Ageu Luminiţa Ştefania, Levai Codrina Mihaela, Andreescu Nicoleta Ioana, Grigoraş Mirela Loredana, Hogea Lavinia Maria, Chiriac Daniela Veronica, Folescu Roxana, Bredicean Ana Cristina, Nussbaum Liliana Maria, Enătescu Virgil Radu, Poroch Vladimir, Lupu Viorel, Puiu Maria, Nussbaum Laura Alexandra
Discipline of Anatomy and Embryology, "Victor Babes" University of Medicine and Pharmacy, Timisoara, Romania;
Rom J Morphol Embryol. 2018;59(1):165-173.
Antidepressant medication influences cellular lipogenesis, being associated with metabolic side effects including weight gain. Due to the increasing use of antidepressants in children and adolescents, their metabolic and endocrine adverse effects are of particular concern, especially within this pediatric population that appears to be at greater risk. Genetic factors with a possible influence on antidepressant's adverse effects include CYP [cytochrome P450 (CYP450)] polymorphisms. We target to evaluate the efficacy of the pharmacogenetic testing, when prescribing antidepressants, in correlation with the occurrence of adverse events and weight gain. Our research was performed between the years 2010 and 2016, in the University Clinic of Child and Adolescent Psychiatry, Timisoara, Romania. We recruited 80 patients, children and adolescents with depressive disorders. Our study sample was divided in two groups: G1 - 40 patients took treatment after pharmacogenetic testing, and G2 - 40 patients without pharmacogenetic testing before the treatment election. Our results show statistically significant differences concerning the weight gain for groups G1 (with pharmacogenetic testing) and G2 (without pharmacogenetic testing). The CYP genotype and the pharmacogenetic testing, for choosing the personalized antidepressant therapy in children and adolescents with depressive disorders, proved to be good predictors for the response to antidepressants and the side effects registered, especially for weight gain. The significant correlations between the CYP polymorphisms for group G2 (without pharmacogenetic testing) and the weight gain/body mass index (BMI) increase, as major side effects induced by antidepressants, proved the fact that the pharmacogenetic screening is needed in the future clinical practice, allowing for individualized, tailored treatment, especially for at-risk pediatric categories.
抗抑郁药物会影响细胞脂肪生成,与包括体重增加在内的代谢副作用相关。由于儿童和青少年中抗抑郁药物的使用日益增加,其代谢和内分泌不良反应备受关注,尤其是在这个似乎风险更高的儿科人群中。可能对抗抑郁药物不良反应有影响的遗传因素包括细胞色素P450(CYP450)基因多态性。我们旨在评估在开具抗抑郁药物时进行药物遗传学检测与不良事件发生及体重增加之间的相关性及疗效。我们的研究于2010年至2016年在罗马尼亚蒂米什瓦拉的儿童和青少年精神病学大学诊所进行。我们招募了80名患有抑郁症的儿童和青少年患者。我们的研究样本分为两组:G1组 - 40名患者在进行药物遗传学检测后接受治疗,G2组 - 40名患者在选择治疗前未进行药物遗传学检测。我们的结果显示,G1组(进行药物遗传学检测)和G2组(未进行药物遗传学检测)在体重增加方面存在统计学上的显著差异。对于患有抑郁症的儿童和青少年,CYP基因型和药物遗传学检测被证明是抗抑郁药物反应及所记录副作用(尤其是体重增加)的良好预测指标。G2组(未进行药物遗传学检测)的CYP基因多态性与体重增加/体重指数(BMI)升高之间的显著相关性,作为抗抑郁药物引起的主要副作用,证明了在未来临床实践中需要进行药物遗传学筛查,以实现个体化、量身定制的治疗,特别是对于有风险的儿科类别。