Peter Kim Moon
MD Student, expected graduation Spring 2023
All Publications
-
Cerebral volume and diffusion MRI changes in children with sensorineural hearing loss.
NeuroImage. Clinical
2020; 27: 102328
Abstract
Sensorineural hearing loss (SNHL) is the most prevalent congenital sensory deficit in children. Information regarding underlying brain microstructure could offer insight into neural development in deaf children and potentially guide therapies that optimize language development. We sought to quantitatively evaluate MRI-based cerebral volume and gray matter microstructure children with SNHL.We conducted a retrospective study of children with SNHL who obtained brain MRI at 3 T. The study cohort comprised 63 children with congenital SNHL without known focal brain lesion or structural abnormality (33 males; mean age 5.3 years; age range 1 to 11.8 years) and 64 age-matched controls without neurological, developmental, or MRI-based brain macrostructure abnormality. An atlas-based analysis was used to extract quantitative volume and median diffusivity (ADC) in the following brain regions: cerebral cortex, thalamus, caudate, putamen, globus pallidus, hippocampus, amygdala, nucleus accumbens, brain stem, and cerebral white matter. SNHL patients were further stratified by severity scores and hearing loss etiology.Children with SNHL showed higher median ADC of the cortex (p = .019), thalamus (p < .001), caudate (p = .005), and brainstem (p = .003) and smaller brainstem volumes (p = .007) compared to controls. Patients with profound bilateral SNHL did not show any significant differences compared to patients with milder bilateral SNHL, but both cohorts independently had smaller brainstem volumes compared to controls. Children with unilateral SNHL showed greater amygdala volumes compared to controls (p = .021), but no differences were found comparing unilateral SNHL to bilateral SNHL. Based on etiology for SNHL, patients with Pendrin mutations showed higher ADC values in the brainstem (p = .029, respectively); patients with Connexin 26 showed higher ADC values in both the thalamus (p < .001) and brainstem (p < .001) compared to controls.SNHL patients showed significant differences in diffusion and volume in brain subregions, with region-specific findings for patients with Connexin 26 and Pendrin mutations. Future longitudinal studies could examine macro- and microstructure changes in children with SNHL over development and potential predictive role for MRI after interventions including cochlear implant outcome.
View details for DOI 10.1016/j.nicl.2020.102328
View details for PubMedID 32622314
-
Association of Pediatric Acute-Onset Neuropsychiatric Syndrome With Microstructural Differences in Brain Regions Detected via Diffusion-Weighted Magnetic Resonance Imaging
JAMA Network Open
2020
View details for DOI 10.1001/jamanetworkopen.2020.4063
-
Significance of Nodal Metastasis in Parotid Gland Acinar Cell Carcinoma
The Laryngoscope
2020
View details for DOI 10.1002/lary.28966
-
Revisiting IDO and its value as a predictive marker for anti-PD-1 resistance
JOURNAL OF TRANSLATIONAL MEDICINE
2019; 17
View details for DOI 10.1186/s12967-019-1784-8
View details for Web of Science ID 000456257700002
-
Macrophage de novo NAD(+) synthesis specifies immune function in aging and inflammation
NATURE IMMUNOLOGY
2019; 20 (1): 50-+
View details for DOI 10.1038/s41590-018-0255-3
View details for Web of Science ID 000456273900014
-
Reexamining IFN-gamma Stimulation of De Novo NAD+ in Monocyte-Derived Macrophages
INTERNATIONAL JOURNAL OF TRYPTOPHAN RESEARCH
2018; 11
View details for DOI 10.1177/1178646918773067
View details for Web of Science ID 000434098500001
-
Teasing apart NAD(+) metabolism in inflammation: commentary on Zhou et al. (2016). Br J Pharmacol 173: 2352-2368.
British journal of pharmacology
2017; 174 (3): 281–83
View details for PubMedID 28092923
View details for PubMedCentralID PMC5241388
-
Reevaluating the role of IDO1: Examining NAD+ metabolism in inflammation
Journal of Neuroimmunology
2017; 307: 31-32
View details for DOI 10.1016/j.jneuroim.2017.03.016