4.7 Article

Association between Seminal Oxidation-Reduction Potential and Sperm DNA Fragmentation-A Meta-Analysis

Journal

ANTIOXIDANTS
Volume 11, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/antiox11081563

Keywords

oxidative stress; male infertility; oxidation-reduction potential; sperm DNA fragmentation; meta-analysis

Funding

  1. School of Medicine Pilot Funding Award 2021 (Tulane University, New Orleans, LA, USA)

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This study conducted a systematic review and meta-analysis to evaluate the relationship between seminal ORP and SDF. The results showed a significant positive correlation between ORP and SDF, indicating the role of oxidative stress in sperm DNA damage. Further exploration of the clinical value of these sperm function tests is warranted.
Seminal oxidative stress and sperm DNA damage are potential etiologies of male factor infertility. The present study aims to evaluate the relationship between oxidation-reduction potential (ORP), a measure of oxidative stress, and sperm DNA fragmentation (SDF) by conducting a systematic review and meta-analysis of relevant clinical data. A literature search was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The COVIDENCE tool was used to screen and identify studies evaluating seminal ORP and SDF. Studies (n = 7) that measured seminal ORP and SDF of 3491 semen samples were included in the analysis. The fixed-effects model revealed a significant pooled correlation coefficient (r = 0.24; p < 0.001) between seminal ORP and SDF. Furthermore, subgroup analyses indicated that the pooled correlation coefficient between ORP and sperm chromatin dispersion (SCD) assay was less than other SDF assays (0.23 vs. 0.29). There was a moderate level of heterogeneity (I-2 = 42.27%) among the studies, indicating a lack of publication bias. This is the first meta-analysis to reveal a positive correlation between seminal ORP and SDF. Furthermore, this study indicates the role of oxidative stress in the development of sperm DNA damage and thus warrants prospectively exploring the clinical value of these sperm function tests.

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