Department of Global Public Health, Karolinska Institute, Stockholm, Sweden.
School of Public Health, The University of Queensland, Herston, Australia.
Soc Sci Med. 2021 Apr;275:113811. doi: 10.1016/j.socscimed.2021.113811. Epub 2021 Mar 4.
The developmental origins of ischemic heart disease (IHD) have been widely documented but little is known about their persistence across more than one generation. This study aimed to investigate whether the effects of early life disadvantages on adult IHD have changed between generations and are mediated by adult socioeconomic circumstances, and further explore the transgenerational effects of grandparental and parental exposures to disadvantaged circumstances on adult offspring's IHD.
We used register-based data from the Uppsala Multigenerational Study, Sweden. The study populations were the parents born 1915-1929 and their offspring born 1932-1972 with available obstetric data. The offspring were further linked to grandparents who had their socioeconomic and demographic data recorded. The outcome was incident IHD assessed at ages 32-75 during a follow-up from January 1, 1964 till December 31, 2008. The exposures included birthweight standardized-for-gestational age, ponderal index, gestational length, and parental socioeconomic position (SEP). Education and income were analyzed as mediators. Potential transgenerational associations were explored by linking offspring IHD to parents' standardized birthweight and gestational length, grandparental SEP, and to grandmothers' age, parity, and marital status at parental birth. All associations were examined in Cox proportional hazard regression models.
Lower standardized birthweight and lower parental SEP were found to be associated with higher IHD rates in both generations, with no evidence of effect modification by generation. Education and income did not mediate the association between standardized birthweight and IHD. Disadvantaged grandparental SEP, younger and older childbearing ages of grandmothers, and paternal preterm birth affected offspring's IHD independent of parental education, income, or IHD history.
The findings point to similar magnitudes of IHD inequalities by early life disadvantages across two historical periods and the existence of transgenerational effects on IHD. Epigenetic dysregulation involving the germline is a plausible candidate mechanism underlying the transgenerational associations that warrant further research.
缺血性心脏病(IHD)的发育起源已被广泛记录,但对其在两代以上的持续存在知之甚少。本研究旨在探讨早期生活劣势对成年 IHD 的影响是否在两代人之间发生了变化,并受成年社会经济环境的影响,并进一步探讨祖辈和父母接触不利环境对成年后代 IHD 的跨代影响。
我们使用了来自瑞典乌普萨拉多代研究的基于登记的资料。研究人群为 1915-1929 年出生的父母及其 1932-1972 年出生的可获得产科资料的后代。这些后代与有社会经济和人口资料记录的祖辈进一步联系起来。结果是在 1964 年 1 月 1 日至 2008 年 12 月 31 日的随访期间,在 32-75 岁时发生的 IHD。暴露包括按胎龄标准化的出生体重、体质指数、妊娠期长度以及父母的社会经济地位(SEP)。教育和收入被分析为中介因素。通过将后代的 IHD 与父母的标准化出生体重和妊娠长度、祖辈的 SEP 以及父母出生时祖母的年龄、产次和婚姻状况联系起来,探讨了潜在的跨代关联。所有关联都在 Cox 比例风险回归模型中进行了检验。
发现较低的标准化出生体重和较低的父母 SEP 与两代人较高的 IHD 发生率相关,而且没有证据表明两代人之间存在效应修饰。教育和收入并不能介导标准化出生体重与 IHD 之间的关联。不利的祖辈 SEP、祖母较年轻和较年长的生育年龄以及父亲的早产,独立于父母的教育、收入或 IHD 病史,影响后代的 IHD。
这些发现表明,在两个历史时期,由早期生活劣势导致的 IHD 不平等程度相似,并且存在 IHD 的跨代效应。涉及种系的表观遗传失调是跨代关联的一个可能机制,值得进一步研究。