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A Genetic Analytics Approach for Risk Variant Identification to Support Intervention Strategies for People Susceptible to Polygenic Obesity and Overweight

机译:遗传分析方法用于风险变异识别,以支持易感多基因肥胖和超重人群的干预策略

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Obesity is a growing epidemic that has increased steadily over the past several decades. It affects significant parts of the global population and this has resulted in obesity being high on the political agenda in many countries. It represents one of the most difficult clinical and public health challenges worldwide. While eating healthy and exercising regularly are obvious ways to combat obesity, there is a need to understand the underlying genetic constructs and pathways that lead to the manifestation of obesity and their susceptibility metrics in specific individuals. In particular, the interpretation of genetic profiles will allow for the identification of Deoxyribonucleic Acid variations, known as Single Nucleotide Polymorphism, associated with traits directly linked to obesity and validated with Genome-Wide Association Studies. Using a robust data science methodology, this paper uses a subset of the TwinsUK dataset that contains genetic data from extremely obese individuals with a BMI ≥ 40, to identify significant obesity traits for potential use in genetic screening for disease risk prediction. The paper posits an approach for methodical risk variant identification to support intervention strategies that will help mitigate long-term adverse health outcomes in people susceptible to obesity and overweight.
机译:肥胖是一种日益增长的流行病,在过去的几十年中一直稳定增长。它影响了全球人口的很大一部分,这导致肥胖症在许多国家的政治议程中占据重要位置。它代表着全球最困难的临床和公共卫生挑战之一。虽然健康饮食和定期运动是对抗肥胖的明显方法,但有必要了解导致肥胖在特定个体中表现出来及其易感性指标的潜在遗传结构和途径。尤其是,遗传学特征的解释将有助于鉴定脱氧核糖核酸变异(称为单核苷酸多态性),该变异与直接与肥胖相关的性状有关,并已通过全基因组关联研究验证。通过使用可靠的数据科学方法,本文使用了TwinsUK数据集的子集,该子集包含BMI≥40的极端肥胖个体的遗传数据,以鉴定重要的肥胖特征,可用于遗传筛查疾病风险预测。本文提出了一种有条理的风险变量识别方法,以支持干预策略,该策略将有助于减轻易患肥胖和超重人群的长期不良健康后果。

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