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2012 (English)In: PLOS ONE, E-ISSN 1932-6203, Vol. 7, no 4, p. e34292-Article in journal (Refereed) Published
Abstract [en]
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.
Place, publisher, year, edition, pages
Public Library of Science, 2012
National Category
Neurosciences
Identifiers
urn:nbn:se:umu:diva-54207 (URN)10.1371/journal.pone.0034292 (DOI)000305297500024 ()22506016 (PubMedID)2-s2.0-84859582344 (Scopus ID)
2012-04-192012-04-192024-07-02Bibliographically approved