Young male patients undergoing cardiac surgery may require oral anticoagulation with warfarin either lifelong, such as after mechanical valve replacement, or for a limited postoperative period, for example following valve repair or bioprosthetic valve implantation. Although the teratogenic effects of warfarin during pregnancy are well established, prospective clinical data on the potential impact of warfarin therapy on male reproductive health are scarce. This gap is particularly relevant for patients of reproductive age who may have a present or future desire for fatherhood. Warfarin acts as a vitamin K antagonist by inhibiting the vitamin K epoxide reductase complex, thereby reducing the availability of functional vitamin K. Beyond its role in coagulation, vitamin K is increasingly recognized as an important regulator of spermatogenesis, mitochondrial function, oxidative balance, and steroid hormone synthesis. Experimental and translational evidence suggests that disruption of vitamin K-dependent pathways may impair sperm quality, DNA integrity, mitochondrial bioenergetics, and reproductive hormone homeostasis. In addition, warfarin exposure has been associated with increased oxidative stress and inflammatory responses, both of which are known contributors to male infertility. Despite these biologically plausible mechanisms, no prospective observational studies have systematically evaluated semen parameters, sperm DNA fragmentation, hormonal profiles, inflammatory markers, and advanced molecular sperm alterations in men exposed to warfarin after cardiac surgery. Consequently, structured andrological assessment is rarely incorporated into routine preoperative counseling or postoperative follow-up in this population. This prospective pilot observational study aims to investigate the association between warfarin therapy and male reproductive health in patients undergoing elective cardiac surgery. Male patients aged 18 to 50 years will be enrolled and observed in three cohorts based on clinical indication for anticoagulation: (1) long-term warfarin therapy following mechanical valve replacement; (2) short-term warfarin therapy (approximately three months) after selected cardiac procedures; and (3) a control cohort undergoing cardiac surgery without an indication for long-term oral anticoagulation beyond standard perioperative prophylaxis. Participants will undergo comprehensive andrological assessments at baseline and during follow-up up to 12 months after surgery. Evaluations will include semen analysis according to World Health Organization guidelines, assessment of sperm DNA fragmentation, reproductive hormonal profiles, and seminal inflammatory markers. Exploratory analyses will assess mitochondrial function, oxidative stress, and molecular alterations in spermatozoa. Detailed warfarin exposure data, including dose, cumulative exposure, international normalized ratio values, and time in therapeutic range, will be collected to explore potential exposure-response relationships. As a pilot study, the primary aims are to assess feasibility and generate preliminary clinical evidence to inform future larger studies. The findings may contribute to improved clinical counseling, fertility preservation strategies, and integration of reproductive health considerations into the multidisciplinary management of young male cardiac surgery patients.
This prospective, comparative, pilot observational study is designed to investigate the effects of warfarin therapy on male reproductive health in patients undergoing elective cardiac surgery, integrating conventional andrological assessment with inflammatory, hormonal, and exploratory molecular analyses. Young male patients undergoing cardiac surgery may require oral anticoagulation with warfarin either lifelong, most commonly after mechanical heart valve replacement, or for a limited postoperative period following selected procedures such as valve repair or bioprosthetic valve implantation. Although the teratogenic effects of warfarin during pregnancy are well established, prospective clinical data addressing its potential impact on male reproductive health are scarce. This knowledge gap is particularly relevant for patients of reproductive age who may have a present or future desire for fatherhood and for whom fertility-related counseling is increasingly important. Warfarin exerts its anticoagulant effect through inhibition of the vitamin K epoxide reductase (VKOR) complex, resulting in reduced availability of biologically active vitamin K. Beyond its role in coagulation, vitamin K-dependent pathways are involved in key aspects of male reproductive physiology, including spermatogenesis, mitochondrial bioenergetics, oxidative stress regulation, inflammatory signaling, and steroid hormone synthesis. Experimental and translational evidence suggests that disruption of these pathways may impair semen quality, sperm DNA integrity, mitochondrial function, and endocrine homeostasis, while promoting oxidative stress and inflammatory responses known to contribute to male infertility. However, these mechanisms have not been systematically explored in prospective clinical studies involving men exposed to warfarin after cardiac surgery. The study adopts a prospective cohort design with a comparative approach and includes three groups of male patients stratified according to clinical indication for anticoagulation: (1) patients receiving long-term warfarin therapy following mechanical valve replacement; (2) patients receiving short-term postoperative warfarin therapy, typically for approximately three months, after