Correlations between abnormalities of morphological details and DNA fragmentation in human sperm

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Clin Exp Reprod Med. 2022;49(1):40-48

Publication date (electronic) : 2022 February 24

doi : https://doi.org/10.5653/cerm.2021.04777

Hiep Tuyet Thi Nguyen¹, Hong Nhan Thi Dang¹, Thai Thanh Thi Nguyen¹, Trung Van Nguyen¹, Thuan Cong Dang², Quoc Huy Vu Nguyen³, Minh Tam Le^,1,3

¹Center for Reproductive Endocrinology and Infertility, Hue University, Hue, Vietnam

²Departments of Histology, Embryology, and Pathology, Hue University of Medicine and Pharmacy, Hue University, Hue, Vietnam

³Department of Obstetrics and Gynecology, Hue University of Medicine and Pharmacy, Hue University, Hue, Vietnam

Corresponding author: Minh Tam Le Department of Obstetrics and Gynecology, Hue University of Medicine and Pharmacy, Hue University, 6 Ngo Quyen st, Hue, Viet Nam Tel: +84-23-4626-9696 Fax: +84-23-4382-2173 E-mail: leminhtam@hueuni.edu.vn

*Hiep Tuyet Thi Nguyen was funded by Vingroup Joint Stock Company and was supported by the Domestic Master/ PhD Scholarship Program of Vingroup Innovation Foundation (VINIF), Vingroup Big Data Institute (VINBIGDATA), code VINIF. 2020.TS.44.

Received 2021 June 21; Revised 2021 August 13; Accepted 2021 September 6.

Abstract

Introduction

Infertility is a reproductive health problem that affects approximately 15% of reproductive-aged couples worldwide; male factors contribute as a unique cause in approximately 30% of infertility cases [1]. Male factor infertility results from pre-testicular, testicular, or post-testicular abnormalities. However, in some cases, no reason for diminished sperm quality can be identified [2]. Conventional semen analysis is routinely performed according to standard criteria in the World Health Organization (WHO) guidelines and is accepted as the first step in evaluating male fertility [3]. Further, sperm DNA fragmentation (SDF) tests have recently gained interest as a way to assess sperm quality in the context of recurrent miscarriage, unexplained infertility, varicocele, or recurrent implantation failure after in vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) [2].

During spermiogenesis, when spermatids transform into spermatozoa, the chromatin of sperm cells can be damaged by endogenous and exogenous factors [4,5]. Due to chromatin compaction, the substantial reduction in cell cytoplasm leads to a limited self-repair process for fragmentation [5]. Severe DNA fragmentation may occur after spermatogenesis is completed, during the time in the epididymis and other ducts. Lifestyle-related risk factors (e.g., alcohol consumption and smoking, or toxic and hot environments) may also lead to increased concentrations of oxygen free radicals, thereby increasing the levels of sperm DNA damage [6-8]. SDF is correlated with apoptosis and dysfunction of sperm mitochondrial membrane potential, which is in turn negatively related to motility and normal morphology [9].

A high percentage of abnormal sperm, especially abnormalities of structural details, may result from a defective mechanism associated with spermatogenesis and/or sperm maturation. Abnormal sperm morphology is associated with a decrease in routine semen parameters [10] as well as signs of sperm damage (e.g., DNA fragmentation levels) and increased concentrations of reactive oxygen species (ROS) [11].

To date, the relationship between sperm morphology and SDF remains unclear. Furthermore, very few results have been obtained from fresh or prepared samples using different techniques, and sperm morphology has not been assessed in detail [12-14]. Additional information on the detailed characteristics of sperm morphology and information regarding sperm cells may be helpful for predicting sperm quality and advising patients. Therefore, the goal of this study was to determine the relationship between abnormalities of morphological details and DNA integrity of human spermatozoa using the sperm chromatin dispersion (SCD) assay.

Methods

2. Semen analysis

Fresh semen samples were obtained and tested in accordance with the 2010 WHO standards [3]. Sperm motility was analyzed manually using phase-contrast microscopy at ×400 magnification; sperm viability was assessed by eosin staining. For morphological assessment, after staining with Giemsa, the morphology of the sperm head shape, acrosomal region, sperm neck, midpiece, tail, and cytoplasmic droplets was determined under a microscope at ×1,000 magnification, according to the WHO 2010 guidelines. Head defects included abnormal head shapes and vacuolation, abnormal acrosomal areas, double heads, or any combination thereof. Neck and midpiece defects included a folding neck, an irregular thick, thin or a sharply bent midpiece. Principal piece defects included short, multiple, broken, smooth hairpin bends, sharply angulated bends, an irregular width, coiled structure, or any combination thereof. Excess residual cytoplasm (ERC) was recorded when the cytoplasm was larger than one-third of the sperm head size [3]. The images of abnormal sperm were taken using an Olympus CX41 microscope (Cebu, Philippines) and Infinity 1 Lumenera software (Ottawa, Canada) and shown in Figure 1. Based on the morphology results, the samples were separated into normal (normal morphology rate ≥4%) and abnormal (normal morphology rate <4%) morphology groups.

