Effects of Tissue Temperature and Injury on ADC during Therapeutic Hypothermia in Newborn Hypoxic-Ischemic Encephalopathy

被引：0

作者：

Zenobi, C. ^{[1
]}

Wisnowski, J. L. ^{[2
,4
]}

Tamrazi, B. ^{[2
,5
]}

Wong, A. M-C ^{[6
,7
]}

Chapman, R. ^{[4
]}

Bluml, S. ^{[2
,3
,5
]}

Wu, T-W ^{[3
,4
]}

机构：

[1] USC, Keck Sch Med, Los Angeles Cty USC Med Ctr, Los Angeles, CA USA

[2] USC, Keck Sch Med, Dept Radiol & Pediat, Los Angeles, CA USA

[3] USC, Keck Sch Med, Dept Pediat, Los Angeles, CA USA

[4] Childrens Hosp Los Angeles, Fetal & Neonatal Inst, Div Neonatol, Los Angeles, CA 90027 USA

[5] Childrens Hosp Los Angeles, Dept Radiol, Los Angeles, CA 90027 USA

[6] Chang Gung Mem Hosp, Dept Med Imaging & Intervent, Keelung, Taiwan

[7] Chang Gung Univ, Dept Diagnost Radiol, Taoyuan, Taiwan

来源：

AMERICAN JOURNAL OF NEURORADIOLOGY | 2022年 / 43卷 / 03期

基金：

美国国家卫生研究院;

关键词：

APPARENT DIFFUSION-COEFFICIENT; BRAIN TEMPERATURE; MR SPECTROSCOPY;

D O I：

10.3174/ajnr.A7413

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

BACKGROUND AND PURPOSE: ADC changes are useful in detecting ischemic brain injury, but mechanisms other than tissue pathology may affect the kinetic movement and diffusion of water molecules. We aimed to determine the effects of brain temperature on the corresponding ADC in infants undergoing therapeutic hypothermia. MATERIALS AND METHODS: Brain temperature and ADC values in the basal ganglia, thalamus, cortical GM, and WM were analyzed during and after therapeutic hypothermia. The study cohort was categorized as having no-injury or injury. Among infants without injury, the correlation between ADC values and temperature was analyzed using the Pearson correlation. Intrasubject comparison of ADC changes during and after therapeutic hypothermia were analyzed, excluding patients who had an MR image interval of >5?days to minimize the effects of injury evolution. RESULTS: Thirty-nine infants with hypoxic-ischemic encephalopathy were enrolled (23 no-injury; 16 injury). The median ADC was significantly lower during therapeutic hypothermia (837; interquartile range, 771?928, versus 906; interquartile range, 844?1032 ?10(?6)mm(2)/s; P < .001). There was no difference in the ADC between the no-injury and injury groups during therapeutic hypothermia (823; interquartile range, 782?868, versus 842; interquartile range, 770?1008 ?10(?6)mm(2)/s; P ?=?.4). In the no-injury group, in which ADC is presumed least affected by the evolution of injury, the median ADC was significantly lower during therapeutic hypothermia (826; interquartile range, 771?866, versus 897; interquartile range, 846?936 ?10(?6)mm(2)/s; P ?<?.001). There was a moderate correlation between temperature and ADC in the no-injury group (during therapeutic hypothermia: Spearman ?, 0.48; P ?<?.001; after therapeutic hypothermia: ?, 0.4; P ?<?.001). CONCLUSIONS: Aside from brain injury, reduced tissue temperature may also contribute to diffusion restriction on MR imaging in infants undergoing therapeutic hypothermia.

引用

页码：462 / 467

页数：6