Spinal cord injured (SCI) men, para or tetraplegic, most often have an infertility, caused among others by a deficiency of sperm quality particularly motility and vitality. Several mechanisms have been proposed: low frequency of ejaculation, recurrent urinary tract and seminal infections, presence of an inflammatory syndrome (IS) and an oxidative stress (OS). However, no French study of sperm quality has been conducted in this population that could identify aggravating factors of sperm quality and a way to prevent them. Hypothesis: Sperm parameters decrease rapidly following spinal cord injury and next stabilise. However, unidentified yet risk factors could influence long-term evolution of sperm parameters. The objective is to study the evolution of sperm parameters during 18 months taking into account bladder management, recurrent urinary tract and bladder infections, IS and OS. The evaluation of these parameters and their consequences will be indicative to determine one or more risk factors of sperm degradation and determine a strategy for long term support to avoid the use of ART either by sperm cryopreservation and/or by preventing risk factors
SCI men are mostly young adults who have not completed their parental project. Infertility has many causes: erectile dysfunction, anejaculation (85% of SCI ) and altered sperm parameters. Penile vibratory stimulation allows 75 % of the sperm collection. If sperm quality is sufficient, intravaginal insemination of their partner at home is possible. The use of AMP remains common, which is damaging to men non sterile priori. In SCI, sperm concentration remains satisfactory but mobility and vitality are impaired. The installation of this irreversible degradation likely occurs very quickly after the trauma. The possible deterioration of sperm parameters with time is not known. The following pathophysiological mechanisms have been proposed: i) increased scrotal temperature, ii) decreased ejaculatory frequency, iii) recurrent urinary tract and seminal infections, iv ) inflammation and oxidative stress in the semen. Patients, and even rehabilitation doctors often submit an application for preventive sperm conservation but in the absence of prospective longitudinal data on the evolution of sperm quality of SCI men over the time and identified risk factors of degradation, the indication and timing of preventive cryopreservation remain to be defined. Hypothesis: The sperm parameters, mobility and vitality, in SCI patients with or without penile vibratory stimulation (PVS), decrease in the immediate aftermath of trauma and next stabilize out the occurrence of intercurrent medical events or symptomatic urogenital infections. However, unidentified yet risk factors could influence long-term evolution of these sperm parameters. Main objective: Monitoring the evolution of sperm parameters for 18 months: concentration, mobility, vitality, sperm morphology, inflammatory syndrome and oxidative stress on 4 ejaculates collected by masturbation or SVP at 6-month intervals. Secondary objectives: In case of impaired sperm quality, identify risk factors for this change. SCI men will have 4 medical visits associated to sperm retrieval spaced to 6 months during 18 months. At each visit medical and reproductive informations will be collected. Knowledge of the evolution of sperm parameters and risk factors of its degradation over time must answer with the criteria of "evidence based medicine" the request of sperm cryopreservation frequently expressed by SCI patients. This study should lead to the optimization of the management of infertility in patients with spinal cord injuries and giving directions for research aiming to prevent the degradation of sperm parameters. Finally, this study should provide the rationale for future research on clinical risk factors and / or biological degradation of sperm and biological markers of risk of degradation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
35
penile vibratory stimulation (PVS) or masturbation
Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Department of Biology of Reproduction
Paris, France
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart.
Time frame: 18 month
spermogram
Sperm concentration, mobility and morphology
Time frame: 18 months
elastase
Measure of inflammation
Time frame: 6 month
DNA fragmentation
Sperm DNA integrity, measures oxidative stress
Time frame: 18 months
8 Hydroxydesoxyguanosine (8OHdG)
Oxydative stress
Time frame: 18 months
Seminal biochemistry
Secretion of seminal tract
Time frame: 18 months
Urinary and seminal infections
Bacteriological analysis of sperm and urine
Time frame: 18 months
Mode of urinary catheter
Time frame: 18 months
Spinal cord injury type
Type and level of the lesion
Time frame: 0 months
Concomitant treatments
Time frame: 18 months
Patient age and time to spinal cord injury
Time frame: 18 months
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart.
Time frame: 6 months
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart.
Time frame: 12 months
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart.
Time frame: 0 months
elastase
Measure of inflammation
Time frame: 0 month
elastase
Measure of inflammation
Time frame: 12 month
elastase
Measure of inflammation
Time frame: 18 month
spermogram
Sperm concentration, mobility and morphology
Time frame: 0 months
spermogram
Sperm concentration, mobility and morphology
Time frame: 6 months
spermogram
Sperm concentration, mobility and morphology
Time frame: 12 months
DNA fragmentation
Sperm DNA integrity, measures oxidative stress
Time frame: 0 month
DNA fragmentation
Sperm DNA integrity, measures oxidative stress
Time frame: 6 months
DNA fragmentation
Sperm DNA integrity, measures oxidative stress
Time frame: 12 months
8 Hydroxydesoxyguanosine (8OHdG)
Oxydative stress
Time frame: 0 months
8 Hydroxydesoxyguanosine (8OHdG)
Oxydative stress
Time frame: 6 months
Seminal biochemistry
Secretion of seminal tract
Time frame: 0 months
Seminal biochemistry
Secretion of seminal tract
Time frame: 6 months
Seminal biochemistry
Secretion of seminal tract
Time frame: 12 months
Urinary and seminal infections
Bacteriological analysis of sperm and urine
Time frame: 0 months
Urinary and seminal infections
Bacteriological analysis of sperm and urine
Time frame: 6 months
Urinary and seminal infections
Bacteriological analysis of sperm and urine
Time frame: 12 months
Mode of urinary catheter
Time frame: 0 months
Mode of urinary catheter
Time frame: 6 months
Mode of urinary catheter
Time frame: 12 months
Concomitant treatments
Time frame: 0 month
Concomitant treatments
Time frame: 6 months
Concomitant treatments
Time frame: 12 months
Patient age and time to spinal cord injury
Time frame: 0 month
Patient age and time to spinal cord injury
Time frame: 6 months
Patient age and time to spinal cord injury
Time frame: 12 months
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