Department of Biochemistry, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Center, Jalan Yaacob Latif, Cheras, Kuala Lumpur 56000, Malaysia.
Faculty of Medicine and Defence Health, National Defence University of Malaysia, Kem Sungai Besi, Kuala Lumpur 57000, Malaysia.
Cells. 2021 Jun 27;10(7):1611. doi: 10.3390/cells10071611.
The mechanism of cognitive aging at the molecular level is complex and not well understood. Growing evidence suggests that cognitive differences might also be caused by ethnicity. Thus, this study aims to determine the gene expression changes associated with age-related cognitive decline among Malay adults in Malaysia. A cross-sectional study was conducted on 160 healthy Malay subjects, aged between 28 and 79, and recruited around Selangor and Klang Valley, Malaysia. Gene expression analysis was performed using a HumanHT-12v4.0 Expression BeadChip microarray kit. The top 20 differentially expressed genes at < 0.05 and fold change (FC) = 1.2 showed that PAFAH1B3, HIST1H1E, KCNA3, TM7SF2, RGS1, and TGFBRAP1 were regulated with increased age. The gene set analysis suggests that the Malay adult's susceptibility to developing age-related cognitive decline might be due to the changes in gene expression patterns associated with inflammation, signal transduction, and metabolic pathway in the genetic network. It may, perhaps, have important implications for finding a biomarker for cognitive decline and offer molecular targets to achieve successful aging, mainly in the Malay population in Malaysia.
分子水平上认知老化的机制很复杂,目前还不是很清楚。越来越多的证据表明,认知差异也可能是由种族引起的。因此,本研究旨在确定与马来西亚马来成年人年龄相关的认知能力下降相关的基因表达变化。在马来西亚雪兰莪和巴生谷地区,进行了一项横断面研究,共纳入了 160 名年龄在 28 岁至 79 岁之间的健康马来成年人。使用 HumanHT-12v4.0 Expression BeadChip 微阵列试剂盒进行基因表达分析。在 < 0.05 和倍数变化 (FC) = 1.2 的条件下,前 20 个差异表达基因显示,PAFAH1B3、HIST1H1E、KCNA3、TM7SF2、RGS1 和 TGFBRAP1 的表达随着年龄的增长而增加。基因集分析表明,马来成年人易发生与年龄相关的认知能力下降,可能是由于遗传网络中与炎症、信号转导和代谢途径相关的基因表达模式的变化所致。这或许对寻找认知能力下降的生物标志物以及实现成功老龄化的分子靶点具有重要意义,特别是在马来西亚的马来人群体中。