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Infertility is defined as the inability of a couple to conceive despite trying for a year, and it affects approximately 15% of the reproductive-age population. It is considered a genetically lethal factor, as the family lineage stops at that individual with no progeny produced. A genetic defect associated with an infertile individual cannot be transmitted to the offspring, ensuring the maintenance of reproductive fitness of the species. However, with the advent of assisted reproductive techniques (ART), we are now able to overcome sterility and bypass nature’s protective mechanisms that developed through evolution to prevent fertilization by defective or deficient sperm.
The causes of male factor infertility are multifactorial, with estimates reaching 50% due to, or contributed by, genetic abnormalities (Table 1, Refs. 2–11).1 Although the majority of the genetic causes of male infertility are still unknown, genetic defects, such as cystic fibrosis, have important implications for offspring conceived through intracytoplasmic sperm injection (ICSI). However, in the absence of a comprehensive clinical evaluation, many of these genetic etiologies may go undiagnosed.
The foundation of diagnosis for males is the routine semen analysis (SA), where sperm concentration, motility, morphology, and the presence of other cells are evaluated. Indicators of patency and function of the male genital tract are assessed including semen volume, liquefaction time, pH, and the presence or absence of fructose. While the routine SA evaluates the ejaculate for abnormalities in the sperm number, morphology, and motility, it only provides clues and suggestions to indicate the need to pursue further testing. Current genetic testing performed for male infertility includes karyotype, CFTR gene analysis, PCR testing for Y-chromosome microdeletions, and sperm FISH analysis for specific chromosome aberrations.
The primary goals of the evaluation of the male presenting with infertility are to identify etiological conditions that can be reversed with resulting improvement of fertility status, medically significant and potentially dangerous diagnoses underlying the male’s infertility, genetic etiologies that may have implications for the patient and/or his offspring; and irreversible conditions that may be best managed with the use of assisted reproductive techniques (ART) or the recommendation of donor insemination or adoption. The genetic basis of male infertility, although relatively poorly understood, may ultimately represent one of the most clinically important aspects of male infertility (Table 2, Ref. 12). However, with the advent of IVF/ICSI, while these hurdles of infertility can be overcome, the underlying causes of infertility–defective genes–have the potential to be transmitted to offspring.
When faced with the evaluation of a man with azoospermia, the focus should be placed on deciphering between whether the azoospermia is a result of abnormal spermatogenesis or obstruction (Fig. 1).
In Mendelian recessive inheritance, each parent contributes one of two mutant alleles for a disease trait. However, if a mutant allele has a dominant effect, it requires inheritance of only one parental allele. If the genotypes of both parents in a genetic cross are known, Mendel’s principles of segregation and independent assortment can be used to determine the distribution of phenotypes expected for the population of offspring.
There are relatively few diagnosed genetic causes of male infertility. Diagnoses are largely descriptive and reflect the lack of understanding of the factors that regulate sperm production, maturation, and function. Endocrine factors are one of the components that are relatively well-established and have become an essential component of the male evaluation, with either an abnormal physical examination suggestive of a disorder in testosterone production and action, an abnormal semen examination, or evidence of impaired sexual dysfunction (Table 3). However, true endocrinologic causes of male infertility are relatively uncommon, being present in less than 3% of cases13 (Table 4).
The hypothalamic–pituitary–adrenal (HPA) axis, and the hormonal reproductive system, that is, the hypothalamic–pituitary–gonadal (HPG) axis, are intimately interlinked. The HPG axis is an important mediator of infertility. Stress can inhibit the HPG axis and negatively impact fertility. Abnormal development of the HPG axis can result in acquired hypogonadotropic hypogonadism (IHH) and Kallman syndrome (KS). Finally, spontaneously occurring mutations in the genes involved in the HPG axis, can also contribute to infertility.14,15
Kallmann syndrome (MIM308700) is a rare condition characterized by isolated hypogonadotropic hypogonadism (HH) and anosmia due to agenesis of the olfactory bulb; it occurs in approximately 1 in 10,000–60,000 live births.16 A subset of Kallmann syndrome, inherited in an X-linked fashion, is caused by a mutation of the KAL1 gene, which produces a cell adhesion molecule.17–19 Autosomal dominant inheritance is caused by mutations in FGFR1, FGFR8, PROKR2, and PROK2 genes.20–22 In about 75–80% of KS patients, the causative gene is unknown.
