Measured with Sperm Chromatin Dispersion (SCD) Technique: Will DNA Integrity in Spermatozoa Increase After Micronutrient Supplementation? Comparative Controlled Study

Author:

Eidenberger Fiona1,Huber Kim-Lien2ORCID,Fuchs Patricia2ORCID,Simkovicova Nikola2,Imhof Martin13ORCID

Affiliation:

1. Karl Landsteiner Institute for Cell-Focused Therapy in Gynecology, Wiener Ring 3–5, 2100 Korneuburg, Vienna, Austria

2. Medical Students at the Medical University of Vienna, Spitalgasse 23, 1090 Vienna, Austria

3. Department of Obstetrics and Gynecology, General Public Hospital Korneuburg, Wiener Ring 3–5, 2100 Korneuburg, Vienna, Austria

Abstract

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.

Publisher

World Scientific Pub Co Pte Lt

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