TY - JOUR
T1 - Engaging dystonia networks with subthalamic stimulation
AU - Butenko, Konstantin
AU - Neudorfer, Clemens
AU - Dembek, Till A.
AU - Hollunder, Barbara
AU - Meyer, Garance M.
AU - Li, Ningfei
AU - Oxenford, Simón
AU - Bahners, Bahne H.
AU - Al-Fatly, Bassam
AU - Lofredi, Roxanne
AU - Gordon, Evan M.
AU - Dosenbach, Nico U.F.
AU - Ganos, Christos
AU - Hallett, Mark
AU - Jinnah, Hyder A.
AU - Starr, Philip A.
AU - Ostrem, Jill L.
AU - Wu, Yiwen
AU - Zhang, Chen Cheng
AU - Fox, Michael D.
AU - Horn, Andreas
N1 - Publisher Copyright:
Copyright © 2025 the Author(s).
PY - 2025/1/14
Y1 - 2025/1/14
N2 - Deep brain stimulation is an efficacious treatment for dystonia. While the internal pallidum serves as the primary target, recently, stimulation of the subthalamic nucleus (STN) has been investigated. However, optimal targeting within this structure and its surroundings have not been studied in depth. Indeed, historical targets that have been used for surgical treatment of dystonia are directly adjacent to the STN. Further, multiple types of dystonia exist, and outcomes are variable, suggesting that not all types would profit maximally from the same target. Therefore, a thorough investigation of neural substrates underlying stimulation effects on dystonia signs and symptoms is warranted. Here, we analyze a multicenter cohort of isolated dystonia patients with subthalamic implantations (N = 58) and relate their stimulation sites to improvements of appendicular and cervical symptoms as well as blepharospasm. Stimulation of the ventral oral posterior nucleus of thalamus and surrounding regions were associated with improvements in cervical dystonia, while stimulation of the dorsolateral STN was associated with improvements in limb dystonia and blepharospasm. This dissociation was matched by structural connectivity analysis, where the cerebellothalamic, corticospinal, and pallidosubthalamic tracts were associated with improvements of cervical dystonia, while hyperdirect and subthalamopallidal pathways with alleviation of limb dystonia and blepharospasm. On the level of functional networks, improvements of limb dystonia were associated with connectivity to the corresponding somatotopic regions in the primary motor cortex, while alleviation of cervical dystonia to the cingulo-opercular network. These findings shed light on the pathophysiology of dystonia and may guide DBS targeting and programming in the future.
AB - Deep brain stimulation is an efficacious treatment for dystonia. While the internal pallidum serves as the primary target, recently, stimulation of the subthalamic nucleus (STN) has been investigated. However, optimal targeting within this structure and its surroundings have not been studied in depth. Indeed, historical targets that have been used for surgical treatment of dystonia are directly adjacent to the STN. Further, multiple types of dystonia exist, and outcomes are variable, suggesting that not all types would profit maximally from the same target. Therefore, a thorough investigation of neural substrates underlying stimulation effects on dystonia signs and symptoms is warranted. Here, we analyze a multicenter cohort of isolated dystonia patients with subthalamic implantations (N = 58) and relate their stimulation sites to improvements of appendicular and cervical symptoms as well as blepharospasm. Stimulation of the ventral oral posterior nucleus of thalamus and surrounding regions were associated with improvements in cervical dystonia, while stimulation of the dorsolateral STN was associated with improvements in limb dystonia and blepharospasm. This dissociation was matched by structural connectivity analysis, where the cerebellothalamic, corticospinal, and pallidosubthalamic tracts were associated with improvements of cervical dystonia, while hyperdirect and subthalamopallidal pathways with alleviation of limb dystonia and blepharospasm. On the level of functional networks, improvements of limb dystonia were associated with connectivity to the corresponding somatotopic regions in the primary motor cortex, while alleviation of cervical dystonia to the cingulo-opercular network. These findings shed light on the pathophysiology of dystonia and may guide DBS targeting and programming in the future.
KW - cervical dystonia
KW - deep brain stimulation
KW - limb dystonia
KW - structural connectivity
KW - sweet-spot analysis
UR - http://www.scopus.com/inward/record.url?scp=85214999995&partnerID=8YFLogxK
U2 - 10.1073/pnas.2417617122
DO - 10.1073/pnas.2417617122
M3 - Article
C2 - 39773021
AN - SCOPUS:85214999995
SN - 0027-8424
VL - 122
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 2
M1 - e2417617122
ER -