The effects of omega-3 fatty acids on Wnt activity in iPSC-derived neural stem cells from adult ADHD patients

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Authors: Cristine M. Yde Ohki, Natalie M. Walter, Louisa C. Dury, Letizia Del Campana, Romane Lasmarrigues, Rhiannon V. McNeill, Zora Schickardt, Lukasz Smigielski, Susanne Walitza, Sarah Kittel‐Schneider, Edna Grünblatt
Cited by: 1
References: 59

Abstract

and genetic evidence suggests an association between attention-deficit/hyperactivity disorder (ADHD) and abnormalities in the Wnt pathway. Prior research from our group indicated heightened basal Wnt activity in neural stem cells (NSCs) derived from induced pluripotent stem cells (iPSCs) of pediatric ADHD patients and showed that methylphenidate (MPH) and omega-3 polyunsaturated fatty acids (ω-3 PUFAs) can modulate this pathway. While MPH is a first-line treatment for ADHD, ω-3 PUFAs are under investigation as a potential non-pharmacological supplement. Using the same functionality-based reporter technology, we assessed Wnt activity in iPSC-derived NSCs from 5 adult ADHD patients and 5 healthy controls. We examined whether ω-3 fatty acids (EPA and DHA), alone or combined, and DHA with MPH can modulate Wnt activity in these NSCs. Basal Wnt responsiveness did not differ between adult ADHD and control lines, although genetic risk for ADHD was associated with increased Wnt activity. EPA showed no statistically significant effects, while DHA strongly increased Wnt activity in both groups. DHA combined with EPA increased Wnt activity in ADHD lines, whereas DHA with MPH caused group-specific responses: enhancing Wnt signaling in ADHD but reducing it in controls. Compared to NSCs derived from children, adult-derived NSCs behave differently and show distinct responses to EPA and DHA, suggesting a potential route toward refined therapeutic strategies for adults.

Fields of Study & Subjects

Fatty Acid Research and Health Neurogenesis and neuroplasticity mechanisms Nerve injury and regeneration

Publication details

Journal / source
Neuroscience Applied
Publisher
Elsevier BV
Volume
5
Pages
107005–107005
Publication date
1 January 2026
Language
EN