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‘Infertile’ studies on mitochondrial DNA variation in asthenozoospermic Tunisian men

机译:弱精症突尼斯男子线粒体DNA变异的“不育”研究

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摘要

We reviewed five studies undertaken by the same research group on the possible links between mitochondrial DNA (mtDNA) variation and asthenozoospermia, all carried out on Tunisian men. A thorough assessment of these articles reveals that all five studies were carried out on virtually the same cohort of patients, although this information was concealed by the authors. Thus, the results were ‘sliced’ in order to unjustifiably maximize the number of publications. In addition, a phylogenetic analysis of their data indicates that the reported results are notably incomplete and deficient. Overall, contrary to the original claims, the association of mtDNA variants with asthenozoospermia finds no support on this saga on Tunisian infertile men. Highlights ? We re-analyze the seeming association of mtDNA with infertility in Tunisians. ? The existing data are incomplete and deficient. ? The data do not support association of mtDNA and infertility.
机译:我们回顾了同一研究小组针对线粒体DNA(mtDNA)变异与弱精子症之间的可能联系进行的五项研究,所有研究均在突尼斯男子身上进行。对这些文章的透彻评估表明,尽管作者掩盖了这些信息,但所有五项研究实际上都是针对同一组患者进行的。因此,为了不合理地使出版物数量最大化,对结果进行了“切片”。此外,对其数据的系统发育分析表明,报告的结果明显不完整且不足。总体而言,与最初的主张相反,mtDNA变体与弱精子症的关联对突尼斯不育男性的这一传奇没有任何支持。强调 ?我们重新分析了突尼斯人中mtDNA与不育的表面联系。 ?现有数据不完整且不足。 ?数据不支持mtDNA与不育的关联。

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