Hou Yuyang, Wang Jingjie, Pan Mengyue, Zhou Yanfen, Wang Yupeng, Chen Jiaxi, Zhong Mengling, Li Xin, Zhang Qi
College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing, 211816, The People's Republic of China.
School of Pharmaceutical Sciences, Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing, 211816, The People's Republic of China.
J Assist Reprod Genet. 2024 Nov;41(11):3161-3171. doi: 10.1007/s10815-024-03294-4. Epub 2024 Oct 21.
Obese men have a significantly increased risk of developing asthenozoospermia. Sperm motility is directly related to cellular energy supply and metabolic status. Sperm metabolomics research based on Gas chromatography-mass spectrometry (GC-MS) technology can provide useful information for the pathological mechanism, diagnosis, and treatment of obesity-associated asthenozoospermia.
Sperm samples were obtained from a healthy control group (n = 49) and patients with obesity-associated asthenozoospermia (n = 40). After the analysis of sperm samples using GC-MS, various multivariate statistical methods such as principal component analysis (PCA), partial least squares-discriminant analysis (PLS-DA), and orthogonal partial least squares-discriminant analysis (OPLS-DA) were conducted.
A total of 56 metabolites were identified in the sperm samples. Among them, 19 differential metabolites were found between the two groups. Metabolites such as glutamic acid, fumaric acid, and cysteine were significantly downregulated in the sperm of patients with obesity-associated asthenozoospermia, while metabolites like palmitic acid, stearic acid, and alanine were significantly upregulated. The differential metabolites were enriched in D-glutamine and D-glutamate metabolism; proline, aspartate, and glutamate metabolism; glutathione metabolism and the other metabolic pathways.
Obesity may influence the composition of metabolic products in sperm, and metabolomic analysis proves beneficial for the future diagnosis and treatment of obesity-associated asthenozoospermia.
肥胖男性患弱精子症的风险显著增加。精子活力与细胞能量供应和代谢状态直接相关。基于气相色谱 - 质谱(GC-MS)技术的精子代谢组学研究可为肥胖相关性弱精子症的病理机制、诊断和治疗提供有用信息。
从健康对照组(n = 49)和肥胖相关性弱精子症患者(n = 40)中获取精子样本。使用GC-MS对精子样本进行分析后,进行了主成分分析(PCA)、偏最小二乘判别分析(PLS-DA)和正交偏最小二乘判别分析(OPLS-DA)等多种多元统计方法。
在精子样本中总共鉴定出56种代谢物。其中,两组之间发现了19种差异代谢物。肥胖相关性弱精子症患者精子中的谷氨酸、富马酸和半胱氨酸等代谢物显著下调,而棕榈酸、硬脂酸和丙氨酸等代谢物显著上调。差异代谢物在D-谷氨酰胺和D-谷氨酸代谢;脯氨酸、天冬氨酸和谷氨酸代谢;谷胱甘肽代谢及其他代谢途径中富集。
肥胖可能影响精子中代谢产物的组成,代谢组学分析对未来肥胖相关性弱精子症的诊断和治疗有益。