The Danish Aging Research Center and The Danish Twin Registry, Epidemiology and Biostatistics Unit, Institute of Public Health, University of Southern Denmark, Odense.
Department of Clinical Genetics, Odense University Hospital.
J Gerontol A Biol Sci Med Sci. 2019 Nov 13;74(12):1853-1860. doi: 10.1093/gerona/glz070.
Aging is a multifactorial trait caused by early as well as late-life circumstances. A society trend that parents deliberately delay having children is of concern to health professionals, for example as advanced parental age at conception increases disease risk profiles in offspring. We here aim to study if advanced parental age at conception affects mitochondrial DNA content, a cross-species biomarker of general health, in adult human twin offspring and in a model organism. We find no deteriorated mitochondrial DNA content at advanced parental age at conception, but human mitochondrial DNA content was higher in females than males, and the difference was twofold higher at advanced maternal age at conception. Similar parental age effects and sex-specific differences in mitochondrial DNA content were found in Drosophila melanogaster. In addition, parental longevity in humans associates with both mitochondrial DNA content and parental age at conception; thus, we carefully propose that a poorer disease risk profile from advanced parental age at conception might be surpassed by superior effects of parental successful late-life reproduction that associate with parental longevity.
衰老是一种多因素特征,由早期和晚期生活环境共同导致。例如,父母有意延迟生育的社会趋势引起了健康专家的关注,因为受孕时父母年龄较大会增加后代的疾病风险。在这里,我们旨在研究受孕时父母年龄较大是否会影响线粒体 DNA 含量,即一种通用健康的跨物种生物标志物,在人类双胞胎后代和模式生物中进行研究。我们发现受孕时父母年龄较大不会导致线粒体 DNA 含量恶化,但人类线粒体 DNA 含量在女性中高于男性,而在受孕时母亲年龄较大时,这种差异要高出两倍。在黑腹果蝇中也发现了类似的与父母年龄相关的线粒体 DNA 含量的作用和性别特异性差异。此外,人类的父母寿命与线粒体 DNA 含量和受孕时父母年龄都有关联;因此,我们谨慎地提出,受孕时父母年龄较大带来的较差疾病风险状况可能会被与父母长寿相关的父母成功晚年生育的优越效应所超越。