Medical Theraphy of Idiopathic OAT Hyun-Joo Kim M.D. Department of Urology Pochon CHA University
Medical Theraphy of Idiopathic OAT Current Treatment Modalities Considerations Mission
OAT as a Diagnosis? Concept of OAT ≒ FEVER OAT is a Phenomenon !
Criteria of OAT on Semen Analysis Oligospermia<20x10 6 /ml (WHO) severe<5x10 6 /ml crypto<1x10 6 /ml a fewmotile or immotile Astheno<50% (WHO) severe<10% Terato<30% (WHO) <14% (Strict Criteria) severe< 4%(Strict Criteria)
Idiopathic v.s Specific Specific Causes Secondary Hypogonadism Varicocele Retrograde Ejaculation Infections Immunologic Infertility Idiopathic Causes All unknown causes
Prevalence of Male Infertility Normal/OAT84.3% Azoospermia15.7% a Obstructive 6.3% b Non-obstructive 9.4% c a. 981/6242 semen analysis ( ) b. 165/416 testis bx ( ) c. 251/416 testis bx ( ) from CHA
Prevalence of Abnormal Semen Parameters All parameter43% Motility39% Oligospermia10% Morphology 8% from Greenberg, 1987
Specific Causes v.s Idiopathic Varicocele39% Obstructive 8% Mechanical 8% Endocrine 6% Developmental 5% Immunologic 1% Idiopathic33% from Schlegel and Pavlovich, 1997
Current Management Modality of Idiopathic OAT Pharmacological Sperm processing ART
Management Idiopathic OAT: Pharmacological Treatment Hormonal Treatment GnRH HCG/HMG Purified or recombinant FSH Androgens Anti-Estrogens Non-Hormonal Treatment Kallikrein Bromocriptine Anti-Oxidant: Vit. C or E
Spermatogenesis I
Meta-Analysis of Medical Treatment in OAT Antiestrogens n=459 FSH n=223 Androgens n=1025 Kinin enhancing agents n=197 odds ratio
Role of FSH ( in Monkey) Normal Normal + FSH Hypophysectomy + T Hypophysectomy + T + FSH
FSH on Spermatogenesis I Quantitative Influence Increase A-pale spermatogonia Spermatocyte, Spermatid Qualititative Influence Restore defective spermatozoal maturation (esp. acrosomal cap) For adequate concentration of intratubular Testosterone LH for T, FSH for ABP
FSH on Spermatogenesis II Stimulate Sertoli cell to enhance FSH dependent functions Support spermatogenesis without interfering negatively with Leydig cell physiology and without locally increasing Estrogen level Modulate intra-testicular paracrine and autocrine mechanism
Variable Results of FSH Treatment Dose: may not high enough Frequency : short half-life Duration : too short Reduction in FSH receptor activity Low proliferative activity of A-pale spermatogonia Elevated endogenous level of FSH
Management Plan for Idiopathic OAT I Considerations: Female factor, Severity of OAT, Previous Treatment, P/E Oligo: T.Vol.(normal), FF(-): Empirical Tx > 3mos. T.Vol.<10cc or FF(+): ART Severe OAT: ART A few motile/immotile: ICSI p.r.n) oocyte freezing Astheno: >10%, FF(-): Empirical Tx > 3mos. or IUI 3mos. or ICSI p.r.n) T-Bx 0%: Vital >20-30% : ICSI Vital <10% : TESE-culture
Management Plan for Idiopathic OAT II Terato: General condition control Empirical Tx > 3mos. + IUI Severe Terato: General condition control Empirical Tx > 3mos. p.r.n) IUI or ICSI FF(+): ICSI
Treatment of Male Infertility? Relative Concept of FERTILITY Consider Cumulative P.R Natural Pregnancy or ART?
Cumulative Live Birth Rate 52.5%/36mos. 25.2%/36mos. From Kamischke, 1999
Male Fecundity from Schrader, 1988 Intra-and inter-individual variation of semen parameters in human, coefficient of variation Semen parameters COA of Individual Intra – individual Inter- Individual Concentration4479 Normal forms1419 Motile sperm4526 Linear progression 1619
Drugs, Chemical, and Metabolites possible to exert toxic actions on the male gonad Parent compoundUsageMetabolites Amiodaroneanti-arrhythmiaDesethylamiodarone Cephalosporin analoguesanti-microbial drugN-Methyltetrazolethiol Valproic acidanti-epileptic drugIsomers of 2-ethyl hexanol(?) Diethylhexyl phthalateplasticizerMono-ethylhexylphthalate (MEHP) (DEHP)2-ethyl hexanol(?) DibromochloropropanefungicideDichloropropene derivatives (?) (DBCP) Ethylene glycolindustrial solvent2-Methoxyacetaldehyde (MALD) monoethyl ether n-Hexaneenvironmental toxicant2,5-Hexanedione Acrylamideindustrial useN-Methylacrylamide, N-isopropylacrylamide VinclozolinfungicideButenoic acid derivatives enanilide metabolite 1. Only substituent is a testicular toxin, not cephalosporin 2. Questionable testicular toxin but probably teratogenic from Thomas, 1996
Environmental/Lifestyle factors to affect male fertility Cigarette smoke Ingestion of female sex hormones Exposure to heavy metals(i.e. lead, arsenic) Alcohol Marijuana, anabolic steroids, cocaine Cancer chemotherapeutics Radiation exposure Increased testicular temperature Stress Lack of exercise Caffeine
Medical Treatment of OAT : Anti-Estrogens
Medical Treatment of OAT : FSH
Causes of Male Infertility Pre-Testicular Disorders of H-P-G axis Testicular Spermatogenic Defects Post-Testicular Epididymal Dysfunction Obstructive change of passage Infection of Accessary glands
Prevalence of Male Infertility Pre-Testicular 8% Testicular80% (Idiopathic > 25%) Post-Testicular12% from Sigman, 1987
Spermatogenesis I
Testicular Causes: Spermatogenic Defects Germ cell Defects Somatic cell Defects Communications Defects
Testicular expression of cytokines CytokinesProductionReceptor Leydig cellSertoli cellGerm cells IL-1L, S,G+++ IL-6L, S,++? TNFa G?+? IFN P,S,Gnnn c-kit ligand S+n+ EGF/TGFaL,P,S,G+++ TGFb P,S+++ ActivinL,P,S+++ InhibinL, S+++ IGF-IL,P,S,G+++ FGFL,P,S,G+++ NGF Gn+- PDGFL, S++-
Function of Testis Dependent on Gonadotropins and Correct action of local growth factors Major system Endocrine System Local factors depend on Endocrine system “act as an adjusted fine local relay for the endocrine system”
Spermatogenic Defects OAT from Inadequate Gonadotropin activity Imbalance in the intratesticular paracrine regulation Mystery
Possible Diagnostic Tools of Spermatogenic Defects Sperm chromosomal study Gonadotropin assay Germ cell and Somatic cell activity study Receptors study
Medical Treatment of idiopathic OAT For the good results of treatment, Pt. SELECTION by Correct Diagnosis is mandatory !