Disturbed spontaneous brain-activity pattern in patients with optic neuritis using amplitude of low-frequency fluctuation: a functional magnetic resonance imaging study.

OBJECTIVE: To use the amplitude of low-frequency fluctuation (ALFF) technique to investigate the local features of spontaneous brain activity in optic neuritis (ON) and their relationship with behavioral performance.
MATERIALS AND METHODS: Twelve patients with ON (four male, eight female) and twelve age-, sex-, and education status-matched healthy controls (HCs) (four male, eight female) underwent resting-state functional magnetic resonance imaging (rs-fMRI) scans. The ALFF technique was used to assess local features of spontaneous brain activity. Correlation analysis was used to explore the relationship between the observed mean ALFF values of the different areas and visual evoked potentials (VEPs) in patients with ON.
RESULTS: Compared with HCs, patients with ON had significantly decreased ALFF values in the posterior and anterior lobes of the right cerebellum, right putamen, right inferior frontal gyrus, right insula, right supramarginal gyrus, right inferior parietal lobule, left medial frontal gyrus, left superior temporal gyrus, bilateral anterior cingulate/medial frontal gyrus, and bilateral precuneus, and significantly increased ALFF values in the posterior lobes of the left and right cerebellum, right inferior temporal gyrus, right inferior temporal/fusiform gyrus, left parahippocampal gyrus, left fusiform gyrus, left calcarine fissure, left inferior parietal lobule, and left cuneus. We found negative correlations between the mean ALFF signal value of the left parahippocampal gyrus and the VEP amplitude of the right eye in ON (r=-0.584, P=0.046), and a positive correlation between the mean ALFF signal value of the bilateral precuneus and the best-corrected visual acuity of the left eye (r=0.579, P=0.048) in patients with ON.
CONCLUSION: ON mainly seems to involve dysfunction in the default-mode network, cerebellum, and limbic system, which may reflect the underlying pathologic mechanism of ON.

Introduction

Optic neuritis (ON) is an inflammation of the optic nerve, which is caused by inflammatory demyelination of the optic nerve, infection, or nonspecific inflammation. The main clinical manifestations include pain during eye movement, sudden vision loss in one or both eyes, visual field defects, relative afferent pupillary obstacle, and papilledema.1 Studies have estimated the annual incidence of ON in the USA at 5–6.4 per 100,000, with an epidemic level of 115 per 100,000.2 ON results in lesions of the optic nerve axons and apoptosis of retinal ganglion cells. Clinically, it can occur as an isolated condition or as a symptom of several systemic autoimmune diseases, such as multiple sclerosis (MS) or neuromyelitis optica.

Optical coherence tomography (OCT) is a noninvasive, high-resolution method that measures the thickness of the retinal nerve-fiber layer. Previous studies have shown that the retinal fiber side is attenuated in patients with ON, which indicates axonal and retinal ganglion-cell loss.3–5 In addition, visual evoked potential (VEP) has greater sensitivity than OCT as a diagnostic test for ON. A previous study showed that ON led to reduction in multifocal VEP amplitude.6 VEP and OCT can also detect axonal degeneration and demyelination of the optic nerve in ON. Magnetic resonance imaging (MRI) is another important clinical test for diagnosing ON, and detects inflammation of the optic nerve and optic papilla by detecting high-density shadows in the optic papilla and anatomy of the optic nerve.7 This may reveal ON demyelination and the potential existence of underlying MS.8

Functional MRI (fMRI) has been used in ON research. A previous fMRI study found decreased functional connectivity in the visual system after acute ON.9 Diffusion-tensor imaging can accurately measure fractional anisotropy (FA) and mean diffusivity of the visual pathway. Previous research has shown significantly decreased mean FA in the affected nerves of patients with idiopathic demyelinating ON.10 In the acute phase of ON, activation of the lateral geniculate nucleus during visual stimulation of the affected eye was shown to be significantly reduced.11 Other evidence has demonstrated that the optic nerve of patients with ON has reduced white-matter FA and decreased fiber structure.12 Although these findings have demonstrated that there are neuronal morphological changes in the ON, there is far less evidence for neuromechanical changes.