Androgen insensitivity syndrome (AIS, MIM300068) is an X-linked disorder caused by mutations in the androgen receptor (AR) gene (MIM313700), resulting in end-organ resistance to androgens. More than 800 different AR gene mutations, resulting in AIS have been reported. However, the mutation–receptor structure–function relationship is not yet fully understood. Thus, the phenotypes resulting from these mutations are not always predictable. The vast majority of androgen receptor mutations are single base substitutions, while deletions or insertions are rare. Most of these mutations are located in a few “hot spots” in the ligand-binding domain of the AR protein. About two thirds of these androgen receptor mutations are inherited in an X-linked fashion. The remainders of these mutations are either germ line or somatic de novo mutations. Somatic mutations can result in somatic mosaicism, where both mutant and wild-type receptors are expressed in different proportions.23
AIS is a disorder affecting sexual differentiation in variable severity, ranging from phenotypic females (complete AIS, CAIS) to defective spermatogenesis in otherwise normal males (partial AIS, PAIS, or minimal AIS, MAIS) depending on the type and localization of these mutations.24,25 Haploinsufficiency of the AR gene due to complete or partial gene deletions or nonsense and frameshift mutations usually lead to complete AIS. Splicing mutations or missense mutations, on the other hand, can result in diverse phenotypes that are impossible to predict. Alternative factors that can influence the phenotype include defects in the protein coactivators and corepressors, somatic mosaicism, and the length of polyglutamine (PolyGln) repeats in exon 1. There are at least 864 mutations known, of which 724 associated with AIS have been reported in the AR mutation database (www.mcgill.ca/androgendb). Until now, only 91 mutations have been reported in exon 1 of the AR gene in patients suffering from any form of AIS, despite the fact that it encodes for more than half of the AR protein. Interestingly, many patients presenting with clinical features of AIS do not have documented mutations in the AR gene and may have alternative defects in androgen signaling pathway. For example, defects in coregulators such as transcriptional intermediary factor 2 (TIF2)26–28 and AR coactivators29 are also implicated in the pathogenesis of AIS. Reduced AR transcription was also found in patients with AIS.30 Several mutations have been identified in the AR gene linked to endocrine dysfunction. Most of these mutations are due to loss-of-function of AR activity.
The expansion of the CAG trinucleotide repeats encoding the polyglutamine (PolyGln) tract, including the amino terminal transactivation domain of the AR protein, is involved in various neurodegenerative disorders. Spinal and bulbar muscular atrophy (SBMA, MIM313200) or Kennedy’s disease (Kennedy-Alter-Sung disease) is a rare inherited X-linked neurodegenerative disorder of motor neurons.31,32 SBMA usually affects males in the third decade. It is characterized by muscle cramps, fasciculations followed by weakness, and atrophy of the proximal limb and bulbar muscles.33–35 The severity of the disease correlates with the increased number of CAG repeats of the AR gene. Expansion over 38–62 repeats leads to degeneration of facial, hypoglossal, and spinal motor neurons with neurogenic wasting of the corresponding skeletal muscle. Clinically, patients with SBMA present with progressive AIS, severe oligozoospermia, infertility, testicular atrophy, and gynecomastia.32,36,37
SBMA is a member of a new class of trinucleotide repeat disorders (or PolyGln-related) and inherited neurodegenerative diseases38,39 that include Huntington’s disease (HD), several spinocerebellar ataxias (SCAs),40 and dentatorubral-pallidoluysian atrophy (DRPLA).41,42 These conditions are caused by gain-of-function mutations leading to accumulation of abnormal proteins with the PolyGln tract that produce neurotoxic effects and cause cell death of motor neurons,38 mostly in the anterior horns of the spinal cord and in the bulbar region of the brain stem.
