Impact of advanced paternal age on the intracytoplasmic sperm injection (ICSI) outcomes in donor egg cycles
Original Article

Impact of advanced paternal age on the intracytoplasmic sperm injection (ICSI) outcomes in donor egg cycles

Gianmartin Cito1#, Maria Elisabetta Coccia2#, Rita Picone2, Andrea Cocci1, Giorgio Ivan Russo3, Giulio Garaffa4, Rossella Fucci2, Francesco Bertocci2, Elena Borrani2, Valentina Basile2, Elisabetta Micelli5, Luciana Criscuoli2, Sergio Serni1, Marco Carini1, Alessandro Natali1

1Department of Urology, 2Assisted Reproductive Technology Centre, Careggi Hospital, University of Florence, Florence, Italy; 3Department of Urology, Vittorio Emanuele II, University of Catania, Catania, Italy; 4Institute of Urology, University College London Hospitals, London, UK; 5Department of Obstetrics and Gynecology, Santa Chiara Hospital, University of Pisa, Pisa, Italy

Contributions: (I) Conception and design: G Cito, ME Coccia, A Natali; (II) Administrative support: L Criscuoli, S Serni, M Carini; (III) Provision of study materials or patients: A Cocci, GI Russo; (IV) Collection and assembly of data: E Micelli, F Bertocci, E Borrani, V Basile; (V) Data analysis and interpretation: R Fucci, R Picone, G Garaffa; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

#These authors contributed equally to this work.

Correspondence to: Gianmartin Cito. Department of Urology, Careggi Hospital, University of Florence, Largo Brambilla, 3, 50134 Florence, Italy. Email:

Background: The purpose of this study is to assess the impact of paternal age on the oocyte-donation outcomes in intracytoplasmic sperm injection (ICSI) cycles.

Methods: Two hundred and seventy-eight infertile couples were retrospectively involved. Inclusion criteria were: infertility from almost 1 year, normal or sub-fertile seminal parameters, overall oocyte survival rate greater than 85%. Baseline characteristics included male age, recipient age, male body mass index (BMI), smoking, drinking status. Main outcome measures: fertilization rate (FR), cleavage rate (CR), pregnancy rate (PR).

Results: Patients were categorized in group 1 ≤45, group 2 >45 years. A total of 1,724 frozen oocytes were included. After warming, 1,642 oocytes survived. Median overall oocyte survival rate was 100% [interquartile range (IQR), 85–100%]. Median male age was 44±5.60 years (IQR, 31–70 years). Median recipients age was 42±3.62 years (IQR, 29–50 years). Group 1 included 166 men, group 2 112 men. Two hundred and seventy-eight fresh ICSI cycle were performed. “Two-pronuclear” (2PN) FR was 72.6%±0.20%, CR 93.0%±0.16%, PR 39.6%. Miscarriage rate was 25.5%. Live birth rate per cycles was 29.5%. Comparison between group 1, group 2 and ICSI outcomes confirmed an association with FR, resulting 80.0% (IQR, 67.0–83.0%) and 67.0% (IQR, 50.0–80.0%), respectively (P<0.01). There were no significant differences between the two groups with respect to seminal parameters.

Conclusions: It would be recommended more emphasis on the advancing male age when counselling older couples who undergo egg donation program.

Keywords: Aging male; infertility; intracytoplasmic sperm injection (ICSI)

Submitted Oct 16, 2018. Accepted for publication Dec 26, 2018.

doi: 10.21037/tau.2018.12.13


The last two decades have been characterized by a steady increase of paternal and maternal age (1). This phenomenon is likely to be secondary to a variety of factors, including increased life expectancy, the changing role of women in society, the absence of supportive family policies, economic uncertainty and the availability of assisted reproductive technologies (ARTs) (2).

While the impact of advancing female age on reproduction is widely recognized, very little is known regarding the influence of paternal age (3,4). Advanced maternal age is proved to be associated with decreased fertilization and implantation rates, just like higher miscarriages rates. This could be a consequence of the increase of chromosomal abnormalities in oocytes and embryos (5-8). Also increased rates of pregnancy complications, congenital anomalies or perinatal mortality were reported in literature (9,10). On the other hand, the effect of paternal age on both sperm characteristics and reproductive outcomes has not been adequately investigated.

