Introduction
For much of the twentieth century, functional neurological (conversion) disorder (FND) was marginalized across neurology and psychiatry despite being the second most common reason for neurological referral and incurring significant healthcare costs (Barsky, Orav, & Bates, Reference Barsky, Orav and Bates2005; Hallett, Reference Hallett2006; Stone et al., Reference Stone, Carson, Duncan, Roberts, Warlow, Hibberd and Sharpe2010a). Patients with FND have symptoms not explained by traditional neurological conditions, including limb weakness, tremor, gait abnormalities, seizures, sensory deficits, fatigue, pain, and cognitive difficulties (Espay et al., Reference Espay, Aybek, Carson, Edwards, Goldstein, Hallett and Morgante2018a). FND has received renewed interest following increased recognition of physical examination signs and semiologic features that are specific for the diagnosis (Avbersek & Sisodiya, Reference Avbersek and Sisodiya2010; Daum, Hubschmid, & Aybek, Reference Daum, Hubschmid and Aybek2014). Improved diagnostic specificity offers an opportunity to elucidate the neurobiology of FND, decrease stigma, and develop biologically-informed treatments.
Though in its early stages compared to other neuropsychiatric disorders, functional magnetic resonance imaging (MRI) studies of FND have characterized several differences compared to healthy subjects including: (1) amygdalar and periaqueductal gray (PAG) hyperreactivity to negatively-valenced stimuli (Aybek et al., Reference Aybek, Nicholson, Zelaya, O'Daly, Craig, David and Kanaan2014b; Aybek et al., Reference Aybek, Nicholson, O'Daly, Zelaya, Kanaan and David2015; Hassa et al., Reference Hassa, Sebastian, Liepert, Weiller, Schmidt and Tüscher2017; Voon et al., Reference Voon, Brezing, Gallea, Ameli, Roelofs, LaFrance and Hallett2010a); (2) increased amygdalar and cingulo-insular connectivity to motor control areas (Diez et al., Reference Diez, Ortiz-Teran, Williams, Jalilianhasanpour, Ospina, Dickerson and Perez2019; Espay et al., Reference Espay, Maloney, Vannest, Norris, Eliassen, Neefus and Szaflarski2018c; van der Kruijs et al., Reference van der Kruijs, Bodde, Vaessen, Lazeron, Vonck, Boon and Jansen2012; Voon et al., Reference Voon, Brezing, Gallea, Ameli, Roelofs, LaFrance and Hallett2010a); (3) right temporoparietal junction hypoactivation and altered connectivity with sensorimotor cortices (Baek et al., Reference Baek, Donamayor, Morris, Strelchuk, Mitchell, Mikheenko and Voon2017; Maurer et al., Reference Maurer, LaFaver, Ameli, Epstein, Hallett and Horovitz2016a; Voon et al., Reference Voon, Gallea, Hattori, Bruno, Ekanayake and Hallett2010b); and (4) motor deficits (Voon, Brezing, Gallea, & Hallett, Reference Voon, Brezing, Gallea and Hallett2011). Quantitative MRI has also elucidated gray matter abnormalities in FND, including increased amygdalar volume (Maurer et al., Reference Maurer, LaFaver, Limachia, Capitan, Ameli, Sinclair and Horovitz2018), cingulo-insular atrophy (Labate et al., Reference Labate, Cerasa, Mula, Mumoli, Gioia, Aguglia and Gambardella2011; Perez et al., Reference Perez, Williams, Matin, LaFrance, Costumero-Ramos, Fricchione and Dickerson2017b; Perez et al., Reference Perez, Matin, Williams, Tanev, Makris, LaFrance and Dickerson2018; Vasta et al., Reference Vasta, Cerasa, Sarica, Bartolini, Martino, Mari and Labate2018), decreased pituitary volume (Atmaca, Baykara, Mermi, Yildirim, & Akaslan, Reference Atmaca, Baykara, Mermi, Yildirim and Akaslan2016), and sensorimotor and striato-thalamic alterations (Aybek et al., Reference Aybek, Nicholson, Draganski, Daly, Murphy, David and Kanaan2014a; Espay et al., Reference Espay, Maloney, Vannest, Norris, Eliassen, Neefus and Szaflarski2018c; Maurer et al., Reference Maurer, LaFaver, Limachia, Capitan, Ameli, Sinclair and Horovitz2018; Nicholson et al., Reference Nicholson, Aybek, Kempton, Daly, Murphy, David and Kanaan2014).
