Molecular Biology & Clinical Neuroscience Division, National Neurosciences Centre, Calcutta, Peerless Hospital (2nd floor), 360, Panchasayar, Kolkata, 700094, India.
Department of Neurology, National Neurosciences Centre, Calcutta, Kolkata, India.
Neuromolecular Med. 2024 Oct 14;26(1):41. doi: 10.1007/s12017-024-08808-y.
The circadian variation in stroke occurrence is a well-documented phenomenon. However, the circadian effect on stroke outcome, particularly on post-stroke cognition, has not yet been fully elucidated. We aim to evaluate the influence of diurnal variation of stroke onset upon post-stroke cognition and development of post-stroke depression. Based on 4-hourly time period of stroke occurrence, 249 recruited cohorts were categorized into 6 groups. Several clinical and cognitive parameters were compared among the groups. Then, the mRNA expression of core clock genes in Peripheral Blood Mononuclear Cells were quantified and correlated with post-stroke outcomes among 24 acute phase cases with day-time or night-time stroke occurrence. Furthermore, the genetic susceptibility towards a higher number of cases in the morning was examined by genotyping CLOCK (rs1801260T/C, rs4580704G/C) and CRY2 (rs2292912C/G) genes variants in cases and 292 controls. In our study, the peak for highest incidence although observed during the early morning from 4 to 8 am, the nocturnal-onset stroke cases showed more severity (12.2 ± 5.67) at the time of admission irrespective of arterial territory involved. The night onset cases were also found to be more susceptible to develop language impairment and post-stroke depression in due course of time. Upon transcript analysis, circadian genes (BMAL1 and CRY1) were found to be downregulated in night-time cases than day-time ones during the acute phase of onset. In addition, those mRNA levels also showed a correlation with raw scores for language and depression. However, the difference in incidence frequency along a day did not reveal any genetic correlation. Therefore, we suggest night-time stroke to be positively associated with higher immediate severity and poor cognitive outcome than day-time injury and propose downregulation of circadian genes during the acute phase could be the underlying molecular mechanism for this.
卒中发生的昼夜变化是一个有据可查的现象。然而,昼夜节律对卒中结局的影响,特别是对卒中后认知的影响,尚未得到充分阐明。我们旨在评估卒中发作的昼夜变化对卒中后认知和卒中后抑郁发展的影响。根据卒中发生的 4 小时时间间隔,将 249 名入组队列分为 6 组。比较各组间的若干临床和认知参数。然后,在 24 例急性期中日间或夜间卒中发作的病例中,定量检测外周血单个核细胞中核心时钟基因的 mRNA 表达,并将其与卒中后结局相关联。此外,通过对病例和 292 例对照的 CLOCK(rs1801260T/C、rs4580704G/C)和 CRY2(rs2292912C/G)基因变异进行基因分型,研究了早晨出现更多病例的遗传易感性。尽管我们的研究中观察到最高发病率的峰值出现在清晨 4 点至 8 点之间,但无论涉及的动脉区域如何,夜间发作的卒中病例在入院时的严重程度更高(12.2±5.67)。随着时间的推移,夜间发作的病例也更容易出现语言障碍和卒中后抑郁。在转录分析中,昼夜节律基因(BMAL1 和 CRY1)在发病急性期的夜间病例中表达下调,低于日间病例。此外,这些 mRNA 水平也与语言和抑郁的原始评分相关。然而,一天中发病率的差异并没有显示出任何遗传相关性。因此,我们认为夜间卒中与更高的即刻严重程度和较差的认知结局相关,而白天的损伤则与之相反,并提出在急性期下调昼夜节律基因可能是其潜在的分子机制。