International Association of Athletics Federations, IAAF-Medical and Antidoping Commission, Monte Carlo, Monaco,
Sports Med. 2013 Oct;43(10):965-77. doi: 10.1007/s40279-013-0075-4.
During the last 2 decades, progress in deciphering the human gene map as well as the discovery of specific defective genes encoding particular proteins in some serious human diseases have resulted in attempts to treat sick patients with gene therapy. There has been considerable focus on human recombinant proteins which were gene-engineered and produced in vitro (insulin, growth hormone, insulin-like growth factor-1, erythropoietin). Unfortunately, these substances and methods also became improper tools for unscrupulous athletes. Biomedical research has focused on the possible direct insertion of gene material into the body, in order to replace some defective genes in vivo and/or to promote long-lasting endogenous synthesis of deficient proteins. Theoretically, diabetes, anaemia, muscular dystrophies, immune deficiency, cardiovascular diseases and numerous other illnesses could benefit from such innovative biomedical research, though much work remains to be done. Considering recent findings linking specific genotypes and physical performance, it is tempting to submit the young athletic population to genetic screening or, alternatively, to artificial gene expression modulation. Much research is already being conducted in order to achieve a safe transfer of genetic material to humans. This is of critical importance since uncontrolled production of the specifically coded protein, with serious secondary adverse effects (polycythaemia, acute cardiovascular problems, cancer, etc.), could occur. Other unpredictable reactions (immunogenicity of vectors or DNA-vector complex, autoimmune anaemia, production of wild genetic material) also remain possible at the individual level. Some new substances (myostatin blockers or anti-myostatin antibodies), although not gene material, might represent a useful and well-tolerated treatment to prevent progression of muscular dystrophies. Similarly, other molecules, in the roles of gene or metabolic activators [5-aminoimidazole-4-carboxamide 1-β-D-ribofuranoside (AICAR), GW1516], might concomitantly improve endurance exercise capacity in ischaemic conditions but also in normal conditions. Undoubtedly, some athletes will attempt to take advantage of these new molecules to increase strength or endurance. Antidoping laboratories are improving detection methods. These are based both on direct identification of new substances or their metabolites and on indirect evaluation of changes in gene, protein or metabolite patterns (genomics, proteomics or metabolomics).
在过去的 20 年中,人类基因图谱的破译以及发现某些严重人类疾病中特定缺陷基因编码特定蛋白质的进展,导致了尝试使用基因治疗来治疗患病患者。人们一直关注经过基因工程改造并在体外产生的人类重组蛋白,这些蛋白包括胰岛素、生长激素、胰岛素样生长因子-1、促红细胞生成素。不幸的是,这些物质和方法也成为了无良运动员的不当工具。生物医学研究的重点是将基因物质直接插入体内,以替代体内某些有缺陷的基因和/或促进内源性合成缺乏的蛋白质。从理论上讲,糖尿病、贫血、肌肉营养不良、免疫缺陷、心血管疾病和许多其他疾病都可以从这种创新的生物医学研究中受益,尽管还有很多工作要做。考虑到最近发现的特定基因型与身体表现之间的关联,人们很想让年轻的运动员接受基因筛查,或者通过人工基因表达调节来改变基因。为了实现安全地将遗传物质转移到人类身上,已经进行了大量的研究。这一点至关重要,因为无控制地生产特定编码蛋白可能会导致严重的继发性不良反应(红细胞增多症、急性心血管问题、癌症等)。在个体水平上,还可能发生其他不可预测的反应(载体或 DNA 载体复合物的免疫原性、自身免疫性贫血、野生遗传物质的产生)。一些新物质(肌肉生长抑制素阻滞剂或抗肌肉生长抑制素抗体),虽然不是基因物质,但可能代表一种有用且耐受良好的治疗方法,可预防肌肉营养不良的进展。同样,其他分子(基因或代谢激活剂[5-氨基咪唑-4-甲酰胺 1-β-D-核糖呋喃糖苷(AICAR)、GW1516])可能会同时改善缺血条件下和正常条件下的耐力运动能力。毫无疑问,一些运动员会试图利用这些新分子来提高力量或耐力。反兴奋剂实验室正在改进检测方法。这些方法既基于对新物质或其代谢物的直接鉴定,也基于对基因、蛋白质或代谢物图谱变化的间接评估(基因组学、蛋白质组学或代谢组学)。