The exact knowledge of paternal age role is fundamental for the correct counselling of older couples, in order to predict the successful chances of an ART treatment.

Previous studies have demonstrated that the quality of the semen in terms of volume (11), total sperm count (12), sperm motility (13), sperm morphology (14) or sperm DNA integrity (15) is inversely related with male age. This aspect can be possibly explained by sperm DNA damage due to methylation (16) and to exposure to reactive oxygen species (ROS) (17-19). Some recent papers indicate a direct correlation between men age and risk of DNA damage (20), spontaneous abortion (21), stillbirth (22), foetal death (23), birth defects (24), low birth weight, impaired neurocognitive development, epilepsy, schizophrenia, and several types of malignancies (25).

Although the evidence shows that age negatively affects seminal parameters, results of the impact of male age on the outcomes of assisted reproduction are conflicting (26,27).

This is because it can be difficult to assess the impact of paternal age by examining the reproductive outcomes in the whole population or in couples undergoing autologous in vitro fertilization (IVF) cycles. In this regard, maternal age and ovarian hyperstimulation, as well as embryo development represent possible bias (28). For this reason, the ovum donation model represents a better model since all the oocytes are collected from young women, reducing the confounding factor associated with the oocyte quality. Nevertheless, it is not possible to eliminate the adverse effects caused by endometrial aging or uterine factors (29).

Overall, the majority of reports assessing the effect of male aging on reproductive outcomes have not found statistically significant correlation between male age and rate of fertilization, implantation, pregnancy, miscarriage, or live birth (30-34).

Thus, the aim of our study was to assess the impact of paternal age on the oocyte-donation outcomes in intracytoplasmic sperm injection (ICSI) cycles, after selecting only cycles with overall oocyte survival rate greater than 85%.


Study population

Data of 278 couples who underwent fertility treatment at the ARTs Centre of the University of Florence (Italy) between January 2016 and December 2017 were retrospectively reviewed. All the patients gave a written consent to agree on having their data included into the study. All couples had a history of primary infertility with a severe female infertility factor, including diminished ovarian reserve, poor response to ovarian stimulation, chromosome aberration, repeated failure of IVF cycles or premature ovarian failure. In all cases, a donor egg was utilized to perform an ICSI cycle using ejaculated spermatozoa by fresh. Only couples with a donor egg program were included in this series in order to standardize female characteristics and to reduce all possible confounding factors associated with egg quality.

All anonymous oocyte donors were <25 years of age (range, 18–25 years) at the time of participation and fulfilled the standard screening criteria as outlined by the American Society of Reproductive Medicine (ASRM). All these women were healthy, had normal menstrual cycles and no gynaecological pathologies.

Inclusion criteria were: infertility from almost one year, presence of normal or sub-fertile seminal parameters in almost two seminal analyses (according to 2010 WHO guidelines), an overall oocyte survival rate after thawing greater than 85%. Only couples who underwent ICSI with fresh sperm were included in this series. Azoospermia, hypogonadism, varicocele, retractile testes or previous testicular torsion, concomitant urogenital infections, previous chemotherapy or radiotherapy, hematologic disorders, chronic inflammatory disease and drug therapy were exclusion criteria.

All couples performed a complete medical work-up including gynaecological evaluation and andrological assessment. Baseline characteristics of participants included recipient age, male age, height and weight with body mass index (BMI) count, smoking and drinking status. Drug consumption, previous diseases or surgery, history of cryptorchidism, medication, and comorbidities were extrapolated from the medical records. All men underwent a preliminary physical examination to assess testicular size and to exclude anomalies in the seminal tract. The hormonal profile, including follicle stimulating hormone (FSH), luteinizing hormone (LH), total testosterone (TT), estradiol (E2) and prolactin (PRL) was checked in all patients. Genetic screening to detect karyotype anomalies was carried out in all patients. Urine analysis and urine culture was carried out to rule out the presence of urinary tract infections. A semen culture test was performed when leukocyte cells were detected in the seminal fluid. Infection from human immunodeficiency virus, hepatitis B virus, hepatitis C virus, Cytomegalovirus, Treponema pallidum and Syphilis was excluded in all patients.