By contrast, white matter investigations in FND are in their infancy (Ding et al., Reference Ding, An, Liao, Li, Wu, Xu and Chen2013; Hernando, Szaflarski, Ver Hoef, Lee, & Allendorfer, Reference Hernando, Szaflarski, Ver Hoef, Lee and Allendorfer2015; Lee et al., Reference Lee, Allendorfer, Gaston, Griffis, Hernando, Knowlton and Ver Hoef2015; Tomic et al., Reference Tomic, Agosta, Sarasso, Petrovic, Basaia, Pesic and Filippi2018), despite non-specific white matter lesions being common in this population (Bolen, Koontz, & Pritchard, Reference Bolen, Koontz and Pritchard2016) and reported links between subcortical hyperintensities and the development of somatic symptom disorders (Inamura et al., Reference Inamura, Shinagawa, Nagata, Tagai, Nukariya and Nakayama2015). This literature gap, if clarified, can help contextualize the broadly-distributed, multi-network findings described in FND. By measuring the diffusion of water molecules, diffusion tensor imaging (DTI) allows for the in vivo characterization of white matter microstructural integrity. Fractional anisotropy (FA) is a global microstructural integrity measure, with reduced FA linked to decreased white matter integrity. In 44 patients with functional dystonia compared to healthy controls, FA reductions in the uncinate fasciculus, cingulum bundle, corpus callosum, corticospinal tract, anterior thalamic radiations, and brainstem structures were identified using tract-based spatial statistics (Tomic et al., Reference Tomic, Agosta, Sarasso, Petrovic, Basaia, Pesic and Filippi2018); this study also showed robust white matter differences in those with fixed functional dystonia compared to mobile functional dystonia patients and healthy controls. DTI studies in 8 (Hernando et al., Reference Hernando, Szaflarski, Ver Hoef, Lee and Allendorfer2015) and 16 (Lee et al., Reference Lee, Allendorfer, Gaston, Griffis, Hernando, Knowlton and Ver Hoef2015) individuals with psychogenic nonepileptic seizures (PNES, a.k.a. dissociative seizures) showed microstructural differences in the uncinate fasciculus compared to controls; the internal/external capsules and corona radiata also showed group-level differences in one PNES study (Lee et al., Reference Lee, Allendorfer, Gaston, Griffis, Hernando, Knowlton and Ver Hoef2015). A study performed in 17 patients with PNES showed altered (more lattice-like) structural connectivity profiles compared to controls, including disruptions in sensorimotor, attentional, default mode, and subcortical networks (Ding et al., Reference Ding, An, Liao, Wu, Xu, Zhou and Chen2014). These studies, however, did not adjust for comorbid depression and anxiety, and FA profiles inconsistently correlated with clinical data.
In this DTI study, we performed graph theory and tractography analyses to examine white matter integrity in 32 patients with FND compared to 36 healthy controls. First, a white matter-based graph theory analysis was performed to identify the cortico-subcortical areas, and associated fiber bundles originating from these identified brain regions, exhibiting microstructural differences in patients compared to controls. Second, probabilistic tractography was employed to quantify within-tract FA differences in patients with FND compared to controls. Within-group tractography analyses also investigated relationships between FA profiles, patient-reported FND severity, physical disability, and illness duration. In this cohort, we previously characterized gray matter and resting-state salience network alterations (Diez et al., Reference Diez, Ortiz-Teran, Williams, Jalilianhasanpour, Ospina, Dickerson and Perez2019; Perez et al., Reference Perez, Matin, Barsky, Costumero-Ramos, Makaretz, Young and Dickerson2017a, Reference Perez, Williams, Matin, LaFrance, Costumero-Ramos, Fricchione and Dickerson2017b, Reference Perez, Matin, Williams, Tanev, Makris, LaFrance and Dickerson2018), theorizing that impaired multimodal integration and emotion dysregulation play important roles in the pathophysiology of FND (Perez et al., Reference Perez, Dworetzky, Dickerson, Leung, Cohn, Baslet and Silbersweig2015; Pick, Goldstein, Perez, & Nicholson, Reference Pick, Goldstein, Perez and Nicholson2019). Thus, we hypothesized that individuals with FND would exhibit reduced limbic white matter integrity compared to controls, and that reduced FA in these tracts would correlate with symptom severity, disability and illness duration.
Materials and methods
Participants and questionnaires
Thirty-two subjects with FND (22 women, 10 men; mean age = 40.9 ± 13.1; average illness duration = 3.5 ± 4.5 years) were recruited from the Massachusetts General Hospital FND Clinic between 2014 and 2018 following a ‘rule-in’ FND diagnosis in accord with the Diagnostic and Statistical Manual of Mental Disorders 5th Edition criteria (American Psychiatric Association, 2013; Stone, LaFrance, Levenson, & Sharpe, Reference Stone, LaFrance, Levenson and Sharpe2010b). Four additional patients were enrolled but excluded following image acquisition and preprocessing (see online Supplementary Methods). Given the overlap across the FND spectrum (Perez et al., Reference Perez, Dworetzky, Dickerson, Leung, Cohn, Baslet and Silbersweig2015), we used a transdiagnostic approach that included clinically-established functional movement disorders [n = 17; five tremor, five gait, one jerky movements, one paroxysmal truncal/head movements, five mixed (including one with functional dystonia)], functional weakness (n = 13), and documented (n = 13) or clinically-established (n = 1) PNES. Eleven of 32 subjects had mixed phenotypes. Exclusion criteria included major neurological comorbidities with MRI abnormalities (e.g. encephalomalacia), epilepsy, poorly controlled medical problems with known central nervous system consequences, active substance dependence, history of mania or psychosis, and/or active suicidality. Comorbid psychiatric diagnoses assessed using the Structured Clinical Interview (SCID-I) for DSM-IV-TR were present in 29 of 32 participants. Fourteen were on selective serotonin reuptake inhibitors (SSRIs) and/or serotonin-norepinephrine reuptake inhibitors (SNRIs). See online Supplementary Table S1 for clinical information. Thirty-six healthy controls (24 women, 12 men; mean age = 39.2 ± 11.8) were recruited through local advertisements, and all screened negative for SCID-I major psychiatric comorbidities (one had past depression not-otherwise-specified). Four additional controls were enrolled but excluded due to lifetime major psychiatric comorbidities. All subjects signed informed consent and the Partners Human Research Committee approved this study.
