Cammisa Ignazio, Rigante Donato, Cipolla Clelia
Department of Life Sciences and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.
Department of Life Sciences and Public Health, Università Cattolica Sacro Cuore, 20123 Rome, Italy.
Children (Basel). 2025 Apr 11;12(4):495. doi: 10.3390/children12040495.
BACKGROUND/OBJECTIVES: Growth in childhood and adolescence is influenced by a complex interaction of genetic, environmental, and hormonal factors, with growth hormone (GH) and insulin-like growth factor 1 (IGF-1) playing crucial roles in linear growth and development. However, chronic inflammation, often detected in situations like inflammatory bowel disease and juvenile idiopathic arthritis, can significantly disrupt the GH/IGF-1 axis, causing a relevant growth impairment.
We conducted a retrospective review focusing on the role of cytokines in the GH-IGF-1 axis and growth.
Inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6 have been shown to contribute to GH resistance through an array of mechanisms that involve the downregulation of GH receptors and alterations in IGF-1 metabolism. This disruption negatively impacts the growth plate, particularly by impairing chondrocyte proliferation and differentiation, which are essential for proper bone elongation. This review delves into the intricate relationship among growth, chronic inflammation, and GH-IGF-1 axis, emphasizing the contribution of inflammatory cytokines in modulating GH signaling. It also highlights how cytokines can interfere with the molecular pathways that regulate skeletal growth, ultimately leading to growth disturbances in children suffering from chronic inflammatory diseases.
The findings underscore the importance of controlling inflammation in affected individuals to mitigate its detrimental effects on growth and ensure that children may reach their growth full potential.
背景/目的:儿童和青少年时期的生长受到遗传、环境和激素因素复杂相互作用的影响,生长激素(GH)和胰岛素样生长因子1(IGF-1)在线性生长和发育中起着关键作用。然而,在炎症性肠病和青少年特发性关节炎等情况下经常检测到的慢性炎症,会显著扰乱GH/IGF-1轴,导致相关的生长障碍。
我们进行了一项回顾性研究,重点关注细胞因子在GH-IGF-1轴和生长中的作用。
肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和IL-6等炎性细胞因子已被证明通过一系列机制导致GH抵抗,这些机制包括GH受体的下调和IGF-1代谢的改变。这种破坏对生长板产生负面影响,特别是通过损害软骨细胞增殖和分化,而软骨细胞增殖和分化对骨骼正常伸长至关重要。本综述深入探讨了生长、慢性炎症和GH-IGF-1轴之间的复杂关系,强调了炎性细胞因子在调节GH信号传导中的作用。它还强调了细胞因子如何干扰调节骨骼生长的分子途径,最终导致患有慢性炎症性疾病的儿童生长紊乱。
研究结果强调了控制受影响个体炎症的重要性,以减轻其对生长的有害影响,并确保儿童能够充分发挥其生长潜力。