From the Departments of Psychiatry and Psychology.
Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
J Clin Psychopharmacol. 2023;43(5):428-433. doi: 10.1097/JCP.0000000000001747.
The purpose of this study was to review the association between the SLC6A4 5-HTTLPR polymorphism and antidepressant (AD)-associated treatment emergent mania (TEM) in bipolar disorder alongside starting a discussion on the merits of developing risk stratification models to guide when not to provide AD treatment for bipolar depression.
Studies that examined the association between clinical and genetic risk factors, specifically monoaminergic transporter genetic variation, and TEM were identified. A meta-analysis was performed using the odds ratio to estimate the effect size under the Der-Simonian and Laird model.
Seven studies, referencing the SLC6A4 5-HTTLPR polymorphism and TEM (total N = 1578; TEM+ =594, TEM- = 984), of 142 identified articles were included. The time duration between the start of the AD to emergence of TEM ranged from 4 to 12 weeks. There was a nominally significant association between the s allele of the 5-HTTLPR polymorphism and TEM (odds ratio, 1.434; 95% confidence interval, 1.001-2.055; P = 0.0493; I2 = 52%). No studies have investigated norepinephrine or dopamine transporters.
Although the serotonin transporter genetic variation is commercially available in pharmacogenomic decision support tools, greater efforts, more broadly, should focus on complete genome-wide approaches to determine genetic variants that may contribute to TEM. Moreover, these data are exemplary to the merits of developing risk stratification models, which include both clinical and biological risk factors, to guide when not to use ADs in bipolar disorder. Future studies will need to validate new risk models that best inform the development of personalized medicine best practices treating bipolar depression.
本研究旨在回顾 5-羟色胺转运体基因(SLC6A4)5-HTTLPR 多态性与双相障碍患者抗抑郁药(AD)相关治疗性转躁(TEM)之间的关系,并探讨开发风险分层模型的意义,以指导何时不对双相障碍抑郁患者使用 AD 治疗。
本研究检索了与临床和遗传风险因素(特别是单胺能转运体遗传变异)与 TEM 相关的研究。采用比值比(OR)进行 Meta 分析,以估计在 Der-Simonian 和 Laird 模型下的效应量。
共纳入了 142 篇文章中 7 项研究,涉及 SLC6A4 5-HTTLPR 多态性与 TEM(总 N=1578;TEM+=594,TEM-=984)。AD 起始至 TEM 出现的时间间隔为 4-12 周。5-HTTLPR 多态性的 s 等位基因与 TEM 之间存在显著关联(OR,1.434;95%置信区间,1.001-2.055;P=0.0493;I2=52%)。尚无研究探讨去甲肾上腺素或多巴胺转运体。
尽管血清素转运体的遗传变异在药物基因组学决策支持工具中具有商业可用性,但应更广泛地努力全面开展全基因组研究,以确定可能导致 TEM 的遗传变异。此外,这些数据为开发风险分层模型提供了有力支持,该模型包括临床和生物学风险因素,以指导何时不对双相障碍患者使用 AD 治疗。未来的研究需要验证新的风险模型,以最佳地为制定治疗双相障碍抑郁的个性化医学最佳实践提供信息。