Congenital sensorineural hearing loss affects the development of corpus callosum
Weiwei Men1, Tianbing Song2, Shuang Xia3, Yaoyu Zhang1, Jing Che4, and Jia-Hong Gao1

1Center for MRI Research, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China, People's Republic of, 2Beijing cancer hospital, Beijing, China, People's Republic of, 3Tianjing First Central Hospital, Tianjing, China, People's Republic of, 4Aerospace Central Hospital, Beijing, China, People's Republic of

Synopsis

Congenital sensorineural hearing loss (CSHL) is a common disease in newborns, which can affect the development of corpus callosum (CC). In this study, a novel method of CC thickness analysis was employed to compare the CC difference between deaf and control groups. The results indicate that after 24 months deaf group has thinner CC thickness in the anterior splenium of CC compared to control group, which means the development of deaf anterior splenium is slowed down. Our study suggests that 12~24 month old is the best time period for CSHL treatment and intervention.

Targeted audience

Researchers and clinicians interested in brain development.

PURPOSE

Congenital sensorineural hearing loss (CSHL) is a common disease in newborns, with an incidence rate of 0.1 ~ 0.3 %1. Underdeveloped corpus callosum (CC) caused by CSHL, however, has been rarely reported. Being the largest inter-hemispheric commissure of the human brain, CC contains nerve fibers crossing through and connecting most brain regions of the two hemispheres, including bilateral auditory cortices2. At present, cochlear implantation stays the best treatment for CSHL, so the purpose of this study is to investigate the effect of CSHL on CC and find the best time point for treatment and intervention, using a novel CC thickness analysis method.

METHODS

Twenty nine deaf children (age 6~45 m, mean 22.56 ± 12.61 m, 10 female, 19 male) were included in this study. The hearing screening results of the auditory brain stem response (ABR) test of all deaf children were larger than 90 dnBL. Eighteen children (age 4~48 m, mean 27.62 ± 11.97 m, 4 female, 14 male) with normal hearing served as the control group. There was no statistically significant difference for age and gender between the two groups. Informed consent was obtained from the parent of every infant and all the checks were agreed by the ethics committee of Tianjin first central hospital. All children were scanned on a Siemens 3T scanner (Trio Tim, Siemens Healthcare) with a 32-channel head coil. For sedation, all children were given oral administration of 10% chloral hydrate (0.6 ml/kg) prior to MRI examination. The MPRAGE sequence was employed for CC thickness analysis with the following parameters: TR/TE/TI = 1900 ms / 2.53 ms / 900 ms, flip angle = 9º, FOV = 250 × 250 mm2, voxel size = 0.98 × 0.98 × 1 mm3, 176 slices. The intensity of images was corrected by N3 method after converting the DICOM files to NIFTI format; all images were reoriented according to MNI space. The method of CC thickness measurement was followed as described by Weiwei Men, et al3. In this study, both deaf and control groups were subdivided into two subgroups: 4~24 m and 25~48 m. The two-sample T test was used to compare the difference of the registered CC thickness between deaf and control groups. An area of significant difference was observed. The mean CC thickness of this area was calculated for every infant, and fitting plots were given for both groups. We finally conducted intra- and inter-group comparisons among the mean CC thickness of each subgroup with the same T test.

RESULTS

Before 24 month old, there are no difference in CC thickness between deaf and control groups, see Fig. 1. Between 25~48 month old, the CC thickness of deaf group is significant thinner than that of control group, see Fig. 2. Overall, the anterior splenium of deaf group develops slower than that of control group, especially after 24 month old, see Fig. 3 and 4.

DISCUSSION

The results of this study indicate that CSHL will affect the development of CC anterior splenium, where nerve fibers cross through and connect with bilateral auditory cortices2, especially after 24 month old. The auditory cortices of deaf group have not been stimulated sufficiently, which can lead to delay of brain development. The method of CC thickness analysis is more prominent than other analysis method due to better registration in CC space and rubus, allowing the display of significant difference among CC of the subgroups.

CONCLUSION

Our study suggests that 12~24 month old is the best time period for CSHL treatment and intervention.

Acknowledgements

No acknowledgement found.

References

1. Han, Y., Huang, L., Zhang, W., Zhang, Y., Jia, X., Ni, T., Sun, H., Liang, P., Yu, H., Guo, Y., Zhang, A., Li, J., Zhang, H., 2015. Cost-effectiveness of three-stage newborns hearing screening in Beijing. Zhonghua Liu Xing Bing Xue Za Zhi 36, 455-459.

2. Chao, Y.P., Cho, K.H., Yeh, C.H., Chou, K.H., Chen, J.H., Lin, C.P., 2009. Probabilistic topography of human corpus callosum using cytoarchitectural parcellation and high angular resolution diffusion imaging tractography. Human Brain Mapping 30, 3172-3187.

3. Men, W., Falk, D., Sun, T., Chen, W., Li, J., Yin, D., Zang, L., Fan, M., 2014. The corpus callosum of Albert Einstein‘s brain: another clue to his high intelligence? Brain 137, e268.

Figures

Fig. 1. Subgroup 4~24 m CC thickness comparison. There is no significant difference between deaf and control groups.

Fig. 2. Subgroup 25~48 m CC thickness comparison. The CC thickness of deaf group is significant thinner than that of control group in the anterior splenium of CC.

Fig.3. Fitting plots of CC thickness in the anterior splenium of both deaf and control groups. The growth rate of CC thickness in deaf group is slower than that of control group, especially after 24 month old.

Fig. 4. The intra- and inter-group comparisons of the mean CC thickness among each subgroup (* indicate p<0.05, ** indicate p<0.001).



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