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MALE INFERTILITY
Edited by Anu Bashamboo
and Kenneth David McElreavey
Male Infertility
Edited by Anu Bashamboo and Kenneth David McElreavey
Published by InTech
Janeza Trdine 9, 51000 Rijeka, Croatia
Copyright © 2012 InTech
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First published April, 2012
Printed in Croatia
A free online edition of this book is available at www.intechopen.com
Additional hard copies can be obtained from orders@intechopen.com
Male Infertility, Edited by Anu Bashamboo and Kenneth David McElreavey
p. cm.
ISBN 978-953-51-0562-6
Contents
Preface IX
Chapter 1 Obstructive and Non-Obstructive Azoospermia 1
Antonio Luigi Pastore, Giovanni Palleschi, Luigi Silvestri,
Antonino Leto and Antonio Carbone
Chapter 2 Gene Mutations Associated with Male Infertility 21
Kamila Kusz-Zamelczyk, Barbara Ginter-Matuszewska,
Marcin Sajek and Jadwiga Jaruzelska
Chapter 3 Apoptosis, ROS and Calcium Signaling in
Human Spermatozoa: Relationship to Infertility 51
Ignacio Bejarano, Javier Espino, Sergio D. Paredes, Águeda Ortiz,
Graciela Lozano, José Antonio Pariente, Ana B. Rodríguez
Chapter 4 The Role of PDE5 Inhibitors in the
Treatment of Testicular Dysfunction 77
Fotios Dimitriadis, Dimitrios Baltogiannis, Sotirios Koukos,
Dimitrios Giannakis, Panagiota Tsounapi, Georgios Seminis,
Motoaki Saito, Atsushi Takenaka and Nikolaos Sofikitis
Chapter 5 Effectiveness of Assisted Reproduction
Techniques as an Answer to Male Infertility 107
Sandrine Chamayou and Antonino Guglielmino
Chapter 6 Makings of the Best Spermatozoa:
Molecular Determinants of High Fertility 133
Erdogan Memili, Sule Dogan, Nelida Rodriguez-Osorio,
Xiaojun Wang, Rodrigo V. de Oliveira, Melissa C. Mason,
Aruna Govindaraju, Kamilah E. Grant, Lauren E. Belser,
Elizabeth Crate, Arlindo Moura and Abdullah Kaya
Chapter 7 A Systems Biology Approach to
Understanding Male Infertility 171
Nicola Bernabò, Mauro Mattioli and Barbara Barboni
Preface
In recent years there has been an increasing concern about possible decline in
reproductive health with an estimate of one in seven couples worldwide having
problems conceiving. Despite high and increasing rates of human infertility, our
understanding of the genetic pathways and basic molecular mechanisms involved in
gonadal development and function remains limited. A genetic contribution to
spermatogenic failure is indicated by several families with multiple infertile or
subfertile men. In some of these families an autosomal recessive mutation appears to
be responsible whilst in others an autosomal dominant mutation with sex-limited
expression is likely. In other families the genetic cause is known to involve either
chromosomal anomalies or Y chromosome microdeletions. However, only a significant
minority of the cases of male infertility and subfertility may be explained by the
genetic causes. This raises the question of environmental contribution to male
infertility and subfertility.
Prospective cross-sectional studies have indicated a general birth cohort decline in
sperm quantity and quality as well as an increase in incidence of Testicular germ cell
cancer during the last 50 years. These phenotypes, together with undescended testis
and anomalies of the male external genitalia are termed "testicular dysgenesis
syndrome” (TDS) and may have a common aetiology resulting from disruption of the
gonadal environment during fœtal life. The rapid, often synchronous, rise in the
incidence of TDS suggests an environmental aetiology possibly in genetically
susceptible individuals. Emerging data suggest that exposure of a developing male
foetus to a number of environmental factors, including but not limited to endocrine
disruptors, can negatively regulate testicular development and function. Several
studies show that this detrimental effect of environmental toxins on male germ cells
may be epigenetic resulting in aberrant DNA methylation of key genes. Several reports
suggest that the epigenetic landscape may be altered in some men with reduced sperm
counts but relationship between these changes and infertility remains unclear.
The increase in incidence of male infertility is associated with an increase in demand
for infertility treatments. These include intracytoplasmic sperm injection (ICSI) and in
vitro fertilization (IVF). In some European countries, such as Denmark, more than 6%
of children are born with assisted reproductive techniques (ARTs). There is a
suggestion that children conceived using ARTs might show a higher prevalence of
X Preface
genetic and epigenetic anomalies. This raises the question of complete molecular
characterization of sperm that will be eventually used for ARTs. Our understanding of
the molecular landscape of the sperm is likely to increase dramatically in the coming
future with the advent of new technologies that permit high throughput and detailed
molecular analysis. OMICS involving the exploration of genetic, epigenetic,
transcriptomic and proteomic modifications and their interaction with each other is
fast becoming a tool of choice to understand and interpret complex biological
phenomenon and may be used to understand key molecular events involved in the
development of the normal male germ cell lineages and their pathological
counterparts. A combination of these approaches together with strict diagnostic
criteria will increase the likelihood of success in understanding male infertility and
use of ARTs.
