Association of Brain Iron Overload With Brain Edema and Brain Atrophy After Intracerebral Hemorrhage.
Association of Brain Iron Overload With Brain Edema and Brain Atrophy After Intracerebral Hemorrhage.
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DOI:
10.3389/fneur.2020.602413
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发表时间:
2020
影响因子:
3.4
通讯作者:
Huang Y
中科院分区:
文献类型:
--
作者:
Liu R;Zhang H;Cheng S;Sun Y;Li H;Xiao J;Huang Y
Objective: This study evaluated iron overload after intracerebral hemorrhage (ICH) using ESWAN sequences. Methods: This single-center prospective observational cohort study enrolled supratentorial ICH patients. MRI was obtained with a 3.0-T scanner at day 1, day 14, day 30, and follow-up (300 days or later). R2* mapping was generated based on the ESWAN. R2* value of the ipsilateral side represented iron deposition, and the R2* value of the contralateral side served as control. R2* value was adjusted by volume and used to assess total iron overload. Brain edema was measured on T2 FLAIR-weighted images. Brain atrophy was calculated as the contralateral hemisphere volume minus the injured hemisphere volume. Results: Twnety-seven patients with a spontaneous supratentorial ICH were included in this analysis. The ipsilateral R2* value was 40.27 ± 11.62, 41.92 ± 13.56, and 60.89 ± 14.09 at days 1, 14, and 30, respectively. The R2* value was significantly higher in the ICH side than the contralateral side (p < 0.01). Increased R2* value was seen on day 30 compared to day 14 (p < 0.01). The R2* value showed logistic decay with the distance to the hematoma margin (p < 0.01). Brain edema at day 14 and brain atrophy at follow-up correlated with R2* value adjusted by volume at day 14 (p < 0.01). Conclusions: After ICH, the iron deposition in the perihematomal region was progressively increased during the first month. R2* value adjusted by volume predicted acute brain edema and chronic brain atrophy.
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DOI:
10.1523/jneurosci.3252-09.2009
发表时间:
2009-12-02
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Fjell AM;Walhovd KB;Fennema-Notestine C;McEvoy LK;Hagler DJ;Holland D;Brewer JB;Dale AM
通讯作者:
Dale AM
影响因子:
8.3
作者:
Mehdiratta, Manu;Kumar, Sandeep;Selim, Magdy
通讯作者:
Selim, Magdy
影响因子:
8.3
作者:
Wu, JM;Hua, Y;Xi, GH
通讯作者:
Xi, GH
影响因子:
4.1
作者:
Nakamura, T;Keep, RF;Xi, GH
通讯作者:
Xi, GH
影响因子:
9.9
作者:
Knudsen, KA;Rosand, J;Greenberg, SM
通讯作者:
Greenberg, SM