The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Prenatal and early life influences on epigenetic age in children: a study of mother–offspring pairs from two cohort studies
Open accessAbstract
DNA methylation-based biomarkers of aging are highly correlated with actual age. Departures of methylation-estimated age from actual age can be used to define epigenetic measures of child development or age acceleration (AA) in adults. Very little is known about genetic or environmental determinants of these epigenetic measures of aging. We obtained DNA methylation profiles using Infinium HumanMethylation450 BeadChips across five time-points in 1018 mother-child pairs from the Avon Longitudinal Study of Parents and Children. Using the Horvath age estimation method, we calculated epigenetic age for these samples. AA was defined as the residuals from regressing epigenetic age on actual age. AA was tested for associations with cross-sectional clinical variables in children. We identified associations between AA and sex, birth weight, birth by caesarean section and several maternal characteristics in pregnancy, namely smoking, weight, BMI, selenium and cholesterol level. Offspring of non-drinkers had higher AA on average but this difference appeared to resolve during childhood. The associations between sex, birth weight and AA found in ARIES were replicated in an independent cohort (GOYA). In children, epigenetic AA measures are associated with several clinically relevant variables, and early life exposures appear to be associated with changes in AA during adolescence. Further research into epigenetic aging, including the use of causal inference methods, is required to better our understanding of aging.
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“Placental and offspring epigenetic signatures, telomere biology and mitochondrial function provide measurable molecular readouts of prenatal exposure at birth or during childhood [116,117,118].”
From Placental Pathophysiology and Developmental Programming of Adult Cardiometabolic Risk: A Narrative Review of Pregnancy Exposures (2026) · cites this paper as [116]
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DNA methylation age of human tissues and cell types
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Common SNPs explain a large proportion of the heritability for human height
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Genome-wide methylation profiles reveal quantitative views of human aging rates
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Self-citationCohort Profile: The Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort
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Self-citationHeritability in the genomics era — concepts and misconceptions
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DNA methylation age of blood predicts all-cause mortality in later life
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Self-citationThe Danish National Birth Cohort - its background, structure and aim
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DNA methylation-based biomarkers and the epigenetic clock theory of ageing
Horvath, S., & Raj, K. (2018) · Nature Reviews Genetics · doi:10.1038/s41576-018-0004-3 · Cited by 3,095
Self-citationDNA methylation aging clocks: challenges and recommendations
Bell, C. G., Lowe, R., Adams, P. D., Baccarelli, A. A., Beck, S., Bell, J. T., Christensen, B. C., Gladyshev, V. N., Heijmans, B. T., Horvath, S., et al. (2019) · Genome Biology · doi:10.1186/s13059-019-1824-y · Cited by 1,025
Self-citationAn epigenetic clock analysis of race/ethnicity, sex, and coronary heart disease
Horvath, S., Gurven, M., Levine, M. E., Trumble, B. C., Kaplan, H. S., Allayee, H., Ritz, B. R., Chen, B. H., Lu, A. T.-H., Rickabaugh, T. M., et al. (2016) · Genome biology · doi:10.1186/s13059-016-1030-0 · Cited by 749
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Epigenetic clock: A promising biomarker and practical tool in aging
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Metadata
- Authors
- Simpkin, A. J., Hemani, G., Suderman, M., Gaunt, T. R., Lyttleton, O., Mcardle, W. L., Ring, S. M., Sharp, G. C., Tilling, K., Horvath, S., Kunze, S., Peters, A., Waldenberger, M., Ward-Caviness, C., Nohr, E. A., Sørensen, T. I. A., Relton, C. L., & Smith, G. D.
- Affiliations
- MRC Integrative Epidemiology Unit (GB)
- University of Bristol (GB)
- University of California, Los Angeles (US)
- Helmholtz Munich (DE)
- University of Southern Denmark (DK)
- University of Copenhagen (DK)
- Corresponding author
- Simpkin, Andrew J.
- ORCID
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-11-05
- Volume
- 25
- Issue
- 1
- Pages
- 191-201
- ISSN
- 0964-6906 (ISSN-L)
- 1460-2083
- PMC
- PMC4690495
- OpenAlex
- W2158554646
- Cited by
- 246
- References
- 31
- Citations by year
- 2026: 14 · 2025: 7 · 2024: 24 · 2023: 22 · 2022: 18 · 2021: 30 · 2020: 57 · 2019: 19 · 2018: 22 · 2017: 21 · 2016: 11 · 2015: 1
- FWCI
- 7.96
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Human Molecular Genetics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Bristol Research (University of Bristol) (publishedVersion, cc-by)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Site cant be reached (submittedVersion, cc-by)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Explore Bristol Research (submittedVersion, cc-by)
- Newcastle University ePrints (Newcastle Univesity) (cc-by)
- Funders
- UK Economic & Social Research Council (RES-060-23-0011)
- UK Medical Research Council (G0601625, G0600705 and MR/L011824/1)
- European Research Council (269874)
- the BBSRC (BBI025751/1 and BB/I025263/1)
- the Medical Research Council (MRC) and the Wellcome Trust (102215/2/13/1)
- NIH
- the auspices of the MRC Integrative Epidemiology Unit at the University of Bristol (MC_UU_12013/2, MC_UU_12013/8, MRC_UU_12013/9)
- German Federal Ministry of Education and Research (01ZX1313A-2014)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
- Keywords
- epigenetic age, accelerated aging, DNA methylation, prenatal exposure, early life exposure, mother-child pairs, birth weight, cesarean section, maternal smoking, maternal cholesterol, sex differences, adolescence, child development, Avon Longitudinal Study of Parents and Children
- MeSH terms
- Aging, Birth Weight, Child, Humans, Longitudinal Studies, Mothers, Cohort Studies, DNA Methylation, Epigenesis, Genetic
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