Bousquet Audrey, Sanderson Keia, O'Shea T Michael, Fry Rebecca C
Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.
Department of Internal Medicine, School of Medicine, University of North Carolina, Chapel Hill, NC 27599, USA.
Children (Basel). 2023 Oct 13;10(10):1683. doi: 10.3390/children10101683.
Individuals born preterm have shorter lifespans and elevated rates of chronic illness that contribute to mortality risk when compared to individuals born at term. Emerging evidence suggests that individuals born preterm or of low birthweight also exhibit physiologic and cellular biomarkers of accelerated aging. It is unclear whether, and to what extent, accelerated aging contributes to a higher risk of chronic illness and mortality among individuals born preterm. Here, we review accelerated aging phenotypes in adults born preterm and biological pathways that appear to contribute to accelerated aging. We highlight biomarkers of accelerated aging and various resiliency factors, including both pharmacologic and non-pharmacologic factors, that might buffer the propensity for accelerated aging among individuals born preterm.
与足月出生的个体相比,早产个体的寿命较短,慢性病发病率较高,这些因素会增加死亡风险。新出现的证据表明,早产或低出生体重的个体也表现出加速衰老的生理和细胞生物标志物。目前尚不清楚加速衰老是否以及在多大程度上导致早产个体患慢性病和死亡的风险更高。在此,我们综述了早产成年人的加速衰老表型以及似乎导致加速衰老的生物学途径。我们强调了加速衰老的生物标志物和各种弹性因素,包括药物和非药物因素,这些因素可能会缓冲早产个体加速衰老的倾向。