Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Horm Res Paediatr. 2011;76(2):99-103. doi: 10.1159/000327369. Epub 2011 Jul 7.
Considering the high prevalence of congenital hypothyroidism (CH) in Isfahan, the possible involvement of endothelial dysfunction in the pathogenesis of CH and the lack of studies in this field, the aim of this study was to determine the endothelial function in CH patients.
During this case-control study, the endothelial function in CH neonates and in those with normal screening results was evaluated during a CH screening program in Isfahan. Peripheral blood samples were obtained for measurement of the von Willebrand factor (vWf), and intercellular and vascular cell adhesion molecule (ICAM and VCAM). In CH patients these biomarkers were measured twice: before and 4 weeks after treatment.
In this study, 56 neonates were evaluated: 30 of them were neonates with normal screening results and 26 were diagnosed with CH and classified into two groups according to their TSH levels. The mean ICAM and VCAM were higher in CH patients than in the control group (p < 0.05). The mean ICAM and VCAM decreased significantly after treatment in CH patients (p < 0.05). There is no significant relationship between TSH, ICAM, VCAM and vWf (p > 0.05).
The findings of this study demonstrate the possible involvement of the endothelial system in the pathogenesis of CH and its cardiovascular complications. Further studies with a larger sample size and with the measurement of other endothelial function markers are needed.
鉴于先天性甲状腺功能减退症 (CH) 在伊斯法罕的高患病率、内皮功能障碍可能参与 CH 的发病机制以及该领域缺乏研究,本研究旨在确定 CH 患者的内皮功能。
在这项病例对照研究中,在伊斯法罕的 CH 筛查计划中评估了 CH 新生儿和筛查结果正常的新生儿的内皮功能。采集外周血样本测量血管性血友病因子 (vWf)、细胞间和血管细胞粘附分子 (ICAM 和 VCAM)。在 CH 患者中,这些生物标志物测量了两次:治疗前和治疗后 4 周。
本研究共评估了 56 名新生儿:其中 30 名新生儿筛查结果正常,26 名被诊断为 CH,并根据 TSH 水平分为两组。CH 患者的平均 ICAM 和 VCAM 高于对照组 (p < 0.05)。CH 患者治疗后 ICAM 和 VCAM 明显下降 (p < 0.05)。TSH、ICAM、VCAM 和 vWf 之间无显著相关性 (p > 0.05)。
本研究结果表明内皮系统可能参与 CH 的发病机制及其心血管并发症。需要进一步研究,样本量更大,并测量其他内皮功能标志物。