Frequently, A43 and myotonic dystrophy (DM) (MIM160900) are associated with idiopathic azoospermia.44 DM is caused by a CTG trinucleotide repeat expansion in the 3′-untranslated region of the DM protein kinase gene (DMPK, MIM605377, 19q13.3). However, the results are controversial since one report found more than 18 repeats at the DM locus in azoospermia patients, and not in controls,45 while others have failed to find any differences.44 A less frequent cause of DM is an expansion of the CCTG repeat in intron 1 of zinc finger protein 9 (ZNF9, MIM116955, 3q13.3).46
Rare instances of isolated HH can also result from rare dominant or recessive mutations in GNRHR, KISS1R, NROB1, LEPR, TAC3, and TACR3 affecting the various components of the HPG axis.15 The effect of inactivating mutations of GNRHR has been associated with impaired LH/FSH secretion, HH, and delayed puberty in both males and females. Male patients present with microphallus and undescended testes in childhood. Inactivating mutations of LH receptors have also been described in both sexes. In men, the phenotype ranges from female genitalia to micropenis. Testicular biopsies show various degrees of Leydig cell hypoplasia with resultant oligozoospermia. Isolated selective LH hormone deficiency has been described in consanguineous families due to mutations in the luteinizing hormone β (LHB) gene, resulting in hypogonadism in both sexes.47 Recently, a polymorphism in the promoter of the follicle stimulating hormone β (FSHB) gene, which is associated with hypogonadism has been identified in a young Estonian cohort.48
Prader-Willi syndrome (PWS) (MIM176270) is a complex genetic disorder caused by deficiency of one or more paternally expressed imprinted transcripts within chromosome 15q11-q13, affecting 1:25,000 live births. Thus, PWS is not usually inherited in a Mendelian fashion. PWS is characterized by hypothalamic dysfunction resulting in hypogonadism associated with delayed puberty, obesity, hypotonia, developmental delay, behavioral abnormalities, short stature, and genital abnormalities that include cryptorchidism, scrotal hypoplasia, and microphallus.49,50 PWS is a phenotypically variable disorder with regards to sexual maturation. Pubertal variability is common in most of the individuals who are unable to complete puberty, likely due to degeneration of GnRH secreting neurons.50,51 Fertility has not been documented in any male PWS patients to date. PWS infertility could be a result of multiple factors, including low pituitary-testicular axis hormones including FSH, LH, estradiol, testosterone, and inhibin B.52,53 PWS patients have low sexual libido with testicular histology varying from normal to Sertoli cell only.54
Klinefelter’s syndrome is the most common cause of hypogonadism and infertility in males (1 in 500). The classic Klinefelter’s syndrome is associated with a 47, XXY karyotype due to maternal or paternal meiotic nondisjunction. Maternal nondisjunction is associated with advanced maternal age.55 A variety of mosaic patterns constitute nearly 15% of the cases, most common being 46,XY/47,XXY and the remainder of cases are due to polysomy of X chromosome (48, XXXY or 49,XXXXY). Rare cases of Klinefelter syndrome are caused by isochromosome Xq i (Xq), or X-Y translocations in 0.3–0.9% of males with X chromosome polysomies.56,57 Clinically, patients with this syndrome present with azoospermia or severe oligozoospermia, gynecomastia in late puberty, atrophy and hyalinization of the seminiferous tubules, and elevated urinary gonadotropin levels.
