Skip to main content

ORIGINAL RESEARCH article

Front. Neurosci., 07 December 2022
Sec. Perception Science
This article is part of the Research Topic Hemispheric Asymmetries in the Auditory Domain, Volume II View all 5 articles

Lateralization of cerebral blood flow in the auditory cortex of patients with idiopathic tinnitus and healthy controls: An arterial spin labeling study

\r\nXiaoshuai Li&#x;Xiaoshuai Li1†Yansheng Zhao&#x;Yansheng Zhao2†Ying HuiYing Hui1Yuntao WuYuntao Wu3Qian ChenQian Chen1Huijing ShiHuijing Shi4Han LvHan Lv1Mengning LiMengning Li2Pengfei ZhaoPengfei Zhao1Wenfei ZhangWenfei Zhang2Xinyu ZhaoXinyu Zhao5Jing Li*Jing Li1*Liufu Cui*Liufu Cui4*Zhenchang Wang*Zhenchang Wang1*
  • 1Department of Radiology, Beijing Friendship Hospital, Capital Medical University, Beijing, China
  • 2Department of MRI Room, Kailuan General Hospital, Tangshan, Hebei, China
  • 3Department of Cardiology, Kailuan General Hospital, Tangshan, Hebei, China
  • 4Department of Rheumatology and Immunology, Kailuan General Hospital, Tangshan, Hebei, China
  • 5Clinical Epidemiology and Evidence-Based Medicine Unit, Beijing Friendship Hospital, Capital Medical University, Beijing, China

Objectives: To assess the lateralization of cerebral blood flow (CBF) in the auditory cortex of idiopathic tinnitus patients and healthy controls (HCs) using 3D pseudocontinuous arterial spin labeling (pcASL).

Methods: Thirty-six patients with idiopathic tinnitus and 43 sex- and age-matched HCs underwent 3D-pcASL scanning using a 3.0 T MRI system. For both groups, region of interest analysis was performed on the primary auditory cortex (PAC), auditory associative cortex (AAC), and secondary auditory cortex (SAC). The clinical data of all subjects were analyzed.

Results: In both tinnitus patients and HCs, CBF of the left PAC was significantly higher than that of the right (HCs: P = 0.02; patients: P = 0.043), but CBF of the right AAC and SAC was significantly higher than that of the left (AAC: HCs, P < 0.001; patients: P < 0.001. SAC: HCs, P < 0.001; patients: P = 0.001). Compared with HCs, tinnitus patients exhibited significantly higher CBF in the bilateral PAC (right: P = 0.008; left: P = 0.022). CBF in the left PAC was positively correlated with tinnitus severity (r = 0.399, P = 0.016).

Conclusion: This study confirms the asymmetry of the auditory cortex and investigates the underlying neuropathology of idiopathic tinnitus in terms of CBF.

Introduction

Idiopathic tinnitus is a subjective auditory perception that occurs in the absence of external sound stimuli. In adults, the incidence of idiopathic tinnitus is as high as 15% and increases with age; consequently, idiopathic tinnitus has become a major health issue worldwide (Conlon et al., 2020; Henton and Tzounopoulos, 2021). This condition seriously affects quality of life and can lead to depression, sleep disturbance, anxiety and even suicide.

The etiology of idiopathic tinnitus remains unclear. It is considered to originate from abnormal neuronal activity in the auditory cortex (AC) (Hayes et al., 2021). In animal models of tinnitus, auditory cortical neurons exhibit increased spontaneous firing rates (Basura et al., 2015; Takacs et al., 2017), and functional magnetic resonance imaging (fMRI) has revealed similar findings in the human AC (Chen et al., 2017; Han et al., 2018). The AC is one of the most plastic cerebral cortexes and is involved in the processing of sound information. Long-term abnormal neural activity can cause structural and functional plasticity of the AC, resulting in persistent tinnitus (Adjamian et al., 2014). The inhibitory gating mechanism, a system that prevents tinnitus signals from reaching the AC, is also thought to be related to the development of tinnitus (Rauschecker et al., 2010). Under normal conditions, abnormal neural activity associated with tinnitus is counteracted at the thalamic level by inhibitory feedback loops from the limbic system. However, compromise of the inhibitory gating mechanism results in transmission of abnormal activity to the AC and its perception as tinnitus (Adjamian et al., 2014). Therefore, the AC plays a key role in the mechanism of tinnitus.

