Champigny Camille, Morin-Parent Florence, Bellehumeur-Lefebvre Laurence, Çaku Artuela, Lepage Jean-François, Corbin François
Department of Biochemistry and Functional Genomics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
Centre de Recherche du CHUS (CRCHUS), Sherbrooke, QC, Canada.
Front Psychiatry. 2022 Jan 4;12:762967. doi: 10.3389/fpsyt.2021.762967. eCollection 2021.
Limited success of previous clinical trials for Fragile X syndrome (FXS) has led researchers to consider combining different drugs to correct the pleiotropic consequences caused by the absence of the Fragile X mental retardation protein (FMRP). Here, we report the results of the LovaMiX clinical trial, the first trial for FXS combining two disease-modifying drugs, lovastatin, and minocycline, which have both shown positive effects when used independently. The main goals of the study were to assess the safety and efficacy of a treatment combining lovastatin and minocycline for patients with FXS. Pilot Phase II open-label clinical trial. Patients with a molecular diagnostic of FXS were first randomized to receive, in two-step titration either lovastatin or minocycline for 8 weeks, followed by dual treatment with lovastatin 40 mg and minocycline 100 mg for 2 weeks. Clinical assessments were performed at the beginning, after 8 weeks of monotherapy, and at week 20 (12 weeks of combined therapy). The primary outcome measure was the Aberrant Behavior Checklist-Community (ABC-C) global score. Secondary outcome measures included subscales of the FXS specific ABC-C (ABC-C), the Anxiety, Depression, and Mood Scale (ADAMS), the Social Responsiveness Scale (SRS), the Behavior Rating Inventory of Executive Functions (BRIEF), and the Vineland Adaptive Behavior Scale second edition (VABS-II). Twenty-one individuals out of 22 completed the trial. There were no serious adverse events related to the use of either drugs alone or in combination, suggesting good tolerability and safety profile of the combined therapy. Significant improvement was noted on the primary outcome measure with a 40% decrease on ABC-C global score with the combined therapy. Several outcome measures also showed significance. The combination of lovastatin and minocycline is safe in patients for FXS individuals and appears to improve several elements of the behavior. These results set the stage for a larger, placebo-controlled double-blind clinical trial to confirm the beneficial effects of the combined therapy.
以往针对脆性X综合征(FXS)的临床试验成效有限,这促使研究人员考虑联合使用不同药物,以纠正因脆性X智力低下蛋白(FMRP)缺失所导致的多效性后果。在此,我们报告LovaMiX临床试验的结果,这是首个针对FXS联合使用两种疾病修饰药物——洛伐他汀和米诺环素的试验,这两种药物单独使用时均已显示出积极效果。该研究的主要目的是评估洛伐他汀和米诺环素联合治疗对FXS患者的安全性和有效性。II期开放性试点临床试验。经分子诊断为FXS的患者首先被随机分为两组,采用两步滴定法,一组接受洛伐他汀治疗8周,另一组接受米诺环素治疗8周,随后两组均接受40毫克洛伐他汀和100毫克米诺环素的联合治疗2周。在试验开始时、单药治疗8周后以及第20周(联合治疗12周后)进行临床评估。主要疗效指标是异常行为检查表-社区版(ABC-C)的总体评分。次要疗效指标包括FXS特异性ABC-C(ABC-C)的各个子量表、焦虑、抑郁和情绪量表(ADAMS)、社会反应量表(SRS)、执行功能行为评定量表(BRIEF)以及文兰适应行为量表第二版(VABS-II)。22名患者中有21名完成了试验。未出现与单独使用或联合使用这两种药物相关的严重不良事件,表明联合治疗具有良好的耐受性和安全性。联合治疗使主要疗效指标有显著改善,ABC-C总体评分降低了40%。几个疗效指标也显示出显著变化。洛伐他汀和米诺环素联合使用对FXS患者是安全的,并且似乎改善了行为的多个方面。这些结果为开展更大规模的、安慰剂对照双盲临床试验奠定了基础,以证实联合治疗的有益效果。