Resting-state fMRI (rs-fMRI) is a functional brain-imaging technique that can be used to reveal brain activity that occurs when a subject is not performing any appointed tasks.13 The rs-fMRI method is suitable for investigating the brain’s functional organization and for examining whether it is changed in neurologic or psychiatric diseases.14 Resting-state functional connectivity research has explored many networks that are consistently found in healthy subjects, in different stages of consciousness, and across species, and represent a particular mode of synchronous activity.15 Amplitude of low-frequency fluctuation (ALFF) is an rs-fMRI analysis technique used to measure spontaneous fluctuations in blood oxygen level-dependent fMRI-signal intensity for nervous activity, reflecting the intensity of regional spontaneous brain activity at rest. Whole-brain ALFF shows higher signals in the posterior cingulate, precuneus, and medial prefrontal areas of the default-mode network (DMN).16 The DMN is a “resting-state” network, which shows higher activity at rest, and tends to have a negative correlation with activity in task-positive networks. The DMN is believed to support such processes as implicit learning, autobiographical memory, prospection, and monitoring of the external environment. However, the functional connectivity of the DMN is significantly decreased in patients with Alzheimer’s disease.17 ALFF has been used as a reliable biomarker to investigate neurological conditions, such as schizophrenia,18 Parkinson’s disease,19 and glaucoma,20 and provide useful information for the understanding of these diseases. The current study is the first to our knowledge to investigate regional spontaneous brain activity in the ON and its relationship with VEP.

Materials and methods

Subjects

Twelve patients with ON (four male, eight female) were recruited from the Ophthalmology Department of the First Affiliated Hospital of Nanchang University. The diagnostic criteria of idiopathic ON21 were: 1) acute loss of vision with or without eye pain; 2) visual field abnormalities associated with damage to nerve fibers; 3) relative pupillary conduction block or abnormal VEPs; 4) no clinical or laboratory evidence of compressive, ischemic, toxic, genetic, metabolic, or invasive optic neuropathy; 5) acute vision loss due to retinal disease, sympathetic ophthalmia, or nervous system disease; 6) no treatment with any drugs before rs-fMRI scanning; 7) no obvious abnormality in brain parenchyma by brain MRI; 8) no history of congenital or acquired diseases, such as psychiatric disorder, hypertension, diabetes mellitus, or coronary artery disease, and no addictions such as heroin, smoking, or alcohol; 9) no receipt of organ transplant; and 10) moderate body shape and weight (body mass index between 18.5 and 24.9 kg/m2).

Twelve healthy controls (HCs; four male, eight female) who were age-, sex-, and education status-matched to the patients with the ON group were also recruited for this study. All HCs met the following criteria: 1) no abnormalities in visual pathways or brain parenchyma detected by brain MRI; 2) no ocular disease, naked eye or corrected visual acuity (VA) >1.0; 3) sex and age consistent with the ON group; 4) normal nervous system, with no headache and no psychiatric disorder; and 5) no contraindications for MRI. This study was authorized by the First Affiliated Hospital of Nanchang University ethics committee. All research methods followed the Declaration of Helsinki, and conformed to the principles of medical ethics. For each subject, the study protocol and procedure were fully explained, and consent was obtained, according to the Ethics Committee of the First Affiliated Hospital of Nanchang University.

