Background and Objective: In adults, leukocyte telomere length (LTL) is variable, familial, and longer in women and in offspring conceived by older fathers. Although short LTL is associated with atherosclerotic cardiovascular disease, long LTL is associated with major cancers. The prevailing notion is that LTL is a "telomeric clock, " whose movement (expressed in LTL attrition) reflects the pace of aging. Accordingly, individuals with short LTL are considered to be biologically older than their peers. Recent studies suggest that LTL is largely determined before adulthood. We examined whether factors that largely characterize LTL in adults also influence LTL in newborns. METHODS: LTL was measured in blood samples from 490 newborns and their parents. RESULTS: LTL (mean ± SD) was longer (9.50 ± 0.70 kb) in newborns than in their mothers (7.92 ± 0.67 kb) and fathers (7.70 ± 0.71 kb) (both P
CITATION STYLE
Factor-Litvak, P., Susser, E., Kezios, K., McKeague, I., Kark, J. D., Hoffman, M., … Aviv, A. (2016). Leukocyte telomere length in newborns: Implications for the role of telomeres in human disease. Pediatrics, 137(4). https://doi.org/10.1542/peds.2015-3927
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