Patients completed the Conversion Disorder subscale of the Screening for Somatoform Symptoms-7 scale (SOMS:CD) (Rief & Hiller, Reference Rief and Hiller2003) and the Patient Health Questionnaire-15 (PHQ15) (Kroenke, Spitzer, & Williams, Reference Kroenke, Spitzer and Williams2002) as patient-reported FND symptom severity measures. The SOMS:CD is a 14-item measure of FND symptoms within the past 7 days scored on a 5-point scale. The PHQ15 is a 15-item measure of somatic complaints within the past 4 weeks scored on a 3-point scale. To reduce the number of statistical tests, a SOMS:CD–PHQ15 composite was created by averaging the z-scores of the two scales consistent with our previously published approach (Diez et al., Reference Diez, Ortiz-Teran, Williams, Jalilianhasanpour, Ospina, Dickerson and Perez2019). Patients also completed the Short Form Health Survey 36 (SF-36) as a questionnaire of health-related quality of life, and the composite physical health score was used as a physical disability measure (Ware & Sherbourne, Reference Ware and Sherbourne1992). Subjects also completed the Beck Depression Inventory-II (BDI) and the Spielberger State-Trait Anxiety Inventory (STAI).
Data acquisition and preprocessing
See online Supplementary Methods for T1-weighted and diffusion-weighted MRI scan acquisition parameters. Data preprocessing is also outlined in the online Supplementary Methods. Note: the total head motion index was computed as a covariate of non-interest to account for possible head motion confounds (Yendiki, Koldewyn, Kakunoori, Kanwisher, & Fischl, Reference Yendiki, Koldewyn, Kakunoori, Kanwisher and Fischl2014).
Weighted-degree and link-level graph theory analyses
Graph theory was used to delineate white matter integrity profiles in relation to cortico-subcortical structures (Rubinov & Sporns, Reference Rubinov and Sporns2010; van den Heuvel & Sporns, Reference van den Heuvel and Sporns2011). The first step to study the structural connectome is to create an individual-subject graph. These graphs are composed of nodes (brain regions of interest) and links (defining the connectivity property of interest). For the nodes, an 87 region brain parcellation was used: 68 cortical and 16 subcortical regions from the Desikan atlas, the midbrain and pons structures from the brainstem parcellation (Iglesias et al., Reference Iglesias, Van Leemput, Bhatt, Casillas, Dutt and Schuff2015), and the PAG from a probabilistic map (Keuken et al., Reference Keuken, Bazin, Crown, Hootsmans, Laufer, Muller-Axt and Forstmann2014).
The next step to generate an individual-subject structural connectome is to select the metric defining the link connectivity measure between each pair of 87 regions (van den Heuvel & Sporns, Reference van den Heuvel and Sporns2011). Commonly used DTI metrics are the mean FA of all the fiber connections between each pair of nodes and fiber density (how many fibers connect each pair of nodes). We focused on the mean FA (a proxy of microstructural integrity) to identify less efficacious connectivity patterns (van den Heuvel & Sporns, Reference van den Heuvel and Sporns2011), as well as to allow the graph theory and within-tract analyses (see below) to use the same diffusion parameter. To complement the FA graph analysis, the fiber density (streamline) metric was also used as an additional link connectivity measure in a secondary analysis.
To compute the path of the fibers connecting each pair of regions (nodes), the PROBTRACKX2 tool was used taking 100 samples from the range of possible principal diffusion directions within each voxel. To remove low probability voxels from the density map (a map defining how many fibers pass through each voxel connecting two regions), we eliminated those voxels in the path containing less than 0.1% of all the fibers starting in the seed region. To compute the mean FA of the above defined path at the individual-subject level, the FA values in each voxel were weighted by the probability of fibers passing through that voxel when connecting a pair of regions. Thus, FA values of the voxels with highest probability were given a greater weight when computing the FA values defining the connectivity of two regions. An 87 × 87 connectivity matrix was obtained for each subject.
