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速度基因研究:方法、研究设计和初步结果。

The speed-gene study: methods, study design and preliminary results.

机构信息

Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.

Human Movement Performance Enhancement Research Unit, Faculty of Sports Science, Chulalongkorn University, Bangkok, Thailand.

出版信息

BMC Res Notes. 2023 Nov 22;16(1):345. doi: 10.1186/s13104-023-06617-3.

Abstract

The Speed-Gene study aims to identify genetic variants influencing athletic performance and human locomotion using motion capture technology. Currently, 60 female participants have completed the testing protocol, and the overall aim is to recruit 283 moderately trained, healthy Southeast Asian individuals (18-45 y, BMI < 30). Participants will undergo biomechanical analysis and genetic testing. Several analyses will be performed, including (but not limited to) linear and angular kinematic analysis using motion capture technology, force plate dynamometry and genetic analyses to define novel power/torque related outcomes that would be more sensitive to allele-specific differences in athletic performance. Pretesting beverages will be provided, and activity history and current activity levels will be assessed by a questionnaire. The kinematic data will be obtained using a Qualisys Track Manager (QTM) system, and DNA will be extracted from white blood cells. The participants serve as their own controls. Although the Speed-Gene study is tightly controlled, our preliminary findings still indicate considerable individual variability. More participants and further genetic analysis are required to allow the investigation of potential underlying genetic mechanisms responsible for this individual variability.

摘要

《速度基因》研究旨在利用运动捕捉技术鉴定影响运动表现和人体运动的遗传变异。目前,已有 60 名女性参与者完成了测试方案,总体目标是招募 283 名训练有素、健康的东南亚个体(18-45 岁,BMI<30)。参与者将接受生物力学分析和基因测试。将进行多项分析,包括(但不限于)使用运动捕捉技术进行线性和角度运动学分析、力量板测力和基因分析,以确定更能敏感地反映与运动表现相关的特定等位基因差异的新型功率/扭矩相关结果。将提供预测试饮料,并通过问卷评估活动历史和当前活动水平。运动学数据将使用 Qualisys Track Manager(QTM)系统获得,DNA 将从白细胞中提取。参与者充当自己的对照。尽管《速度基因》研究受到严格控制,但我们的初步发现仍表明存在相当大的个体差异。需要更多的参与者和进一步的遗传分析,以研究潜在的遗传机制,这些机制负责造成这种个体差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da79/10664269/316481bbce01/13104_2023_6617_Fig1_HTML.jpg

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