Song Yuan-Zong, Li Bing-Xiao, Hao Hu, Xin Ruo-Lei, Zhang Ting, Zhang Chun-Hua, Kobayashi Keiko, Wang Zi-Neng, Zheng Xiao-Ying
Department of Pediatrics, First Affiliated Hospital, Jinan University, Guangzhou 510630, China.
Clin Biochem. 2008 May;41(7-8):616-20. doi: 10.1016/j.clinbiochem.2008.01.025. Epub 2008 Feb 12.
Urease pretreatment-gas chromatography-mass spectrometry (UP-GC-MS) has become a valuable tool in the field of metabolome research, including analysis of inborn errors of metabolism (IEMs) and acquired metabolic disturbances secondary to nutrition or drugs. This research aims to screen IEMs in Chinese patients and to explore the cause of neural tube defects (NTDs), a congenital malformation very common in North China.
Urine samples from 618 patients at high risk of IEMs in China were collected, and UP-GC-MS was performed in the selective screening. Urinary methylmalonate (MMA) levels in pregnancy with and without NTDs fetus, respectively, at Luliang district, a countryside region with NTDs incidence 227/10,000, Shanxi Province, North China, were analyzed by GC-MS-selective ion monitoring, and compared with that from control region.
Among the 618 patients, 22 kinds and 59 cases of IEM were found. Methylmalonic aciduria (MMAuria) is on top of the list, followed by neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD), phenylketonuria (PKU), multiple carboxylase deficiency (MCD), etc. Satisfactory therapeutic effects have been achieved in patients such as NICCD, MCD, and galactosemia. At Luliang district, urinary MMA levels in pregnancy, no matter NTDs-affected or unaffected, are both significantly (P<0.01) higher than that in normal control, while serum B(12) levels in NTDs-affected pregnancy are significantly lower than that both in NTDs-unaffected group (P<0.01) and in normal control (P<0.01). Furthermore, B(12) <52.5 pmol/L is associated with a 7.78-fold increased NTDs risk (P<0.01) at Luliang district.
Selective screening for IEMs by UP-GC-MS provides valuable evidences for the diagnosis of IEMs. MMAuria secondary to B(12) deficiency is quite common at Luliang district, suggesting B(12) deficiency is involved in the development of NTDs in the specific population. This metabolome research by UP-GC-MS provides valuable epidemiological information that helps to understand the prevalence and the possible intervention strategy of NTDs and IEMs, especially in Chinese population.
脲酶预处理-气相色谱-质谱联用技术(UP-GC-MS)已成为代谢组学研究领域的一项重要工具,可用于分析先天性代谢缺陷病(IEMs)以及由营养或药物引起的后天性代谢紊乱。本研究旨在筛查中国患者中的IEMs,并探究神经管缺陷(NTDs)的病因,NTDs是中国北方一种非常常见的先天性畸形。
收集了618例中国IEMs高危患者的尿液样本,并采用UP-GC-MS进行选择性筛查。在中国北方山西省吕梁地区(NTDs发病率为227/10000的农村地区),分别对有和没有NTDs胎儿的孕妇尿液中的甲基丙二酸(MMA)水平进行气相色谱-质谱选择性离子监测分析,并与对照地区进行比较。
在618例患者中,发现了22种类型共59例IEMs。甲基丙二酸血症(MMAuria)位居榜首,其次是由citrin缺乏引起的新生儿肝内胆汁淤积症(NICCD)、苯丙酮尿症(PKU)、多种羧化酶缺乏症(MCD)等。NICCD、MCD和半乳糖血症等患者已取得了满意的治疗效果。在吕梁地区,无论胎儿是否患有NTDs,孕妇尿液中的MMA水平均显著高于正常对照组(P<0.01),而患有NTDs的孕妇血清维生素B12水平显著低于未患NTDs组(P<0.01)和正常对照组(P<0.01)。此外,在吕梁地区,维生素B12<52.5 pmol/L与NTDs风险增加7.78倍相关(P<0.01)。
通过UP-GC-MS对IEMs进行选择性筛查为IEMs的诊断提供了有价值的证据。吕梁地区因维生素B12缺乏继发的MMAuria相当常见,提示维生素B12缺乏与特定人群中NTDs的发生有关。这项采用UP-GC-MS的代谢组学研究提供了有价值的流行病学信息,有助于了解NTDs和IEMs的患病率及可能的干预策略,尤其是在中国人群中。