selected cardiac surgical procedures; and (3) a control group undergoing cardiac surgery without indication for long-term oral anticoagulation beyond standard perioperative prophylaxis. This design allows evaluation of different exposure patterns, including chronic exposure, transient exposure, and non-exposure, and supports exploratory assessment of exposure-response relationships and reversibility after treatment discontinuation. Participants undergo structured and standardized andrological evaluations at baseline (preoperative) and during longitudinal follow-up up to 12 months after surgery. Conventional semen analysis is performed according to World Health Organization (WHO) guidelines and includes assessment of sperm concentration, progressive motility, morphology, and related semen parameters. Sperm DNA integrity is evaluated through measurement of the sperm DNA fragmentation index (DFI) using the sperm chromatin dispersion (SCD) assay. Reproductive endocrine function is assessed through serial measurement of serum reproductive hormones, including follicle-stimulating hormone (FSH), luteinizing hormone (LH), total testosterone, sex hormone-binding globulin (SHBG), prolactin, and thyroid-stimulating hormone (TSH), using standardized laboratory immunoassay methods. Local inflammatory processes within the male reproductive tract are investigated through assessment of seminal inflammatory mediators, including interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), prostaglandin E2 (PGE2), and prostaglandin F2α (PGF2α). These biomarkers are measured using standardized enzyme-linked immunosorbent assay (ELISA) techniques and evaluated in relation to semen quality parameters. To provide mechanistic insight beyond conventional clinical and laboratory assessments, exploratory molecular analyses are performed on spermatozoa. These analyses include evaluation of mitochondrial function and bioenergetics, assessment of oxidative stress-related parameters, and analysis of selected proteins involved in sperm energy metabolism and motility, using validated laboratory techniques. These exploratory investigations are intended to characterize molecular alterations potentially associated with warfarin exposure and to generate hypotheses for future mechanistic studies. Detailed warfarin exposure data are collected prospectively from clinical records and anticoagulation monitoring systems, including daily and cumulative dosing information, international normalized ratio (INR) measurements, and quality of anticoagulation control over time as reflected by time in therapeutic range (TTR). These exposure variables are used to support exploratory correlation analyses with reproductive, inflammatory, and molecular outcomes, as well as evaluation of potential reversibility of observed alterations in patients receiving short-term warfarin therapy after treatment discontinuation. Sexual and reproductive function is further characterized through validated questionnaires assessing sexual function, including the International Index of Erectile Function-5 (IIEF-5), and through collection of exploratory reproductive outcomes, such as desire for paternity and occurrence of partner pregnancies during follow-up. As a pilot study, the primary objectives are to assess feasibility, characterize longitudinal changes in male reproductive parameters, and generate preliminary clinical and mechanistic data to inform the design of future larger-scale studies. The findings are expected to contribute to improved fertility-related counseling, consideration of fertility preservation strategies, and integration of reproductive health assessment into the multidisciplinary management of young male patients undergoing cardiac surgery.
Study Type
OBSERVATIONAL
Enrollment
90
Participants undergo standardized study assessments including semen analysis according to WHO criteria, sperm DNA fragmentation assessment, hormonal blood tests, andrological ultrasound, and exploratory molecular analyses of spermatozoa (mitochondrial function, oxidative stress markers, inflammatory mediators, and protein expression). All assessments are performed for observational and research purposes only and do not guide or modify clinical treatment.
Città di Lecce Hospital - Department of Cardiac Surgery
Lecce, LE, Italy
Change in sperm concentration over time
Change in sperm concentration expressed as millions of spermatozoa per milliliter (millions/mL), assessed by standard semen analysis performed according to World Health Organization (WHO) guidelines. Correlation between warfarin exposure status (long-term exposure, short-term exposure, or no exposure) and changes in sperm concentration over time will be evaluated.
Time frame: Baseline (T0) to 6 months (T2) and 12 months (T3)
Change in progressive sperm motility over time
Change in progressive sperm motility expressed as percentage (%), assessed by standard semen analysis according to World Health Organization (WHO) guidelines. Correlation between warfarin exposure status (long-term exposure, short-term exposure, or no exposure) and changes in progressive sperm motility over time will be evaluated.
Time frame: Baseline (T0) to 6 months (T2) and 12 months (T3)
Change in sperm morphology over time
Change in the percentage (%) of spermatozoa with normal morphology, assessed using strict criteria as part of standard semen analysis according to World Health Organization (WHO) guidelines. Correlation between warfarin exposure status (long-term exposure, short-term exposure, or no exposure) and changes in sperm morphology over time will be evaluated.
