不同年龄阶段成人认知、脑源性神经营养因子血浆水平和炎症选定指标的年龄相关变化。

Q4 Medicine
Sheu Kadiri Rahamon, Abiodun Olaide Yusuff, Olatunde Olayinka Ayinde, Funmilola Taiwo
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引用次数: 0

摘要

衰老与以认知障碍为特征的神经系统疾病有关。有报道表明脑源性神经营养因子(BDNF)参与神经发生和神经可塑性。同样,与衰老相关的慢性炎症在免疫衰老中起着重要作用。然而,关于BDNF水平和炎症的年龄相关变化的信息缺乏。因此,本研究旨在确定不同年龄成人的认知、血浆BDNF水平和选定的炎症指标。88名成年人被分成4组;本横断面研究分为I组(30 ~ 39岁)、II组(40 ~ 49岁)、III组(50 ~ 59岁)和IV组(≥60岁)。采用简易精神状态检查(MMSE)评估认知功能。采用ELISA和分光光度法测定血浆BDNF和一氧化氮(NO)水平。采用标准方法进行白细胞计数和白细胞分化,适当计算中性粒细胞淋巴细胞比(NLR)。随着寿命的增加,认知评分和血浆BDNF水平显著下降。神经认知得分都显著高于在我组,第二组,第三组与组第四。同样,BDNF的平均血浆水平明显高于在我组与组III和IV。此外,平均混合数明显高于静脉组与组相比我虽然说等离子体水平没有明显高于第二和第三组与组即回归分析显示年龄与认知负相关(R2 = 0.522,p = 0.000)和BDNF水平(R2 = 0.095, p = 0.003)。此外,BDNF与i组神经认知评分呈显著正相关。随着寿命的增加,血浆BDNF水平和认知评分逐渐降低。这可能表明随着年龄的增长,血浆BDNF水平可以预测神经认知功能障碍的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age-Related Changes in Cognition, Plasma Levels of Brain-Derived Neurotrophic Factors and Selected Indices of Inflammation in Adults at Different Decades of Life.

Ageing is associated with neurological disorders that are characterized by cognitive impairment. Reports have shown that brain-derived neurotrophic factor (BDNF) is involved in neurogenesis and neuroplasticity. Similarly, chronic inflammation-associated with ageing plays important roles in immunosenescence. However, there is the dearth of information on age-related changes in BDNF level and inflammation. This study was thus, designed to determine cognition, plasma levels of BDNF and selected indices of inflammation in adults at different decades of life. Eighty-eight adults sub-divided into 4 groups; Group I (30 - 39 years), Group II (40 - 49 years), Group III (50 - 59 years) and Group IV (≥60 years) were enrolled into this cross-sectional study. Cognitive function was assessed using the Mini-mental state examination (MMSE). Plasma levels of BDNF and nitric oxide (NO) were determined using ELISA and spectrophotometry. White blood cell count and differentials were done using standard methods and neutrophil-lymphocyte ratio (NLR) was calculated appropriately. There was significant progressive reduction in cognitive score and plasma levels of BDNF as decades of life increase. The neurocognitive scores were significantly higher in Group I, Group II, and Group III compared with Group IV. Similarly, the median plasma level of BDNF was significantly higher in Group I compared with Groups III and IV. Also, the mean mixed count was significantly higher in Group IV compared with Group I while the mean plasma level of NO was significantly higher in Groups II and III compared with Group I. Regression analysis showed that age negatively related with cognition (R2 = 0.522, p = 0.000) and BDNF level (R2 = 0.095, p = 0.003). Furthermore, BDNF had significant positive correlation with the neurocognitive score in Group I. There is progressive reduction in plasma BDNF level and cognitive score with increasing decades of life. This may indicate that plasma BDNF level could predict susceptibility to neurocognitive dysfunction as ageing progresses.

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来源期刊
Nigerian Journal of Physiological Sciences
Nigerian Journal of Physiological Sciences Medicine-Physiology (medical)
CiteScore
0.80
自引率
0.00%
发文量
23
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