Optimal deep brain stimulation sites and networks for stimulation of the fornix in Alzheimer’s disease
Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer’s Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode pl...
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| Veröffentlicht in: | Nature communications Jg. 13; H. 1; S. 7707 - 14 |
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
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London
Nature Publishing Group UK
14.12.2022
Nature Publishing Group Nature Portfolio |
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| ISSN: | 2041-1723, 2041-1723 |
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| Abstract | Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer’s Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement (
R
= 0.53,
p
< 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures (
R
= 0.48,
p
< 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes (
R
= 0.48,
p
< 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming.
Deep brain stimulation has been investigated as a potential treatment for cognitive impairments in Alzheimer’s disease. Here the authors carry out post hoc analysis of multi-center cohorts to investigate the anatomical and functional correlates of effective deep brain stimulation, and find that stimulating circuit of Papez, fornix and bed nucleus of the stria terminalis, and a multi-region functional network, were associated with clinical improvement. |
|---|---|
| AbstractList | Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer's Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement (R = 0.53, p < 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures (R = 0.48, p < 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes (R = 0.48, p < 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming.Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer's Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement (R = 0.53, p < 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures (R = 0.48, p < 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes (R = 0.48, p < 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming. Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer’s Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement (R = 0.53, p < 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures (R = 0.48, p < 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes (R = 0.48, p < 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming.Deep brain stimulation has been investigated as a potential treatment for cognitive impairments in Alzheimer’s disease. Here the authors carry out post hoc analysis of multi-center cohorts to investigate the anatomical and functional correlates of effective deep brain stimulation, and find that stimulating circuit of Papez, fornix and bed nucleus of the stria terminalis, and a multi-region functional network, were associated with clinical improvement. Deep brain stimulation has been investigated as a potential treatment for cognitive impairments in Alzheimer’s disease. Here the authors carry out post hoc analysis of multi-center cohorts to investigate the anatomical and functional correlates of effective deep brain stimulation, and find that stimulating circuit of Papez, fornix and bed nucleus of the stria terminalis, and a multi-region functional network, were associated with clinical improvement. Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer’s Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement ( R = 0.53, p < 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures ( R = 0.48, p < 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes ( R = 0.48, p < 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming. Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer's Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement (R = 0.53, p < 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures (R = 0.48, p < 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes (R = 0.48, p < 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming. Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer’s Disease. Outcomes from randomized clinical trials have shown that cognitive function improved in some patients but deteriorated in others. This could be explained by variance in electrode placement leading to differential engagement of neural circuits. To investigate this, we performed a post-hoc analysis on a multi-center cohort of 46 patients with DBS to the fornix (NCT00658125, NCT01608061). Using normative structural and functional connectivity data, we found that stimulation of the circuit of Papez and stria terminalis robustly associated with cognitive improvement ( R = 0.53, p < 0.001). On a local level, the optimal stimulation site resided at the direct interface between these structures ( R = 0.48, p < 0.001). Finally, modulating specific distributed brain networks related to memory accounted for optimal outcomes ( R = 0.48, p < 0.001). Findings were robust to multiple cross-validation designs and may define an optimal network target that could refine DBS surgery and programming. Deep brain stimulation has been investigated as a potential treatment for cognitive impairments in Alzheimer’s disease. Here the authors carry out post hoc analysis of multi-center cohorts to investigate the anatomical and functional correlates of effective deep brain stimulation, and find that stimulating circuit of Papez, fornix and bed nucleus of the stria terminalis, and a multi-region functional network, were associated with clinical improvement. |
| ArticleNumber | 7707 |
