain limited in sensitivity and accessibility, there is a critical need for novel, non-invasive biomarkers aiding early detection. Non-coding RNAs (ncRNAs), including long non-coding RNAs (lncRNAs),...

Full description

Saved in:
Bibliographic Details
Main Authors: Ruomin Xin, Elizabeth Kim, Wei Tse Li, Jessica Wang-Rodriguez, Weg M. Ongkeko
Format: Article
Language:English
Published: MDPI AG 2025-06-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/15/6/806
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850156039690780672
author Ruomin Xin
Elizabeth Kim
Wei Tse Li
Jessica Wang-Rodriguez
Weg M. Ongkeko
author_facet Ruomin Xin
Elizabeth Kim
Wei Tse Li
Jessica Wang-Rodriguez
Weg M. Ongkeko
author_sort Ruomin Xin
collection DOAJ
description Alzheimer’s disease (AD) is a leading cause of dementia worldwide. As current diagnostic approaches remain limited in sensitivity and accessibility, there is a critical need for novel, non-invasive biomarkers aiding early detection. Non-coding RNAs (ncRNAs), including long non-coding RNAs (lncRNAs), PIWI-interacting RNAs (piRNAs), and small nucleolar RNAs (snoRNAs), have emerged as promising candidates due to their regulatory roles in gene expression and association with diseases. In this study, we systematically profiled ncRNA expression from RNA sequencing data of 48 AD and 22 control blood tissue samples, aiming to evaluate their utility as biomarkers for AD classification. Differential expression analysis revealed widespread dysregulation of lncRNAs and piRNAs, with over 5000 lncRNAs and nearly 1000 piRNAs significantly upregulated in AD. Weighted gene co-expression network analysis (WGCNA) identified multiple ncRNA modules associated with the AD phenotype. Using supervised machine learning approaches, we evaluated the diagnostic potential of ncRNA expression profiles, including single-gene, multi-gene, and module-level models. Random Forest models trained on individual genes identified 121 ncRNAs with AUROC > 0.8. Feature importance analysis emphasized ncRNAs such as lnc-MYEF2-3, lnc-PRKACB2, and HBII-115 as major contributors to diagnostic accuracy. These findings support the potential of ncRNA signatures as reliable and non-invasive biomarkers for AD diagnosis.
format Article
id doaj-art-9f2b776d27a440a7aadaee2fefd55101
institution OA Journals
issn 2218-273X
language English
publishDate 2025-06-01
publisher MDPI AG
record_format Article
series Biomolecules
spelling doaj-art-9f2b776d27a440a7aadaee2fefd551012025-08-20T02:24:42ZengMDPI AGBiomolecules2218-273X2025-06-0115680610.3390/biom15060806Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s DiseaseRuomin Xin0Elizabeth Kim1Wei Tse Li2Jessica Wang-Rodriguez3Weg M. Ongkeko4Department of Otolaryngology—Head and Neck Surgery, University of California, La Jolla, San Diego, CA 92093, USADepartment of Otolaryngology—Head and Neck Surgery, University of California, La Jolla, San Diego, CA 92093, USADepartment of Otolaryngology—Head and Neck Surgery, University of California, La Jolla, San Diego, CA 92093, USADepartment of Pathology, University of California, La Jolla, San Diego, CA 92093, USADepartment of Otolaryngology—Head and Neck Surgery, University of California, La Jolla, San Diego, CA 92093, USAAlzheimer’s disease (AD) is a leading cause of dementia worldwide. As current diagnostic approaches remain limited in sensitivity and accessibility, there is a critical need for novel, non-invasive biomarkers aiding early detection. Non-coding RNAs (ncRNAs), including long non-coding RNAs (lncRNAs), PIWI-interacting RNAs (piRNAs), and small nucleolar RNAs (snoRNAs), have emerged as promising candidates due to their regulatory roles in gene expression and association with diseases. In this study, we systematically profiled ncRNA expression from RNA sequencing data of 48 AD and 22 control blood tissue samples, aiming to evaluate their utility as biomarkers for AD classification. Differential expression analysis revealed widespread dysregulation of lncRNAs and piRNAs, with over 5000 lncRNAs and nearly 1000 piRNAs significantly upregulated in AD. Weighted gene co-expression network analysis (WGCNA) identified multiple ncRNA modules associated with the AD phenotype. Using supervised machine learning approaches, we evaluated the diagnostic potential of ncRNA expression profiles, including single-gene, multi-gene, and module-level models. Random Forest models trained on individual genes identified 121 ncRNAs with AUROC > 0.8. Feature importance analysis emphasized ncRNAs such as lnc-MYEF2-3, lnc-PRKACB2, and HBII-115 as major contributors to diagnostic accuracy. These findings support the potential of ncRNA signatures as reliable and non-invasive biomarkers for AD diagnosis.https://www.mdpi.com/2218-273X/15/6/806Alzheimer’s diseasenon-coding RNAdisease diagnosticstranscriptomicsgene regulationliquid biopsy
spellingShingle Ruomin Xin
Elizabeth Kim
Wei Tse Li
Jessica Wang-Rodriguez
Weg M. Ongkeko
Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease
Biomolecules
Alzheimer’s disease
non-coding RNA
disease diagnostics
transcriptomics
gene regulation
liquid biopsy
title Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease
title_full Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease
title_fullStr Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease
title_full_unstemmed Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease
title_short Non-Coding RNAs: lncRNA, piRNA, and snoRNA as Robust Plasma Biomarkers of Alzheimer’s Disease
title_sort non coding rnas lncrna pirna and snorna as robust plasma biomarkers of alzheimer s disease
topic Alzheimer’s disease
non-coding RNA
disease diagnostics
transcriptomics
gene regulation
liquid biopsy
url https://www.mdpi.com/2218-273X/15/6/806
work_keys_str_mv AT ruominxin noncodingrnaslncrnapirnaandsnornaasrobustplasmabiomarkersofalzheimersdisease
AT elizabethkim noncodingrnaslncrnapirnaandsnornaasrobustplasmabiomarkersofalzheimersdisease
AT weitseli noncodingrnaslncrnapirnaandsnornaasrobustplasmabiomarkersofalzheimersdisease
AT jessicawangrodriguez noncodingrnaslncrnapirnaandsnornaasrobustplasmabiomarkersofalzheimersdisease
AT wegmongkeko noncodingrnaslncrnapirnaandsnornaasrobustplasmabiomarkersofalzheimersdisease