Cystic fibrosis transmembrane conductance regulator (CFTR) gene-related disorders encompass a disease spectrum from focal male reproductive tract involvement in congenital bilateral absence of the vas deferens (CBAVD) to multiorgan involvement in classic cystic fibrosis. CFTR-related disorders are inherited in an autosomal recessive manner. Severe dysfunction of the CFTR gene causes cystic fibrosis (CF), a life-threatening disease manifesting with progressive lung disease. CBAVD, resulting in primary obstructive azoospermia is a well-recognized cause of male infertility.
The CFTR gene (MIM602421) is located on the long arm of chromosome 7q31.2 and contains 27 coding exons that spread over 230 kb.58 Its normal allele produces a 6.5-kb mRNA that encodes a 1480-amino acid integral membrane protein that functions as a regulated chloride channel in a variety of epithelial cells. The most common gene mutation is a 3-bp deletion, resulting in loss of a phenylalanine at amino acid position 508 of the CFTR polypeptide (ΔF508); this mutation accounts for about 30–80% of all mutant alleles depending on the ethnic group.59 CBAVD commonly results from the combination of two mutant alleles, one allele with severe CFTR mutation and a second allele with either a mild CFTR mutation or the common splicing mutant allele 5T.60
Young’s syndrome (MIM279000) is a condition characterized by respiratory infections, ranging from simple bronchitis to bronchiectasis, and obstructive azoospermia secondary to inspissated secretions, although spermatogenesis is unaffected. Due to the similarities, parallels to CBAVD secondary to mutations in the CFTR gene were noted; however, further investigations concluded that classical Young’s syndrome was unlikely associated with defects in CFTR.61,62
Men without clinically apparent pulmonary manifestations of CF may have CBAVD. Hypoplasia or aplasia of the vas deferens and seminal vesicles may occur either bilaterally or unilaterally. CBAVD does not pose a health risk per se to the affected men, and testicular development, function, and spermatogenesis are usually normal. CBAVD is commonly identified during evaluation of infertility or as an incidental finding at the time of a surgical procedure, such as orchidopexy. However, the genetic fundamental basis of CBAVD has a significant impact on ART. For fathers with CBAVD, spermatogenesis may be normal, though it is imperative to determine whether the female partner is a carrier of the CFTR mutation as their offspring will be at increased risk of transmitting infertility to their male offspring or cystic fibrosis to both male and female offspring.
The treatment options include both microsurgical epididymal sperm aspiration (MESA) and testicular sperm extraction (TESE), or donor sperm in conjunction with ICSI to treat men with obstructive azoospermia (Fig. 1). Genetic counseling is standard in family planning for male factor couples with CBAVD.
Asthenozoospermia (AZS) or reduced sperm motility is defined by the proportion of motile spermatozoa in semen (usually <40%). It is one of the four major semen defects found in at least half of infertile men. AZS is one of the phenotypes present in primary ciliary dyskinesia (PCD) (MIM242650), a predominantly autosomal recessive condition characterized by ciliary dysfunction and impaired mucociliary clearance that causes respiratory tract infections and infertility. The most severe form, Kartagener’s syndrome (KS), presents in combination with situs inversus (MIM244400). The incidence of PCD is estimated at 1:16,000 births with KS accounting for 50% of the cases. A high percentage of PCD males are infertile, and the majority of cases of KS are due to immotility or dysmotility of the spermatozoa; however, the penetrance of the defect varies among individuals. PCD is caused by different structural abnormalities in dynein arms of axoneme, the internal structure of cilia and flagella responsible for their motility. The axonemal structure is highly conserved through evolution and consists of a complex made of a central pair of two microtubules and nine outer-doublet microtubules with attached inner and outer dynein arms (9 + 2 structure).63 There are more than 250 genes involved in the structure, assembly, and regulation of a cilium; however, only three genes have been associated with PCD: DNAI1 (MIM603332; 9p21-p13), DNAH5 (MIM603335; 5p15.2), and DNAH11 (MIM603339; 7p21). Recent screening in 90 non-syndromic AZS patients and 200 controls revealed one mutation in each of the three dynein genes in seven patients, all inherited from their mothers.64