While different graph analysis metrics are available (Konigs et al., Reference Konigs, van Heurn, Bakx, Vermeulen, Goslings, Poll-The and Pouwels2017; Rubinov & Sporns, Reference Rubinov and Sporns2010; van den Heuvel & Sporns, Reference van den Heuvel and Sporns2011), weighted-degree is an index that sums all the weights of the links starting in a given node (i.e. one of the 87 regions-of-interest). The weighted-degree calculation is defined as:
$${\rm W}{\rm D}_i = \mathop \sum \limits_{\,j = 1}^n {\rm FAM}\lpar {i,j} \rpar $$where the weighted-degree for the node i is computed as the sum of all the FA values of the links starting in node i and ending in the rest of the n nodes of the brain. Thus, the weighted-degree FA value is a proxy of the integrity of white matter originating from a given node (brain area).
To examine between-group differences in the weighted-degree FA maps, a general linear model was performed controlling for age, gender, and head motion, and findings were corrected for multiple comparisons using a false-discovery-rate (FDR) q = 0.05. This identified cortical-subcortical brain areas showing differential fiber integrity in patients with FND compared to controls.
To identify altered links, a general linear model was again performed examining between-group differences at the link level. These analyses controlled for age, gender, and head motion, and findings were corrected for multiple comparisons using an FDR q = 0.05 considering all possible links. To restrict the results to the weighted-degree findings, only the resulting links starting in regions that showed group differences in the weighted-degree FA analysis were displayed.
To label altered links in patients with FND v. controls onto anatomically-defined fiber bundles, the following procedures were performed: first, we created a probabilistic white matter atlas of the 36 healthy controls by computing all the tracts defined in the query language for each of the healthy subjects (Wassermann et al., Reference Wassermann, Makris, Rathi, Shenton, Kikinis, Kubicki and Westin2016), and then the resulting probabilistic density maps were transformed to MNI space. Thereafter, the mean of these density maps across all controls was computed for each fiber bundle. Second, to map statistically significant link-level findings in relation to the created fiber bundle probabilistic atlas, we computed the density map of the fibers passing through both the starting and end points for all controls, transformed the data to MNI space, and computed the mean density map containing fibers connecting two regions. Finally, this link-level probability map was compared with the created atlas to label these links as belonging to the highest probability fiber bundle.
Tractography analyses
As a complementary analysis, we used query language informed tractography to characterize the location of FA alterations within specific fiber bundles (Colby et al., Reference Colby, Soderberg, Lebel, Dinov, Thompson and Sowell2012; Wassermann et al., Reference Wassermann, Makris, Rathi, Shenton, Kikinis, Kubicki and Westin2016). This approach incorporates information from the starting and end points of each white matter tract as well as brain areas that the tract passes through (i.e. way points). Two limbic tracts not defined in the previously published query language were constructed as follows: stria terminalis/fornix – starting in the amygdala/hippocampus and passing superior to the thalamus and through the ventral diencephalon (Kamali et al., Reference Kamali, Yousem, Lin, Sair, Jasti, Keser and Hasan2015); medial forebrain bundle/PAG – fibers starting in the PAG as defined from a 7T probabilistic atlas (Ezra, Faull, Jbabdi, & Pattinson, Reference Ezra, Faull, Jbabdi and Pattinson2015). A nonlinear transformation was subsequently applied to the tracts to project them to MNI152 space using MRtrix3 software. To generate templates for each tract to project the results, fibers from healthy controls were combined into group-based fiber bundles. Thereafter, to account for false positives we eliminated fibers with low probability (<0.1%) and high curvature (>70%). To remove crossing fibers, we computed a histogram for each voxel with the probability of the passing fibers going through each possible direction. Fibers with a probability lower than 5% of going within ±15° of the highest probability direction were removed. Additionally, fibers passing through voxels with a probability lower than 0.1% were removed.
To investigate between-group within-tract differences in FA values at the voxel-level, a general linear model was used. All between-group analyses were controlled for age, gender, and head motion. Separate secondary analyses also adjusted between-group findings for: (1) BDI and STAI-trait anxiety scores; (2) SSRI and/or SNRI use (yes/no); and (3) motor FND subtypes (PNES, functional movement disorders, or functional weakness). Correction for multiple comparisons used Monte Carlo simulation cluster-wise correction with 10 000 iterations and α value of 0.05, applied to a whole-brain white matter mask.
In addition, within-group tractography analyses were performed using a general linear model to characterize relationships between fiber tract FA values and indices of FND symptom severity (SOMS:CD–PHQ15 composite scores), physical disability (SF-36 physical health component scores), and illness duration. Within-group analyses controlled for age, gender, and head motion, and separate secondary analyses also adjusted for: (1) BDI and STAI-trait anxiety scores; (2) SSRI and/or SNRI use; and (3) motor FND subtypes. Correction for multiple comparisons used Monte Carlo simulation cluster-wise correction with 10 000 iterations and α value of 0.05, applied to a whole-brain white matter mask.