MRI parameters

MRI scanning was performed on a 3 T MR scanner (Trio; Siemens AG, Berlin, Germany) as previously described.20 Functional data were acquired with a three-dimensional spoiled gradient-recalled echo sequence with the following parameters: 176 images (repetition time =1,900 ms, echo time =2.26 ms, thickness =1.0 mm, gap =0.5 mm, acquisition matrix =256×256, field of view =250×250 mm, flip angle =9°) were obtained. Also, 240 functional images (repetition time =2,000 ms, echo time =30 ms, thickness =4.0 mm, gap =1.2 mm, acquisition matrix =64×64, flip angle =90°, field of view =220×220 mm, 29 axial) were obtained.

fMRI data analysis

Functional data were classified by MRIcro software (www.mricro.com) to eliminate incomplete data. The first ten volumes were discarded due to magnetization equilibration. The rest of the data preprocessing was performed by DPARSFA (http://rfmri.org/DPARSF) software, including Digital Imaging and Communications in Medicine form transformation, slice timing, head-motion correction, spatial normalization, and smoothening with a Gaussian kernel of 6×6×6 mm3 full width at half maximum. Subjects who had more than 1.5 mm maximum shift in x, y, or z and 1.5° of angular motion were dismissed. Friston six head-motion parameters were used to regress out head-motion effects, based on recent work showing that higher-order models were more effective in removing head-motion effects.22,23 Linear regression was also applied to remove other sources of false variables, which contained the signal from ventricular and from a region centered in the brain white matter.24 After head-motion correction, the functional images were spatially normalized to the Montreal Neurological Institute space using the standard echo-planar imaging template. ALFF calculation was performed as per a previous study.16 To reduce the global effects of variability across the participants, the ALFF of each voxel was divided by the global mean ALFF value for each participant. A general linear model analysis was performed with the SPM8 toolkit to investigate the group differences in resting brain entropy between patients with ON and HCs, after controlling for the effects of age and sex. The significance level was set at P<0.05, Gaussian random-field theory-corrected, minimum z>2.3.

Brain–behavior correlation analysis

Based on the ALFF findings, the different brain regions between groups were classified as regions of interest with REST software. For each region of interest, the mean ALFF value was extracted by averaging the ALFF value over all voxels. Finally, correlation analysis was performed to investigate the relationship between the mean ALFF value in each of those different areas in the ON group and the related behavioral performances. P<0.005 was considered statistically significant.

Clinical data analysis

All patients underwent pattern-reversal VEP stimulation (RETIport electrophysiological instrument; Roland Consult Stasche & Finger GmbH, Brandenburg an der Havel, Germany) in a dark and quiet room. All the patients were in a quiet state. Three active skin electrodes were placed on the scalp along the midline (over the inion) and on lateral positions (right and left). VEP recording was performed at 100 cm distance from the screen. All patients underwent monocular recording with the untested eye covered.

Using stimulus mode with pattern-reversal VEP stimulation, the parameters were set as: stimulus frequency =1.0 and 100 Hz; interphase =500 ms; number of stimulations =100; average screen brightness =5 cd/m2; spatial frequency =50 ms/s; and contrast ratio =90%. Amplitude and latency VEP values were studied at different angular dimensions of the stimulus (120′, 60′, and 15′ for stimuli with small, medium, and large spatial frequencies of stimulation, respectively). VEPs were characterized by a series of N75, P100, and N135 peaks, each characterized by a specific amplitude and latency.

Results

Demographics and visual measurements

There were no obvious differences in weight (P=0.648), age (P=0.827), height (P=0.632), or body mass index (P=0.956) between the patients with ON and the HCs. There were significant differences in best-corrected VA – right (P<0.001) and best-corrected VA – left (P=0.021) between patients with ON and the HCs. Details are presented in Table 1.

Table 1

Characteristics of participants included in the study

Characteristics	ON	HCs	t	P-values
Male/female	4/8	4/8	NA	NA
Age (years)	44.83±10.71	45.83±11.38	−0.222	0.827
Weight (kg)	57.08±7.30	58.33±5.85	−0.463	0.648
Height (cm)	160.81±9.31	161.38±6.28	−0.485	0.632
BMI (kg/m2)	21.13±1.62	21.17±1.27	−0.056	0.956
Duration of ON (days)	4.67±3.26	NA	NA	NA
Duration from onset of ON to rs-fMRI scan (days)	5.42±2.94	NA	NA	NA
Best-corrected VA, right	0.25±0.32	1.30±0.31	−8.138	,0.001#
Best-corrected VA, left	0.85±0.52	1.28±0.32	−2.481	0.021*
Latency (ms), right of the VEP	112.94±16.27	NA	NA	NA
Amplitudes (μV), right of the VEP	6.56±3.15	NA	NA	NA
Latency (ms), left of the VEP	104.78±7.13	NA	NA	NA
Amplitudes (μV), left of the VEP	12.51±6.38	NA	NA	NA

Notes:

P<0.05;

P<0.001; independent t-test, P-values between ON and HCs.