Sperm motility requires an increase in the concentration of intracellular calcium ions.65 Several calcium channel genes residing in the sperm may be responsible for infertility. The CATSPER gene family (CATSPER1–4) is a unique cation channel expressed exclusively in sperm. CATSPER2 (MIM607249) (expressed in the sperm and inner ear) together with STRC, KIAA0377, and CKMT1B are associated with deafness-infertility syndrome (DIS) (MIM61102) due to a homozygous contiguous gene deletion at 15q15.3. Four families have been identified with homozygous deletions in this area that cause deafness and sperm dysmotility.66,67 CATSPER1 (MIM606389; 11q12.1), a gene responsible for infertility in mice due to lack of sperm motility, has been mutated in infertile men of two consanguineous families.68,69 Two separate insertion mutations that lead to frameshifts and a premature stop codon in CATSPER1 were found in three infertile Iranian men, and absent in 576 Iranian controls.68
SPAG16 (MIM612173; 2q34), which encodes a protein from the axoneme central apparatus, is associated with ciliary dyskinesia and mouse infertility due to impaired sperm motility.70 In humans, two fertile males heterozygous for the SPAG16 mutation were reported with only one having sperm count and motility levels significantly below the normal range. SPAG16 likely influences the stability of protein interactions in the sperm axoneme; however, it may be not significant enough to cause infertility.71
Another family of proteins important for axoneme stability and structure are the tektins, playing a fundamental role in ciliary movement. A screening of 90 nonsyndromic AZS patients for TEKT2 (MIM608953; 1p35.3-p34.1) revealed a heterozygous mutation in one patient that was maternally inherited.72 Dysplasia of the fibrous sheath (DFS) is a genetic sperm defect with hypertrophy and hyperplasia of random fibrous sheath associated with classical dynein arm deficiency in spermatozoa. Mutations in the cyclic-dependent protein kinases AKAP3 (MIM604689; 12p13.3) and AKAP4 (MIM300185; Xp11.2), the most abundant structural proteins of the sheath, were found in an AZS patient indicating the importance of motility of the sperm for fertility.73 These are examples of Mendelian inheritance of nonsyndromic male infertility. Most of the mutations are heterozygous displayed by the variable penetrance.
Currently, there are numerous mouse models described that manifest asthenozoospermia (Table 5). These models provide growing evidence that a myriad of the gene products influence spermatozoal motility in mammals, and defects in many human genes could result in spermatozoal immotility. Moreover, recent proteomic studies estimate that several hundred genes encode structural proteins of the flagellum, the axoneme fibrous sheath, outer dense fibers, and enzymes of the glycolytic machinery in spermatozoa and could therefore be considered as additional gene candidates for AZS in human males.74,75
Oligozoospermia (OZS), or reduced sperm count, is one of the most common categories of semen defects and is found in nearly half of infertile men. According to the World Health Organization, OZS is defined as a sperm concentration with less than 20 × 106 sperm/mL.125 However, several prominent studies indicate that the diagnosis of OZS must reflect the inherent intra- and inter-individual variability of sperm concentration, and therefore OZS should be divided into subcategories that are more specifically defined, that is, severe OZS with concentration < 1 × 106 sperm/mL, moderate OZS with 1–10 × 106 sperm/mL, and mild OZS >10 × 106 to 20 × 106 sperm/mL.126–128 Other major semen categories are absence of sperm (azoospermia) and morphology defects (teratozoospermia). Clinically, azoospermia overlaps with severe oligozoospermia. To date, only a limited number of genes are associated with low sperm count and male infertility.
One of the first successful studies reported is an association of nonsense mutations in SYCP3 with azoospermia and severe OZS in infertile patients.129 SYCP3 encodes a DNA-binding protein and is an important structural component of the synaptonemal complex, which mediates the synapsis of homologous chromosomes pairing during meiosis in male germ cells. The Sycp3 knockout mouse model exhibits meiosis arrest during spermatogenesis and resultant azoospermia and male infertility.130 The patients selected for this analysis represented a highly selected group of men with a meiotic arrest phenotypically similar to that observed in the mouse model.
