# Low Testosterone and Sperm Quality Alterations: A Prospective Study of Sperm DNA Fragmentation and Chromatin Condensation in Infertile Men

**Authors:** Asmaa Serbouti, Kenza Berrada, Samy Housbane, Noureddine Louanjli, Rachid Aboutaieb

PMC · DOI: 10.3390/biology15030287 · Biology · 2026-02-06

## TL;DR

Low testosterone in men is linked to poor sperm quality and increased DNA damage, contributing to infertility.

## Contribution

This study establishes a direct link between low testosterone levels and impaired sperm DNA integrity and semen quality in infertile men.

## Key findings

- Low testosterone is associated with increased sperm DNA fragmentation and chromatin decondensation.
- Testosterone levels positively correlate with sperm concentration, motility, morphology, and vitality.
- Men with low testosterone show significantly worse semen parameters compared to those with normal testosterone.

## Abstract

Male infertility represents an important public health problem worldwide. There are many factors behind male infertility, including endocrine dysfunctions. Hormones play a crucial role in the male reproductive system. In particular, testosterone, which seems to be the principal hormone implicated in testicular function, specifically regulates spermatogenesis. This study aimed to determine the relationship between testosterone and DNA fragmentation, chromatin condensation, and semen parameters. This was a prospective study that included 214 men aged 25–45 undergoing infertility evaluation. Participants were classified into two groups according to serum testosterone levels: low testosterone and normal testosterone. The results of the present study indicate that low testosterone levels are associated with increased DNA damage. Furthermore, reduced testosterone levels are linked to global alteration of the sperm quality, particularly affecting concentration, motility, morphology, and vitality of spermatozoa.

(1) Background: Testosterone plays a key role in spermatogenesis and in maintaining semen quality and sperm DNA integrity. Consequently, reduced testosterone levels may disrupt these processes and contribute to male infertility. This study aimed to evaluate the impact of low testosterone levels on semen parameters, sperm DNA fragmentation, and chromatin condensation; (2) Methods: This was a prospective study that included 214 men aged 25–45 years undergoing infertility evaluation. Participants were classified into two groups according to serum testosterone levels: low testosterone and normal testosterone. Total testosterone was determined using electrochemiluminescence immunoassay. Semen analysis was carried out according to the WHO 2021 guidelines. The DNA fragmentation index was assessed using the TUNEL assay. The sperm decondensation index was evaluated by aniline blue staining; (3) Results: Men with low serum total testosterone levels (<2.64 ng/mL) exhibited significantly impaired semen parameters compared with those with normal testosterone levels. Serum total testosterone was positively correlated with sperm concentration (rs = 0.43, p < 0.001), total motility (rs = 0.20, p = 0.005), normal morphology (rs = 0.25, p < 0.001), and sperm vitality (rs = 0.173, p = 0.014). In contrast, testosterone levels were negatively correlated with the DNA fragmentation index (rs = −0.221, p = 0.0017) and the chromatin decondensation index (rs = −0.19, p = 0.0086). A higher proportion of pathological DFI (>15%) was observed in the low testosterone group. (4) Conclusions: These findings support the essential role of testosterone in sustaining spermatogenesis, semen quality, and sperm DNA integrity and highlight the crucial importance of testosterone assessment in the diagnosis and pathophysiological understanding of male infertility.

## Full-text entities

- **Diseases:** male infertility (MESH:D007248), infertility (MESH:D007246)
- **Chemicals:** aniline blue (MESH:C017006), Testosterone (MESH:D013739)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12896868/full.md

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Source: https://tomesphere.com/paper/PMC12896868