A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia. Issue 3 (26th November 2019)

• Record Type: Journal Article
• Authors: Kang, Lulu; Liu, Yupeng; Shen, Ming; Liu, Yi; He, Ruxuan; Song, Jinqing; Jin, Ying; Li, Mengqiu; Zhang, Yao; Dong, Hui; Liu, Xueqin; Yan, Hui; Qin, Jiong; Zheng, Hong; Chen, Yongxing; Li, Dongxiao; Wei, Haiyan; Zhang, Huifeng; Sun, Liying; Zhu, Zhijun; Liang, Desheng; Yang, Yanling
• Is Part Of: Journal of inherited metabolic disease. Volume 43:Issue 3(2020)
• Page Start: 409
• Page End: 423
• Publication Date: 2019-11-26
• Subjects: adenosylcobalamin (AdoCbl) -- methylmalonic acid -- methylmalonic acidemia (MMA) -- methylmalonyl‐CoA mutase -- MMUT -- propionylcarnitine; Metabolism, Inborn errors of -- Periodicals; Metabolism -- Disorders -- Periodicals; 616.39042
• DOI: 10.1002/jimd.12183
• Languages: English
• ISSNs: 0141-8955

Abstract

Abstract: Methylmalonic acidemia (MMA) is the most common organic acidemia in China. This study aimed to characterise the genotypic and phenotypic variabilities, and the molecular epidemiology of Chinese patients with isolated MMA. Patients (n = 301) with isolated MMA were diagnosed by clinical examination, biochemical assays, and genetic analysis. Fifty‐eight patients (19.3%) were detected by newborn screening and 243 patients (80.7%) were clinically diagnosed after onset. Clinical onset ranged from the age of 3 days to 23 years (mean age = 1.01 ± 0.15 years). Among 234 MMA patients whose detailed clinical data were available, 170 (72.6%) had early onset disease (before the age of 1 year), and 64 (27.4%) had late‐onset disease. The 234 MMA patients manifested with neuropsychiatric impairment (65.4%), haematological abnormality (31.6%), renal damage (8.5%), and metabolic crises (67.1%). Haematological abnormality was significantly more common in early‐onset patients than that in late‐onset patients. The incidence of metabolic crises was significantly high ( P < 0.001) in patients with mut type than those with other types of isolated MMA. Variations (n = 122) were identified in MMUT, MMAA, MMAB, MMADHC, SUCLG1, and SUCLA2, of which 45 were novel. c.729_730insTT was the most frequent MMUT mutation, with a significantly higher frequency in our patients than that in 151 reported European patients. The frequency of c.914T>C in MMUT in our cohort was also higher than that in 151 European patients. MMUT mutations c.729_730insTT and c.914T>C are specific for the Chinese population. Our study expanded the spectrum of phenotypes and genotypes in isolated MMA.