Likewise, mutations in two related genes, CREM and FHL5 (formerly ACT, activator of CREM in testis), were shown to be responsible for azoospermia and OZS in men.131,132 CREM encodes a testis-specific transcription factor, cAMP responsive element modulator protein, and a CREM recognition site was found in the promoters of many testis-specific genes. Crem knockout mice show round spermatid arrest leading to male infertility.133,134 FHL5 protein contains a four-and-a-half LIM (FHL) domain that binds to CREM as a cofactor and modulates its activity. The Flh5 knockout mouse model demonstrates severe OZS and abnormal cell morphology, resulting in subfertility.135
Similarly, investigation of PRM1 gene mutations in infertile patients with severe OZS, abnormal morphology, and DNA damage revealed nonsense and missense alterations.136–138 PRM1 encodes protamine 1, which functions to compact, stabilize, and protect the DNA-protein complexes in the nucleus during spermatid development. The study was prompted by the Prm1 haploinsufficiency effect in mice, which causes abnormal sperm compaction, DNA damage, OZS, and male infertility.139 Recently, NALP14 mutations were identified in patients with AS and severe OZS.140 The study was initiated by delineation of gene-candidate disrupted by chromosome aberrations identified in patient with OZS.141 The gene was mapped to the chromosome 11p15 region. NALP14 displays testis-specific expression and encodes protein that plays important roles in apoptosis.
One noteworthy alternative approach for the OZS research is the RNA-based study of human kelch-like 10 (KLHL10) in infertile OZS patients.142 It employs the presence of stable mRNAs in human ejaculate spermatozoa. Our investigations focused on the detection of missense and splicing KLHL10 mutations in male germline mRNAs obtained from semen samples of OZS infertile men. We identified seven KLHL10 missense and splicing mutations out of 550 (1.2%) OZS patients examined. A concurrent study of 400 normozoospermic controls did not reveal these described KLHL10 mutations. Using reverse transcription-polymerase chain reaction (RT-PCR), we demonstrated that the splicing mutation caused a frameshift of the KLHL10 open reading frame. Pathogenic effects of the identified KLHL10 missense mutations were confirmed using a functional assay, an in vitro yeast 2-hybrid screen, which showed abnormal protein dimerization of mutant proteins. These findings were consistent with earlier mouse studies. KLHL10 is germ cell-specific protein involved in protein ubiquitination and is critical for maturation of mouse spermatozoa. Male mice heterozygous for a deletion in the Klhl10 gene demonstrate a failure of spermatozoal maturation, resulting in severe oligozoospermia.143,144
Despite a low frequency of described gene defects in OZS, significance of mutations in SYCP3, CREM1, FLH5, NALP14, PRM1, and KLHL10 were supported by statistical and/or functional evidence. However, many other investigations report limited statistical or functional evidence to support the pathological roles of the gene mutations in oligozoospermia; these include DDX25, PRM2, PRM3, TNP1, TNP2, UBE2B, USP26, FKBP6, mitochondrial ATPase8, and ATPase6.136,138,145–151
Teratozoospermia (TZS) is a condition characterized by the presence of sperm with abnormal morphology that affects fertility in males. Despite its relatively high occurrence, the progress toward understanding TZS has been slow. To date, there are only a few dozen genes that exhibit abnormal spermatozoal morphology in mouse knockout models,12 and even fewer genes show an association with TZS in infertile men.
