Rwatambuga F A, Ali E R, Bramble M S, Gosschalk J E, Kim Morris, Yandju D L, Okitundu L A, Boivin M J, Banea J P, Westaway S K, Larry D, Vilain Eric, Mumba Ngoyi D, Tshala-Katumbay D D
Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, OR, USA.
Department of Biology, University of Kinshasa, Congo.
Food Chem Toxicol. 2021 Feb;148:111917. doi: 10.1016/j.fct.2020.111917. Epub 2020 Dec 6.
A case-control design determined whether konzo, an upper motoneuron disease linked to food (cassava) toxicity was associated with protein carbamoylation and genetic variations. Exon sequences of thiosulfate sulfurtransferase (TST) or mercaptopyruvate sulfurtransferase (MPST), plasma cyanide detoxification rates, and 2D-LC-MS/MS albumin carbamoylation were assessed in 40 children [21 konzo-affected and 19 putatively healthy controls, mean (SD) age: 9.2 (3.0) years] subjected to cognition and motor testing using the Kaufman Assessment Battery and the Bruininks/Oseretsky Test, respectively. Konzo was significantly associated with higher levels of carbamoylated peptides 206-219 (LDELRDEGKASSAK, pep1) after adjusting for age, gender, albumin concentrations and BUN [regression coefficient: 0.03 (95%CI:0.02-0.05), p = 0.01]. Levels of pep1 negatively correlated with performance scores at all modalities of motor proficiency (r = 0.38 to 0.61; all p < 0.01) or sequential processing (memory)(r = - 0.59, p = 0.00) and overall cognitive performance (r = - 0.48, p = 0.00) but positively with time needed for cyanide detoxification in plasma (r = 0.33, p = 0.04). Rare potentially damaging TST p.Arg206Cys (rs61742280) and MPST p.His317Tyr (rs1038542246) heterozygous variants were identified but with no impact on subject phenotypes. Protein carbamoylation appears to be a reliable marker for cassava related neurodegeneration.
一项病例对照研究确定了与食物(木薯)毒性相关的上运动神经元疾病——痉挛性截瘫是否与蛋白质氨甲酰化及基因变异有关。对40名儿童[21名患痉挛性截瘫儿童和19名假定健康的对照儿童,平均(标准差)年龄:9.2(3.0)岁]的硫代硫酸盐硫转移酶(TST)或巯基丙酮酸硫转移酶(MPST)外显子序列、血浆氰化物解毒率以及二维液相色谱-串联质谱法测定的白蛋白氨甲酰化情况进行了评估,这些儿童分别使用考夫曼儿童能力成套测验和布吕尼inks/奥塞列茨基运动技能测验进行认知和运动测试。在对年龄、性别、白蛋白浓度和血尿素氮进行校正后,痉挛性截瘫与氨甲酰化肽206 - 219(LDELRDEGKASSAK,pep1)水平升高显著相关[回归系数:0.03(95%置信区间:0.02 - 0.05),p = 0.01]。pep1水平与所有运动熟练度模式(r = 0.38至0.61;所有p < 0.01)或顺序加工(记忆)(r = - 0.59,p = 0.00)以及总体认知表现(r = - 0.48,p = 0.00)的表现得分呈负相关,但与血浆中氰化物解毒所需时间呈正相关(r = 0.33,p = 0.04)。鉴定出了罕见的可能具有损害性的TST p.Arg206Cys(rs61742280)和MPST p.His317Tyr(rs1038542246)杂合变异,但对受试者表型无影响。蛋白质氨甲酰化似乎是木薯相关神经变性的可靠标志物。