Results
Weighted-degree and link-level graph theory
Patients with FND compared to controls showed white matter differences originating from the following brain areas: bilateral amygdala, insula, parahippocampal gyri, temporal poles, precentral gyri, superior parietal lobules, putamen, periaqueductal gray, midbrain, pons and right hippocampus, entorhinal cortex, and the isthmus of the cingulate gyrus. Based on link-level analyses, seven fiber bundles showed reduced FA in patients with FND compared to controls: (1) stria terminalis/fornix; (2) medial forebrain bundle/PAG projections; (3) uncinate fasciculus; (4) extreme capsule; (5) cingulum bundle; (6) corpus callosum; and (7) striatal-postcentral gyrus projections (see Fig. 1). See online Supplementary Fig. S1 for a description of all links surviving multiple comparison correction. No statistically significant links with higher FA in FND v. controls were found. Using the fiber density (streamline) metric, there were no statistically-significant group-level weighted-degree differences.
Weighted-degree and link-level graph theory white matter analyses in patients with FND. Left panel shows cortico-subcortico-limbic-brainstem origins of the fiber bundles showing decreased FA in patients with FND compared to healthy controls (HC). Only results surviving to FDR q = 0.05 adjusting for age, gender, and head motion are displayed. The origins of the regions showing microstructural alterations in FND included the bilateral amygdala, insula, parahippocampal gyri, temporal poles, precentral gyri, superior parietal lobules, putamen, periaqueductal gray, midbrain, pons and right hippocampus, entorhinal cortex, and the isthmus of the cingulate gyrus. The middle panel displays the connectogram identifying the altered fiber bundles starting in the regions previously identified in the initial weighted-degree graph theory analyses and connecting to other brain areas; only results surviving to FDR q = 0.05 adjusting for age, gender, and head motion are displayed. Each tract was labeled based on the maximum probability of fiber identified using query language. The seven fiber bundles showing between-group alterations included: the stria terminalis/fornix, medial forebrain bundle, uncinate fasciculus, extreme capsule, cingulum bundle, corpus callosum, and striatal to postcentral gyrus projections.
Between-group tractography
Probabilistic tractography also showed reduced FA in the above identified seven white matter tracts (see Fig. 2). In secondary analyses adjusting separately for depression and anxiety scores, antidepressant use, and motor FND subtypes, all tracts remained significant except for the stria terminalis/fornix FA reductions that were no longer significant after adjusting for group-level depression and anxiety scores.
Probabilistic tractography differences in patients with FND compared to healthy controls (HC). Patients with FND in tractography analyses showed decreased FA in the following fiber bundles: stria terminalis/fornix, medial forebrain bundle, uncinate fasciculus, extreme capsule, cingulum bundle, corpus callosum, and striatal to postcentral gyrus projections. Only results surviving multiple comparisons are shown adjusting for age, gender, and head motion. Results from secondary analyses adjusting for between-group differences in depression [Beck Depression Inventory-II (BDI)] and trait anxiety [Spielberger State Trait Anxiety Inventory (STAI-T)] are also displayed.
Within-group tractography
In patients with FND, probabilistic tractography identified that physical disability and longer illness durations correlated with reduced stria terminalis/fornix fiber bundle integrity (see Fig. 3). Decreased FA in the medial forebrain bundle/PAG projections also correlated with physical disability. These within-group findings remained statistically significant when adjusting separately for individual differences in depression and anxiety scores, antidepressant use, and motor FND subtypes. There were no statistically significant findings associated with the SOMS:CD–PHQ15 composite score.
Individual differences in stria terminals/fornix and medial forebrain bundle microstructural integrity correlated with physical disability and illness duration in patients with FND. In within-group analyses, the magnitude of patient-reported physical disability (impaired SF-36 physical health) inversely correlated with stria terminalis/fornix and medial forebrain bundle FA values; illness duration also negatively correlated with stria terminalis/fornix white matter integrity. Only results surviving multiple comparisons are shown adjusting for age, gender, and head motion; all within-group findings also remained significant in secondary analyses adjusting separately for depression and anxiety, antidepressant medication use, and motor FND subtypes. Note: SF-36 scores were inverted so that higher scores represent greater physical disability.
Discussion
Consistent with hypotheses, individuals with FND compared to controls showed reduced white matter integrity in the stria terminalis/fornix, medial forebrain bundle, extreme capsule, uncinate fasciculus, cingulum bundle, corpus callosum, and striatal-postcentral gyrus projections. With the exception of the stria terminalis/fornix, these differences remained significant adjusting for group-level depression and anxiety scores. In within-group analyses, the magnitude of patient-reported physical disability (SF-36 physical health) correlated with reduced stria terminalis/fornix and medial forebrain bundle FA values; illness duration also negatively correlated with stria terminalis/fornix white matter integrity. The SOMS:CD–PHQ15 composite score did not show any statistically significant relationship with fiber bundle integrity. All significant within-group findings held adjusting for individual differences in depression and anxiety, antidepressant medication use, and motor FND subtypes. Notably, weighted-degree and link-level graph theory analyses connected the identified white matter alterations to cortico-subcortical-limbic-brainstem areas commonly implicated in the pathophysiology of FND including the amygdala, insula, parahippocampus, precentral gyrus, putamen, and PAG among other regions (Pick et al., Reference Pick, Goldstein, Perez and Nicholson2019; Voon et al., Reference Voon, Cavanna, Coburn, Sampson, Reeve and LaFrance2016).