Time frame: Baseline (T0) to 6 months (T2) and 12 months (T3)
Change in sperm DNA fragmentation index (DFI)
Change in sperm DNA fragmentation index (DFI), assessed using a validated assay (sperm chromatin dispersion method), between baseline and follow-up timepoints in warfarin-exposed and control groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in serum follicle-stimulating hormone (FSH) levels
Change in serum follicle-stimulating hormone (FSH) levels, measured in international units per liter (IU/L) using standard immunoassay methods, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in serum luteinizing hormone (LH) levels
Change in serum luteinizing hormone (LH) levels, measured in international units per liter (IU/L) using standard immunoassay methods, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in serum total testosterone levels
Change in serum total testosterone levels, measured in nanograms per deciliter (ng/dL) using standard immunoassay methods, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in serum sex hormone-binding globulin (SHBG) levels
Change in serum sex hormone-binding globulin (SHBG) levels, measured in nanomoles per liter (nmol/L) using standard immunoassay methods, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in serum prolactin levels
Change in serum prolactin levels, measured in nanograms per milliliter (ng/mL) using standard immunoassay methods, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in serum thyroid-stimulating hormone (TSH) levels
Change in serum thyroid-stimulating hormone (TSH) levels, measured in milli-international units per liter (mIU/L) using standard immunoassay methods, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between mean daily warfarin dose and changes in semen parameters
Correlation between mean daily warfarin dose, expressed in milligrams per day (mg/day), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines, in warfarin-exposed patients.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between cumulative warfarin dose and changes in semen parameters
Correlation between cumulative warfarin dose, expressed in milligrams (mg), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines, in warfarin-exposed patients.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between time in therapeutic range and changes in semen parameters
Correlation between time in therapeutic range (TTR), expressed as percentage (%), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines, in warfarin-exposed patients.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between warfarin exposure and changes in sperm DNA fragmentation index
Correlation between warfarin exposure variables (mean daily dose \[mg/day\], cumulative dose \[mg\], and time in therapeutic range \[%\]) and changes from baseline in sperm DNA fragmentation index (DFI), expressed as percentage (%), assessed using the sperm chromatin dispersion (SCD) assay.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Reversibility of changes in semen parameters after short-term warfarin discontinuation
Evaluation of reversibility of changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines, between 3 and 6 months after surgery (T1 to T2), in patients receiving short-term warfarin therapy.
Time frame: From 3 to 6 months after surgery (T1 to T2)
Reversibility of changes in sperm DNA fragmentation index after short-term warfarin discontinuation
Evaluation of reversibility of changes from baseline in sperm DNA fragmentation index (DFI), expressed as percentage (%), assessed using the sperm chromatin dispersion (SCD) assay, between 3 and 6 months after surgery (T1 to T2), in patients receiving short-term warfarin therapy.
Time frame: From 3 months (T1) to 6 months (T2) after surgery
Correlation between seminal interleukin-6 (IL-6) levels and semen parameters
Correlation between seminal interleukin-6 (IL-6) concentration, measured using a standardized enzyme-linked immunosorbent assay (ELISA), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between seminal tumor necrosis factor-alpha (TNF-α) levels and semen parameters
Correlation between seminal tumor necrosis factor-alpha (TNF-α) concentration, measured using a standardized enzyme-linked immunosorbent assay (ELISA), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between seminal prostaglandin E2 (PGE2) levels and semen parameters
Correlation between seminal prostaglandin E2 (PGE2) concentration, measured using a standardized enzyme-linked immunosorbent assay (ELISA), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Correlation between seminal prostaglandin F2α (PGF2α) levels and semen parameters
Correlation between seminal prostaglandin F2α (PGF2α) concentration, measured using a standardized enzyme-linked immunosorbent assay (ELISA), and changes from baseline in semen parameters assessed by standard semen analysis according to World Health Organization (WHO) guidelines.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Exploratory assessment of mitochondrial function in spermatozoa
Exploratory evaluation of mitochondrial function in spermatozoa, assessed using validated bioenergetic assays evaluating mitochondrial respiratory activity and related functional parameters.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Exploratory assessment of oxidative stress markers in spermatozoa
Exploratory evaluation of oxidative stress-related parameters in spermatozoa, assessed using validated assays measuring reactive oxygen species production and lipid peroxidation markers.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Exploratory assessment of sperm protein expression involved in bioenergetics and motility
Exploratory evaluation of the expression of selected sperm proteins involved in bioenergetics and motility, assessed using validated protein analysis techniques.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Change in sexual function assessed by the International Index of Erectile Function-5 (IIEF-5)
Change in sexual function assessed using the International Index of Erectile Function-5 (IIEF-5) questionnaire, expressed as total score on a validated scale, evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Desire for paternity over time
Assessment of desire for paternity, recorded as a categorical variable (presence or absence of desire for fatherhood), evaluated over time and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
Occurrence of partner pregnancies during follow-up
Occurrence of partner pregnancies during the follow-up period, assessed as incidence of pregnancies reported by participants and compared between study groups.
Time frame: Baseline (T0), 3 months (T1), 6 months (T2), and 12 months (T3)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.