Toward precision nutrition: A cross‐sectional study on the genetic risks of nutrients deficiencies and eating behaviors among the Orang Asli and Malays

IF 0.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Nurul Ain Bt Khoruddin, W. Lim, L. Teh, Mohd Nur Fakhruzzaman Noorizhab, F. Z. Mohd Yusof, M. Z. Salleh
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引用次数: 0

Abstract

This cross‐sectional study aimed to profile 15 genetic markers associated with the risks of nutrient deficiencies and eating disinhibition behaviors that could lead to obesity among the Orang Asli (OA) and the Malays. The whole‐genome sequences of 98 OA and 96 Malay individuals were mined for these 15 genetic variants. The distributions of risk allele frequencies were then compared with other world populations to determine the impact of these genetic variations on the wellness of the two cohorts. The risk alleles include rs2025804 G, rs1800497 T, rs4680 G, rs602662 G, rs174547 C, and rs4654748 C, were commonly found among the OA and Malays and are likely to be pathogenic genetics variants for obesity. The risk allele frequencies differed significantly between the studied and the other five populations (p < .05). We believe that this is the first reported study on the genetic variants associated with nutrient deficiencies and eating disinhibition behaviors that are likely to increase risks of obesity among the OA and Malays.
走向精准营养:一项关于原住民和马来人营养缺乏和饮食行为遗传风险的横断面研究
这项横断面研究旨在对奥兰阿斯利人(OA)和马来人中可能导致肥胖的营养缺乏和饮食去抑制行为风险相关的15个遗传标记进行分析。对98名OA和96名马来人的全基因组序列进行了这15种遗传变异的挖掘。然后将风险等位基因频率的分布与世界其他人群进行比较,以确定这些基因变异对两个队列健康的影响。风险等位基因包括rs2025804 G、rs1800497 T、rs4680 G、rs602662 G、rs174547 C和rs4654748 C,常见于OA和马来人,可能是肥胖的致病性遗传变异。风险等位基因频率在研究人群和其他五个人群之间存在显著差异(p < .05)。我们认为,这是首次报道与营养缺乏和饮食去抑制行为相关的基因变异的研究,这些行为可能会增加OA和马来人肥胖的风险。
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来源期刊
Precision Medical Sciences
Precision Medical Sciences MEDICINE, RESEARCH & EXPERIMENTAL-
自引率
0.00%
发文量
33
审稿时长
15 weeks
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