Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy

Background: Identifying an effective method for the early diagnosis of neonatal hypoxic-ischemic encephalopathy (HIE) would be beneficial for effective therapies. Methods: We studied blood biomarkers before 6 h after birth to correlate the degree of neonatal HIE. A total of 80 patients were divided...

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Main Authors: Inn-Chi Lee, Swee-Hee Wong, Xing-An Wang, Chin-Sheng Yu
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/11/5/897
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author Inn-Chi Lee
Swee-Hee Wong
Xing-An Wang
Chin-Sheng Yu
author_facet Inn-Chi Lee
Swee-Hee Wong
Xing-An Wang
Chin-Sheng Yu
author_sort Inn-Chi Lee
collection DOAJ
description Background: Identifying an effective method for the early diagnosis of neonatal hypoxic-ischemic encephalopathy (HIE) would be beneficial for effective therapies. Methods: We studied blood biomarkers before 6 h after birth to correlate the degree of neonatal HIE. A total of 80 patients were divided into group 1 (mild HIE) and group 2 (moderate or severe HIE). Then, 42 patients from group 2 received hypothermia therapy and were further divided into group 3 (unremarkable or mild MRI results) and group 4 (severe MRI results). Results: Between groups 1 and 2, lactate, creatinine, white blood cells, and lactate dehydrogenase (LDH) were significantly different. Between groups 3 and 4, lactate, prothrombin time, and albumin were significantly different. Sarnat staging was based on our observation that more than 45 mg/dL of lactate combined with more than 1000 U/L of LDH yielded the highest positive predictive value (PPV) (95.7%; odds ratio, 22.00), but a low negative predictive value (NPV) for moderate or severe HIE. Using more than 45 mg/dL of lactate yielded the highest NPV (71.4%) correlated with moderate or severe HIE. Conclusions: Lactate combined with LDH before 6 h after birth yielded a high PPV. Using combined biomarkers to exclude mild HIE, include moderate or severe HIE, and initialize hypothermia therapy is feasible.
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spelling doaj.art-41eb17d73411425dbd38aa053f5114d92023-11-21T20:15:25ZengMDPI AGDiagnostics2075-44182021-05-0111589710.3390/diagnostics11050897Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic EncephalopathyInn-Chi Lee0Swee-Hee Wong1Xing-An Wang2Chin-Sheng Yu3Division of Pediatric Neurology, Department of Pediatrics, Chung Shan Medical University Hospital, Taichung 40201, TaiwanDivision of Pediatric Neurology, Department of Pediatrics, Chung Shan Medical University Hospital, Taichung 40201, TaiwanInstitute of Medicine, School of Medicine, Chung Shan Medical University, Taichung 40201, TaiwanDepartment of Information Engineering and Computer Science, and Master’s Program in Biomedical Informatics and Biomedical Engineering, Feng Chia University, Taichung 40201, TaiwanBackground: Identifying an effective method for the early diagnosis of neonatal hypoxic-ischemic encephalopathy (HIE) would be beneficial for effective therapies. Methods: We studied blood biomarkers before 6 h after birth to correlate the degree of neonatal HIE. A total of 80 patients were divided into group 1 (mild HIE) and group 2 (moderate or severe HIE). Then, 42 patients from group 2 received hypothermia therapy and were further divided into group 3 (unremarkable or mild MRI results) and group 4 (severe MRI results). Results: Between groups 1 and 2, lactate, creatinine, white blood cells, and lactate dehydrogenase (LDH) were significantly different. Between groups 3 and 4, lactate, prothrombin time, and albumin were significantly different. Sarnat staging was based on our observation that more than 45 mg/dL of lactate combined with more than 1000 U/L of LDH yielded the highest positive predictive value (PPV) (95.7%; odds ratio, 22.00), but a low negative predictive value (NPV) for moderate or severe HIE. Using more than 45 mg/dL of lactate yielded the highest NPV (71.4%) correlated with moderate or severe HIE. Conclusions: Lactate combined with LDH before 6 h after birth yielded a high PPV. Using combined biomarkers to exclude mild HIE, include moderate or severe HIE, and initialize hypothermia therapy is feasible.https://www.mdpi.com/2075-4418/11/5/897newbornhypoxic-ischemic encephalopathybiomarkerMRIlactate
spellingShingle Inn-Chi Lee
Swee-Hee Wong
Xing-An Wang
Chin-Sheng Yu
Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy
Diagnostics
newborn
hypoxic-ischemic encephalopathy
biomarker
MRI
lactate
title Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy
title_full Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy
title_fullStr Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy
title_full_unstemmed Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy
title_short Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy
title_sort identifying early diagnostic biomarkers associated with neonatal hypoxic ischemic encephalopathy
topic newborn
hypoxic-ischemic encephalopathy
biomarker
MRI
lactate
url https://www.mdpi.com/2075-4418/11/5/897
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AT chinshengyu identifyingearlydiagnosticbiomarkersassociatedwithneonatalhypoxicischemicencephalopathy