Abbreviations: ON, optic neuritis; HCs, healthy controls; NA, not applicable; BMI, body mass index; rs-fMRI, resting-state functional magnetic resonance imaging; VA, visual acuity; VEP, visual evoked potential.

ALFF differences

Compared with HCs, patients with ON had significantly decreased ALFF values in the anterior and posterior lobes of the right cerebellum, and the right putamen, right inferior frontal gyrus, right insula, right supramarginal gyrus, right inferior parietal lobule, left medial frontal gyrus, left superior temporal gyrus, bilateral anterior cingulate/medial frontal gyrus, and bilateral precuneus (Figure 1 [blue] and Table 2).

Figure 1

Significant differences in spontaneous brain activity between the ON group and HCs.

Notes: The different brain regions are seen in the bilateral cerebellum posterior lobe, right cerebellum anterior lobe, right putamen, right inferior frontal gyrus, right insula, left medial frontal gyrus, left superior temporal gyrus, right supramarginal gyrus, bilateral anterior cingulate/medial frontal gyrus, bilateral precuneus, right inferior parietal lobule, left cerebellum posterior lobe, right inferior temporal gyrus, left parahippocampal gyrus, right inferior temporal/fusiform gyrus, left fusiform gyrus, left calcarine fissure, left inferior parietal lobule, and left cuneus. The red areas denote higher ALFF brain regions, and the blue areas denote lower ALFF brain regions (P<0.05 for multiple comparisons using Gaussian random-field theory (z>2.3, cluster-wise P<0.05 corrected).

Abbreviations: ON, optic neuritis; HCs, healthy controls; ALFF, amplitude of low-frequency fluctuation; L, left; R, right.

Table 2

Brain regions with significant differences in ALFF between the ON and HC groups

ON group and HCs				MNI coordinates
Brain areas	BA	t-score of peak voxels	Voxels	x	y	z
ON < HCs
Right cerebellum posterior lobe	–	−2.686	21	33	−66	−21
Right cerebellum anterior lobe	–	−3.890	35	15	−48	−21
Right putamen	–	−3.657	35	21	9	−3
Right inferior frontal gyrus	47	−4.642	33	51	42	−3
Right insula	48	−3.048	33	33	12	3
Left medial frontal gyrus	10	−4.711	146	−6	60	18
Left superior temporal gyrus	39	−3.387	23	−60	−57	24
Right supramarginal gyrus	40	−3.656	29	54	−48	24
Bilateral anterior cingulate/medial frontal gyrus	32, 10, 6, 8	−5.489	341	−3	36	30
Bilateral precuneus	7, 31	−3.728	91	12	−51	33
Right supramarginal gyrus	40	−3.724	48	63	−30	39
Right inferior parietal lobule	40, 42, 48	−3.254	32	48	−57	51
ON > HCs
Left cerebellum posterior lobe	–	4.516	116	−48	−69	−33
Right cerebellum posterior lobe	–	4.101	39	24	−78	−54
Right inferior temporal gyrus	20	3.155	28	42	−6	−45
Left parahippocampal gyrus	20, 36	3.803	101	−36	−24	−21
Right inferior temporal/fusiform gyrus	20, 37	3.387	79	45	−21	−24
Left fusiform gyrus	37	4.018	20	−30	−45	−18
Left parahippocampal gyrus	20	3.677	36	−30	−54	−6
Left calcarine fissure	19	5.999	41	−24	−75	6
Left inferior parietal lobule	42, 48	4.219	31	−51	−36	21
Left cuneus	19	3.491	38	−15	−90	33

Notes: Statistical threshold set at voxels with P<0.05 for multiple comparisons using Gaussian random-field theory (z>2.3, cluster-wise P<0.05 corrected).

