Author
Listed:
- Yiheng Tu
(Harvard Medical School
Massachusetts General Hospital, Harvard Medical School)
- Zening Fu
(Tri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, Emory University)
- Cuiping Mao
(Harvard Medical School
Second Affiliated Hospital of Xi’An Jiao Tong University)
- Maryam Falahpour
(University of California San Diego)
- Randy L. Gollub
(Harvard Medical School)
- Joel Park
(Harvard Medical School)
- Georgia Wilson
(Harvard Medical School)
- Vitaly Napadow
(Massachusetts General Hospital, Harvard Medical School)
- Jessica Gerber
(Massachusetts General Hospital, Harvard Medical School)
- Suk-Tak Chan
(Massachusetts General Hospital, Harvard Medical School)
- Robert R. Edwards
(Harvard Medical School)
- Ted J. Kaptchuk
(Harvard Medical School)
- Thomas Liu
(University of California San Diego)
- Vince Calhoun
(Tri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, Emory University)
- Bruce Rosen
(Massachusetts General Hospital, Harvard Medical School)
- Jian Kong
(Harvard Medical School
Massachusetts General Hospital, Harvard Medical School)
Abstract
Thalamocortical dysrhythmia is a key pathology of chronic neuropathic pain, but few studies have investigated thalamocortical networks in chronic low back pain (cLBP) given its non-specific etiology and complexity. Using fMRI, we propose an analytical pipeline to identify abnormal thalamocortical network dynamics in cLBP patients and validate the findings in two independent cohorts. We first identify two reoccurring dynamic connectivity states and their associations with chronic and temporary pain. Further analyses show that cLBP patients have abnormal connectivity between the ventral lateral/posterolateral nucleus (VL/VPL) and postcentral gyrus (PoCG) and between the dorsal/ventral medial nucleus and insula in the less frequent connectivity state, and temporary pain exacerbation alters connectivity between the VL/VPL and PoCG and the default mode network in the more frequent connectivity state. These results extend current findings on thalamocortical dysfunction and dysrhythmia in chronic pain and demonstrate that cLBP pathophysiology and clinical pain intensity are associated with distinct thalamocortical network dynamics.
Suggested Citation
Yiheng Tu & Zening Fu & Cuiping Mao & Maryam Falahpour & Randy L. Gollub & Joel Park & Georgia Wilson & Vitaly Napadow & Jessica Gerber & Suk-Tak Chan & Robert R. Edwards & Ted J. Kaptchuk & Thomas Li, 2020.
"Distinct thalamocortical network dynamics are associated with the pathophysiology of chronic low back pain,"
Nature Communications, Nature, vol. 11(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17788-z
DOI: 10.1038/s41467-020-17788-z
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