Hanson M A, Gluckman P D
Academic Unit of Human Development and Health, University of Southampton, and NIHR Nutrition Biomedical Research Centre, University Hospital, Southampton, United Kingdom; and Liggins Institute and Gravida (National Centre for Growth and Development), University of Auckland, Auckland, New Zealand.
Physiol Rev. 2014 Oct;94(4):1027-76. doi: 10.1152/physrev.00029.2013.
Extensive experimental animal studies and epidemiological observations have shown that environmental influences during early development affect the risk of later pathophysiological processes associated with chronic, especially noncommunicable, disease (NCD). This field is recognized as the developmental origins of health and disease (DOHaD). We discuss the extent to which DOHaD represents the result of the physiological processes of developmental plasticity, which may have potential adverse consequences in terms of NCD risk later, or whether it is the manifestation of pathophysiological processes acting in early life but only becoming apparent as disease later. We argue that the evidence suggests the former, through the operation of conditioning processes induced across the normal range of developmental environments, and we summarize current knowledge of the physiological processes involved. The adaptive pathway to later risk accords with current concepts in evolutionary developmental biology, especially those concerning parental effects. Outside the normal range, effects on development can result in nonadaptive processes, and we review their underlying mechanisms and consequences. New concepts concerning the underlying epigenetic and other mechanisms involved in both disruptive and nondisruptive pathways to disease are reviewed, including the evidence for transgenerational passage of risk from both maternal and paternal lines. These concepts have wider implications for understanding the causes and possible prevention of NCDs such as type 2 diabetes and cardiovascular disease, for broader social policy and for the increasing attention paid in public health to the lifecourse approach to NCD prevention.
大量的实验动物研究和流行病学观察表明,早期发育过程中的环境影响会影响后期与慢性疾病(尤其是非传染性疾病,NCD)相关的病理生理过程的风险。这一领域被公认为健康与疾病的发育起源(DOHaD)。我们讨论了DOHaD在多大程度上代表了发育可塑性生理过程的结果,这可能在以后的NCD风险方面产生潜在的不良后果,或者它是否是早期生命中起作用的病理生理过程的表现,只是在以后才表现为疾病。我们认为,证据表明是前者,这是通过在正常发育环境范围内诱导的调节过程起作用的,并且我们总结了所涉及的生理过程的当前知识。后期风险的适应性途径符合进化发育生物学中的当前概念,特别是那些关于亲代效应的概念。在正常范围之外,对发育的影响可能导致非适应性过程,我们回顾了它们的潜在机制和后果。我们还回顾了有关疾病的破坏性和非破坏性途径中涉及的潜在表观遗传和其他机制的新概念,包括来自母系和父系的风险跨代传递的证据。这些概念对于理解2型糖尿病和心血管疾病等NCD的病因和可能的预防、更广泛的社会政策以及公共卫生中对NCD预防的生命历程方法日益增加的关注具有更广泛的意义。