Detection of urine metabolites in patients with inherited metabolic diseases by nuclear magnetic resonance spectroscopy
10.3760/cam.j.cn114452-20210226-00125
- VernacularTitle:利用核磁共振波谱技术检测遗传代谢病患者尿液代谢产物
- Author:
Siyu CHANG
1
;
Xia ZHAN
;
Lianshu HAN
;
Huiwen ZHANG
;
Xiaolan GAO
;
Ting CHEN
;
Feng XU
;
Xuefan GU
Author Information
1. 上海交通大学医学院附属新华医院 上海市儿科医学研究所小儿内分泌遗传代谢科，上海 200092
- Keywords:
Inherited metabolic disease;
Nuclear magnetic resonance spectroscopy;
Gas chromatography mass spectrometry;
Organic acids;
Methylmalonic acid
- From:
Chinese Journal of Laboratory Medicine
2021;44(10):931-936
- CountryChina
- Language:Chinese
-
Abstract:
Objective:Nuclear magnetic resonance spectroscopy (NMR) was used to detect the species and content of metabolites in urine of patients with inherited metabolic diseases, and to explore the application value of NMR technology in the diagnosis of inherited metabolic diseases.Methods:Urine samples were collected from 20 patients with inherited metabolic diseases diagnosed in Xinhua Hospital, Shanghai Jiaotong University School of Medicine from March to June 2019, including 9 cases of methylmalonic acidemia (MMA). NMR pulse length-based concentration determination and Gas chromatography mass spectrometry (GC/MS) semi-quantitative method were used to detect the composition of metabolites in urine samples of patients with inherited metabolic diseases, and the levels of abnormal metabolites in the two methods were analyzed.Results:NMR technology can detect the levels of characteristic metabolites significantly increased in the urine of patients with MMA, isovalerinemia, glutaric acidemia, propionic acidemia, 3-methylcrotonyl-CoA carboxylase deficiency, ornithine carbamyltransferase deficiency, Citrin deficiency, Canavan disease, tyrosinemia and lysinuria protein intolerance. The average is 8 times of the upper limit of the reference value, and the highest is 545 times. Compared to GC/MS, NMR technology can detect the levels of various metabolites such as organic acids, amino acids and sugars. In 9 cases of untreated MMA,the median levels of methylmalonic acid and 3-hydroxypropionic acid in NMR [1 800 (180-12 000) and 50 (0-270) mmol/mol Cr] were higher than the reference values (0-31, 0-35). The median levels of methylmalonic acid and methylmalonic acid in GC/MS [136.56 (43.79-518.67) and 4.87 (1.52-7.52)] were higher than the reference values (0-4 and 0-0.7).Conclusions:NMR and GC/MS technologies are specific for the diagnosis of organic acidemia. The primary component detected by GC/MS is organic acid. NMR technology can break through this limitation and measure the level of various metabolites in urine, which provides a more theoretical basis for the diagnosis and research of inherited metabolic disease.
