Department of Clinical Epidemiology, Leiden University Medical Center, Leiden 2300 RC, The Netherlands.
Population Health Sciences, German Center for Neurodegenerative Diseases (DZNE), Bonn 53175, Germany.
Hum Mol Genet. 2023 May 5;32(10):1741-1752. doi: 10.1093/hmg/ddad020.
Tandem cytosine-adenine-guanine (CAG) repeat sizes of 36 or more in the huntingtin gene (HTT) cause Huntington's disease (HD). Apart from neuropsychiatric complications, the disease is also accompanied by metabolic dysregulation and weight loss, which contribute to a progressive functional decline. Recent studies also reported an association between repeats below the pathogenic threshold (<36) for HD and body mass index (BMI), suggesting that HTT repeat sizes in the non-pathogenic range are associated with metabolic dysregulation. In this study, we hypothesized that HTT repeat sizes < 36 are associated with metabolite levels, possibly mediated through reduced BMI. We pooled data from three European cohorts (n = 10 228) with genotyped HTT CAG repeat size and metabolomic measurements. All 145 metabolites were measured on the same targeted platform in all studies. Multilevel mixed-effects analysis using the CAG repeat size in HTT identified 67 repeat size metabolite associations. Overall, the metabolomic profile associated with larger CAG repeat sizes in HTT were unfavorable-similar to those of higher risk of coronary artery disease and type 2 diabetes-and included elevated levels of amino acids, fatty acids, low-density lipoprotein (LDL)-, very low-density lipoprotein- and intermediate density lipoprotein (IDL)-related metabolites while with decreased levels of very large high-density lipoprotein (HDL)-related metabolites. Furthermore, the associations of 50 metabolites, in particular, specific very large HDL-related metabolites, were mediated by lower BMI. However, no mediation effect was found for 17 metabolites related to LDL and IDL. In conclusion, our findings indicate that large non-pathogenic CAG repeat sizes in HTT are associated with an unfavorable metabolomic profile despite their association with a lower BMI.
亨廷顿病(HD)由 huntingtin 基因(HTT)中的串联胞嘧啶-腺嘌呤-鸟嘌呤(CAG)重复大小为 36 或更大引起。除了神经精神并发症外,该疾病还伴有代谢失调和体重减轻,这导致功能逐渐下降。最近的研究还报告了 HD 致病阈值(<36)以下的重复与体重指数(BMI)之间的关联,表明非致病范围内的 HTT 重复大小与代谢失调有关。在这项研究中,我们假设 HTT 重复大小<36 与代谢物水平有关,可能通过降低 BMI 来介导。我们汇集了三个欧洲队列(n=10228)的数据,这些队列具有 HTT CAG 重复大小和代谢组学测量的基因分型。所有 145 种代谢物都在所有研究中使用相同的靶向平台进行测量。使用 HTT 中的 CAG 重复大小进行多层次混合效应分析确定了 67 个重复大小代谢物关联。总的来说,与 HTT 中较大 CAG 重复大小相关的代谢组学特征不利-类似于冠心病和 2 型糖尿病的更高风险-包括氨基酸、脂肪酸、低密度脂蛋白(LDL)-极低密度脂蛋白(VLDL)和中间密度脂蛋白(IDL)相关代谢物水平升高,而非常大高密度脂蛋白(HDL)相关代谢物水平降低。此外,50 种代谢物的关联,特别是特定的非常大 HDL 相关代谢物的关联,是由较低的 BMI 介导的。然而,对于与 LDL 和 IDL 相关的 17 种代谢物没有发现中介效应。总之,我们的研究结果表明,尽管与较低的 BMI 相关,但 HTT 中的大非致病性 CAG 重复大小与不利的代谢组学特征有关。