The stria terminalis, carrying efferent amygdalar projections to the hypothalamus and septal nuclei, and the fornix, connecting the diencephalon and basal forebrain to the hippocampus, showed reduced microstructural integrity in patients with FND compared to controls. Disruptions in the integrity of the stria terminalis/fornix fiber bundle also correlated with greater physical disability and longer illness durations. These novel, clinically relevant findings can be contextualized based on the neuroimaging, neuroendocrine, and autonomic literature in FND. Across several functional MRI studies, patients with FND exhibited heightened amygdalar reactivity to affective-valenced stimuli (Aybek et al., Reference Aybek, Nicholson, O'Daly, Zelaya, Kanaan and David2015; Hassa et al., Reference Hassa, Sebastian, Liepert, Weiller, Schmidt and Tüscher2017; Voon et al., Reference Voon, Brezing, Gallea, Ameli, Roelofs, LaFrance and Hallett2010a), suggesting a neurobiological correlate of emotional dysregulation. Increased amygdalar volume was also observed in an FND cohort compared to controls (Maurer et al., Reference Maurer, LaFaver, Limachia, Capitan, Ameli, Sinclair and Horovitz2018), and individual differences in amygdalar gray matter volume positively correlated with elevated trait anxiety and mental health disability in our FND cohort (Perez et al., Reference Perez, Williams, Matin, LaFrance, Costumero-Ramos, Fricchione and Dickerson2017b). Furthermore, some patients with FND exhibit exaggerated startle responses (Seignourel et al., Reference Seignourel, Miller, Kellison, Rodriguez, Fernandez, Bauer and Okun2007) and heightened sympathetic tone in cardiac-related autonomic measures (Maurer et al., Reference Maurer, Liu, LaFaver, Ameli, Wu, Toledo and Hallett2016b). Studies have also characterized elevated skin conductance (Pick, Mellers, & Goldstein, Reference Pick, Mellers and Goldstein2016) and cortisol profiles in patients with FND, including links between heightened salary cortisol levels and negative attentional biases (Bakvis, Spinhoven, & Roelofs, Reference Bakvis, Spinhoven and Roelofs2009). Similarly, reduced hippocampal activity has been reported during stressful life event processing in individuals with FND (Aybek et al., Reference Aybek, Nicholson, Zelaya, O'Daly, Craig, David and Kanaan2014b), and adverse life event burden and maladaptive coping styles correlated with decreased hippocampal volumes (Perez et al., Reference Perez, Matin, Barsky, Costumero-Ramos, Makaretz, Young and Dickerson2017a; Williams et al., Reference Williams, Jalilianhasanpour, Matin, Fricchione, Sepulcre, Keshavan and Perez2018). While important for declarative memory, the fornix and hippocampus are also implicated in anxiety (Bannerman et al., Reference Bannerman, Rawlins, McHugh, Deacon, Yee, Bast and Feldon2004), and fornix integrity inversely correlated with somatization scores in individuals exposed to verbal abuse (Choi, Jeong, Rohan, Polcari, & Teicher, Reference Choi, Jeong, Rohan, Polcari and Teicher2009). Our findings, together with the literature, suggest convergent gray matter, white matter and activity-based amygdalar-hippocampal abnormalities in patients with FND. More research is needed to determine if the stria terminalis/fornix findings are FND specific or more closely tied to psychiatric comorbidities.
The medial forebrain bundle is a brainstem and subcortical fiber tract connecting the deep cerebellar nuclei, PAG, hypothalamus, and ventral striatum, among other structures. PAG tractography studies have verified that the medial forebrain bundle connects the PAG to the hypothalamus (Ezra et al., Reference Ezra, Faull, Jbabdi and Pattinson2015). Our finding of group-level reductions in medial forebrain bundle microstructural integrity, and correlations between decreased FA in this tract and greater physical disability, are consistent with the literature implicating the PAG in the pathophysiology of FND. Neurobiologically, the PAG is involved in defensive behaviors, pain modulation, stress responses, and homeostasis (Roelofs, Reference Roelofs2017). In FND, increased PAG activity was identified during negative emotion processing (Aybek et al., Reference Aybek, Nicholson, O'Daly, Zelaya, Kanaan and David2015), and our laboratory has characterized enhanced laterobasal amygdala-to-PAG resting state connectivity (Diez et al., Reference Diez, Ortiz-Teran, Williams, Jalilianhasanpour, Ospina, Dickerson and Perez2019). Individual differences in PAG volume also correlated with mental health disability in patients with FND (Perez et al., Reference Perez, Williams, Matin, LaFrance, Costumero-Ramos, Fricchione and Dickerson2017b). By measuring postural sway, a marker of the freezing response, one study identified impaired automatic defensive behaviors in patients with FND compared to controls (Zito, Apazoglou, Paraschiv-Ionescu, Aminian, & Aybek, Reference Zito, Apazoglou, Paraschiv-Ionescu, Aminian and Aybek2018). Together with the autonomic and neuroendocrine literature (Pick et al., Reference Pick, Goldstein, Perez and Nicholson2019), amygdala–hypothalamus and PAG–hypothalamus interactions appear to play roles in the pathophysiology of FND.
