Increased activation of precuneus and posterior cingulate cortex in resting state fMRI in patients with functional movement disorders after undergoing a motor retraining program
Kwan-Jin Jung1, Sarah Mufti2, and Kathrin LaFaver2

1Radiology, University of Louisville, Louisville, KY, United States, 2Neurology, University of Louisville, Louisville, KY, United States

Synopsis

Functional movement disorders (FMD) can be significantly reduced with a one-week motor retraining program. Our study compared resting state fMRI before and after treatment of 6 FMD patients. We found increased activity in the posterior default mode network, specifically the precuneus and posterior cingulate cortex, in 4 out of 6 patients after treatment, which correlated with clinical improvement of motor symptoms. Our findings suggest that restoration of normal movements in FMD patients are accompanied by increased default mode network activation.

Background

Functional movement disorders (FMD) are characterized by involuntary tremor, hyperkinetic movements or astasia-abasia. Prior neuroimaging studies in FMD patients using SPECT1 and fMRI found abnormal activation within motor areas2, the amygdala3 and the right temporal parietal junction4. In these studies, FMD patients were compared with control subjects or the same patient was compared during voluntary and involuntary movements. We set out to compare resting state fMRI activity before and after patients underwent a recently developed treatment program for FMD symptoms using motor retraining strategies.5

Methods

Resting state fMRI was obtained from 6 FMD patients with moderate to severe symptoms before and after undergoing a one-week motor retraining program in an inpatient setting. Symptoms were self-rated at the beginning and end of the program (Table 1). During resting state fMRI, patients were instructed to look at a fixation cross on a blue background. The scan time was 8 min 32 s with a repetition time = 2 s, an echo time = 28 ms and an isotropic voxel size = 3.2 mm x 3.2 mm x 3.2 mm. The temporal resolution of fMRI data was doubled using the half-TR method6 followed by a motion correction to address the expected involuntary motion of the FMD patients. The pre- and post-treatment sessions were analyzed using a multi-session tensor independent component analysis (ICA) program of FSL7 into 30 ICA components for the contrast at the two time points in each subject. The meaningful ICA components were identified manually in each subject by a trained and experienced analyst. Among the brain regions with a signal change between the pre- and post- treatments at the selected meaningful ICA component, only brain regions consistent over at least 3 subjects were manually identified.

Results

All 6 patients underwent the one-week treatment program as planned. Symptom improvement at the end of the treatment intervention was noticeable except in one participant (number 5) as listed in Table 1. The patients were able to maintain stillness of the head except for steady tremor vibrational motion in 4 scan sessions among 12 scan sessions (Fig. 1). The half-Tr method helped limit the image volume with motion artifacts and estimated the motion more accurately. Additionally, the ICA separated the motion from the default mode activation. The multi-session tensor ICA demonstrated increased activation in the precuneus and posterior cingulated cortex (PCC) in 4 out of 6 patients after treatment (Table 2, Fig. 2 and Fig. 3). No change in activation was found in 2 subjects, one of whom reported no change in clinical symptoms at the end of the therapy intervention. Other brain areas were activated together with the precuneus cortex and PCC as included in the same ICA component (Fig. 3).

Conclusions

Patients with FMD showed significant clinical improvement after a one-week inpatient rehabilitation program employing motor retraining strategies. Resting state fMRI before and after the program demonstrated a more active engagement of the precuneus and posterior cingulated cortex after treatment. The precuneus is involved in visuospatial monitoring and increased activation after treatment may reflect improved control of movements.8 The findings from this study may help in better understanding of FMD pathophysiology and treatment approaches.

Acknowledgements

This study was partially supported by an internal grant from Department of Neurology at University of Louisville.

References

1. Czarnecki K, et al. SPECT perfusion patterns distinguish psychogenic from essential tremor. Parkinsonism Relat Disord 2011;17(5):328-332.

2. Voon V, et al. Aberrant supplementary motor complex and limbic activity during motor preparation in motor conversion disorder. Mov Disord 2011;26(13):2396-2403.

3. Voon V, et al. Emotional stimuli and motor conversion disorder. Brain : a journal of neurology 2010;133(Pt 5):1526-1536.

4. Voon V, et al. The involuntary nature of conversion disorder. Neurology 2010;74(3):223-228.

5. Czarnecki K, et al. Functional movement disorders: successful treatment with a physical therapy rehabilitation protocol. Parkinsonism Relat Disord 2012;18(3):247-251.

6. Jung K-J. An Alternative Method of Slice-timing Correction: Temporal Upsampling of Functional MRI Using a Half-TR Method. Int Soc Magn Reson Med: Functional MRI Workshop2014.

7. Beckmann CF, Smith SM. Tensorial extensions of independent component analysis for multisubject FMRI analysis. Neuroimage 2005;25(1):294-311.

8. Cavanna AE, Trimble MR. The precuneus: a review of its functional anatomy and behavioural correlates. Brain : a journal of neurology 2006;129(Pt 3):564-583.

Figures

Table 1. Self-rating of motor symptom severity before and after treatment intervention. The symptom severity scale was: 1=no symptoms, 2=borderline symptoms, 3=mild symptoms, 4=moderate symptoms, 5=marked symptoms, 6=severe symptoms, 7 = very severe symptoms.

Table 2. Selected brain regions with increased activity after the treatment intervention in multi-session tensor ICA analysis of the resting state fMRI.

Fig. 1. Motion during the pre-treatment scan of subject 5. A vibrational motion was observed.

Fig. 2. Increased activity in the precuneus cortex of subject 1 (top panel) and 2 (bottom panel). MNI coordinates (in mm) of the precuneus cortex were (6, -66, 30) and (16, -68, 44).

Fig. 3. Increased activity in the precuneus cortex of subject 3 (top panel) and 6 (bottom panel). MNI coordinates (in mm) of the precuneus cortex were (12, -56, 34) and (0, -64, 28).



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
3789