Currently, the lateralization of the AC in idiopathic tinnitus patients remains unclear. Geven et al. (2014) used positron emission tomography (PET) to describe the lateralized activation of the AC in tinnitus patients; the primary AC (PAC) undergoes leftward lateralization, while the auditory associative cortex (AAC) and secondary AC (SAC) undergo rightward lateralization. However, the sample size of the study by Geven et al. was small, and no statistical analysis of activation of the bilateral AC was performed to provide additional evidence. Several fMRI studies of sound-evoked neuronal activity in tinnitus patients have demonstrated lateralized activation of the AC (Smits et al., 2007; Lanting et al., 2014). But, experimental auditory stimuli may interfere with resting-state activity of the AC. Thus, quantitative assessment of lateralization in the AC in tinnitus at rest is an important topic.

Neuronal activity is closely coupled to cerebral blood flow (CBF), and increased neuronal activity leads to increased CBF (Raichle and Mintun, 2006; Lanting et al., 2009). Arterial spin labeling (ASL) can non-invasively measure CBF by using endogenous arterial blood protons as contrast agents. Compared with PET, computed tomography perfusion, and dynamic contrast-enhanced MRI, ASL is non-invasive, simple, and has high repeatability. Moreover, the accuracy of this technique has been verified (Dolui et al., 2020). Due to its increased signal-to-noise ratio, 3D pseudocontinuous ASL (pcASL) is widely used to identify CBF changes under different pathological conditions, including tinnitus (Li et al., 2020, 2021; Xia et al., 2020).

Thus, the aim of this study was to assess the lateralization of CBF in the AC in idiopathic tinnitus patients and healthy controls (HCs) using 3D-pcASL. In addition, we explored the differences in CBF in the AC between patients with tinnitus and HCs, and the correlation of altered CBF with clinical data.

Materials and methods

Subjects

This research was approved by the Medical Research Ethics Committees. Written informed consent was acquired from each participant in accordance with the Declaration of Helsinki.

In this study, 36 bilateral tinnitus patients and 43 sex- and age-matched HCs were enrolled from Kailuan community. Patients were included if the following criteria were met: persistent idiopathic tinnitus, self-reported normal audiology, no prior history of central nervous system disorders or head trauma, and no MRI contraindications. Subjects were excluded if they had pulsatile tinnitus, hyperacusis, prior stroke, systemic diseases, or a history of drug or alcohol abuse in the previous 3 months. Tinnitus is divided into 6 grades according to its severity: grade 1, in which tinnitus is seemingly non-existent; grade 2, in which tinnitus is only experienced in quiet environments; grade 3, in which tinnitus is experienced in daily environments and does not affect quality of life; grade 4, in which tinnitus is experienced in noisy environments and affects sleep; grade 5, in which tinnitus seriously affects sleep and work; and grade 6, in which tinnitus leads to anxiety and depression.

Magnetic resonance imaging scanning

All subjects were scanned on a GE 750W 3.0 T MR scanner (General Electric, Milwaukee, WI, USA). We used earplugs and foam padding to reduce scanner noise and head motion, respectively. All participants were instructed to close their eyes and avoid thinking of anything. Structural images were obtained using a brain volume sequence (echo time (TE) = 2.8 ms; inversion time (TI) = 450 ms; repetition time (TR) = 7.5 ms; flip angle (FA) = 15°; slice thickness = 1 mm; matrix = 256 × 256; and field of view (FOV) = 256 mm × 256 mm). Perfusion data were acquired by a 3D-pcASL sequence (TE = 10.7 ms; TR = 5313 ms; slice thickness = 4 mm; post-label delay (PLD), 2525 ms; and FA = 111°; FOV, 240 mm × 240 mm; and in-plane resolution, 3.37 × 3.37 mm). The acquisition time of ASL was 4 min and 45 s.

Data preprocessing

In the AW4.6 workstation, the ASL difference images were derived by pairwise subtraction of the control and label images; subsequently, the CBF map was obtained from the ASL difference images. Details of the processing procedures were described in a previous study (Li et al., 2022). The CBF maps of all patients and HCs were coregistered to MNI space using SPM8 software. Subsequently, we standardized the CBF of each voxel by dividing it by the mean CBF of the whole brain (Aslan and Lu, 2010). Finally, the 8-mm FWHM Gaussian kernel was used to smooth the standardized CBF maps.

