Department of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Chemistry and Center for Innovative Technology, Vanderbilt University, Nashville, TN, USA.
J Huntingtons Dis. 2024;13(1):103-111. doi: 10.3233/JHD-231511.
Huntington's disease (HD) is a neurodegenerative disorder caused by expanded cytosine-adenine-guanine (CAG) repeats in the Huntingtin gene, resulting in the production of mutant huntingtin proteins (mHTT). Previous research has identified urea as a key metabolite elevated in HD animal models and postmortem tissues of HD patients. However, the relationship between disease course and urea elevations, along with the molecular mechanisms responsible for these disturbances remain unknown.
To better understand the molecular disturbances and timing of urea cycle metabolism across different stages in HD.
We completed a global metabolomic profile of cerebrospinal fluid (CSF) from individuals who were at several stages of disease: pre-manifest (PRE), manifest (MAN), and late manifest (LATE) HD participants, and compared to controls.
Approximately 500 metabolites were significantly altered in PRE participants compared to controls, although no significant differences in CSF urea or urea metabolites were observed. CSF urea was significantly elevated in LATE participants only. There were no changes in the urea metabolites citrulline, ornithine, and arginine.
Overall, our study confirms that CSF elevations occur late in the HD course, and these changes may reflect accumulating deficits in cellular energy metabolism.
亨廷顿病(HD)是一种由亨廷顿基因中胞嘧啶-腺嘌呤-鸟嘌呤(CAG)重复扩展引起的神经退行性疾病,导致突变亨廷顿蛋白(mHTT)的产生。先前的研究已经确定尿素是在 HD 动物模型和 HD 患者死后组织中升高的关键代谢物。然而,疾病进程与尿素升高之间的关系以及导致这些紊乱的分子机制尚不清楚。
更好地了解 HD 不同阶段尿素循环代谢的分子紊乱和时间进程。
我们对处于疾病几个阶段的个体(即无症状前(PRE)、有症状(MAN)和晚期有症状(LATE)HD 参与者)的脑脊液(CSF)进行了全面代谢组学分析,并与对照组进行了比较。
与对照组相比,PRE 参与者的大约 500 种代谢物明显改变,尽管 CSF 尿素或尿素代谢物没有观察到显著差异。仅在 LATE 参与者中 CSF 尿素显著升高。尿素代谢物瓜氨酸、精氨酸和鸟氨酸没有变化。
总的来说,我们的研究证实 CSF 升高发生在 HD 病程的晚期,这些变化可能反映了细胞能量代谢的累积缺陷。