Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/25515
Title: Telomere tracking from birth to adulthood and residential traffic exposure
Authors: BIJNENS, Esmee 
Zeegers, Maurice P.
Derom, Catherine
MARTENS, Dries 
Gielen, Marij
HAGEMAN, Geja 
Thiery, Evert
Vlietinck, Robert
PLUSQUIN, Michelle 
NAWROT, Tim 
Issue Date: 2017
Source: BMC medicine, 15(1), (Art N° 205)
Abstract: Background: Telomere attrition is extremely rapid during the first years of life, while lifestyle during adulthood exerts a minor impact. This suggests that early life is an important period in the determination of telomere length. We investigated the importance of the early-life environment on both telomere tracking and adult telomere length. Methods: Among 184 twins of the East Flanders Prospective Twin Survey, telomere length in placental tissue and in buccal cells in young adulthood was measured. Residential addresses at birth and in young adulthood were geocoded and residential traffic and greenness exposure was determined. Results: We investigated individual telomere tracking from birth over a 20 year period (mean age (SD), 22.6 (3.1) years) in association with residential exposure to traffic and greenness. Telomere length in placental tissue and in buccal cells in young adulthood correlated positively (r = 0.31, P < 0.0001). Persons with higher placental telomere length at birth were more likely to have a stronger downward shift in telomere ranking over life (P < 0.0001). Maternal residential traffic exposure correlated inversely with telomere length at birth. Independent of birth placental telomere length, telomere ranking between birth and young adulthood was negatively and significantly associated with residential traffic exposure at the birth address, while traffic exposure at the residential address at adult age was not associated with telomere length. Conclusions: Longitudinal evidence of telomere length tracking from birth to adulthood shows inverse associations of residential traffic exposure in association with telomere length at birth as well as accelerated telomere shortening in the first two decades of life.
Notes: [Bijnens, Esmee M.; Martens, Dries S.; Plusquin, Michelle; Nawrot, Tim S.] Hasselt Univ, Ctr Environm Sci, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium. [Bijnens, Esmee M.; Zeegers, Maurice P.; Gielen, Marij] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Dept Complex Genet, Maastricht, Netherlands. [Zeegers, Maurice P.] Maastricht Univ, CAPHRI Sch Publ Hlth & Primary Care, Maastricht, Netherlands. [Derom, Catherine] Ghent Univ Hosp, Dept Obstet & Gynecol, Ghent, Belgium. [Derom, Catherine; Vlietinck, Robert] Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium. [Hageman, Geja J.] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Dept Toxicol, Maastricht, Netherlands. [Thiery, Evert] Ghent Univ Hosp, Dept Neurol, Ghent, Belgium. [Nawrot, Tim S.] Leuven Univ KU Leuven, Dept Publ Hlth, Leuven, Belgium.
Keywords: telomere length; traffic; tracking
Document URI: http://hdl.handle.net/1942/25515
ISSN: 1741-7015
e-ISSN: 1741-7015
DOI: 10.1186/s12916-017-0964-8
ISI #: 000415874400001
Rights: © The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Category: A1
Type: Journal Contribution
Validations: ecoom 2018
Appears in Collections:Research publications

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