| Author | Wolk, David A. Smith, Gwenn S. Ríos, Ana Sofía Mari, Zoltan Foote, Kelly D. Rosenberg, Paul B. Oxenford, Simón Germann, Jurgen Amaral, Robert Almeida, Leonardo Brito de Chakravarty, M. Mallar Lyketsos, Constantine G. Salloway, Stephen Butenko, Konstantin Elias, Gavin J. B. Lozano, Andres M. Okun, Michael S. Ponce, Francisco A. Neudorfer, Clemens Rajamani, Nanditha Deeb, Wissam Wang, Fuyixue Burke, Anna D. Horn, Andreas Salvato, Bryan Loh, Aaron Li, Ningfei Setsompop, Kawin Tang-Wai, David F. Anderson, William S. Sabbagh, Marwan N. Boutet, Alexandre |
| Author_xml | – sequence: 1 givenname: Ana Sofía surname: Ríos fullname: Ríos, Ana Sofía organization: Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin – sequence: 2 givenname: Simón orcidid: 0000-0003-2989-3861 surname: Oxenford fullname: Oxenford, Simón organization: Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin – sequence: 3 givenname: Clemens surname: Neudorfer fullname: Neudorfer, Clemens organization: Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin – sequence: 4 givenname: Konstantin surname: Butenko fullname: Butenko, Konstantin organization: Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin – sequence: 5 givenname: Ningfei orcidid: 0000-0003-3315-3591 surname: Li fullname: Li, Ningfei organization: Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin – sequence: 6 givenname: Nanditha surname: Rajamani fullname: Rajamani, Nanditha organization: Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin – sequence: 7 givenname: Alexandre orcidid: 0000-0001-6942-5195 surname: Boutet fullname: Boutet, Alexandre organization: Division of Neurosurgery, Department of Surgery, University Health Network and University of Toronto, Krembil Research Institute, University of Toronto, Joint Department of Medical Imaging, University of Toronto – sequence: 8 givenname: Gavin J. B. orcidid: 0000-0002-7495-550X surname: Elias fullname: Elias, Gavin J. 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Martinos Center for Biomedical Imaging, Department of Radiology, Harvard Medical School, Massachusetts General Hospital, Harvard-MIT Health Sciences and Technology, MIT – sequence: 13 givenname: Kawin surname: Setsompop fullname: Setsompop, Kawin organization: Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Harvard Medical School, Massachusetts General Hospital, Harvard-MIT Health Sciences and Technology, MIT, Department of Radiology, Stanford University – sequence: 14 givenname: Bryan surname: Salvato fullname: Salvato, Bryan organization: University of Florida Health Jacksonville – sequence: 15 givenname: Leonardo Brito de surname: Almeida fullname: Almeida, Leonardo Brito de organization: Norman Fixel Institute for Neurological Diseases, Departments of Neurology and Neurosurgery, University of Florida – sequence: 16 givenname: Kelly D. orcidid: 0000-0002-2436-4138 surname: Foote fullname: Foote, Kelly D. organization: Norman Fixel Institute for Neurological Diseases, Departments of Neurology and Neurosurgery, University of Florida – sequence: 17 givenname: Robert surname: Amaral fullname: Amaral, Robert organization: Cerebral Imaging Centre, Douglas Research Centre – sequence: 18 givenname: Paul B. surname: Rosenberg fullname: Rosenberg, Paul B. organization: Department of Psychiatry and Behavioral Sciences and Richman Family Precision Medicine Center of Excellence, School of Medicine, Johns Hopkins University – sequence: 19 givenname: David F. surname: Tang-Wai fullname: Tang-Wai, David F. organization: Krembil Research Institute, University of Toronto, Department of Medicine, Division of Neurology, University Health Network and University of Toronto – sequence: 20 givenname: David A. surname: Wolk fullname: Wolk, David A. organization: Department of Neurology, University of Pennsylvania – sequence: 21 givenname: Anna D. surname: Burke fullname: Burke, Anna D. organization: Barrow Neurological Institute – sequence: 22 givenname: Stephen orcidid: 0000-0002-2631-0942 surname: Salloway fullname: Salloway, Stephen organization: Department of Psychiatry and Human Behavior and Neurology, Alpert Medical School of Brown University, Memory & Aging Program, Butler Hospital – sequence: 23 givenname: Marwan N. surname: Sabbagh fullname: Sabbagh, Marwan N. organization: Barrow Neurological Institute – sequence: 24 givenname: M. Mallar surname: Chakravarty fullname: Chakravarty, M. 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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36517479$$D View this record in MEDLINE/PubMed |
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| DOI | 10.1038/s41467-022-34510-3 |
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| Snippet | Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer’s Disease. Outcomes from randomized clinical trials... Deep brain stimulation (DBS) to the fornix is an investigational treatment for patients with mild Alzheimer's Disease. Outcomes from randomized clinical trials... Deep brain stimulation has been investigated as a potential treatment for cognitive impairments in Alzheimer’s disease. Here the authors carry out post hoc... |
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| SubjectTerms | 59 59/36 59/57 692/308/575 692/699/375/132/1283 Alzheimer Disease - therapy Alzheimer's disease Brain Brain - diagnostic imaging Circuits Clinical trials Cognitive ability Deep Brain Stimulation Fornix Fornix, Brain - diagnostic imaging Fornix, Brain - physiology Health services Humanities and Social Sciences Humans multidisciplinary Neural networks Neurodegenerative diseases Patients Randomized Controlled Trials as Topic Science Science (multidisciplinary) Stimulation Stria terminalis Structure-function relationships Thalamus |
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| Title | Optimal deep brain stimulation sites and networks for stimulation of the fornix in Alzheimer’s disease |
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