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Editorial
Copyright: ©Author(s) 2026.
World J Stem Cells. Oct 26, 2026; 18(10): 119872
Published online Oct 26, 2026. doi: 10.4252/wjsc.119872
Table 1 Comparison of neuromodulation modalities relevant to brain-function regulation
Modality
Core physical carrier
Typical biological “entry points”
Strengths for dementia-relevant brain regulation
Key constraints/risks
Photonic, e.g., photobiomodulationLight (red/NIR)Mitochondrial cytochrome c oxidase, redox signaling, cerebral blood flowNon-invasive; potential metabolic and vascular effects; clinically scalableUncertain dose window; limited tissue penetration; heterogeneous protocols[18-20]
Electrical, e.g., tDCS/tACSElectric fields/currentsMembrane polarization, oscillatory entrainmentLow cost; portable; growing evidence base from RCTs and meta-analyses in cognitive impairment/dementiaVariable field delivery; modest effect sizes; placebo sensitivity; montage heterogeneity[21-23]
Magnetic, e.g., rTMSMagnetic pulses inducing electric fieldsCortical excitability, circuit plasticityCan target circuits; clinical infrastructure existsProtocol variability; challenging sham-controlled designs; mixed durability of effects[24-26]
Acoustic, e.g., transcranial ultrasound stimulationFocused ultrasound pressure wavesMechanosensitive channelsDeep targeting capability; emerging precision and focalitySafety standards still evolving; parameter sensitivity; limited clinical data[27-29]
AcupunctureMechanical stimulation at acupoints; afferent nerve activationAfferent nerve activation; peripheral-central neuroimmune and autonomic pathways; local niche modulation (e.g., miR-124/Notch-Wnt signaling)Engages whole-body systems; modulates inflammation and metabolism; suitable for repeated dosing; potential to prime stem-cell nicheProtocol heterogeneity; blinding difficulties; need for rigorous mechanism-based controls[30-33]


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