Figure 1.

(A) Normal sperm cell. (B) Pyriform-head sperm cell. (C) Sperm cell with a tapered head, thick insertion midpiece, and coiled tail. (D) Tapered-head sperm cell and an amorphous-head sperm cell. (E) Round-head sperm cell without an acrosome. (F) Sperm cell with a small acrosomal area. (G) Round-head sperm cell with vacuolation and an amorphous-head sperm cell with vacuolation and excess residual cytoplasm. (H) Pyriform sperm head with bent midpiece and coiled tail. (I) Sperm cell with a bent neck and excess residual cytoplasm greater than one-third of the head. (Giemsa stain, ×1,000)

3. SCD test

All fresh semen samples were tested for fragmented DNA using the Halosperm HT-HS10 system (Halotech DNA, Madrid, Spain). A 20-μL sperm sample was added to 40 μL of low-melting agarose and mixed evenly. Subsequently, an 8-μL aliquot was placed on a slide and refrigerated at 4°C for 10 minutes to solidify the agarose. The slide was then immersed respectively in an acid denaturant for 7 minutes and lysis solution for 25 minutes. After that, the slide was rinsed in distilled water for 5 minutes, dehydrated in ethanol baths at concentrations of 70% (2 minutes) and 100% (2 minutes), and air-dried. Giemsa staining was used to stain the sperm at the end. The slides were examined under phase-contrast microscopy at ×1,000 magnification. The DNA fragmentation index (DFI) was estimated as the sum of DNA fragmentation spermatozoa per 500 spermatozoa. Spermatozoa without DNA fragmentation included sperm cells with a large halo (halo width equal to or higher than the diameter of the core) or medium halo (halo size between large and small). Spermatozoa with fragmented DNA included any sperm cells with small halos (halo width equal to or smaller than one-third of the diameter of the core) or no halo, as well as those that were degraded (no halo and presenting a core that was irregularly or weakly stained). To prevent bias, the slide observations were recorded and then assessed by two experienced andrologists (NTHT and DTHN). The images of sperm halos were taken using an Olympus CX41 microscope and Infinity 1 Lumenera software, as shown in Figure 2. The normal DFI group was defined as those with a DFI ≤15%, while a DFI >15% was considered abnormal.

Figure 2.

Classification of human sperm DNA fragmentation using the Halosperm test. The normal group included (A) sperm with a large halo and (B) sperm with a medium halo; while the abnormal group included (C) sperm with a small halo, (D) sperm without a halo, and (E) degraded sperm. (Giemsa stain, ×1,000)

Results

In total, 130 semen samples from 130 infertile men were collected for this study. As shown in Table 1, they ranged in age from 25 to 51 years old (mean, 34.16±5.72 years). The following results were obtained for semen parameters: semen volume, 2.33±0.88 mL; pH, 7.31±0.47; sperm progressive motility (PR), 28.55%±9.88%; concentration, 34.35±18.34 ×10⁶/mL; vitality, 83.02%±9.06%; normal morphology, 4.75%± 3.06%; and sperm DFI, 34.57%±22.42%.

Table 1.

Comparison of semen parameters and sperm DFI between normal and abnormal sperm morphology groups

Statistically significant differences were found between the normal and aberrant morphology groups in terms of PR (31.35%±9.13% vs. 24.73%±9.66%, p=0.000), sperm concentration (38.40±18.08 ×10⁶/mL vs. 28.84±17.37 ×10⁶/mL, p=0.003), viability rate (84.81%±5.31% vs. 80.58%±12.11%, p=0.018), abnormal head rate (85.20%±7.73% vs. 91.96%±7.27%, p=0.00), pyriform rate (18.41%±10.44% vs. 12.56%±10.74%, p=0.002), and ERC rate (0.73%±1.43% vs. 3.20%±4.69%, p=0.000). Amorphous morphology was the most common head abnormality, at 29.66%±13.46%; however, only a trend towards significance was observed between the two morphological groups (p=0.051). Regarding the characteristics of SDF, no statistically significant differences in the halo characteristics were found between the normal and abnormal morphology groups.

Table 2 shows the results for the relationship of semen characteristics with the two groups (DFI ≤15% and DFI >15%); the results revealed no statistically significant difference between the two groups in terms of routine semen parameters and abnormalities of morphological details. Table 3 presents the relationship between DNA fragmentation characteristics and semen parameters. A weak positive correlation was found between large halos and semen pH. Further, the absence of a halo was negatively correlated with viability (r=–0.301, p=0.000), and the incidence of degraded sperm was also negatively correlated with the rate of PR (r=–0.332, p=0.000) and viability (r=–0.205, p=0.019); in general, the DFI was negatively correlated with the viability of spermatozoa (r=–0.188, p=0.033).

Table 2.

Comparison semen parameters and detailed sperm morphology in two groups of sperm DFI

Table 3.