Tinnitus has been confirmed to originate from abnormal neuronal activity in the AC (Hayes et al., 2021). Thus, we performed ROI analysis of the AC in tinnitus patients, including the AAC, PAC, and SAC (Figure 1). Brodmann’s area (BA) template was used to extract the bilateral AAC (BA22), PAC (BA41), and SAC (BA42). The CBF in each ROI in tinnitus patients and HCs was extracted based on the above templates.

FIGURE 1
www.frontiersin.org

Figure 1. Region of interest (ROI) analysis for quantitative evaluation of CBF in the auditory cortex. SAC, secondary auditory cortex; AAC, auditory associative cortex; PAC, primary auditory cortex; CBF, cerebral blood flow; R, right; L, left.

The lateralization index (LI), which was calculated as: (left–right)/(left+right) (Seghier, 2008), was used to assess the symmetry of CBF in the bilateral AC. The LI ranged between −1 and 1. A negative LI represented higher CBF in the right AC, and a positive LI indicated higher CBF in the left AC.

Statistical analysis

The chi-square test and two-sample t-test were performed to identify group differences in demographic data. CBF differences in the bilateral AC of each group were explored using the paired samples t-test. We used one-sample t-test as the comparison point to investigate the LI difference in the AC of each group. The analysis of covariance was used to compare the difference in CBF and LI in each AC between patients and HCs, with age and sex as covariates. In addition, we analyzed the correlations of altered CBF with the duration and severity of tinnitus. All results were presented without correction for multiple comparisons.

Results

Sample characteristics

The baseline information for all subjects is shown in Table 1. There were no significant differences in age, sex, and handedness between the two groups. The duration of tinnitus was 41.3 ± 24.6 months. There were 6 patients with grade 1, 10 patients with grade 2, 9 patients with grade 3, 5 patients with grade 4, and 6 patients with grade 5.

TABLE 1
www.frontiersin.org

Table 1. Sample characteristics of patients with tinnitus and HCs.

Cerebral blood flow analysis

The CBF in the AC in each group of subjects is shown in Figure 2. In both HCs and tinnitus patients, CBF of the left PAC was significantly higher than that of the right (HCs: 0.942 ± 0.102 vs. 0.911 ± 0.089, P = 0.02; patients: 0.996 ± 0.077 vs. 0.969 ± 0.089, P = 0.043), but CBF of the right AAC and SAC was significantly higher than that of the left (AAC: HCs, 0.908 ± 0.057 vs. 1.093 ± 0.066, P < 0.001; patients: 0.919 ± 0.079 vs. 1.073 ± 0.071, P < 0.001. SAC: HCs, 1.075 ± 0.084 vs. 1.193 ± 0.074, P < 0.001; patients: 1.109 ± 0.101 vs. 1.163 ± 0.096, P = 0.001). In addition, compared with HCs, patients with tinnitus exhibited significantly higher CBF in the bilateral PAC (right: 0.969 ± 0.089 vs. 0.911 ± 0.089, P = 0.008; left: 0.996 ± 0.077 vs. 0.942 ± 0.102, P = 0.022).

FIGURE 2
www.frontiersin.org

Figure 2. Normalized CBF according to ROI analysis of the auditory cortex in tinnitus patients and HCs. AAC, auditory associative cortex; SAC, secondary auditory cortex; PAC, primary auditory cortex; CBF, cerebral blood flow; HC, healthy control; ROI, region of interest; L, left; R, right. *Statistical significance.

Figure 3 shows the LI of the AC in the two groups. CBF was lateralized to the left in the PAC and lateralized to the right in the SAC and AAC in both tinnitus patients and HCs. One-sample t-test showed that in each group, the LI of the PAC was significantly higher than 0 (HCs: P = 0.023; patients: P = 0.037), while the LI of the SAC and AAC were significantly lower than 0 (SAC: HCs, P < 0.001; patients, P = 0.001; AAC: HCs, P < 0.001; patients, P < 0.001). In addition, tinnitus patients had significantly lower LI in SAC than HCs (P = 0.008), and no significant LI difference was found in PAC and AAC between the two groups (P > 0.05).

FIGURE 3
www.frontiersin.org

Figure 3. Lateralization index of cerebral blood flow in the auditory cortex in the two groups. AAC, auditory associative cortex; SAC, secondary auditory cortex; PAC, primary auditory cortex; HC, healthy control; R, right; L, left. *Statistical significance.

