Department of Human Biology, University of Wrocław, Ul. Przybyszewskiego 63, 51-148, Wrocław, Poland.
Sci Rep. 2023 Aug 30;13(1):14231. doi: 10.1038/s41598-023-41065-w.
Previous studies showed that intrauterine growth restrictions, resulting in smaller body size at birth, are associated with altered development and the risk of age-related diseases in adult life. Thus, prenatal development may predict aging trajectories in humans. The study aimed to verify if body size at birth is related to biological age in adult men. The study sample consisted of 159 healthy, non-smoking men with a mean age of 35.24 (SD 3.44) years. Birth weight and length were taken from medical records. The ponderal index at birth was calculated. Biological age was evaluated based on serum levels of s-Klotho, hsCRP, DHEA/S, and oxidative stress markers. Pregnancy age at birth, lifestyle, weight, cortisol, and testosterone levels were controlled. The results showed no relationship between birth size and s-Klotho, DHEA/S level, inflammation, or oxidative stress. Also, men born as small-for-gestational-age (N = 49) and men born as appropriate-for-gestational-age (N = 110) did not differ in terms of biological age markers levels. The results were similar when controlled for pregnancy week at birth, chronological age, BMI, testosterone, or cortisol level. The results suggest that there is no relationship between intrauterine growth and biomarkers of aging in men aged 30-45 years from the affluent population.
先前的研究表明,宫内生长受限导致出生时体型较小,与成年后发育改变和与年龄相关疾病的风险相关。因此,产前发育可能可以预测人类的衰老轨迹。本研究旨在验证出生时的体型是否与成年男性的生物年龄有关。研究样本包括 159 名健康、不吸烟的男性,平均年龄为 35.24 岁(标准差为 3.44 岁)。出生体重和长度取自病历。出生时的体质量指数( ponderal index)通过计算得出。生物年龄根据血清 s-Klotho、hsCRP、DHEA/S 和氧化应激标志物的水平进行评估。控制了出生时的孕期年龄、生活方式、体重、皮质醇和睾酮水平。结果显示,出生时的体型与 s-Klotho、DHEA/S 水平、炎症或氧化应激之间没有关系。此外,出生时为小于胎龄儿(N=49)和出生时为适于胎龄儿(N=110)的男性在生物年龄标志物水平方面没有差异。当控制出生时的孕周、实际年龄、BMI、睾酮或皮质醇水平时,结果相似。这些结果表明,在富裕人群中,30-45 岁男性的宫内生长与衰老生物标志物之间没有关系。