University Medical Center Groningen, The Netherlands.
Physiol Behav. 2012 Jul 16;106(5):691-700. doi: 10.1016/j.physbeh.2011.12.008. Epub 2011 Dec 22.
This paper integrates the cumulative stress hypothesis with the mismatch hypothesis, taking into account individual differences in sensitivity to programming. According to the cumulative stress hypothesis, individuals are more likely to suffer from disease as adversity accumulates. According to the mismatch hypothesis, individuals are more likely to suffer from disease if a mismatch occurs between the early programming environment and the later adult environment. These seemingly contradicting hypotheses are integrated into a new model proposing that the cumulative stress hypothesis applies to individuals who were not or only to a small extent programmed by their early environment, while the mismatch hypothesis applies to individuals who experienced strong programming effects. Evidence for the main effects of adversity as well as evidence for the interaction between adversity in early and later life is presented from human observational studies and animal models. Next, convincing evidence for individual differences in sensitivity to programming is presented. We extensively discuss how our integrated model can be tested empirically in animal models and human studies, inviting researchers to test this model. Furthermore, this integrated model should tempt clinicians and other intervenors to interpret symptoms as possible adaptations from an evolutionary biology perspective.
本文将累积应激假说与不匹配假说相结合,同时考虑了个体对编程的敏感性差异。根据累积应激假说,随着逆境的积累,个体更容易患上疾病。根据不匹配假说,如果早期编程环境与后期成年环境之间不匹配,个体更容易患上疾病。这两个看似矛盾的假说被整合到一个新模型中,该模型提出累积应激假说适用于早期环境对其影响较小或没有影响的个体,而不匹配假说适用于经历过强烈编程效应的个体。来自人类观察研究和动物模型的证据表明了逆境的主要影响以及早期和后期生活中的逆境之间的相互作用。接下来,本文提出了对编程敏感性个体差异的令人信服的证据。我们广泛讨论了如何在动物模型和人类研究中对我们的综合模型进行实证检验,邀请研究人员来检验该模型。此外,该综合模型应该会促使临床医生和其他干预者从进化生物学的角度来解释症状,将其视为可能的适应。