Chary Sowmya, Amrein Karin, Mahmoud Sherif H, Lasky-Su Jessica A, Christopher Kenneth B
Biogen, Inc., Cambridge, MA 02142, USA.
Division of Endocrinology and Diabetology, Medical University of Graz, 8036 Graz, Austria.
Metabolites. 2022 Feb 25;12(3):207. doi: 10.3390/metabo12030207.
Pharmacological interventions are essential for the treatment and management of critical illness. Although women comprise a large proportion of the critically ill, sex-specific pharmacological properties are poorly described in critical care. The sex-specific effects of vitamin D treatment in the critically ill are not known. Therefore, we performed a metabolomics cohort study with 1215 plasma samples from 428 patients from the VITdAL-ICU trial to study sex-specific differences in the metabolic response to critical illness following high-dose oral vitamin D intervention. In women, despite the dose of vitamin D being higher, pharmacokinetics demonstrated a lower extent of vitamin D absorption compared to men. Metabolic response to high-dose oral vitamin D is sex-specific. Sex-stratified individual metabolite associations with elevations in 25(OH)D following intervention showed female-specific positive associations in long-chain acylcarnitines and male-specific positive associations in free fatty acids. In subjects who responded to vitamin D intervention, significant negative associations were observed in short-chain acylcarnitines and branched chain amino acid metabolites in women as compared to men. Acylcarnitines and branched chain amino acids are reflective of fatty acid B oxidation, and bioenergesis may represent notable metabolic signatures of the sex-specific response to vitamin D. Demonstrating sex-specific pharmacometabolomics differences following intervention is an important movement towards the understanding of personalized medicine.
药物干预对于危重病的治疗和管理至关重要。尽管女性在危重病患者中占很大比例,但在重症监护中,针对性别的药理学特性却鲜有描述。维生素D治疗对危重病患者的性别特异性影响尚不清楚。因此,我们进行了一项代谢组学队列研究,使用了来自VITdAL-ICU试验的428例患者的1215份血浆样本,以研究高剂量口服维生素D干预后危重病代谢反应中的性别差异。在女性中,尽管维生素D剂量较高,但与男性相比,药代动力学显示维生素D的吸收程度较低。高剂量口服维生素D的代谢反应具有性别特异性。干预后按性别分层的个体代谢物与25(OH)D升高的关联显示,长链酰基肉碱中存在女性特异性正相关,游离脂肪酸中存在男性特异性正相关。在对维生素D干预有反应的受试者中,与男性相比,女性的短链酰基肉碱和支链氨基酸代谢物中观察到显著的负相关。酰基肉碱和支链氨基酸反映了脂肪酸β氧化,生物能量学可能代表了对维生素D性别特异性反应的显著代谢特征。证明干预后性别特异性药物代谢组学差异是迈向理解个性化医学的重要一步。