On the day of ICSI, fresh semen was obtained by masturbation after 3–5 days of sexual abstinence. Abstinence time, volume, pH, viscosity, total sperm count/mL, total sperm motility (progressive motility and non-progressive motility) and normal sperm morphology were the seminal parameters evaluated. Prior to ICSI cycle, spermatozoa underwent in vitro capacitation in order to select spermatozoa with good morphology and motility and to remove the seminal plasma. After this process, count/mL and motility were collected.

The study was conducted in accordance with the declaration of Helsinki and after obtaining the institutional review board approval (2018-017 CINECA 10189). The analysis did not require any additional exam and had no impact on patients’ health during the study.

The main outcome measures included fertilization rate (FR), cleavage rate (CR), pregnancy rate (PR), miscarriage rate and live birth rate. In order to investigate the impact of paternal age on the outcomes of ICSI, cycles were arbitrarily subdivided according to paternal age in group 1 (≤45 years) and group 2 (>45 years). Moreover, we used 70% FR as cut-off for group distribution according to the international seminar (The Vienna Consensus: report of an expert meeting on the development of ART laboratory performance indicators—ESHRE Special Interest Group of Embryology and Alpha Scientists in Reproductive Medicine), designed to establish consensus on definitions and recommended values for indicators for ART laboratory. Minimum performance values (“competence”) and aspirational values (“benchmarks”) were recommended for a total of 19 indicators, including 12 key performance indicators (KPIs), five performance indicators (PI) and two benchmarks.

Endometrial preparation of recipients, ICSI procedure and outcome measures

The programmed hormone replacement regimen consisted of oral contraceptive pill (OCP) with a single depot-dose of a GnRH agonist (triptorelin) (Decapeptyl® 3.75, Ipsen Spa, Milan, Italy) on days 20–21 of the cycle, followed by oral estradiol valerate (Progynova®, Bayer, Milan) 2 mg/day from day 2 through 6 of the menstrual cycle, 4 mg/day from days 7 to 10 and 6 mg/day on day 11 until embryo transfer. After endometrial preparation with estrogen, women received progesterone supplementation with 400 mg intravaginal capsules (Progeffik®/Proimetrium®) every 12 hours. Supplementation was started on the evening before the egg thawing and continued until the 10th week of gestation in case of pregnancy. All oocytes that had survived the thawing procedure were submitted for ICSI. Injected oocytes were incubated in 20 µL drops. All the zygotes were evaluated 16–18 hours after ICSI to confirm the presence of two distinct pronuclei. Subsequently, all the embryos were evaluated on days 2, 3, and 5 of the development using an inverted microscope with a Hoffmann modulation contrast system. The following parameters were recorded: number of blastomeres, percentage of fragmentation, variation in blastomere symmetry, presence of multinucleation, and defects in the zona pellucida and cytoplasm. High-quality cleavage-stage embryos were defined as those with all of the following characteristics: four cells on day 2 or 8–10 cells on day 3, <15% fragmentation, symmetric blastomeres, absence of multinucleation, colourless cytoplasm with moderate granulation and no inclusions, absence of perivitelline space granularity, and absence of zona pellucida dysmorphism (classified with the score A). Embryos lacking any of these characteristics were considered to be of low quality (score B–C). To evaluate blastocyst formation, embryos were given a score (1 to 4) according to their degree of expansion and hatching status, as follows: 1, an early blastocyst with a blastocoel that was less than half of the volume of the embryo; 2, a blastocyst with a blastocoel that was greater than half of the volume of the embryo; 3, an expanded blastocyst with a blastocoel that completely filled the embryo; 4, a hatching blastocyst. Expanded and hatching blastocysts were classified as complete blastocysts. Thereafter, ICSI outcomes, as well as FR, CR and PR were evaluated. The total and normal oocyte FR was calculated by total number of fertilized oocytes and “two-pronuclear” (2PN) fertilized oocytes by the number of injected oocytes, respectively. The CR was calculated by the number of embryos obtained by the number of normal fertilized oocytes. Embryos were transferred into the uterine cavity 48 to 72 or 120 hours after ICSI procedure. At our centre, embryo transfers are performed under transabdominal ultrasound guidance using a Wallace catheter. Our laboratory policy on transfer of donor oocytes embryos is to transfer two embryos, either on day 3 or 5, based on morphology. Supernumerary embryos are frozen. After 14 days, HCG test was performed. Clinical pregnancy was defined by HCG levels above 50 mU/L and documented by transvaginal ultrasound visualization of an intrauterine gestational sac with a heartbeat at around 5–6 weeks of gestation. Pregnancy loss before 20 weeks of gestation and all biochemical pregnancies were considered as miscarriages. Live birth rate was defined as the percentage of all cycles that lead to live birth.

