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Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury
INTRODUCTION: The apolipoprotein E (APOE) ε4 allele associates with memory impairment in neurodegenerative diseases. Its association with memory after mild traumatic brain injury (mTBI) is unclear. METHODS: mTBI patients (Glasgow Coma Scale score 13–15, no neurosurgical intervention, extracranial Ab...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607554/ https://www.ncbi.nlm.nih.gov/pubmed/28948085 http://dx.doi.org/10.1002/brb3.791 |
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author | Yue, John K. Robinson, Caitlin K. Burke, John F. Winkler, Ethan A. Deng, Hansen Cnossen, Maryse C. Lingsma, Hester F. Ferguson, Adam R. McAllister, Thomas W. Rosand, Jonathan Burchard, Esteban G. Sorani, Marco D. Sharma, Sourabh Nielson, Jessica L. Satris, Gabriela G. Talbott, Jason F. Tarapore, Phiroz E. Korley, Frederick K. Wang, Kevin K.W. Yuh, Esther L. Mukherjee, Pratik Diaz‐Arrastia, Ramon Valadka, Alex B. Okonkwo, David O. Manley, Geoffrey T. |
author_facet | Yue, John K. Robinson, Caitlin K. Burke, John F. Winkler, Ethan A. Deng, Hansen Cnossen, Maryse C. Lingsma, Hester F. Ferguson, Adam R. McAllister, Thomas W. Rosand, Jonathan Burchard, Esteban G. Sorani, Marco D. Sharma, Sourabh Nielson, Jessica L. Satris, Gabriela G. Talbott, Jason F. Tarapore, Phiroz E. Korley, Frederick K. Wang, Kevin K.W. Yuh, Esther L. Mukherjee, Pratik Diaz‐Arrastia, Ramon Valadka, Alex B. Okonkwo, David O. Manley, Geoffrey T. |
author_sort | Yue, John K. |
collection | PubMed |
description | INTRODUCTION: The apolipoprotein E (APOE) ε4 allele associates with memory impairment in neurodegenerative diseases. Its association with memory after mild traumatic brain injury (mTBI) is unclear. METHODS: mTBI patients (Glasgow Coma Scale score 13–15, no neurosurgical intervention, extracranial Abbreviated Injury Scale score ≤1) aged ≥18 years with APOE genotyping results were extracted from the Transforming Research and Clinical Knowledge in Traumatic Brain Injury Pilot (TRACK‐TBI Pilot) study. Cohorts determined by APOE‐ε4(+/−) were assessed for associations with 6‐month verbal memory, measured by California Verbal Learning Test, Second Edition (CVLT‐II) subscales: Immediate Recall Trials 1–5 (IRT), Short‐Delay Free Recall (SDFR), Short‐Delay Cued Recall (SDCR), Long‐Delay Free Recall (LDFR), and Long‐Delay Cued Recall (LDCR). Multivariable regression controlled for demographic factors, seizure history, loss of consciousness, posttraumatic amnesia, and acute intracranial pathology on computed tomography (CT). RESULTS: In 114 mTBI patients (APOE‐ε4(−)=79; APOE‐ε4(+)=35), ApoE‐ε4(+) was associated with long‐delay verbal memory deficits (LDFR: B = −1.17 points, 95% CI [−2.33, −0.01], p = .049; LDCR: B = −1.58 [−2.63, −0.52], p = .004), and a marginal decrease on SDCR (B = −1.02 [−2.05, 0.00], p = .050). CT pathology was the strongest predictor of decreased verbal memory (IRT: B = −8.49, SDFR: B = −2.50, SDCR: B = −1.85, LDFR: B = −2.61, LDCR: B = −2.60; p < .001). Seizure history was associated with decreased short‐term memory (SDFR: B = −1.32, p = .037; SDCR: B = −1.44, p = .038). CONCLUSION: The APOE‐ε4 allele may confer an increased risk of impairment of 6‐month verbal memory for patients suffering mTBI, with implications for heightened surveillance and targeted therapies. Acute intracranial pathology remains the driver of decreased verbal memory performance at 6 months after mTBI. |
format | Online Article Text |
