Division of Pediatrics & DOHaD Laboratory, CHUV University Hospital and University of Lausanne, Lausanne, Switzerland.
MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
J Endocrinol. 2020 Feb;244(2):249-259. doi: 10.1530/JOE-18-0538.
Low weight in early infancy is a known risk factor for cardio-metabolic syndrome in adult life. However, little is known either about developmental programming in subjects of normal birthweight or about events between the ages which separate early programming and the occurrence of disease at late adulthood. We tested the hypothesis that circulating concentrations of leptin, adiponectin and insulin in young, healthy adults, born with a birth size within the normal range, are influenced by early life growth patterns. In an observational study of 188 healthy volunteers aged 18-25 years (97 males, 91 females) we investigated the association of metabolic function with their birth size, their growth during childhood and their body composition. High plasma leptin in early adulthood, a risk factor for cardio-metabolic syndrome, was associated with low weight at age 2 years (correlation coefficient controlled for adult weight = -0.21, P < 0.01). It was also positively associated with pre-prandial insulin and with HOMA (Homeostasis Model Assessment) insulin resistance. Leptin, leptin-adiponectin ratio and insulin correlated with lean mass, fat mass and percent fat (P < 0.0001). In conclusion, high leptin in early adulthood was associated with both low weight at age 2 years and insulin resistance. We speculate that high leptin is developmentally programmed and can contribute to the association between low weight in early infancy and increased cardio-metabolic risk in adulthood in healthy subjects.
婴儿早期体重低是成年后患心血管代谢综合征的已知危险因素。然而,对于正常出生体重的受试者的发育编程,或者在早期编程和成年后期疾病发生之间分隔的年龄之间的事件,人们知之甚少。我们检验了这样一个假设,即在正常范围内出生的年轻健康成年人中,循环中瘦素、脂联素和胰岛素的浓度受到生命早期生长模式的影响。在一项对 188 名年龄在 18-25 岁之间的健康志愿者(97 名男性,91 名女性)的观察性研究中,我们调查了代谢功能与他们的出生体重、儿童时期的生长情况以及身体成分之间的关系。成年后患心血管代谢综合征的危险因素——早期高血浆瘦素与 2 岁时体重低有关(控制成人体重后的相关系数=-0.21,P<0.01)。它还与餐前胰岛素和 HOMA(稳态模型评估)胰岛素抵抗呈正相关。瘦素、瘦素-脂联素比值和胰岛素与瘦体重、脂肪量和脂肪百分比呈正相关(P<0.0001)。总之,成年早期的高瘦素与 2 岁时体重低和胰岛素抵抗有关。我们推测高瘦素是发育编程的,并可能导致婴儿早期体重低与成年后患心血管代谢风险增加之间的关联。