Zhang Zhilei, Wang Xin, Zhang Jingjing, Guan Xianwei, Wang Yanyun, Hong Dongyang, Li Yahong, Yang Peiying, Sun Yun, Jiang Tao
Nanjing Women and Children's Healthcare Hospital, Center of Genetic Medicine, The Affiliated Obstetrics and Gynecology Hospital With Nanjing Medical University, No.123, Tianfei Xiang, Mochou Road, Nanjing, Jiangsu, China.
Orphanet J Rare Dis. 2025 Jan 8;20(1):9. doi: 10.1186/s13023-025-03529-2.
Ornithine transcarbamylase deficiency exhibits a high degree of clinical heterogeneity, making its screening and classification challenging in some instances. In this study, we first established a simple and stable method for testing ornithine transcarbamylase activity using micro blood from newborns, rather than relying on venous blood.
The activity of ornithine transcarbamylase was assessed by measuring the concentration of citrulline produced in the reaction with carbamoyl phosphate and ornithine, using serum, plasma or micro blood. Correlation analysis was evaluated using Sangerbox Tools. The Receiver Operating Characteristic curve was used in SPSS Statistics 17.0 to evaluate the diagnostic efficiency of Ornithine transcarbamylase deficiency.
A strong linear relationship was observed between ornithine transcarbamylase activity and both micro blood volume and reaction time (R = 0.9793, 0.9922 respectively). The intra-coefficient variation and inter-coefficient variation were 11% and 12.5% with a 1-h reaction time, and 6.77% and 9.58% with a 3-h reaction time, respectively. And the inter-coefficient variation was lower than the most widely used colorimetry method (5.1-21.1%). The Limit of Blank was 0.57 nmol/mL/h. The reference interval for normal newborn population is greater than or equal to 39.6 nmol/mL/h. Notably, the method exhibited a 100% sensitivity, surpassing the sensitivity of colorimetry method (94.3%), along with and a specificity of 96.9% for diagnosing ornithine transcarbamylase deficiency.
We pioneered a method for testing OTC activity that normally carried on venous blood can be effectively performed on microblood heel samples. Meanwhile, our method presents a simpler, more stable and reproducible approach compared to colorimetry.
鸟氨酸转氨甲酰酶缺乏症表现出高度的临床异质性,这使得在某些情况下对其进行筛查和分类具有挑战性。在本研究中,我们首先建立了一种简单且稳定的方法,用于使用新生儿微量血检测鸟氨酸转氨甲酰酶活性,而不是依赖静脉血。
通过测量与氨甲酰磷酸和鸟氨酸反应中产生的瓜氨酸浓度,使用血清、血浆或微量血来评估鸟氨酸转氨甲酰酶的活性。使用Sangerbox工具进行相关性分析。在SPSS Statistics 17.0中使用受试者工作特征曲线来评估鸟氨酸转氨甲酰酶缺乏症的诊断效率。
观察到鸟氨酸转氨甲酰酶活性与微量血量和反应时间之间存在强线性关系(分别为R = 0.9793和0.9922)。反应时间为1小时时,组内变异系数和组间变异系数分别为11%和12.5%;反应时间为3小时时,分别为6.77%和9.58%。并且组间变异系数低于最广泛使用的比色法(5.1 - 21.1%)。空白限为0.57 nmol/mL/h。正常新生儿群体的参考区间大于或等于39.6 nmol/mL/h。值得注意的是,该方法表现出100%的灵敏度,超过了比色法的灵敏度(94.3%),并且诊断鸟氨酸转氨甲酰酶缺乏症的特异性为96.9%。
我们开创了一种检测OTC活性的方法,即通常在静脉血上进行的检测可以在足跟微量血样本上有效进行。同时,与比色法相比,我们的方法呈现出一种更简单、更稳定且可重复的方法。