HMN 2025: How Blood test identifies biological markers for teen depression and severity

Biological markers for teen depression
Top DE miRNAs are expressed in the human brain and miR-32 associates negatively with hippocampal volume. A) The microRNA Tissue Expression Database (miTED) revealed human brain expression levels of each of the top DE miRNA. B) TissueAtlas dataset allowed evaluation of top DE miRNA expression in specific human brain regions. C) Hippocampal volume comparison by group does not show statistical differences. D) Partial correlation of miR-32 by hippocampal volume adjusted by intracranial brain volume (ICV) and MDD medication use shows a negative association. Credit: Biological Psychiatry Global Open Science (2025). DOI: 10.1016/j.bpsgos.2025.100505

Using a novel lab method they developed, McGill University researchers have identified nine molecules in the blood that were elevated in teens diagnosed with depression. These molecules also predicted how symptoms might progress over time.

The findings of the clinical study could pave the way for earlier detection, before symptoms worsen and become hard to treat. The work is published in the journal Biological Psychiatry Global Open Science.

“Alarmingly, more and more adolescents are being diagnosed with , and when it starts early, the effects can be long-lasting and severe,” said senior author Cecilia Flores, James McGill Professor in McGill’s Department of Psychiatry, a researcher at the Douglas Research Center and a principal investigator at the Ludmer Center.

“Teens with depression are more likely to struggle with , and experience symptoms that often don’t respond well to treatment.”

Notably, the nine molecules—known as microRNAs—have not been linked to adult depression, suggesting they reflect unique to teens.

Biological markers for teen depression
Comparison of most expressed miRNAs in dried-blood spots in comparison to the miRNA expression in other peripheral fluids suggests resemblance with the serum profile. A) The heatmap of the top 20 expressed microRNAs in the current DBS samples. B) Based on the additional miTED data, we extracted expression profiles for miRNAs in other whole blood related samples, to compare their similarity with DBS proportions. Credit: Biological Psychiatry Global Open Science (2025). DOI: 10.1016/j.bpsgos.2025.100505

A minimally invasive and scalable approach

The study, conducted in collaboration with colleagues at the University of California, Los Angeles and Stanford University, focused on 62 teenagers: 34 with depression and 28 without.

Researchers collected small volumes of blood samples, let them dry, and then froze the samples to preserve molecular integrity over time. Such samples are taken with a simple finger prick and are easy to store and transport, making the approach practical and scalable for broader use.

The McGill team developed the lab method used to extract and analyze microRNAs from the samples.

“Our findings pave the way for using dried blood spots as a practical tool in psychiatric research, allowing us to track early biological changes linked to using a minimally invasive method,” said first author Alice Morgunova, postdoctoral fellow at McGill.

Diagnosing depression mostly relies on self-reported symptoms. The authors say this could delay care, especially if teens don’t recognize the signs or aren’t ready to talk about them. A blood-based screening tool could provide an additional and more objective metric to identify teens at risk.

The researchers plan to validate their findings in larger groups of adolescents and to study how these microRNAs interact with genetic and environmental risk factors.

More information:
Alice Morgunova et al, Peripheral microRNA signatures in adolescent depression, Biological Psychiatry Global Open Science (2025). DOI: 10.1016/j.bpsgos.2025.100505

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McGill University


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