Abbreviations: ALFF, amplitude of low-frequency fluctuation; ON, optic neuritis; HC, healthy control; MNI, Montreal Neurological Institute; BA, Brodmann area; –, not applicable.

Brain areas with significantly increased ALFF values in the ON group were located in the posterior lobes of the left and right cerebellum, and the right inferior temporal gyrus, right inferior temporal/fusiform gyri, left parahippocampal gyrus, left fusiform gyrus, left calcarine fissure, left inferior parietal lobule, and left cuneus (Figure 1 [red] and Table 2). Meanwhile, we showed the mean of altered spontaneous brain activity between the ONs and HCs in Figure 2.

Figure 2

Means of altered spontaneous brain activity between the ON group and HCs.

Abbreviations: ON, optic neuritis; HCs, healthy controls; ALFF, amplitude of low-frequency fluctuation.

Correlation analysis

In the ON group, we found that the mean ALFF signal value of the left parahippocampal gyrus showed a negative correlation with the VEP amplitude of the right eye in patients with ON (r=−0.584, P=0.046), while the mean ALFF value of the bilateral precuneus showed a positive correlation with the best-corrected VA – left (r=0.579, P=0.048). Details are presented in Figure 3.

Figure 3

Correlations between the mean ALFF signal values of the different areas and the behavioral performances.

Notes: The mean ALFF signal value of the left parahippocampal gyrus showed a negative correlation with the VEP amplitude of the right eye in the ON group (r=−0.584, P=0.046) (A), and the mean ALFF value of the bilateral precuneus showed a positive correlation with the left best-corrected VA (r=0.579, P=0.048) (B).

Abbreviations: ALFF, amplitude of low-frequency fluctuation; VEP, visual evoked potential; ON, optic neuritis; VA, visual acuity.

Discussion

This study is the first to our knowledge to evaluate the effect of ON on resting-state brain activity using the ALFF technique. We found that compared with HCs, patients with ON had lower ALFF values in the posterior and anterior lobes of the right cerebellum, and the right putamen, right inferior frontal gyrus, right insula, right supramarginal gyrus, right inferior parietal lobule, left medial frontal gyrus, left superior temporal gyrus, bilateral anterior cingulate/medial frontal gyrus, and bilateral precuneus, while they had higher ALFF values in the cluster of the posterior lobes of the left and right cerebella, and the right inferior temporal gyrus, right inferior temporal/fusiform gyrus, left parahippocampal gyrus, left fusiform gyrus, left calcarine fissure, left inferior parietal lobule, and left cuneus. Furthermore, we observed that the mean ALFF signal value of the left parahippocampal gyrus showed a negative correlation with the VEP amplitude of the right eye in ON (r=−0.584, P=0.046). In addition, we found that the mean ALFF value of the bilateral precuneus showed a positive correlation with the best-corrected VA – left (r=0.579, P=0.048).

The DMN in the brain is continuously activated during a resting-state condition.25 Many brain-function areas are involved in the DMN, including the posterior cingulate cortex, inferior parietal cortex, medial temporal lobes, medial frontal cortex, and anterior cingulate cortex.26,27 The DMN is related to many awareness activities, such as cognition,28 anxiety, and depression.29 Previous studies have identified many diseases that lead to DMN dysfunction, such as Alzheimer’s disease,30 Parkinson’s disease,31 and schizophrenia.32 Toosy et al33 found that patients with ON showed abnormal activation of areas in the bilateral insula–claustrum and frontal and posterior parietal and lateral temporal cortices. Werring et al34 also found that patients with ON showed abnormal activation of areas in the insula–claustrum, lateral temporal and posterior parietal cortices, and the thalamus. ON is the foremost clinical feature in 20% of patients with MS.35 Bonavita et al36 demonstrated that the DMN connectivity of MS was significantly weaker in the anterior cingulate cortex, but stronger in the posterior cingulate cortex compared with healthy subjects. In support of these findings, we found that patients with ON in the present study had lower ALFF values in the left medial frontal gyrus, left superior temporal gyrus, right inferior parietal lobule, bilateral anterior cingulate/medial frontal gyrus, and bilateral precuneus, while they had higher ALFF in the right inferior temporal gyrus and left inferior parietal lobule. ALFF, as an important aspect of rs-fMRI studies, may provide more information to assist in the understanding of ON-related functional reorganization. Therefore, the decreased ALFF in DMN indicates that ON may lead to DMN damage, while the higher ALFF in the right inferior temporal gyrus and left inferior parietal lobule may reflect compensation by the DMN to maintain the stability of the internal network.

