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评估血清/尿液基因组和代谢组学谱以提高勃起功能障碍患者对西地那非治疗的依从性

Evaluation of Serum/Urine Genomic and Metabolomic Profiles to Improve the Adherence to Sildenafil Therapy in Patients with Erectile Dysfunction.

作者信息

Rocca Maria Santa, Vignoli Alessia, Tenori Leonardo, Ghezzi Marco, De Rocco Ponce Maurizio, Vatsellas Giannis, Thanos Dimitris, Padrini Roberto, Foresta Carlo, De Toni Luca

机构信息

Unit of Andrology and Reproduction Medicine-Department of Medicine, University of Padova, Padova, Italy.

Consorzio Interuniversitario Risonanze Magnetiche di Metallo Proteine (CIRMMP), Sesto Fiorentino, Italy.

出版信息

Front Pharmacol. 2020 Dec 10;11:602369. doi: 10.3389/fphar.2020.602369. eCollection 2020.

Abstract

Type V-phosphodiesterase-inhibitors (PDE5i) are the first choice drugs in the treatment of erectile dysfunction (ED), being effective in 60-70% of patients. However, approximately 50% of patients per year discontinue the treatment with PDE5i after reporting poor drug efficacy or major adverse drug reactions (ADR). To identify early markers of efficacy/safety for the treatment of ED with PDE5i, the basal clinical characteristics of patients, integrated with metabolomics analysis of serum and urine and genomic data, were here correlated with the PDE5i efficacy and the occurrence of ADR upon administration. Thirty-six males with new diagnosis of ED were consecutively recruited and characterized at baseline for anthropometrics, blood pressure, blood glucose, lipid profile, serum levels of thyroid/sex hormones and erectile function evaluated by IIEF-15 questionnaire. Targeted Next Generation Sequencing (NGS) was applied to genes involved in PDE5i pharmacodynamics and pharmacokinetics. Fasting metabolic profiles of serum and urine were assessed by nuclear magnetic resonance (NMR)-based metabolomics analysis. Patients were prescribed on-demand therapy with Sildenafil oro-dispersible film and followed-up after 3 months from recruitment. Baseline data were compared with IIEF-15 score at follow-up and with the occurrence of ADR recorded by a dedicated questionnaire. Twenty-eight patients were finally included in the analysis. Serum LDL-cholesterol levels were increased in those reporting ADR (143.3 ± 13.2 mg/dl ADR vs. 133.1 ± 12.4 mg/dl No ADR; = 0.046). NGS data showed that specific variants of and genes were more represented in drug responders (both relative risk = 2.7 [0.9-5.1]; = 0.04). NMR-based metabolomics showed the highest association between serum LDL-cholesterol metabolites and the occurrence of ADR (Hazard ratio = 17.5; = 0.019). The association between lipid profile and the ADR pattern suggests major cues in the tailoring of ED therapy with PDE5i.

摘要

5型磷酸二酯酶抑制剂(PDE5i)是治疗勃起功能障碍(ED)的首选药物,对60%-70%的患者有效。然而,每年约有50%的患者在报告药物疗效不佳或出现严重药物不良反应(ADR)后停止使用PDE5i治疗。为了确定PDE5i治疗ED的疗效/安全性早期标志物,本研究将患者的基础临床特征与血清和尿液的代谢组学分析以及基因组数据相结合,与PDE5i疗效及给药后ADR的发生情况进行关联分析。连续招募了36例新诊断为ED的男性患者,并在基线时对其进行人体测量学、血压、血糖、血脂谱、甲状腺/性激素血清水平以及通过IIEF-15问卷评估的勃起功能等方面的特征分析。对参与PDE5i药效学和药代动力学的基因应用靶向二代测序(NGS)技术。通过基于核磁共振(NMR)的代谢组学分析评估血清和尿液的空腹代谢谱。患者按需服用西地那非口腔崩解膜进行治疗,并在招募后3个月进行随访。将基线数据与随访时的IIEF-15评分以及通过专门问卷记录的ADR发生情况进行比较。最终28例患者纳入分析。报告有ADR的患者血清低密度脂蛋白胆固醇水平升高(ADR组为143.3±13.2mg/dl,无ADR组为133.1±12.4mg/dl;P=0.046)。NGS数据显示,药物反应者中ABCC1和ABCC2基因的特定变体更为常见(相对风险均为2.7[0.9-5.1];P=0.04)。基于NMR的代谢组学显示血清低密度脂蛋白胆固醇代谢物与ADR发生之间的关联最为显著(风险比=17.5;P=0.019)。血脂谱与ADR模式之间的关联表明,在使用PDE5i定制ED治疗方案时存在重要线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb63/7849189/73f8a0b1ed68/fphar-11-602369-g001.jpg

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