Early Glycemic Profile Is Associated with Brain Injury Patterns on Magnetic Resonance Imaging in Hypoxic Ischemic Encephalopathy.
Early Glycemic Profile Is Associated with Brain Injury Patterns on Magnetic Resonance Imaging in Hypoxic Ischemic Encephalopathy.
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DOI:
10.1016/j.jpeds.2018.07.041
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发表时间:
2018-12
期刊:
影响因子:
--
通讯作者:
Massaro AN
中科院分区:
文献类型:
--
作者:
Basu SK;Ottolini K;Govindan V;Mashat S;Vezina G;Wang Y;Ridore M;Chang T;Kaiser JR;Massaro AN
To investigate whether the early glycemic profile in infants with hypoxic ischemic encephalopathy (HIE) is associated with distinct brain injury patterns on magnetic resonance imaging (MRI). We performed a secondary analysis of 178 prospectively enrolled infants who received therapeutic hypothermia for HIE. Glycemic profiles were identified by glucose concentrations within 24 hours after birth: normoglycemia (all glucose concentrations >47 to ≤150 mg/dL; n=62); hypoglycemia (≥1 concentration ≤47 mg/dL; n=17), hyperglycemia (≥1 concentration >150 mg/dL; n=76), and labile glucose (both hypoglycemia and hyperglycemia; n=23). Patterns of brain injury were identified for 151 infants based on Barkovich scores from the post-rewarming brain MRIs on median age of 9 days. Normal brain MRI was reported in 37/62 (60%) infants with normal blood glucose values compared with 37/116 (32%) infants with an abnormal glucose profile (adjusted for Sarnat stage of encephalopathy and Apgar score at 5 minutes, P=.02). The distribution of MRI patterns of brain injury differed among the glycemic groups (P=.03). Odds of predominant watershed or focal-multifocal injury was higher in infants with hypoglycemia (adjusted OR 6; 95% CI 1.5–24.2) and labile glucose (6.6; 1.6–27) compared with infants with normoglycemia. Infants with labile glucose had higher odds (5.6; 1.1–29.3) of predominant basal ganglia or global injury compared with infants with normal blood glucose values. The early glycemic profile in infants with HIE is associated with specific patterns of brain injury on MRI. Further investigation is needed to explore its prognostic significance and role as a phenotype biomarker.
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DOI:
10.1056/nejmoa1112066
发表时间:
2012-05-31
期刊:
The New England journal of medicine
影响因子:
--
作者:
Shankaran S;Pappas A;McDonald SA;Vohr BR;Hintz SR;Yolton K;Gustafson KE;Leach TM;Green C;Bara R;Petrie Huitema CM;Ehrenkranz RA;Tyson JE;Das A;Hammond J;Peralta-Carcelen M;Evans PW;Heyne RJ;Wilson-Costello DE;Vaucher YE;Bauer CR;Dusick AM;Adams-Chapman I;Goldstein RF;Guillet R;Papile LA;Higgins RD;Eunice Kennedy Shriver NICHD Neonatal Research Network
通讯作者:
Eunice Kennedy Shriver NICHD Neonatal Research Network
影响因子:
168.9
作者:
Gluckman, PD;Wyatt, JS;Gunn, AJ
通讯作者:
Gunn, AJ
影响因子:
5.1
作者:
Miller, SP;Ramaswamy, V;Ferriero, DM
通讯作者:
Ferriero, DM
影响因子:
3.6
作者:
Li, Amanda M.;Chau, Vann;Miller, Steven P.
通讯作者:
Miller, Steven P.
DOI:
10.1136/archdischild-2016-311385
发表时间:
2017-07-01
影响因子:
4.4
作者:
Basu, Sudeepta K.;Salemi, Jason L.;Kaiser, Jeffrey R.
通讯作者:
Kaiser, Jeffrey R.