Laboratory of Genetics and Genomics, Institute for Developing Science and Health Initiatives, Mohakhali, Dhaka 1212, Bangladesh.
Department of Genetic Engineering & Biotechnology, University of Dhaka, Dhaka 1000, Bangladesh.
Biomed Res Int. 2019 Jan 6;2019:3460902. doi: 10.1155/2019/3460902. eCollection 2019.
Liquid Chromatography tandem mass spectrometry (LC-MS/MS) is used for the diagnosis of more than 30 inborn errors of metabolisms (IEMs). Accurate and reliable diagnosis of IEMs by quantifying amino acids (AAs) and acylcarnitines (ACs) using LC-MS/MS systems depend on the establishment of age-specific cut-offs of the analytes. This study aimed to (1) determine the age-specific cut-off values of AAs and ACs in Bangladesh and (2) validate the LC-MS/MS method for diagnosis of the patients with IEMs. A total of 570 enrolled healthy participants were divided into 3 age groups, namely, (1) newborns (1-7 days), (2) 8 days-7 years, and (3) 8-17 years, to establish the age-specific cut-offs for AAs and ACs. Also, 273 suspected patients with IEMs were enrolled to evaluate the reliability of the established cut-off values. Quantitation of AAs and ACs was performed on an automated LC-MS/MS system using dried blood spot (DBS) cards. Then the specimens of the enrolled clinically suspected patients were analyzed by the established method. Nine patients came out as screening positive for different IEMs, including two borderline positive cases of medium-chain acyl-CoA dehydrogenase deficiency (MCAD). A second-tier test for confirmation of the screening positive cases was conducted by urinary metabolic profiling using gas chromatography- mass spectrometry (GC-MS). Out of 9 cases that came out as screening positive by LC-MS/MS, seven cases were confirmed by urinary GC-MS analysis including 3 cases with phenylketonuria, 1 with citrullinemia type II, 1 with methylmalonic acidemia, 1 with isovaleric acidemia and 1 with carnitine uptake defect. Two borderline positive cases with MCAD were found negative by urinary GC-MS analysis. In conclusion, along with establishment of a validated LC-MS/MS method for quantitation of AAs and ACs from the DBS cards, the study also demonstrates the presence of predominantly available IEMs in Bangladesh.
液相色谱串联质谱法(LC-MS/MS)用于诊断 30 多种代谢物遗传缺陷(IEMs)。使用 LC-MS/MS 系统定量分析氨基酸(AAs)和酰基肉碱(ACs)以准确可靠地诊断 IEMs,取决于建立分析物的年龄特异性截止值。本研究旨在:(1)确定孟加拉国 AA 和 AC 的年龄特异性截止值,(2)验证 LC-MS/MS 方法用于诊断 IEM 患者。共纳入 570 名健康参与者,分为 3 个年龄组,即(1)新生儿(1-7 天),(2)8 天-7 岁,和(3)8-17 岁,以建立 AA 和 AC 的年龄特异性截止值。此外,还纳入了 273 名疑似 IEM 患者,以评估所建立的截止值的可靠性。使用干血斑(DBS)卡上的自动 LC-MS/MS 系统定量分析 AAs 和 ACs。然后,使用建立的方法分析纳入的临床疑似患者的标本。9 名患者被筛查出患有不同的 IEM,包括 2 例中等链酰基辅酶 A 脱氢酶缺乏症(MCAD)的边界阳性病例。通过气相色谱-质谱联用(GC-MS)进行尿代谢谱分析,对筛查阳性病例进行二级确认测试。在通过 LC-MS/MS 筛查出的 9 例阳性病例中,有 7 例通过尿 GC-MS 分析得到证实,包括 3 例苯丙酮尿症、1 例 citrullinemia type II、1 例甲基丙二酸血症、1 例异戊酸血症和 1 例肉碱摄取缺陷。2 例 MCAD 的边界阳性病例经尿 GC-MS 分析呈阴性。总之,本研究不仅建立了一种从 DBS 卡上定量分析 AA 和 AC 的验证 LC-MS/MS 方法,还表明孟加拉国存在主要的 IEM。