4.6 Article

Brainstem trigeminal fiber microstructural abnormalities are associated with treatment response across subtypes of trigeminal neuralgia

Journal

PAIN
Volume 162, Issue 6, Pages 1790-1799

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/j.pain.0000000000002164

Keywords

Trigeminal neuralgia; Facial pain; Lesion; Multiple sclerosis; Diffusion tensor imaging; Tractography; Treatment response

Funding

  1. Canadian Institutes of Health Research [MOP130555]
  2. Canadian Institutes of Health Research Doctoral Research Award [GSD164127]

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The study utilized diffusion tensor imaging (DTI) to identify microstructural abnormalities in the brainstem trigeminal fibers as a common biomarker of surgical response in trigeminal neuralgia (TN), which may vary across different subtypes of TN. Abnormalities in the affected pontine trigeminal fibers were found to distinguish treatment nonresponders from responders, with the degree of abnormalities associated with the likelihood of surgical response across TN subtypes. This highlights the potential value of DTI as a noninvasive tool for predicting treatment response and understanding differences in TN treatment outcomes.
Neurosurgical treatments for trigeminal neuralgia (TN) can provide long-lasting pain relief; however, some patients fail to respond and undergo multiple, repeat procedures. Surgical outcomes can vary depending on the type of TN, but the reasons for this are not well understood. Neuroimaging studies of TN point to abnormalities in the brainstem trigeminal fibers; however, whether this is a common characteristic of treatment nonresponse across different subtypes of TN is unknown. Here, we used diffusion tensor imaging (DTI) to determine whether the brainstem trigeminal fiber microstructure is a common biomarker of surgical response in TN and whether the extent of these abnormalities is associated with the likelihood of response across subtypes of TN. We studied 98 patients with TN (61 classical TN, 26 TN secondary to multiple sclerosis, and 11 TN associated with a solitary pontine lesion) who underwent neurosurgical treatment and 50 healthy controls. We assessed treatment response using pain intensity measures and examined microstructural features by extracting pretreatment DTI metrics from the proximal pontine segment of the trigeminal nerves. We found that microstructural abnormalities in the affected pontine trigeminal fibers (notably, lower fractional anisotropy and higher radial diffusivity) highlight treatment nonresponders (n = 47) compared with responders (n = 51) and controls, and that the degree of abnormalities is associated with the likelihood of surgical response across subtypes of TN. These novel findings demonstrate the value of DTI as an objective, noninvasive tool for the prediction of treatment response and elucidate the features that distinguish treatment responders from nonresponders in the TN population.

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