Department of Psychiatry, and National Clinical Research Center for Mental Disorders, The Second Xiangya Hospital, Central South University, No 139 Renmin Road, Changsha, Hunan, 410011, P. R. China.
China National Technology Institute on Mental Disorders & Hunan Key Laboratory of Psychiatry and Mental Health, Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, P. R. China.
BMC Psychiatry. 2023 Jan 17;23(1):45. doi: 10.1186/s12888-023-04533-1.
Schizophrenia (SCZ) is a severe and chronic psychiatric disorder with premature age-related physiological changes. However, numerous previous studies examined the epigenetic age acceleration in SCZ patients and yielded inconclusive results. In this study, we propose to explore the epigenetic age acceleration in drug-naive first-episode SCZ (FSCZ) patients and investigate whether epigenetic age acceleration is associated with antipsychotic treatment, psychotic symptoms, cognition, and subcortical volumes.
We assessed the epigenetic age in 38 drug-naive FSCZ patients and 38 healthy controls by using three independent clocks, including Horvath, Hannum and Levine algorithms. The epigenetic age measurements in SCZ patients were repeated after receiving 8 weeks risperidone monotherapy.
Our findings showed significantly positive correlations between epigenetic ages assessed by three clocks and chronological age in both FSCZ patients and healthy controls. Compared with healthy controls, drug-naive FSCZ patients have a significant epigenetic age deceleration in Horvath clock (p = 0.01), but not in Hannum clock (p = 0.07) and Levine clock (p = 0.43). The epigenetic ages of Hannum clock (p = 0.002) and Levine clock (p = 0.01) were significantly accelerated in SCZ patients after 8-week risperidone treatment. However, no significant associations between epigenetic age acceleration and psychotic symptoms, cognitive function, as well as subcortical volumes were observed in FSCZ patients.
These results demonstrate that distinct epigenetic clocks are sensitive to different aspects of aging process. Further investigations with comprehensive epigenetic clock analyses and large samples are required to confirm our findings.
精神分裂症(SCZ)是一种严重的慢性精神障碍,伴有过早的与年龄相关的生理变化。然而,许多先前的研究检查了精神分裂症患者的表观遗传年龄加速,结果并不一致。在这项研究中,我们提出探索未经药物治疗的首发精神分裂症(FSCZ)患者的表观遗传年龄加速,并研究表观遗传年龄加速是否与抗精神病药物治疗、精神病症状、认知和皮质下体积有关。
我们通过使用三种独立的时钟,包括 Horvath、Hannum 和 Levine 算法,评估了 38 名未经药物治疗的 FSCZ 患者和 38 名健康对照者的表观遗传年龄。在接受 8 周利培酮单药治疗后,重复测量 SCZ 患者的表观遗传年龄。
我们的研究结果表明,在 FSCZ 患者和健康对照组中,三种时钟评估的表观遗传年龄与实际年龄呈显著正相关。与健康对照组相比,未经药物治疗的 FSCZ 患者在 Horvath 时钟中表现出明显的表观遗传年龄减速(p=0.01),但在 Hannum 时钟(p=0.07)和 Levine 时钟(p=0.43)中没有明显减速。在接受 8 周利培酮治疗后,SCZ 患者的 Hannum 时钟(p=0.002)和 Levine 时钟(p=0.01)的表观遗传年龄显著加速。然而,在 FSCZ 患者中,表观遗传年龄加速与精神病症状、认知功能以及皮质下体积之间没有显著关联。
这些结果表明,不同的表观遗传时钟对衰老过程的不同方面敏感。需要进一步的综合表观遗传时钟分析和大样本研究来证实我们的发现。