Suzuki Takeshi, Mihara Kazuo, Nagai Goyo, Kagawa Shoko, Nakamura Akifumi, Nemoto Kenji, Kondo Tsuyoshi
Departments of Hospital Pharmacy and.
Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan.
Ther Drug Monit. 2019 Feb;41(1):86-90. doi: 10.1097/FTD.0000000000000577.
In a previous study, the authors had shown that in treatment-resistant depressive disorder, an early therapeutic response to lamotrigine augmentation therapy is dependent on its plasma concentrations. Lamotrigine is mainly metabolized by UGT1A4 and UGT2B7, and polymorphisms of said UGTs that affect enzyme activities have been reported. This study investigated the effect of these polymorphisms on the steady-state plasma concentrations (Css) of lamotrigine in patients with treatment-resistant depressive disorder receiving lamotrigine as augmentation therapy.
The subjects were 103 depressed patients who had already shown insufficient response to at least 3 psychotropics including antidepressants, mood stabilizers, and atypical antipsychotics. The diagnoses were major depressive disorder (n = 46), bipolar II disorder (n = 44), and bipolar I disorder (n = 13). They received augmentation therapy with lamotrigine for 8 weeks. The final doses of lamotrigine were 100 mg/d for 67 subjects who were not taking valproate and 75 mg/d for 36 subjects taking valproate, respectively. Blood sampling was performed at the 8th week. Plasma concentrations of lamotrigine were measured by high-performance liquid chromatography. The genotypes of UGT1A4 142T>G, UGT2B7 -161C>T, and UGT2B7 372A>G were identified by polymerase chain reaction analyses.
There were no significant relationships between these polymorphisms and the Css of lamotrigine in the subjects regardless of valproate comedication.
This study suggests that these genetic polymorphisms do not affect the Css of lamotrigine in patients with treatment-resistant depressive disorder receiving lamotrigine as augmentation therapy.
在之前的一项研究中,作者发现,在难治性抑郁症中,拉莫三嗪增效治疗的早期治疗反应取决于其血浆浓度。拉莫三嗪主要由尿苷二磷酸葡萄糖醛酸基转移酶1A4(UGT1A4)和尿苷二磷酸葡萄糖醛酸基转移酶2B7(UGT2B7)代谢,并且已经报道了影响这些酶活性的UGT基因多态性。本研究调查了这些多态性对接受拉莫三嗪作为增效治疗的难治性抑郁症患者拉莫三嗪稳态血浆浓度(Css)的影响。
研究对象为103例抑郁症患者,这些患者对至少3种精神药物(包括抗抑郁药、心境稳定剂和非典型抗精神病药)反应不足。诊断为重度抑郁症(n = 46)、双相II型障碍(n = 44)和双相I型障碍(n = 13)。他们接受了8周的拉莫三嗪增效治疗。对于67名未服用丙戊酸盐的受试者,拉莫三嗪的最终剂量为100 mg/d,对于36名服用丙戊酸盐的受试者,拉莫三嗪的最终剂量为75 mg/d。在第8周进行采血。通过高效液相色谱法测量拉莫三嗪的血浆浓度。通过聚合酶链反应分析鉴定UGT1A4 142T>G、UGT2B7 -161C>T和UGT2B7 372A>G的基因型。
无论是否合并丙戊酸盐,这些多态性与受试者拉莫三嗪的Css之间均无显著关系。
本研究表明,这些基因多态性不影响接受拉莫三嗪作为增效治疗的难治性抑郁症患者拉莫三嗪的Css。