Correlation analysis

Spearman correlation analysis showed that in tinnitus patients, CBF in the left PAC was positively correlated with the severity of tinnitus (r = 0.399, P = 0.016) (Figure 4). No significant correlations were found between altered CBF in the other AC and the clinical data.

FIGURE 4
www.frontiersin.org

Figure 4. Correlation between the normalized CBF of the left PAC and severity of tinnitus in patients with tinnitus. PAC, primary auditory cortex; CBF, cerebral blood flow. Grades of tinnitus severity.

Discussion

This study investigated the lateralization of CBF in the AC of patients with idiopathic tinnitus using the 3D-pcASL technique. CBF was asymmetric in the AC in both tinnitus patients and HCs. Moreover, CBF in the bilateral PAC was significantly higher in tinnitus patients than in HCs. The higher CBF in the left PAC was positively correlated with tinnitus severity. These findings contribute toward an understanding of the neuropathological mechanisms of tinnitus in terms of CBF.

The AC is responsible for processing auditory information. A previous study demonstrated that the columnar and connective structures of the AC in the left cerebral hemisphere differ anatomically from those in the right hemisphere (Hutsler and Galuske, 2003). Lanting et al. (2014) used fMRI and found that compared with HCs, tinnitus patients showed smaller lateralization for sound stimuli, reaching significance in the right PAC. However, auditory stimuli may interfere with resting-state neural activity in the AC. Geven et al. described the asymmetry of metabolic activity in the AC of tinnitus patients using the PET technique. They found that in both tinnitus patients and HCs, the activity in the right AAC and SAC was higher than that in the left, while the activity in the left PAC was higher than that in the right (Geven et al., 2014). However, because Geven et al. did not investigate significant differences in metabolic activity in the bilateral AC, there is no strong evidence that AC activity is asymmetric.

In the present study, we compared CBF differences in bilateral AC using the 3D-pcASL technique and found that the CBF in the right AAC and SAC was significantly higher than that in the left, while the CBF in the left PAC was significantly higher than that in the right. We also used the LI to confirm the asymmetry of CBF in the AC. These findings suggest that asymmetric CBF in the bilateral AC is a physiological feature of both tinnitus patients and HCs, regardless of the presence or absence of tinnitus.

The CBF in the bilateral PAC was significantly higher in tinnitus patients than in HCs in this study. Auditory stimuli can increase neural activity in the bilateral AC. De Ridder et al. (2007) found a relationship between the degree of PAC reorganization and tinnitus intensity. Previous studies have suggested that tinnitus originates from abnormal activity in the PAC due to hearing loss (Roberts et al., 2013; Roberts, 2018). Since neuronal activity is closely coupled to CBF, it is reasonable that patients with tinnitus have significantly higher CBF in the bilateral PACs. In addition, CBF in the left PAC was positively correlated with the severity of tinnitus. We speculate that tinnitus patients with higher CBF in the left PAC may have greater difficulty adapting to tinnitus and therefore have higher grade. The correlation between the change in CBF in the left PAC and tinnitus severity needs to be studied further to verify this hypothesis.

Several limitations of this study should be noted. The sample size of this study was limited, and more patients need to be enrolled in the future to further verify these results. Second, all patients in this study had bilateral tinnitus, which is the most common type of tinnitus observed in clinical practice. In future work, we will include patients with unilateral tinnitus and evaluate lateralization in the AC. Third, MRI noise may have a potential effect on the results. In this study, we used earplugs and foam pads to reduce scanner noise, thereby minimizing the impact of noise on the results. In the future, we will further explore the effect of noise on CBF in AC. In addition, we will recruit left-handed subjects to eliminate the possible effect of handedness on the results.

Conclusion

In this study, the asymmetry of the AC in tinnitus patients and HCs was identified using the 3D-pcASL technique. CBF in the PAC was left-lateralized in all subjects, and CBF in the SAC and AAC was right-lateralized. Moreover, CBF in the bilateral PAC was higher in tinnitus patients than in HCs. In this study, we not only investigated the underlying neuropathology of tinnitus in terms of CBF but also may have implications for the rationale of tinnitus treatment protocols based on lateralized hyperactivity.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by the Ethics Committee of Beijing Friendship Hospital. The patients/participants provided their written informed consent to participate in this study.

