Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/39778
Title: Sedentary Behaviour and Telomere Length Shortening during Early Childhood: Evidence from the Multicentre Prospective INMA Cohort Study
Authors: Prieto-Botella, Daniel
MARTENS, Dries 
Valera-Gran, Desiree
Subiza-Pérez, Mikel
Tardón, Adonina
Lozano, Manuel
Casas, Maribel
Bustamante, Mariona
Jimeno-Romero, Alba
Fernández-Somoano, Ana
Llop, Sabrina
Vrijheid, Martine
NAWROT, Tim 
Navarrete-Muñoz, Eva-María
Issue Date: 2023
Publisher: MDPI
Source: International Journal of Environmental Research and Public Health, 20 (6) (Art N° 5134)
Abstract: Sedentary behaviour (SB) may be related to telomere length (TL) attrition due to a possible pro-inflammatory effect. This study examined the association between parent-reported sedentary behaviour (SB) and leukocyte TL at the age of 4 and telomere tracking from 4 to 8 years. In the Spanish birth cohort Infancia y Medio Ambiente (INMA) project, we analysed data from children who attended follow-up visits at age 4 (n = 669) and 8 (n = 530). Multiple robust regression models were used to explore the associations between mean daily hours of SB (screen time, other sedentary activities, and total SB) at 4 years categorised into tertiles and TL at 4 years and difference in TL rank between age 4 and 8, respectively. At the age of 4, the results showed that children with the highest screen time (1.6–5.0 h/day) had a shorter TL of −3.9% (95% CI: −7.4, −0.4; p = 0.03) compared with children in the lowest tertile (0.0–1.0 h/day). Between 4 and 8 years, a higher screen time (highest tertile group vs. lowest tertile) was associated with a decrease in the LTL rank of −1.9% (95% CI: −3.8, −0.1; p = 0.03) from 4 to 8 years. Children exposed to a higher screen time at 4 years were more prone to have shorter TL at 4 and between 4 and 8 years of age. This study supports the potential negative effect of SB during childhood on cellular longevity.
Keywords: lifestyle;children;genetics;screen time;epigenetics;cellular longevity
Document URI: http://hdl.handle.net/1942/39778
ISSN: 1661-7827
e-ISSN: 1660-4601
DOI: 10.3390/ijerph20065134
Rights: 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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