Our FND cohort also showed decreased microstructural integrity in the uncinate fasciculus, cingulate bundle, and extreme capsule, fiber bundles implicated in top-down emotion regulation and language functions (Bubb, Metzler-Baddeley, & Aggleton, Reference Bubb, Metzler-Baddeley and Aggleton2018; Makris & Pandya, Reference Makris and Pandya2009; Von Der Heide, Skipper, Klobusicky, & Olson, Reference Von Der Heide, Skipper, Klobusicky and Olson2013). Decreased FA in the uncinate fasciculus and cingulum bundle is consistent with white matter profiles previously reported in functional dystonia (Tomic et al., Reference Tomic, Agosta, Sarasso, Petrovic, Basaia, Pesic and Filippi2018). Reduced integrity of the uncinate fasciculus, a limbic fiber tract connecting the ventromedial and orbitofrontal prefrontal regions to medial temporal structures including the amygdala, has been reported across mood, anxiety, and trauma-related disorders (Jenkins et al., Reference Jenkins, Barba, Campbell, Lamar, Shankman, Leow and Langenecker2016). Interestingly, uncinate fasciculus microstructure disruptions are linked to neuroticism (McIntosh et al., Reference McIntosh, Bastin, Luciano, Maniega, Del, Royle and Deary2013), psychopathologic vulnerability to stress (Hanson, Knodt, Brigidi, & Hariri, Reference Hanson, Knodt, Brigidi and Hariri2015), and exaggerated fear-potentiated startle responses (Fani et al., Reference Fani, King, Brewster, Srivastava, Stevens, Glover and Jovanovic2015); abnormal ventromedial prefrontal cortex engagement is reported in FND populations (Voon et al., Reference Voon, Cavanna, Coburn, Sampson, Reeve and LaFrance2016). Patients with FND also exhibited reduced cingulum bundle FA, particularly in the subgenual and parahippocampal/retrospenial subsections, which have been linked to affective and nociceptive functions (anterior) and memory performance (posterior). The extreme capsule connects fronto-insular areas to the inferior parietal lobule and superior temporal gyrus (Makris & Pandya, Reference Makris and Pandya2009). It is also notable that the most affected white matter sites in the uncinate fasciculus and extreme capsule were adjacent to the insular cortices. Given the functional and gray matter neuroimaging literature identifying insular alterations in FND populations (Espay et al., Reference Espay, Maloney, Vannest, Norris, Eliassen, Neefus and Szaflarski2018b; Perez et al., Reference Perez, Matin, Barsky, Costumero-Ramos, Makaretz, Young and Dickerson2017a; Reference Perez, Williams, Matin, LaFrance, Costumero-Ramos, Fricchione and Dickerson2017b; van der Kruijs et al., Reference van der Kruijs, Bodde, Vaessen, Lazeron, Vonck, Boon and Jansen2012; Vasta et al., Reference Vasta, Cerasa, Sarica, Bartolini, Martino, Mari and Labate2018; Voon et al., Reference Voon, Brezing, Gallea and Hallett2011), we speculate that peri-insular structural and functional alterations relate to deficits in multimodal integration, interoception, and emotional awareness (Perez et al., Reference Perez, Dworetzky, Dickerson, Leung, Cohn, Baslet and Silbersweig2015).
Other findings included microstructural alterations in the corpus callosum and striatal radiations to the post-central gyrus. Notably, temporoparietal (posterior) aspects of the corpus callosum showed FA reductions in patients with FND compared to controls. This finding may relate to impaired hemispheric transfer of information and altered bodily processing and self-agency perceptions that have been implicated in the pathophysiology of FND (Devinsky, Reference Devinsky2000; Voon et al., Reference Voon, Gallea, Hattori, Bruno, Ekanayake and Hallett2010b). Disruptions in striatal–postcentral gyrus connections also warrant more inquiry in relation to sensory gating and attentional mechanisms.