Statistical analysis

The association between male age and both sperm parameters and reproductive outcomes were analysed. Continuous variables are presented as median and interquartile range (IQR) and differences between groups were assessed by the Student independent t-test or the Mann-Whitney U test on the basis of their normal or not-normal distribution, respectively (normality of variables’ distribution was tested by the Kolmogorov-Smirnov test). Age-adjusted linear regression analysis was performed to determine the relationship between numeric dependent and independent parameters, and logistic regression analysis was employed to determine significant predictors of pregnancy, FR >70% and cleavage. The study was conducted at a confidence level of 95%. All statistical analyses were completed using Stata software, version 14 (StataCorp. 2015. Stata Statistical Software: Release 14. College Station, TX, USA: StataCorp LP). For all statistical comparisons, significance was considered as P<0.05.


A total of 278 couples were included in the study. Overall, 1,724 frozen donor oocytes were obtained from Spain. After thawing, 1,642 oocytes survived, resulting viable and mature. Median overall oocyte survival rate was 100% (IQR, 85–100%). Baseline characteristics of the study cohort are depicted in Table 1. Median male age was 44±5.60 years (IQR, 31–70 years). Group 1 (≤45 years) included 166 men, group 2 (>45 years) 112 men. Recipients had a median age of 42±3.62 years (IQR, 29–50 years). No men suffered from medical conditions such as diabetes, cardiovascular disease and cancers. At baseline, all hormonal parameters collected were in the normal range. Mean right testicular volume, detected by Prader orchidometer scale was 18 mL (IQR, 10–25 mL), while mean left testicular volume was 17 mL (IQR, 6–25 mL). All patients had a normal urine analysis with a negative urine-culture and semen culture. Screening for sexual transmitted diseases was negative in all patients. Two hundred and seventy-eight fresh ICSI cycles were performed. “2PN” FR was 72.6%±0.20%. CR was 93.0%±0.16%. Clinical pregnancy per cycle was obtained in 110/278 cycles (overall PR, 39.6%). Miscarriage rate was 25.5%. Live birth rate per cycles was 29.5%. The great majority (89.2%) of the embryo transfers were performed on day 3. As shown in Table 2, comparison between group 1 and group 2 and FRs demonstrated a strong correlation with “2PN” FR, resulting 80.0% (IQR, 67.0–83.0%) and 67.0% (IQR, 50.0–80.0%) respectively (P<0.01). In addition, there were no significant differences between the two groups with respect to seminal parameters, except for a relationship between advanced male age and reduced total sperm motility (P=0.02).

Table 1
Table 1 Baseline characteristics of the study cohort
Full table
Table 2
Table 2 Comparison of clinical variables according to fertilization rate
Full table

As depicted in Table 3, the multivariate logistic regression analysis confirmed that there is a strong correlation between male age and FR (OR 0.87; P<0.01). CR and PR were not found to be related significantly with paternal age (P=0.417, 0.70 respectively). It was highlighted just a mild correlation between smokers (29.5%) and FR (OR 0.44; P=0.05). Comparison of clinical variables according to male age confirmed the significant association between “2PN” FR and age groups (P<0.01) (Table 4). Overall, comparison of clinical variables according to FR revealed that median BMI, smoking status and alcohol consumption were not related with FR (P=0.88, 0.12, 0.71 respectively) (Table 2).

Table 3
Table 3 Multivariate logistic regression analysis for factors associated with fertilization rate, cleavage rate and pregnancy rate
Full table
Table 4
Table 4 Comparison of clinical variables according to male age
Full table


Nowadays, the analysis of the association between male age and ART outcomes represents an important debated issue.

This retrospective study confirmed the impact of paternal age on reproductive outcomes of ICSI cycles with donor oocytes. Indeed, the results demonstrated a significant decline in FRs with advancing paternal age, in contrast with the evidences shown by the majority of previous studies.