Dr. Anu Bashamboo
Dr. Ken McElreavey
Unit of Human Developmental Genetics
Institut Pasteur, Paris
France
[...]... for other male reproductive processes Thousands of genes in these categories are expressed in human testes and any of them can potentially cause infertility when mutated This circumstance makes studies on genetic causes of male infertility extremely complex Therefore, the generation of about 400 mouse models of male infertility in recent years has been very helpful to select the best human candidates... gene mutations are deleterious only in male patients, Aurora Kinase C is highly expressed in both male (Bernard et al., 1998) and female gonads (Yan et al., 2005) These data indicate that, for couples with male infertility caused by AURKC gene mutation, the ISCI approach should not be encouraged 2.2 SPATA16 and DPY19L2 gene mutations in globozoospermia In course of infertility related genome-wide scan,... may not be properly recognized when mutated This issue opens a new field in the research on male infertility and the underlying genetic causes 2 Autosomal single-gene mutations causing non-syndromic male infertility A small number of well documented cases of autosomal gene mutations causing nonsyndromic male infertility are reviewed below Several of theses genes cause a distinct spermatozoa defect in... sperm retrieval Aging Male 2010 Mar;13(1):4450 Sertić J, Cvitković P, Myers A, Saiki RK, Stavljenić Rukavina A Genetic markers of male infertility: Y chromosome microdeletions and cystic fibrosis transmembrane conductance gene mutations Croat Med J 2001 Aug;42(4):416-20 Shah R Surgical sperm retrieval: Techniques and their indications Indian J Urol 2011; 27(1):102-9 20 Male Infertility Sharif K Reclassification... translocation associated with male infertility is the one originating from chromosomes 13 and 14 Also reciprocal translocations are more frequent (4-10-fold) in infertile than in fertile males (for review see O’Flyn O’Brien et al., 2010) In the recent years much attention has been paid to mutations causing male infertility These mutations were identified in genes known to be responsible for male germ cell development... 86% and 93%, while the cumulative spontaneous pregnancy rates range between 52% and 82% The duration of the obstruction appreciably affect the success rate of vasovasostomy When the interval between obstruction and recanalization is shorter than 3 years, patency and spontaneous pregnancies are obtained, respectively, in 97% and 76% of cases, compared with 88% and 53% when the interval is between 3 and. .. to the infertile man J Clin Endocrinol Metab 2007;92(6):1995-2004 Campbell AJ, Irvine DS Male infertility and intracytoplasmic sperm injection (ICSI) Br Med Bull 2000;56(3):616-29 18 Male Infertility Choe JH, Kim JW, Lee JS, Seo JT Routine screening for classical azoospermia factor deletions of the Y chromosome in azoospermic patients with Klinefelter syndrome Asian J Androl 2007 Nov;9(6):815-20 PubMed... families revealed that all homozygous males were infertile whereas homozygous females and heterozygous males were fertile (Dieterich et al., 2007, 2009) This indicates a recessive inheritance model for AURKC mutation transmission with the infertility phenotype restricted to men The c.114delC mutation introduces a frameshift Gene Mutations Associated with Male Infertility 23 p.Leu49TrpfsX22 resulting... processing, and cryopreservation of epididymal and testicular sperm in connection with intracytoplasmic sperm injection J Androl 1998 Sep-Oct;19(5):517-26 McLachlan RI, O'Bryan MK Clinical Review#: State of the art for genetic testing of infertile men J Clin Endocrinol Metab 2010 Mar;95(3):1013-24 Merchant R, Gandhi G, Allahbadia GN In vitro fertilization/intracytoplasmic sperm injection for male infertility. .. diagnostic tool in complicated cases of male infertility J Androl 15 (Supplement):17S-22S, 1994 Dixit R, Dixit K, Jindal S, Shah KV An unusual presentation of immotile-cilia syndrome with azoospermia: Case report and literature review Lung India 2009;26(4):142-5 PubMed PMID: 20532000; PubMed Central PMCID: PMC2876703 Donkol RH Imaging in male- factor obstructive infertility World J Radiol 2010;2(5):172-9 . MALE INFERTILITY
Edited by Anu Bashamboo
and Kenneth David McElreavey
Male Infertility
Edited by Anu Bashamboo and Kenneth David. can be obtained from orders@intechopen.com
Male Infertility, Edited by Anu Bashamboo and Kenneth David McElreavey
p. cm.
ISBN 978-953-51-0562-6
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