id | pubmed-5607554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56075542017-09-25 Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury Yue, John K. Robinson, Caitlin K. Burke, John F. Winkler, Ethan A. Deng, Hansen Cnossen, Maryse C. Lingsma, Hester F. Ferguson, Adam R. McAllister, Thomas W. Rosand, Jonathan Burchard, Esteban G. Sorani, Marco D. Sharma, Sourabh Nielson, Jessica L. Satris, Gabriela G. Talbott, Jason F. Tarapore, Phiroz E. Korley, Frederick K. Wang, Kevin K.W. Yuh, Esther L. Mukherjee, Pratik Diaz‐Arrastia, Ramon Valadka, Alex B. Okonkwo, David O. Manley, Geoffrey T. Brain Behav Original Research INTRODUCTION: The apolipoprotein E (APOE) ε4 allele associates with memory impairment in neurodegenerative diseases. Its association with memory after mild traumatic brain injury (mTBI) is unclear. METHODS: mTBI patients (Glasgow Coma Scale score 13–15, no neurosurgical intervention, extracranial Abbreviated Injury Scale score ≤1) aged ≥18 years with APOE genotyping results were extracted from the Transforming Research and Clinical Knowledge in Traumatic Brain Injury Pilot (TRACK‐TBI Pilot) study. Cohorts determined by APOE‐ε4(+/−) were assessed for associations with 6‐month verbal memory, measured by California Verbal Learning Test, Second Edition (CVLT‐II) subscales: Immediate Recall Trials 1–5 (IRT), Short‐Delay Free Recall (SDFR), Short‐Delay Cued Recall (SDCR), Long‐Delay Free Recall (LDFR), and Long‐Delay Cued Recall (LDCR). Multivariable regression controlled for demographic factors, seizure history, loss of consciousness, posttraumatic amnesia, and acute intracranial pathology on computed tomography (CT). RESULTS: In 114 mTBI patients (APOE‐ε4(−)=79; APOE‐ε4(+)=35), ApoE‐ε4(+) was associated with long‐delay verbal memory deficits (LDFR: B = −1.17 points, 95% CI [−2.33, −0.01], p = .049; LDCR: B = −1.58 [−2.63, −0.52], p = .004), and a marginal decrease on SDCR (B = −1.02 [−2.05, 0.00], p = .050). CT pathology was the strongest predictor of decreased verbal memory (IRT: B = −8.49, SDFR: B = −2.50, SDCR: B = −1.85, LDFR: B = −2.61, LDCR: B = −2.60; p < .001). Seizure history was associated with decreased short‐term memory (SDFR: B = −1.32, p = .037; SDCR: B = −1.44, p = .038). CONCLUSION: The APOE‐ε4 allele may confer an increased risk of impairment of 6‐month verbal memory for patients suffering mTBI, with implications for heightened surveillance and targeted therapies. Acute intracranial pathology remains the driver of decreased verbal memory performance at 6 months after mTBI. John Wiley and Sons Inc. 2017-08-09 /pmc/articles/PMC5607554/ /pubmed/28948085 http://dx.doi.org/10.1002/brb3.791 Text en © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Yue, John K. Robinson, Caitlin K. Burke, John F. Winkler, Ethan A. Deng, Hansen Cnossen, Maryse C. Lingsma, Hester F. Ferguson, Adam R. McAllister, Thomas W. Rosand, Jonathan Burchard, Esteban G. Sorani, Marco D. Sharma, Sourabh Nielson, Jessica L. Satris, Gabriela G. Talbott, Jason F. Tarapore, Phiroz E. Korley, Frederick K. Wang, Kevin K.W. Yuh, Esther L. Mukherjee, Pratik Diaz‐Arrastia, Ramon Valadka, Alex B. Okonkwo, David O. Manley, Geoffrey T. Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
title |
Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
title_full |
Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
title_fullStr |
Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
title_full_unstemmed |
Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
title_short |
Apolipoprotein E epsilon 4 (APOE‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
title_sort | apolipoprotein e epsilon 4 (apoe‐ε4) genotype is associated with decreased 6‐month verbal memory performance after mild traumatic brain injury |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607554/ https://www.ncbi.nlm.nih.gov/pubmed/28948085 http://dx.doi.org/10.1002/brb3.791 |
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