Translational Psychiatry Program, Louis A. Faillace, MD, Faillace Department of Psychiatry & Behavioral Sciences, The University of Texas Health Science Center at Houston, 1941 East Rd, 77054 Houston, TX, USA; Center for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at Houston. 7000 Fannin St, 77030 Houston, TX, USA; Neuroscience Graduate Program, The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA.
Translational Psychiatry Program, Louis A. Faillace, MD, Faillace Department of Psychiatry & Behavioral Sciences, The University of Texas Health Science Center at Houston, 1941 East Rd, 77054 Houston, TX, USA.
Neurosci Biobehav Rev. 2020 May;112:107-116. doi: 10.1016/j.neubiorev.2020.01.035. Epub 2020 Feb 1.
Bipolar disorder (BD) has been associated with clinical signs of accelerated aging, which potentially underlies its association with several age-related medical conditions, such as hypertension, metabolic imbalances, dementia, and cancer. This paper aims to comprehensively review evidence of biological aging in BD and explore findings and controversies related to common biological clocks in patients, including telomere length, DNA methylation, mitochondrial DNA copy number, inflammation, and oxidative stress. Our results suggest a complex interplay between biological markers and a potential key role of environmental factors, such as childhood trauma and psychological stress, in determining premature aging in patients. Moreover, given its multifactorial nature, our summary evidences the need for further studies incorporating clinical evidence with biomarkers of accelerated aging in BD. Results of this review strongly suggest BD as an accelerated aging disease seen in both clinical and molecular aspects. Understanding the pathophysiology of aging in BD may ultimately lead to identification of pathways that can be targeted for prevention of premature aging in patients and early onset of aging-related conditions.
双相情感障碍(BD)与临床加速衰老的迹象有关,这可能是其与多种与年龄相关的疾病(如高血压、代谢失衡、痴呆和癌症)相关的基础。本文旨在全面综述 BD 中的生物学衰老证据,并探讨与患者常见生物钟相关的发现和争议,包括端粒长度、DNA 甲基化、线粒体 DNA 拷贝数、炎症和氧化应激。我们的研究结果表明,生物学标志物之间存在复杂的相互作用,环境因素(如儿童期创伤和心理压力)在确定患者的过早衰老方面可能起着关键作用。此外,鉴于其多因素性质,我们的总结表明需要进一步研究,将 BD 中加速衰老的生物标志物与临床证据相结合。本综述的结果强烈表明,BD 是一种在临床和分子方面都表现出加速衰老的疾病。了解 BD 中衰老的病理生理学可能最终会确定可以针对患者的预防过早衰老和与衰老相关疾病的早期发病的途径。