The correlation between the classification of halo and semen parameters

The correlations between the classification of halo types and abnormal morphology are shown in Table 4. Round-head spermatozoa had a positive correlation with small-halo sperm and the DFI (r=0.243, p=0.005 and r=0.197, p=0.025), respectively. There were no correlations between other halo characteristics and abnormal sperm morphology.

Table 4.

The correlation between the halo types and detailed sperm morphology abnormalities

Discussion

Sperm morphology is the most relevant parameter in conventional semen analysis for predicting fertilization potential [11,15], a prerequisite factor for the successful use of assisted reproductive technology (ART) [16,17]. Our results indicated that abnormal sperm mainly showed changes in head morphology, and that amorphous-head and tapered spermatozoa were more common in the abnormal morphology group. Amorphous heads, tapered heads, and microheads were also reported to predominate abnormal sperm morphology in previous studies [18,19]. However, the relationship between the level of SDF and semen parameters has remained unclear. In some studies, the DFI was associated with some semen parameters such as sperm viability [20], motility [21,22], concentration, and normal morphology [13,22]. However, other studies indicated that DFI was not correlated with conventional fresh semen parameters [12,23]. In this study, no significant difference in semen parameters was found between the groups with a DFI ≤15% and a DFI >15%. However, there was a negative correlation between the viability rate and SDF.

Men with teratozoospermia may show significantly higher rates of ROS production, denatured DNA, and fragmented DNA [18]. Jakubik-Uljasz et al. [13] reported that the DFI was positively correlated with the teratozoospermia index, the proportion of sperm with head, midpiece, and tail abnormalities, and sperm with ERC. Even in pellet swim-up samples, 14% of morphologically abnormal spermatozoa showed fragmented DNA [12]. SDF primarily occurs by defective maturation from spermatids to mature spermatozoa, abortive apoptosis within the testis, and ROS throughout the male reproductive tract [24,25]. Abnormal spermatozoa arise due to failed apoptosis and/or failure to repair DNA strand breaks that appear during early spermatogenesis. Spermatogonia marked for apoptosis escape this process, leading to possible anomalies that may result in abnormal sperm morphology [26]. Therefore, the relationship between sperm morphology and the SDF level is predictable. However, the details regarding the types of anomalies closely related to SDF are still unclear. Our results showed no correlation of DFI or halo type with abnormal sperm morphology in general, except for a positive correlation between small halos and the DFI in round-head sperm cells.

The occurrence of round-head sperm cells, known as globozoospermia, is a severe male infertility disorder that usually causes low fertilization and pregnancy rates [27,28]; furthermore, it has recently been found to show a relationship with the outcome of ART cycles (ART) [29,30]. Globozoospermia can result from mutations, deletion of gene products associated with the Golgi apparatus in cells, formation of the acroplaxome, or attachment of the acrosome to the nucleus in the sperm head [31]. Our results confirmed a relationship between round-head sperm and SDF, highlighting that round-head sperm were positively correlated with the incidence of small halos and DFI in the SCD test; further, the rate of round-head spermatozoa tended to be higher in the high-DFI group (DFI >15%). Dam et al. [32] observed sperm cells by electron microscopy and discovered that in partial globozoospermia, the sperm head has less condensed chromatin, part of the acrosome, and mitochondria, and that round-head sperm are acrosome-less, with disturbed chromatin compaction. This evidence indicates that improperly compacted chromatin is related to round-head spermatozoa, suggesting that more DNA damage is present in globozoospermia [32]. Moreover, using the dUTP nick-end labeling assay and chromomycin A3 staining, another study found that the percentages of SDF and protamine-deficient spermatozoa were higher in men with globozoospermia than in fertile men [33]. Clearly, DNA fragmentation appears to be a contributor to round-head sperm cells.

Although SDF has been recognized as a supporting tool for male fertility assessment by leading research groups, studies using different assays have resulted in inconsistent conclusions [2,24]. Furthermore, the DFI cut-off values are not identical in previous studies. A DFI threshold of 15% was proposed in some recent studies that evaluated the association between the DFI and sperm morphology of infertile patients [12], embryological or clinical IVF/ICSI outcomes [34], blastocyst culture [35], or embryo development [36]. This cut-off value of 15% was also selected for treatment of SDF by micronutrient supplementation [37]. The threshold of >15% as an abnormal DFI selected in this study should be specifically considered when drawing a conclusion. A major strength of our study is the detection of the relationship of round-head sperm with SDF and the classification of halo types. However, our conclusions were drawn from results obtained using the SCD technique alone, which constitutes a limitation of our study. Thus, further studies using different techniques should be performed to confirm this relationship.

In conclusion, the rate of sperm morphological abnormalities in semen analysis was not related to sperm DNA integrity. However, a detailed assessment of sperm morphology revealed an association with SDF with the classification of halos and the DFI using the SCD assay. Specifically, round-head sperm were found to have a strong relationship with SDF and the DFI, and a higher percentage of round-head sperm was observed in the group of men with higher DFI. Therefore, in routine semen analysis, the detailed characteristics of abnormal sperm morphology should be described, together with a SDF assay for a better assessment of male fertility potential.

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