In addition, we found that ALFF signals in the bilateral anterior cingulate/medial frontal gyrus were lower than in other regions. Previous studies have shown that dysfunction of the anterior cingulate cortex is associated with pain37 and depression,38 and thus patients with ON may have abnormal pain and mental depression. Furthermore, the posterior precuneus is primarily involved in visuospatial functions,39,40 and we also found that the mean ALFF value of the bilateral precuneus showed a positive correlation with the best-corrected VA – left (r=0.579, P=0.048). We therefore conclude that the visual loss experienced by patients with ON may relate to dysfunction of the bilateral precuneus.

The cerebellum is involved in balance and motor control, as well as cognitive tasks. Positron-emission tomography and fMRI studies have demonstrated that the functions of the cerebellum include cognition and memory.41 Previous studies have demonstrated that dysfunction of the cerebellum is involved in schizophrenia,42 bipolar disorder,43 and depression.44 Saini et al45 found that there is a reduction in functional connectivity between the left primary motor cortex and the right dentate in patients with MS, while Ceccarelli et al46 demonstrated that patients with primary progressive MS had more obvious activation of the left cerebellum compared with healthy subjects. In support of these findings, we also found that patients with ON had lower ALFF values in the posterior and anterior lobes of the right cerebellum, and had higher ALFF values in the posterior lobes of the left and right cerebellum. The decreased ALFF values in these regions may reflect functional damage, while the increased ALFF values in neighboring brain regions may reflect functional reorganization to compensate for the damaged area. The limbic system is closely related to memory and emotion.47 The classic circuit of the limbic system described by Papez includes the hippocampus, mammillary bodies, anterior thalamic nuclei, cingulate gyrus, and the parahippocampal gyrus.48 Duan et al49 found that patients with relapsing–remitting MS had significant reductions in gray matter in the bilateral thalami, caudate, left parahippocampal gyrus, and right hippocampus, while Audoin et al50 demonstrated that patients with ON had a lower gray-matter transfer ratio in the visual cortex and left hippocampus compared with controls. In the present study, we also found that patients with ON had lower ALFF values in areas in the anterior cingulate, which may suggest that ON has a harmful effect on the limbic system. However, there were higher ALFF values in areas in the left parahippocampal gyrus, which may relate to compensation by the limbic system. Furthermore, we found that the mean ALFF signal value of the left parahippocampal gyrus showed a negative correlation with the VEP amplitude of the right eye in patients with ON (r=−0.584, P=0.046). A previous study showed that patients with ON had delayed P100 VEP latency and reduced P100 VEP amplitude compared with controls,51 and thus, reduced P100 VEP amplitude in ON can to some extent reflect the severity of ON. We therefore conclude that increased ALFF values in the left parahippocampal gyrus may relate to the severity of ON.

Conclusion

In summary, we found that patients with ON had abnormal regional spontaneous activities involved in regional brain changes, which showed negative correlations with the VEP amplitude of the eye in ON. These findings provide important information for the understanding of the neural mechanisms underlying ON. However, there are some limitations to our study, such as the relatively small sample size, the use of a single-center study, and the lack of comparison between patients before and after treatment. In future studies, we will use other techniques to explore changes in brain function in patients with ON.