Evidence map›Paper›PMID 40291595›Full record

ArticleNeuropsychiatric disease and treatment2025

Exploration of Epigenetic Mechanisms and Biomarkers Among Patients with Very-Late-Onset Schizophrenia-Like Psychosis.

Yansha Gan, Weihua Yue, JiaoJiao Sun, DanTing Yang, ChunXia Fang, Zhenhe Zhou, JiaJun Yin, Hongliang Zhou

Abstract read
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Article in Neuropsychiatric disease and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yansha Gan *The Affiliated Mental Health Center of Jiangnan University, Wuxi, Jiangsu, 214151, People's Republic of China.
Weihua Yue *National Clinical Research Center for Mental Disorders, Peking University Sixth Hospital, Beijing, 100191, People's Republic of China.
JiaoJiao SunThe Affiliated Mental Health Center of Jiangnan University, Wuxi, Jiangsu, 214151, People's Republic of China.
DanTing YangThe Affiliated Mental Health Center of Jiangnan University, Wuxi, Jiangsu, 214151, People's Republic of China.
ChunXia FangThe Affiliated Mental Health Center of Jiangnan University, Wuxi, Jiangsu, 214151, People's Republic of China.
Zhenhe ZhouThe Affiliated Mental Health Center of Jiangnan University, Wuxi, Jiangsu, 214151, People's Republic of China.
JiaJun YinThe Affiliated Mental Health Center of Jiangnan University, Wuxi, Jiangsu, 214151, People's Republic of China.ORCID 0000-0001-6778-1524
Hongliang ZhouDepartment of Psychology, The Affiliated Hospital of Jiangnan University, Wuxi City, Jiangsu, 214100, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aimed to identify DNA methylation patterns associated with Very Late-Onset Schizophrenia-like Psychosis (VLOSLP) and to develop methylation-based biomarkers that differentiate VLOSLP from Schizophrenia (SCZ) and Alzheimer's Disease (AD). Methods: We analyzed methylation microarray datasets (n = 1218) from SCZ and AD patients obtained from the GEO database. We then collected blood samples from VLOSLP patients and age-matched healthy controls (n = 80) at the Wuxi Mental Health Center for methylation microarray profiling and bisulfite sequencing validation. Differential methylation analysis and Gene Ontology (GO) enrichment analysis identified candidate loci. We prioritized key methylation sites through integrated analysis of methylation quantitative trait loci (meQTL), linkage disequilibrium (LD) patterns, and blood-brain methylation correlations. Machine learning algorithms generated diagnostic models, with classification performance evaluated using Area Under the Curve (AUC) metrics. Results: Analysis revealed distinct DNA methylation signatures in VLOSLP patients compared to controls. The Conclusion: Specific DNA methylation alterations in VLOSLP are identified as potential diagnostic biomarkers. These findings may contribute to the development of molecular diagnostic tools, though further validation in larger, independent cohorts is warranted.

Indexed as

Alzheimer’s diseasebiomarkersepigenetics schizophreniavery late-onset schizophrenia-like psychosis

Identifiers

PMID40291595
PMCPMC12032967

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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.