Goïta Yaya, Chao de la Barca Juan Manuel, Keïta Asmaou, Diarra Mamadou Bocary, Dembélé Klétigui Casimir, Chabrun Floris, Dramé Boubacar Sidiki Ibrahim, Kassogué Yaya, Diakité Mahamadou, Mirebeau-Prunier Delphine, Cissé Bakary Mamadou, Simard Gilles, Reynier Pascal
Faculté de Pharmacie, Université des Sciences, des Techniques et des Technologies, de Bamako, Mali.
Service de Cardiologie, Centre Hospitalier Universitaire Mère-Enfant (CHUME) et Laboratoire d'analyses de Biologie médicale et Anatomo-Pathologique, Centre Hospitalier Universitaire Hôpital du Mali, Bamako, Mali.
Sci Rep. 2020 May 5;10(1):7517. doi: 10.1038/s41598-020-64329-1.
Metabolomic studies have demonstrated the existence of biological signatures in blood of patients with arterial hypertension, but no study has hitherto reported the sexual dimorphism of these signatures. We compared the plasma metabolomic profiles of 28 individuals (13 women and 15 men) with essential arterial hypertension with those of a healthy control group (18 women and 18 men), using targeted metabolomics. Among the 188 metabolites explored, 152 were accurately measured. Supervised OPLS-DA (orthogonal partial least squares-discriminant analysis) showed good predictive performance for hypertension in both sexes (Qcum = 0.59 in women and 0.60 in men) with low risk of overfitting (p-value-CV ANOVA = 0.004 in women and men). Seventy-five and 65 discriminant metabolites with a VIP (variable importance for the projection) greater than 1 were evidenced in women and men, respectively. Both sexes showed a considerable increase in phosphatidylcholines, a decrease in C16:0 with an increase in C28:1 lysophosphatidylcholines, an increase in sphingomyelins, as well as an increase of symmetric dimethylarginine (SDMA), acetyl-ornithine and hydroxyproline. Twenty-nine metabolites, involved in phospholipidic and cardiac remodeling, arginine/nitric oxide pathway and antihypertensive and insulin resistance mechanisms, discriminated the metabolic sexual dimorphism of hypertension. Our results highlight the importance of sexual dimorphism in arterial hypertension.
代谢组学研究已经证明了动脉高血压患者血液中存在生物学特征,但迄今为止尚无研究报道这些特征的性别差异。我们采用靶向代谢组学方法,比较了28例原发性动脉高血压患者(13名女性和15名男性)与健康对照组(18名女性和18名男性)的血浆代谢组学谱。在所检测的188种代谢物中,152种得到了准确测定。有监督的OPLS-DA(正交偏最小二乘判别分析)显示,该方法对男女高血压均具有良好的预测性能(女性Qcum = 0.59,男性Qcum = 0.60),且过拟合风险较低(女性和男性的p值-CV ANOVA均 = 0.004)。在女性和男性中,分别有75种和65种投影变量重要性(VIP)大于1的判别性代谢物被鉴定出来。男女两性均显示出磷脂酰胆碱显著增加、C16:0减少伴随C28:1溶血磷脂酰胆碱增加、鞘磷脂增加,以及对称二甲基精氨酸(SDMA)、乙酰鸟氨酸和羟脯氨酸增加。29种参与磷脂和心脏重塑、精氨酸/一氧化氮途径以及抗高血压和胰岛素抵抗机制的代谢物,区分了高血压的代谢性别差异。我们的结果突出了性别差异在动脉高血压中的重要性。