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Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults

The objectives were to compare differences in telomere length (TL) among younger (21–54 years) and older adults (≥55) with mild traumatic brain injury (mTBI) to non-injured controls and to examine the association between TL and the severity of post-concussive symptoms over time. We performed a quant...

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Autores principales: Martha, Sarah R., Tolentino, Ernesto J., Bugajski, Andrew A., Thompson, Hilaire J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240314/
https://www.ncbi.nlm.nih.gov/pubmed/37284700
http://dx.doi.org/10.1089/neur.2023.0012
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author Martha, Sarah R.
Tolentino, Ernesto J.
Bugajski, Andrew A.
Thompson, Hilaire J.
author_facet Martha, Sarah R.
Tolentino, Ernesto J.
Bugajski, Andrew A.
Thompson, Hilaire J.
author_sort Martha, Sarah R.
collection PubMed
description The objectives were to compare differences in telomere length (TL) among younger (21–54 years) and older adults (≥55) with mild traumatic brain injury (mTBI) to non-injured controls and to examine the association between TL and the severity of post-concussive symptoms over time. We performed a quantitative polymerase chain reaction to determine the TL (Kb/genome) of peripheral blood mononuclear cell samples (day 0, 3 months, and 6 months) from 31 subjects. The Rivermead Post-Concussion Symptoms Questionnaire was used to assess symptoms. Group-by-time comparisons of TL and symptom severity were evaluated with repeated-measures analysis of variance. Multiple linear regression examined the relationship between TL, group (mTBI and non-injured controls), and symptom severity total and subscale scores. Significant aging-related differences in TL were found within mTBI groups by time (day 0, 3 months, and 6 months; p = 0.025). Older adults with mTBI experienced significant worsening of changes in total symptom severity scores over time (day 0, 3 months, and 6 months; p = 0.016). Shorter TLs were associated with higher total symptom burden among each of the four groups at day 0 (baseline; p = 0.035) and 3 months (p = 0.038). Shorter TL was also associated with higher cognitive symptom burden among the four groups at day 0 (p = 0.008) and 3 months (p = 0.008). Shorter TL was associated with higher post-injury symptom burden to 3 months in both older and younger persons with mTBI. Large-scale, longitudinal studies of factors associated with TL may be useful to delineate the mechanistic underpinnings of higher symptom burden in adults with mTBI.
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spelling pubmed-102403142023-06-06 Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults Martha, Sarah R. Tolentino, Ernesto J. Bugajski, Andrew A. Thompson, Hilaire J. Neurotrauma Rep Original Article The objectives were to compare differences in telomere length (TL) among younger (21–54 years) and older adults (≥55) with mild traumatic brain injury (mTBI) to non-injured controls and to examine the association between TL and the severity of post-concussive symptoms over time. We performed a quantitative polymerase chain reaction to determine the TL (Kb/genome) of peripheral blood mononuclear cell samples (day 0, 3 months, and 6 months) from 31 subjects. The Rivermead Post-Concussion Symptoms Questionnaire was used to assess symptoms. Group-by-time comparisons of TL and symptom severity were evaluated with repeated-measures analysis of variance. Multiple linear regression examined the relationship between TL, group (mTBI and non-injured controls), and symptom severity total and subscale scores. Significant aging-related differences in TL were found within mTBI groups by time (day 0, 3 months, and 6 months; p = 0.025). Older adults with mTBI experienced significant worsening of changes in total symptom severity scores over time (day 0, 3 months, and 6 months; p = 0.016). Shorter TLs were associated with higher total symptom burden among each of the four groups at day 0 (baseline; p = 0.035) and 3 months (p = 0.038). Shorter TL was also associated with higher cognitive symptom burden among the four groups at day 0 (p = 0.008) and 3 months (p = 0.008). Shorter TL was associated with higher post-injury symptom burden to 3 months in both older and younger persons with mTBI. Large-scale, longitudinal studies of factors associated with TL may be useful to delineate the mechanistic underpinnings of higher symptom burden in adults with mTBI. Mary Ann Liebert, Inc., publishers 2023-05-23 /pmc/articles/PMC10240314/ /pubmed/37284700 http://dx.doi.org/10.1089/neur.2023.0012 Text en © Sarah R. Martha et al., 2023; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License [CC-BY] (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Martha, Sarah R.
Tolentino, Ernesto J.
Bugajski, Andrew A.
Thompson, Hilaire J.
Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults
title Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults
title_full Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults
title_fullStr Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults
title_full_unstemmed Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults
title_short Telomere Length Associates With Symptom Severity After Mild Traumatic Brain Injury in Older Adults
title_sort telomere length associates with symptom severity after mild traumatic brain injury in older adults
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240314/
https://www.ncbi.nlm.nih.gov/pubmed/37284700
http://dx.doi.org/10.1089/neur.2023.0012
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