Department of Medical Surgical and Health Sciences, Ospedale di Cattinara, University of Trieste, Trieste, Italy.
Institute for Maternal and Child Health IRCCS 'Burlo Garofolo', Trieste, Italy.
Front Endocrinol (Lausanne). 2022 Jul 15;13:912064. doi: 10.3389/fendo.2022.912064. eCollection 2022.
The cause of short stature remains often unknown. The renin-angiotensin system contributes to growth regulation. Several groups reported that angiotensin-converting enzyme 2 ()-knockout mice weighed less than controls. Our case-control study aimed to investigate if children with short stature had reduced expression as compared to controls, and its significance.
children aged between 2 and 14 years were consecutively recruited in a University Hospital pediatric tertiary care center. Cases were children with short stature defined as height SD ≤ -2 diagnosed with growth hormone deficiency (GHD) or idiopathic short stature (ISS), before any treatment. Exclusion criteria were: acute diseases, kidney disease, endocrine or autoimmune disorders, precocious puberty, genetic syndromes, SGA history. and expression were measured in peripheral blood mononuclear cells, angiotensins were measured by ELISA.
Children with short stature displayed significantly lower expression, being 0.40 fold induction (0.01-2.27) as compared to controls, and higher , with no differences between GHD and ISS. expression was significantly and inversely associated with the risk of short stature, OR 0.26 (0.07-0.82), and it had a moderate accuracy to predict it, with an AUC of 0.73 (0.61-0.84). The cutoff of 0.45 fold induction of expression was the value best predicting short stature, identifying correctly 70% of the children.
Our study confirms the association between the reduction of expression and growth retardation. Further studies are needed to determine its diagnostic implications.
身材矮小的原因仍然常常未知。肾素-血管紧张素系统有助于生长调节。有几个研究小组报告称,血管紧张素转换酶 2 ()-敲除小鼠的体重比对照组轻。我们的病例对照研究旨在调查身材矮小的儿童与对照组相比是否存在 表达降低,并探讨其意义。
在一所大学医院儿科三级保健中心,连续招募了年龄在 2 至 14 岁之间的儿童。病例为身高标准差(SD)≤-2 的身材矮小儿童,诊断为生长激素缺乏症(GHD)或特发性身材矮小(ISS),且在接受任何治疗之前。排除标准为:急性疾病、肾脏疾病、内分泌或自身免疫性疾病、性早熟、遗传综合征、SGA 病史。通过 ELISA 法测量外周血单个核细胞中的 和 表达。
身材矮小的儿童表现出显著降低的 表达,与对照组相比,诱导倍数为 0.40(0.01-2.27),而 则升高,GHD 和 ISS 之间无差异。表达与身材矮小的风险呈显著负相关,OR 0.26(0.07-0.82),且具有中等的预测准确性,AUC 为 0.73(0.61-0.84)。表达诱导倍数降低 0.45 倍是预测身材矮小的最佳值,可正确识别 70%的儿童。
我们的研究证实了 表达降低与生长迟缓之间的关联。需要进一步研究以确定其诊断意义。