Recently, various authors have focused on this topic (26-35). Overall, the majority did not identify a statistically significant association between paternal age and IVF outcomes. In particular, Bellver et al., in their study cohort including 1,412 IVF cycles, did not find any correlation between paternal age, implantation and FRs (26). Girsh et al. showed a tendency for decreased PR with advanced paternal age, but in this series no data about recipient’s age are available (33). A statistically significant correlation between advancing paternal age and FR was identified only in two studies. In particular, Duran et al. reported a statistically significantly reduced FR with advancing male age only in the ICSI case (12). Luna et al. instead found a statistically significantly lower rate of fertilization by conventional insemination in men older than 50 years, but no differences in the outcome of ICSI cycles (34).

In the current study, FRs were significantly lower in men older than 45 years (P<0.001). However, statistical association between paternal age and other IVF outcomes, including cleavage and PRs, was not detected. We arbitrarily divided men into two age groups (> or ≤45 years) in agreement with some previous data available in literature, suggesting an increased male-related infertility in men >40 of years (36).

Although the precise mechanism of how paternal age influences the IVF outcomes still remains unknown, previous research suggested that advancing age has several effects on DNA damage, chromatin integrity, gene mutations and aneuploidy in spermatozoa (37,38). Since it is generally accepted that part of the damaged sperm DNA can be repaired by the oocyte (39), the extent of DNA damage beyond the point of repair by the young oocyte could explain the impact of male age on severe male factor infertility. Moreover, an increased number of mutations in the sperm of older fathers may have subsequently increased adverse embryo development and IVF outcomes (37).

How shown by several studies, increasing male age could be associated with infertility (40), as well as decreased semen motility and volume (19,41). The largest of the studies demonstrated a significant relationship between paternal age and all sperm parameters analysed: for every additional 5 years of age, sperm volume decreased by 0.22 mL (P<0.001), concentration increased by 3.1 million sperm/mL (P=0.003), and percentage of motile spermatozoa decreased by 1.2% (P<0.001) (35). In our study, we found decreased semen volume and motility with increasing age, but we detected a statistically significant association between male age and total sperm motility (P=0.02).

We took as a reference the KPIs established in Vienna Consensus (ESHRE, 2017) and in the previous Alpha Consensus meeting (Alpha Scientists In Reproductive Medicine, 2012). Therefore, FR greater or equal to 70% was considered optimal, and the less than 70% was suboptimal.

In the current series, we selected cycles with overall oocyte survival rate greater than 85%, in order to reduce possible bias. The oocyte donation program represents a good method to reduce the confounding factors, since the quality of donor oocytes should be considered excellent. Nevertheless, other factors related to recipient’s age play a key role in ICSI success, such as the endometrial factor that could affect the outcome through implantation success (42,43). Since our recipients had a median age of 42 years, the endometrial receptivity could become a determinant of clinical pregnancy and explain the absence of correlation between male age and PR, how shown in our records.

In the current study the impact of BMI, smoking status and drinking habits on the outcomes of ICSI were analyzed (44). However, no significant correlation was found.

The current series has some strength and limitations. One strength was the inclusion of cycles with oocyte survival rate greater than 85%. As a result, the sample size of our study cohort was small. The standardization of donor stimulation protocols, recipients’ endometrial preparation and sperm sample evaluation strengthens our results.

However, further larger prospective studies are needed to investigate the relationship between sperm DNA damage, aneuploidy, gene mutations, chromatin integrity and reproductive outcomes in older couples.


This study showed the significant role of paternal age in determining the outcomes of ICSI when the oocytes are young and healthy. FR seemed to be the major determinant of morphological embryo quality in IVF cycles. Accordingly, it would be recommended to pay more emphasis on the advancing male age when counselling older couples who undergo egg donation program.




Conflicts of Interest: The authors have no conflicts of interest to declare.

Ethical Statement: The study was conducted in accordance with the declaration of Helsinki and after obtaining the institutional review board approval (2018-017 CINECA 10189). Written informed consent was obtained from all the patients for publication of this manuscript and any accompanying images.


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Cite this article as: Cito G, Coccia ME, Picone R, Cocci A, Russo GI, Garaffa G, Fucci R, Bertocci F, Borrani E, Basile V, Micelli E, Criscuoli L, Serni S, Carini M, Natali A. Impact of advanced paternal age on the intracytoplasmic sperm injection (ICSI) outcomes in donor egg cycles. Transl Androl Urol 2019;8(Suppl 1):S22-S30. doi: 10.21037/tau.2018.12.13