An unanswered question relates to how to optimally contextualize the fiber bundle differences identified in this study, particularly whether the findings relate to disease mechanisms, predisposing vulnerabilities, psychiatric comorbidities, and/or compensatory processes (Begue, Adams, Stone, & Perez, Reference Begue, Adams, Stone and Perez2019). While studies with larger sample sizes and longitudinal neuroimaging data collection are needed to clarify these issues, it is notable that the integrity of two specific fiber tracts, the stria terminalis/fornix and the medial forebrain bundle, were implicated in patient-reported physical disability and illness duration. Given the high frequency of uncinate fasciculus alterations characterized in studies of mood and anxiety disorders, we speculate that this fiber tract disruption relates more broadly to emotional dysregulation. A particularly important theme warranting additional research is the role of experience and activity-dependent white and gray matter neuroplasticity. Such research in FND populations should consider antenatal and genetic-epigenetic influences, developmental trajectories, life experiences, psychiatric comorbidities, mobility levels, number of relapses, and prior treatments among other factors (Keynejad et al., Reference Keynejad, Frodl, Kanaan, Pariante, Reuber and Nicholson2018; Kozlowska et al., Reference Kozlowska, Griffiths, Foster, Linton, Williams and Korgaonkar2017; Ludwig et al., Reference Ludwig, Pasman, Nicholson, Aybek, David, Tuck and Stone2018; Sampaio-Baptista & Johansen-Berg, Reference Sampaio-Baptista and Johansen-Berg2017).
Limitations include modest sample size, psychiatric comorbidities, psychotropic medication use, phenotypic heterogeneity, and sole reliance on patient-reported symptom severity scales. While between-group and within-group tractography findings were adjusted for depression and anxiety scores which is a study strength, future studies with psychiatric and neurological controls, other FND populations, and functional somatic disorders (e.g. somatic symptom disorder with predominant pain, fibromyalgia, chronic pain disorders etc.) are needed to further contextualize our DTI findings. This is particularly needed given that several of the identified white matter tracts (and associated cortico-subcortical brain areas) are also components of the central pain matrix, suggesting the considerably more research is needed at the intersection of FND and functional somatic disorders (Begue et al., Reference Begue, Adams, Stone and Perez2019; Denk, McMahon, & Tracey, Reference Denk, McMahon and Tracey2014; Ploner, Lee, Wiech, Bingel, & Tracey, Reference Ploner, Lee, Wiech, Bingel and Tracey2011). In addition, while individuals with FND commonly exhibit mixed symptoms and/or develop new symptoms over the course of their illness, the use of a transdiagnostic research approach remains debated. Here, adjusting for FND subtypes did not robustly influence the between-group and within-group findings providing support for a transdiagnostic approach. Furthermore, it is difficult to directly compare the results of our present study with the four prior DTI studies in FND (Ding et al., Reference Ding, An, Liao, Wu, Xu, Zhou and Chen2014; Hernando et al., Reference Hernando, Szaflarski, Ver Hoef, Lee and Allendorfer2015; Lee et al., Reference Lee, Allendorfer, Gaston, Griffis, Hernando, Knowlton and Ver Hoef2015; Tomic et al., Reference Tomic, Agosta, Sarasso, Petrovic, Basaia, Pesic and Filippi2018) given phenotypic and methodological differences, underscoring the need for additional patient cohorts with larger sample sizes and multimodal methodology. Future DTI studies should also seek to combine multiple diffusion parameters to clarity the specific white matter pathology implicated in FND, particularly given that we did not find statistically significant findings using the fiber density (streamline) metric. More research is also needed to combine patient-reported scales with objective performance measures, as well as combining DTI with behavioral, neuroendocrine, and autonomic data. Methodological limitations also included a 2 mm voxel size and low B values which limited our ability to differentiate the stria terminalis and fornix. Similarly, given the proximity of the extreme and external capsules, we cannot exclude external capsule involvement. Higher resolution diffusion-weighted sequences are needed to replicate and further characterize the microstructural alterations in FND populations.
In conclusion, complementary graph theory and tractography analyses identified microstructural alterations in limbic and associative fiber bundles implicated in salience, defensive behaviors, and emotion regulation. Reduced stria terminalis/fornix and medial forebrain bundle integrity were linked to physical disability and illness duration, advancing our understanding of neurocircuit pathways in the pathophysiology of FND.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S0033291719003386
Author contributions
I.D., M.K., N.M., and D.L.P. conceptualized the study. B.W. and D.L.P. collected the data. I.D. and B.W. performed the data analyses supervised by M.K. and N.M. All authors participated in data interpretation. I.D. and D.L.P. drafted the manuscript and all authors critically reviewed, edited, and approved the final version.
Financial support
D.L.P. was funded by the National Institute of Mental Health Grant K23MH111983-02, Massachusetts General Hospital Physician-Scientist Development Award, and the Sidney R. Baer Jr. Foundation. I.D. was supported by postdoctoral fellowship program from the Basque Country Government. This study was also supported by the NIH shared instrument grant S10RR023043.
Conflict of interest
D.L.P. received honoraria from Harvard Medical School, American Academy of Neurology, Movement Disorder Society, and Toronto Western Hospital. All other authors report no conflicts of interests/disclosures.