One of the encouraging discoveries in the genetics of TZS and male infertility has been reported recently. Using a conventional identical-by-descent genetic approach, researchers reported that a testis-expressed gene, aurora kinase C (AURKC), is responsible for TZS in 10 patients with male infertility.152 The study demonstrated that all male patients carried same founder mutation, homozygous single-nucleotide deletion in the AURKC gene. These patients presented with nearly 100% morphologically abnormal spermatozoa, including oversized irregular heads, abnormal midpiece and acrosome, up to six flagella, and large-headed multiflagellar polyploid spermatozoa. In addition, AURKC protein plays an important role in meiotic division during spermatogenesis in mice.153
In another report, investigation focused on globozoospermia, rare form of TZS with characteristic round-headed spermatozoa that lack an acrosome and showed that the gene SPATA16 is responsible for globozoospermia in three related male infertile patients.154 The study described three affected brothers from a consanguineous family, in which each brother is homozygous for mutation in the SPATA16. The gene is testis-specific and SPATA16 specifically located in cytoplasm and involved in acrosome formation.155 However, a follow-up study of unrelated patients with complete or partial globozoospermia failed to identify SPATA16 mutation, highlighting the common difficulty in identifying genetic mutations in such highly heterogeneous etiology as TZS.
The Y chromosome comprises 60 million base pairs with a short arm (Yp) and a long arm (Yq). The sex determining region (SRY) is located on Yp and is an essential member of the group of genes that ultimately determines the fate of the bipotential gonad.156 The Y chromosome contains vital components needed for male differentiation and sperm function. The azoospermia factor region (AZF) on the long arm of the Y chromosome (Yq) is responsible for sperm development. The male-specific Y is the chromosomal material that bridges the two polar pseudoautosomal regions and is unique in the human genome. It comprises approximately 95% of the Y chromosome and houses multiple genes that help drive spermatogenesis such as DAZ, USP9Y, RBMY1, and BPY2.157 The AZF region is subdivided by location into AZFa, AZFb, and AZFc, which correspond to proximal, middle, and distal portions of the chromosome.5 Deletions in these locations are responsible for varying degrees of spermatogenic dysfunction. Entire microdeletions of AZFa or AZFb regions of the Y chromosome portends an exceptionally poor prognosis in sperm retrieval, such that microscopic sperm extraction is predictably negative.158
Depending on the severity of the deletion, a microdeletion in AZFc can result in a spectrum of spermatogenic deficiency including oligospermia and azoospermia.158 Deletions in the Y(q) are too small to be detected with a karyotype and thus are termed microdeletions. These deletions are identified using polymerase chain reaction techniques to analyze sequence tagged sites. Indications for testing AZF microdeletions are sperm concentrations less then 5 million/mL. Importantly, male offspring of patients with Y microdeletions will inherit the abnormal gene, rendering them likely to be infertile. Thus, ICSI with preimplantation genetic diagnosis (PGD) should be discussed.
As additional mouse models are created and high throughput screening approaches are used, we are beginning to understand more about the Mendelian genetics of male infertility. While it is difficult to fully understand the impact of Mendelian genetics on male infertility, the quick evolution of advanced reproductive therapies has allowed the achievement of biological paternity by men, who, by nature’s standard, would have never been permitted to procreate. IVF/ICSI has allowed the technical potential for these men with severe male factor infertility the ability to father children. However, finding a genetic basis and understanding this mishap before proceeding with any surgical or in vitro technology allows appropriate counseling of the couple with regard to immediate and long-term issues not only for the parents, but also for the future offspring that they should be aware of before moving forward.
This study was supported in part by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (P01HD36289), D.J.L. and M.M.M.; 1R01DK078121 to D.J.L.; and 1K12DK083014 Multidisciplinary K12 Urology Research Career Development Program at Baylor to D.J.L., K.H., and C.J.J., from the National Institute of Kidney and Digestive Diseases., and Ko8HD58073 to A.N.Y. R.L.N. is supported by the Edward J. and Josephine G. Hudson Scholar Fund and the Baylor College of Medicine Medical Scientist Training Program.
Conflicts of Interest
The authors declare no conflicts of interest.