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Early-life Conditions and Age at First Pregnancy in British Women

Overview
Journal Proc Biol Sci
Specialty Biology
Date 2010 Nov 12
PMID 21068037
Citations 50
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Abstract

There is growing evidence that the reproductive schedules of female mammals can be affected by conditions experienced during early development, with low parental investment leading to accelerated life-history strategies in the offspring. In humans, the relationships between early-life conditions and timing of puberty are well studied, but much less attention has been paid to reproductive behaviour. Here, we investigate associations between early-life conditions and age at first pregnancy (AFP) in a large, longitudinally studied cohort of British women (n = 4553). Low birthweight for gestational age, short duration of breastfeeding, separation from mother in childhood, frequent family residential moves and lack of paternal involvement are all independently associated with earlier first pregnancy. Apart from that of birthweight, the effects are robust to adjustment for family socioeconomic position (SEP) and the cohort member's mother's age at her birth. The association between childhood SEP and AFP is partially mediated by early-life conditions, and the association between early-life conditions and AFP is partially mediated by emotional and behavioural problems in childhood. The overall relationship between early-life adversities and AFP appears to be approximately additive.

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References
1.
Belsky J, Steinberg L, Houts R, Friedman S, DeHart G, Cauffman E . Family rearing antecedents of pubertal timing. Child Dev. 2007; 78(4):1302-21. DOI: 10.1111/j.1467-8624.2007.01067.x. View

2.
Alvergne A, Faurie C, Raymond M . Developmental plasticity of human reproductive development: effects of early family environment in modern-day France. Physiol Behav. 2008; 95(5):625-32. DOI: 10.1016/j.physbeh.2008.09.005. View

3.
Cameron N, Shahrokh D, Del Corpo A, Dhir S, Szyf M, Champagne F . Epigenetic programming of phenotypic variations in reproductive strategies in the rat through maternal care. J Neuroendocrinol. 2008; 20(6):795-801. DOI: 10.1111/j.1365-2826.2008.01725.x. View

4.
Mousseau T, Fox C . The adaptive significance of maternal effects. Trends Ecol Evol. 2011; 13(10):403-7. DOI: 10.1016/s0169-5347(98)01472-4. View

5.
Mendle J, Turkheimer E, DOnofrio B, Lynch S, Emery R, Slutske W . Family structure and age at menarche: a children-of-twins approach. Dev Psychol. 2006; 42(3):533-42. PMC: 2964498. DOI: 10.1037/0012-1649.42.3.533. View