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Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects
Telomere length shortens with cellular division, and leukocyte telomere length is used as a marker for systemic telomere length. The hippocampus hosts adult neurogenesis and is an important structure for episodic memory, and carriers of the apolipoprotein E ε4 allele exhibit higher hippocampal atrop...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323621/ https://www.ncbi.nlm.nih.gov/pubmed/22506016 http://dx.doi.org/10.1371/journal.pone.0034292 |
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author | Wikgren, Mikael Karlsson, Thomas Lind, Johanna Nilbrink, Therese Hultdin, Johan Sleegers, Kristel Van Broeckhoven, Christine Roos, Göran Nilsson, Lars-Göran Nyberg, Lars Adolfsson, Rolf Norrback, Karl-Fredrik |
author_facet | Wikgren, Mikael Karlsson, Thomas Lind, Johanna Nilbrink, Therese Hultdin, Johan Sleegers, Kristel Van Broeckhoven, Christine Roos, Göran Nilsson, Lars-Göran Nyberg, Lars Adolfsson, Rolf Norrback, Karl-Fredrik |
author_sort | Wikgren, Mikael |
collection | PubMed |
description | Telomere length shortens with cellular division, and leukocyte telomere length is used as a marker for systemic telomere length. The hippocampus hosts adult neurogenesis and is an important structure for episodic memory, and carriers of the apolipoprotein E ε4 allele exhibit higher hippocampal atrophy rates and differing telomere dynamics compared with non-carriers. The authors investigated whether leukocyte telomere length was associated with hippocampal volume in 57 cognitively intact subjects (29 ε3/ε3 carriers; 28 ε4 carriers) aged 49–79 yr. Leukocyte telomere length correlated inversely with left (r(s) = −0.465; p = 0.011), right (r(s) = −0.414; p = 0.025), and total hippocampus volume (r(s) = −0.519; p = 0.004) among APOE ε3/ε3 carriers, but not among ε4 carriers. However, the ε4 carriers fit with the general correlation pattern exhibited by the ε3/ε3 carriers, as ε4 carriers on average had longer telomeres and smaller hippocampi compared with ε3/ε3 carriers. The relationship observed can be interpreted as long telomeres representing a history of relatively low cellular proliferation, reflected in smaller hippocampal volumes. The results support the potential of leukocyte telomere length being used as a biomarker for tapping functional and structural processes of the aging brain. |
format | Online Article Text |
id | pubmed-3323621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33236212012-04-13 Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects Wikgren, Mikael Karlsson, Thomas Lind, Johanna Nilbrink, Therese Hultdin, Johan Sleegers, Kristel Van Broeckhoven, Christine Roos, Göran Nilsson, Lars-Göran Nyberg, Lars Adolfsson, Rolf Norrback, Karl-Fredrik PLoS One Research Article Telomere length shortens with cellular division, and leukocyte telomere length is used as a marker for systemic telomere length. The hippocampus hosts adult neurogenesis and is an important structure for episodic memory, and carriers of the apolipoprotein E ε4 allele exhibit higher hippocampal atrophy rates and differing telomere dynamics compared with non-carriers. The authors investigated whether leukocyte telomere length was associated with hippocampal volume in 57 cognitively intact subjects (29 ε3/ε3 carriers; 28 ε4 carriers) aged 49–79 yr. Leukocyte telomere length correlated inversely with left (r(s) = −0.465; p = 0.011), right (r(s) = −0.414; p = 0.025), and total hippocampus volume (r(s) = −0.519; p = 0.004) among APOE ε3/ε3 carriers, but not among ε4 carriers. However, the ε4 carriers fit with the general correlation pattern exhibited by the ε3/ε3 carriers, as ε4 carriers on average had longer telomeres and smaller hippocampi compared with ε3/ε3 carriers. The relationship observed can be interpreted as long telomeres representing a history of relatively low cellular proliferation, reflected in smaller hippocampal volumes. The results support the potential of leukocyte telomere length being used as a biomarker for tapping functional and structural processes of the aging brain. Public Library of Science 2012-04-10 /pmc/articles/PMC3323621/ /pubmed/22506016 http://dx.doi.org/10.1371/journal.pone.0034292 Text en Wikgren et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wikgren, Mikael Karlsson, Thomas Lind, Johanna Nilbrink, Therese Hultdin, Johan Sleegers, Kristel Van Broeckhoven, Christine Roos, Göran Nilsson, Lars-Göran Nyberg, Lars Adolfsson, Rolf Norrback, Karl-Fredrik Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects |
title | Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects |
title_full | Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects |
title_fullStr | Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects |
title_full_unstemmed | Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects |
title_short | Longer Leukocyte Telomere Length Is Associated with Smaller Hippocampal Volume among Non-Demented APOE ε3/ε3 Subjects |
title_sort | longer leukocyte telomere length is associated with smaller hippocampal volume among non-demented apoe ε3/ε3 subjects |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323621/ https://www.ncbi.nlm.nih.gov/pubmed/22506016 http://dx.doi.org/10.1371/journal.pone.0034292 |
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