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DOI 10.1016/j.clinph.2026.2111878

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2026

Corticomotor inhibition is associated with balance performance in early Parkinson's disease.

Liu Hsin-Hsuan, Lin Yin-Liang, Wang Ray-Yau, Cheng Shih-Jung, Yang Yea-Ru

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Аннотация

OBJECTIVE

This study aimed to explore the relationship between corticomotor inhibition, assessed by transcranial magnetic stimulation (TMS), and balance performance in people with Parkinson's disease (PwPD).

METHODS

Thirty-nine PwPD, ranging from Hoehn and Yahr stages 1 - 3, underwent TMS to assess corticomotor inhibition-specifically GABAergic intracortical inhibition-under three postural conditions: lying, sitting, and standing. Balance performance was evaluated, including static, dynamic, and functional balance.

RESULTS

Participants' ages ranged from 52 to 76, and disease duration ranged from 2 months to 30 years. Most individuals were in the early stages of the disease, with 59% being in stages 1 and 1.5. The results revealed that intracortical inhibition was associated with functional balance performance. Individuals with lower levels of corticomotor inhibition tended to demonstrate poorer balance. TMS measurements in the sitting position were relatively more stable and sensitive in reflecting corticomotor inhibition.

CONCLUSION

Corticomotor inhibition is related to balance performance in PwPD. Across the three postural conditions assessed during TMS measurements, results obtained during the resting state were similar.

SIGNIFICANCE: These findings highlight the potential of corticomotor inhibition as a neurophysiological marker and target for future interventions addressing balance dysfunction in PwPD.

Для цитирования: Liu Hsin-Hsuan, Lin Yin-Liang, Wang Ray-Yau, Cheng Shih-Jung, Yang Yea-Ru. Corticomotor inhibition is associated with balance performance in early Parkinson's disease.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2026. DOI: 10.1016/j.clinph.2026.2111878.

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