Therapeutic Drug Monitoring of Venlafaxine and Impact of Age, Gender, BMI, and Diagnosis

M. Krivosova, M. Kertys, M. Grendár, I. Ondrejka, I. Hrtanek, I. Tonhajzerova, N. Sekaninova, J. Mokrý
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Abstract

Abstract Depression is a common mental disorder affecting more than 264 million people in the world and 5.1% of the Slovak population. Although various antidepressant approaches have been used; still, about 40% of patients do not respond to a first-choice drug administration and one third of patients do not achieve total remission. Therapeutic drug monitoring (TDM) is a method used for quantification and interpreting the drug concentrations in plasma in order to optimize the pharmacotherapy. The aim of this study was to measure the plasma concentrations of venlafaxine, the fourth most prescribed antidepressant in Slovakia, as well as its active metabolite and interpret them with the relevant patients’ characteristics. The study was of retrospective nature and 28 adult patients in total were included. The concentrations of venlafaxine and its active metabolite O-desmethylvenlafaxine (ODV) in plasma were quantified using the validated UHPLC-MS/MS method. The effects of potential influencing factors were evaluated by a multivariate linear regression model. Only 39% of patients reached the venlafaxine active moiety concentrations within the recommended therapeutic range. Plasma concentrations were dependent on age, gender, and duration of the therapy. Venlafaxine metabolism expressed as a metaboliteto-parent concentrations ratio was influenced by a combination of age, gender, and body mass index (BMI). We did not observe any significant difference in plasma concentrations between the patients with a single and recurrent diagnosis of depression. Combining variables made an additive effect on plasma concentrations, for example, active moiety plasma concentrations were higher in older women. In contrast, drug metabolism was higher in older men and men with lower BMI. TDM of venlafaxine is recommended in clinical practice, especially in the elderly when beginning the pharmacotherapy.
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文拉法辛治疗药物监测及其对年龄、性别、BMI和诊断的影响
摘要抑郁症是一种常见的精神障碍,影响着全世界2.64亿人,占斯洛伐克人口的5.1%。尽管已经使用了各种抗抑郁的方法;尽管如此,约40%的患者对首选药物给药没有反应,三分之一的患者没有完全缓解。治疗药物监测(TDM)是一种用于量化和解释血浆中药物浓度以优化药物治疗的方法。本研究的目的是测量斯洛伐克第四大处方抗抑郁药文拉法辛的血浆浓度及其活性代谢产物,并根据相关患者的特征进行解释。该研究具有回顾性,共纳入28名成年患者。使用经验证的UHPLC-MS/MS方法定量血浆中文拉法辛及其活性代谢产物O-去甲基文拉法辛(ODV)的浓度。通过多元线性回归模型评估潜在影响因素的影响。只有39%的患者达到推荐治疗范围内的文拉法辛活性部分浓度。血浆浓度取决于年龄、性别和治疗持续时间。文拉法辛代谢以代谢产物与母体浓度之比表示,受年龄、性别和体重指数(BMI)组合的影响。我们没有观察到单一和反复诊断为抑郁症的患者之间的血浆浓度有任何显著差异。组合变量对血浆浓度产生相加效应,例如,老年女性的活性部分血浆浓度更高。相比之下,老年男性和BMI较低的男性的药物代谢较高。文拉法辛的TDM在临床实践中是推荐的,尤其是在老年人开始药物治疗时。
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来源期刊
European Pharmaceutical Journal
European Pharmaceutical Journal Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
0.60
自引率
0.00%
发文量
16
期刊介绍: European Pharmaceutical Journal publishes only original articles not previously published and articles that are not being considered or have not been submitted for publication elsewhere. If parts of the results have been published as conference abstract or elsewhere, it should be stated in references. The ethical standards of the Helsinki-Tokio Declaration should be kept. This should be mentioned in the Methods of manuscript. Reviews are published only on request. Authors, whose submitted research work was performed with the support of a company, should indicate this in Conflict of Interest.
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