Author contributions

XL, YZ, YH, QC, HS, ML, and WZ performed the experiment and collected, analyzed, or interpreted the data involved in the study. XL preprocessed image data, performed the statistical results, and drafted the manuscript. PZ, HL, XZ, and YW designed the study and ensured the questions related to all aspects of the work. JL, LC, and ZW gave critical comments on the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by the National Natural Science Foundation of China (Nos. 61931013, 82171886, 82202109, and 82272072), China Postdoctoral Science Foundation (No. 2022M712219), and Beijing Postdoctoral Science Foundation (No. 2022-EE-022).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Adjamian, P., Hall, D. A., Palmer, A. R., Allan, T. W., and Langers, D. R. (2014). Neuroanatomical abnormalities in chronic tinnitus in the human brain. Neurosci. Biobehav. Rev. 45, 119–133.

Google Scholar

Aslan, S., and Lu, H. (2010). On the sensitivity of ASL MRI in detecting regional differences in cerebral blood flow. Magn. Reson. Imaging 28, 928–935.

Google Scholar

Basura, G. J., Koehler, S. D., and Shore, S. E. (2015). Bimodal stimulus timing-dependent plasticity in primary auditory cortex is altered after noise exposure with and without tinnitus. J. Neurophysiol. 114, 3064–3075. doi: 10.1152/jn.00319.2015

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, Y. C., Wang, F., Wang, J., Bo, F., Xia, W., Gu, J. P., et al. (2017). Resting-state brain abnormalities in chronic subjective tinnitus: A meta-analysis. Front. Hum. Neurosci. 11:22. doi: 10.3389/fnhum.2017.00022

PubMed Abstract | CrossRef Full Text | Google Scholar

Conlon, B., Langguth, B., Hamilton, C., Hughes, S., Meade, E., Connor, C. O., et al. (2020). Bimodal neuromodulation combining sound and tongue stimulation reduces tinnitus symptoms in a large randomized clinical study. Sci. Transl. Med. 12:eabb2830. doi: 10.1126/scitranslmed.abb2830

PubMed Abstract | CrossRef Full Text | Google Scholar

De Ridder, D., De Mulder, G., Verstraeten, E., Seidman, M., Elisevich, K., Sunaert, S., et al. (2007). Auditory cortex stimulation for tinnitus. Acta Neurochir. Suppl. 97(Pt 2), 451–462.

Google Scholar

Dolui, S., Li, Z., Nasrallah, I. M., Detre, J. A., and Wolk, D. A. (2020). Arterial spin labeling versus (18)F-FDG-PET to identify mild cognitive impairment. Neuroimage Clin. 25:102146. doi: 10.1016/j.nicl.2019.102146

PubMed Abstract | CrossRef Full Text | Google Scholar

Geven, L. I., de Kleine, E., Willemsen, A. T. M., and van Dijk, P. (2014). Asymmetry in primary auditory cortex activity in tinnitus patients and controls. Neuroscience 256, 117–125.

Google Scholar

Han, Q., Zhang, Y., Liu, D. H., Wang, Y., Feng, Y. J., Yin, X. T., et al. (2018). Disrupted local neural activity and functional connectivity in subjective tinnitus patients: Evidence from resting-state fMRI study. Neuroradiology 60, 1193–1201. doi: 10.1007/s00234-018-2087-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Hayes, S. H., Schormans, A. L., Sigel, G., Beh, K., Herrmann, B., and Allman, B. L. (2021). Uncovering the contribution of enhanced central gain and altered cortical oscillations to tinnitus generation. Prog. Neurobiol. 196:101893. doi: 10.1016/j.pneurobio.2020.101893

PubMed Abstract | CrossRef Full Text | Google Scholar

Henton, A., and Tzounopoulos, T. (2021). What’s the buzz? The neuroscience and the treatment of tinnitus. Physiol. Rev. 101, 1609–1632. doi: 10.1152/physrev.00029.2020

PubMed Abstract | CrossRef Full Text | Google Scholar

Hutsler, J., and Galuske, R. A. (2003). Hemispheric asymmetries in cerebral cortical networks. Trends Neurosci. 26, 429–435.

