用精子染色质分散(SCD)技术测量:补充微量营养素后精子中的DNA完整性会增加吗?比较对照研究

Fiona Eidenberger, K. Huber, P. Fuchs, Nikola Simkovicova, M. Imhof
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引用次数: 1

摘要

背景:DNA片段化指数(DFI)升高与男性不育有关;因此,测量精子核DNA的完整性似乎有助于预测精子与卵母细胞受精的能力。目的:评价微量营养素补充对低生育能力男性DFI值的影响。方法:这是一项回顾性/比较研究,包括2011年3月至2017年11月期间咨询诊所的306名低生育能力男性,他们进行了精子染色质分散测试(SCD) -一种用于检测DNA片段的方法-以及初始精液分析。在纳入的人群中,[公式:见文本]146人每天服用两粒口服胶囊的标准化复合微量营养素化合物([公式:见文本],Lenus Pharma,奥地利维也纳),为期三个月,并改变生活方式(研究组)。每粒胶囊含有左旋肉碱、左旋精氨酸、辅酶Q10、锌、维生素E、叶酸、谷胱甘肽和硒。那些没有接受积极治疗但只改变生活方式的人被认为是对照组。两组分别在基线和3个月后进行SCD测试。结果:在第一次统计分析中,考虑初始平均DFI >15%的患者([公式:见文]66[37为研究,29为对照])。3个月后,两组患者的平均DFI值均显著下降。然而,与对照组相比,研究组的下降更为明显(10.54% vs. 14.48%,[公式:见文]0.05;[公式:见正文]0.013)。第二种统计方法考虑了整个人口([公式:见案文]306)。3个月后,只有研究组的平均初始DFI值显著下降(10.16% ~ 6.49%,[公式:见文]< 0.0001);与对照组相比,下降更为明显(6.49% vs. 8.82%,[公式:见文]0.05;[公式:见文]0.000020)。结论:在DFI >15%的低生育能力男性中,两种方案均可显著降低精子DNA断裂;然而,当考虑任何基线DFI值时,只有使用活性标准化微量营养素化合物治疗才能取得明显更好的结果。
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Measured with Sperm Chromatin Dispersion (SCD) Technique: Will DNA Integrity in Spermatozoa Increase After Micronutrient Supplementation? Comparative Controlled Study
Background: An elevated DNA Fragmentation Index (DFI) has been associated with male infertility; therefore measuring the sperm nuclear DNA integrity appears to be useful in predicting the ability of spermatozoa to fertilize oocytes. Aim: To evaluate the effect of micronutrient supplementation over DFI values in subfertile men. Methods: This was a retrospective/comparative study that included a total of 306 subfertile males consulting the clinic from March 2011 to November 2017, who had performed the Sperm Chromatin Dispersion test (SCD) — a method used to detect DNA fragmentation — along with the initial semen analysis. Of the included population, [Formula: see text] 146 had received two daily oral capsules of a standardized combined micronutrient compound ([Formula: see text], Lenus Pharma, Vienna, Austria) for three months plus lifestyle change (study group). Each capsule contains L-carnitine, L-arginine, coenzyme Q10, zinc, vitamin E, folic acid, glutathione and selenium. Those who did not receive the active treatment ([Formula: see text] 160) but only engaged with lifestyle changes were considered controls. The SCD test was performed in both groups at baseline and after 3 months. Results: For the first statistical analysis, patients with an initial mean DFI of >15% were considered ([Formula: see text] 66 [37 were study and 29 were controls]). After 3 months, both groups displayed a significant decrease of mean DFI values. However, this decrease was more evident in the study group as compared to controls (10.54% vs. 14.48%, [Formula: see text] 0.05; [Formula: see text] 0.013). For the second statistical approach the entire population was considered ([Formula: see text] 306). After 3 months, only the study group displayed a significant decrease of the mean initial DFI value (10.16% to 6.49%, [Formula: see text] < 0.0001); decrease that was more evident as compared to controls (6.49% vs. 8.82%, [Formula: see text] 0.05; [Formula: see text] 0.000020). Conclusions: Among subfertile men with a DFI >15%, both regimes significantly decreased sperm DNA fragmentation; however, when any baseline DFI value was considered, only treatment with the active standardized micronutrient compound achieved a significant better result.
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