Mental Health Center, West China University Hospital, Sichuan University, Chengdu 610041, People's Republic of China; Psychosomatic department, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, People's Republic of China.
Psychosomatic department, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu 610072, People's Republic of China.
J Affect Disord. 2019 Jun 1;252:32-38. doi: 10.1016/j.jad.2019.03.080. Epub 2019 Mar 26.
MiRNAs are considered to be significant contributors to the pathogenesis of psychiatric diseases, but little is known about the potential roles of miRNAs in the treatment effect of panic disorder (PD). Therefore, we aimed to identify the miRNAs association with PD over the course of sertraline treatment.
Sixty-seven patients were collected for a 6-week period of sertraline treatment, and evaluated using HAMD-17, HAMA-14 and PDSS both at the baseline and 6 weeks later. Blood samples were collected before and after treatment, respectively. Ten pairs of samples were analyzed using miRNA array, and the differentially expressed miRNAs were further validated using RT-PCR in the whole sample.
miR-451a, miR-144-5p, miR-25-3p and miR-660-5p were found to be significantly up-regulated, while miR-1 and miR-148-5p significantly down-regulated after sertraline treatment. The change of miR-25-3p before and after treatment (△miR-25-3p) was positively related to both the changes of PDSS3 scores (△PDSS3) (p = 0.017, 31.5% contribution) and △ PDSS7 (p = 0.016, 32.3% contribution). The △miR-660-5p was positively related to both the △HAMA5 (p = 0.03, 26% contribution) and △PDSS7 (p = 0.032). The △miR-148-5p was positively related to the △PDSS4 (p = 0.046, 21.5% contribution), but negatively related to the △HAMA13 (p = 0.005, 41.9% contribution). The △miR-144-5p was negatively related to the △HAMA9 (p = 0.032, 25.3% contribution).
These findings might provide some evidences to the involvement of miRNA in the effect of anti-anxiety agents, which contributed to the better understanding the disease and developing new therapeutic genetic targets.
miRNAs 被认为是精神疾病发病机制的重要贡献者,但对于 miRNAs 在惊恐障碍(PD)治疗效果中的潜在作用知之甚少。因此,我们旨在确定与帕罗西汀治疗过程中 PD 相关的 miRNAs。
共收集 67 例患者进行为期 6 周的帕罗西汀治疗,分别在基线和 6 周后采用 HAMD-17、HAMA-14 和 PDSS 进行评估。分别在治疗前后采集血样。用 miRNA 芯片分析 10 对样本,用 RT-PCR 进一步验证全样本中的差异表达 miRNAs。
发现 miR-451a、miR-144-5p、miR-25-3p 和 miR-660-5p 明显上调,而 miR-1 和 miR-148-5p 明显下调。治疗前后 miR-25-3p 的变化(△miR-25-3p)与 PDSS3 评分的变化(△PDSS3)呈正相关(p=0.017,贡献度 31.5%)和△PDSS7(p=0.016,贡献度 32.3%)。△miR-660-5p 与△HAMA5(p=0.03,贡献度 26%)和△PDSS7(p=0.032)呈正相关。△miR-148-5p 与△PDSS4 呈正相关(p=0.046,贡献度 21.5%),但与△HAMA13 呈负相关(p=0.005,贡献度 41.9%)。△miR-144-5p 与△HAMA9 呈负相关(p=0.032,贡献度 25.3%)。
这些发现可能为 miRNA 参与抗焦虑药物的作用提供了一些证据,有助于更好地了解疾病并开发新的治疗遗传靶点。