Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges

BackgroundWernicke encephalopathy (WE) is a severe neurological disorder caused by thiamine (vitamin B1) deficiency. Though often associated with chronic alcohol abuse, it can also arise from other conditions that impair thiamine intake or absorption. The classic triad of symptoms includes ophthalmo...

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Main Authors: Siping Li, Chengzhi Xing
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Neurology
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Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2025.1566366/full
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author Siping Li
Chengzhi Xing
author_facet Siping Li
Chengzhi Xing
author_sort Siping Li
collection DOAJ
description BackgroundWernicke encephalopathy (WE) is a severe neurological disorder caused by thiamine (vitamin B1) deficiency. Though often associated with chronic alcohol abuse, it can also arise from other conditions that impair thiamine intake or absorption. The classic triad of symptoms includes ophthalmoplegia, an abnormal mental state, and gait ataxia, although these may not be present in all patients, leading to underdiagnosis and undertreatment.MethodsThis mini review synthesizes data from clinical studies, autopsy reports, and imaging findings to assess the prevalence, diagnostic challenges, and treatment protocols for WE. It examines the role of various etiological factors, the presentation of atypical symptoms, and the utility of diagnostic tools such as magnetic resonance imaging (MRI) and vitamin B1 assays.ResultsAutopsy studies report a prevalence of WE that ranges from 0.4 to 2.8%, with most patients experiencing alcohol addiction or having other alcohol use disorders. The diagnosis of WE is primarily clinical, based on the Caine criteria in which a person must display at least two of the three classic symptoms or evidence of nutritional deficiency. MRI is a valuable tool for diagnosing WE, typically showing symmetric T2/FLAIR hyperintense signals in specific brain regions. Treatment involves prompt thiamine replacement, with intravenous administration being the most effective method to ensure adequate brain uptake.ConclusionWE remains a challenging condition to diagnose due to its variable presentations and the potential for atypical symptoms. Early recognition and treatment with thiamine are crucial to prevent irreversible neurological damage or death. There is a need for clear diagnostic and treatment guidelines to improve the management of WE and reduce the risk of underdiagnosis and undertreatment.
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spelling doaj-art-d29a0e70cf3a429ea615f99b9a9d33192025-08-20T03:30:23ZengFrontiers Media S.A.Frontiers in Neurology1664-22952025-07-011610.3389/fneur.2025.15663661566366Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challengesSiping Li0Chengzhi Xing1Department of Ultrasound Medicine, Pu’er People’s Hospital, Pu’er, ChinaDepartment of Neurology, Pu’er People’s Hospital, Pu’er, ChinaBackgroundWernicke encephalopathy (WE) is a severe neurological disorder caused by thiamine (vitamin B1) deficiency. Though often associated with chronic alcohol abuse, it can also arise from other conditions that impair thiamine intake or absorption. The classic triad of symptoms includes ophthalmoplegia, an abnormal mental state, and gait ataxia, although these may not be present in all patients, leading to underdiagnosis and undertreatment.MethodsThis mini review synthesizes data from clinical studies, autopsy reports, and imaging findings to assess the prevalence, diagnostic challenges, and treatment protocols for WE. It examines the role of various etiological factors, the presentation of atypical symptoms, and the utility of diagnostic tools such as magnetic resonance imaging (MRI) and vitamin B1 assays.ResultsAutopsy studies report a prevalence of WE that ranges from 0.4 to 2.8%, with most patients experiencing alcohol addiction or having other alcohol use disorders. The diagnosis of WE is primarily clinical, based on the Caine criteria in which a person must display at least two of the three classic symptoms or evidence of nutritional deficiency. MRI is a valuable tool for diagnosing WE, typically showing symmetric T2/FLAIR hyperintense signals in specific brain regions. Treatment involves prompt thiamine replacement, with intravenous administration being the most effective method to ensure adequate brain uptake.ConclusionWE remains a challenging condition to diagnose due to its variable presentations and the potential for atypical symptoms. Early recognition and treatment with thiamine are crucial to prevent irreversible neurological damage or death. There is a need for clear diagnostic and treatment guidelines to improve the management of WE and reduce the risk of underdiagnosis and undertreatment.https://www.frontiersin.org/articles/10.3389/fneur.2025.1566366/fullWernicke encephalopathythiamine deficiencyatypical manifestationsdiagnostic challengesneuroimaging
spellingShingle Siping Li
Chengzhi Xing
Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges
Frontiers in Neurology
Wernicke encephalopathy
thiamine deficiency
atypical manifestations
diagnostic challenges
neuroimaging
title Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges
title_full Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges
title_fullStr Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges
title_full_unstemmed Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges
title_short Wernicke encephalopathy: a mini review of the clinical spectrum, atypical manifestations, and diagnostic challenges
title_sort wernicke encephalopathy a mini review of the clinical spectrum atypical manifestations and diagnostic challenges
topic Wernicke encephalopathy
thiamine deficiency
atypical manifestations
diagnostic challenges
neuroimaging
url https://www.frontiersin.org/articles/10.3389/fneur.2025.1566366/full
work_keys_str_mv AT sipingli wernickeencephalopathyaminireviewoftheclinicalspectrumatypicalmanifestationsanddiagnosticchallenges
AT chengzhixing wernickeencephalopathyaminireviewoftheclinicalspectrumatypicalmanifestationsanddiagnosticchallenges