Google Scholar

Lanting, C. P., de Kleine, E., Langers, D. R., and van Dijk, P. (2014). Unilateral tinnitus: Changes in connectivity and response lateralization measured with FMRI. PLoS One 9:e110704. doi: 10.1371/journal.pone.0110704

PubMed Abstract | CrossRef Full Text | Google Scholar

Lanting, C. P., de Kleine, E., and van Dijk, P. (2009). Neural activity underlying tinnitus generation: Results from PET and fMRI. Hear. Res. 255, 1–13.

Google Scholar

Li, X. S., Xu, N., Dai, C. H., Meng, X. X., Qiu, X. Y., Ding, H. Y., et al. (2022). Altered neurovascular coupling in unilateral pulsatile tinnitus. Front. Neurosci. 15:791436. doi: 10.3389/fnins.2021.791436

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X. S., Zhao, P. F., Qiu, X. Y., Ding, H. Y., Lv, H., Yang, Z. H., et al. (2020). Lateralization effects on cerebral blood flow in patients with unilateral pulsatile tinnitus measured with arterial spin labeling. Front. Hum. Neurosci. 14:591260. doi: 10.3389/fnhum.2020.591260

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X. S., Zhao, P. F., Qiu, X. Y., Lv, H., Ding, H. Y., Yang, Z. H., et al. (2021). Altered cerebral blood flow in patients with unilateral venous pulsatile tinnitus: An arterial spin labeling study. Br. J. Radiol. 94:20200990. doi: 10.1259/bjr.20200990

PubMed Abstract | CrossRef Full Text | Google Scholar

Raichle, M. E., and Mintun, M. A. (2006). Brain work and brain imaging. Annu. Rev. Neurosci. 29, 449–476.

Google Scholar

Rauschecker, J. P., Leaver, A. M., and Mühlau, M. (2010). Tuning out the noise: Limbic-auditory interactions in tinnitus. Neuron 66, 819–826. doi: 10.1016/j.neuron.2010.04.032

PubMed Abstract | CrossRef Full Text | Google Scholar

Roberts, L. E. (2018). Neural plasticity and its initiating conditions in tinnitus. HNO 66, 172–178.

Google Scholar

Roberts, L. E., Husain, F. T., and Eggermont, J. J. (2013). Role of attention in the generation and modulation of tinnitus. Neurosci. Biobehav. Rev. 37, 1754–1773.

Google Scholar

Seghier, M. L. (2008). Laterality index in functional MRI: Methodological issues. Magn. Reson. Imaging 26, 594–601.

Google Scholar

Smits, M., Kovacs, S., de Ridder, D., Peeters, R. R., van Hecke, P., and Sunaert, S. (2007). Lateralization of functional magnetic resonance imaging (fMRI) activation in the auditory pathway of patients with lateralized tinnitus. Neuroradiology 49, 669–679.

Google Scholar

Takacs, J. D., Forrest, T. J., and Basura, G. J. (2017). Noise exposure alters long-term neural firing rates and synchrony in primary auditory and rostral belt cortices following bimodal stimulation. Hear. Res. 356, 1–15. doi: 10.1016/j.heares.2017.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Xia, W. Q., Cui, J. L., Luo, Y., Xu, J. J., Chen, H. Y., Yin, X. D., et al. (2020). Glucose control has an impact on cerebral blood flow alterations in chronic tinnitus patients. Front. Neurosci. 14:623520. doi: 10.3389/fnins.2020.623520

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: tinnitus, auditory cortex, arterial spin labeling, cerebral blood flow, lateralization

Citation: Li X, Zhao Y, Hui Y, Wu Y, Chen Q, Shi H, Lv H, Li M, Zhao P, Zhang W, Zhao X, Li J, Cui L and Wang Z (2022) Lateralization of cerebral blood flow in the auditory cortex of patients with idiopathic tinnitus and healthy controls: An arterial spin labeling study. Front. Neurosci. 16:992758. doi: 10.3389/fnins.2022.992758

Received: 13 July 2022; Accepted: 18 November 2022;
Published: 07 December 2022.

Edited by:

Leighton B. Hinkley, University of California, San Francisco, United States

Reviewed by:

Sara Ponticorvo, University of Salerno, Italy
Xiao-Min Xu, Nanjing Medical University, China

Copyright © 2022 Li, Zhao, Hui, Wu, Chen, Shi, Lv, Li, Zhao, Zhang, Zhao, Li, Cui and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jing Li, lijingxbhtr@163.com; Liufu Cui, cuiliufu@hotmail.com; Zhenchang Wang, cjr.wzhch@vip.163.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.