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19 - Evaluation of Sperm Damage: Beyond the WHO Criteria

from PART II - INFERTILITY EVALUATION AND TREATMENT

Published online by Cambridge University Press:  04 August 2010

Botros R. M. B. Rizk
Affiliation:
University of South Alabama
Juan A. Garcia-Velasco
Affiliation:
Rey Juan Carlos University School of Medicine,
Hassan N. Sallam
Affiliation:
University of Alexandria School of Medicine
Antonis Makrigiannakis
Affiliation:
University of Crete
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Summary

INTRODUCTION

For over twenty-five years, the World Health Organization (WHO) has served to provide a standardized approach to the assessment of the fertility potential of semen sample. These standards are concerned with measurable parameters such as the physical properties of an ejaculate, estimating the count of its cellular content be it sperm or leukocytes, grading sperm morphology and motility, and examining a possible immune interaction between sperm and the content of seminal plasma or the preovulatory mucus produced by the uterine cervix. The adoption of these standards worldwide has been enhanced through local schemes of quality control measures leading to andrology laboratory accreditation and certification. The first andrology laboratory manual published by the WHO in 1981 was the culmination of clinical experience and research in the previous eighty years (1). In its successive editions, the WHO manual portrayed stricter criteria in assessing parameters of interest and as a result values that were thought to be compatible with normal male fertility were modified (2,3). The resounding success of the WHO criteria is met by call for further scrutiny of sperm quality to address numerous concerns born from clinical and research work carried out in more recent years. First, the results of semen analyses can be very subjective and prone to intra- and interobserver variability (4). Second, although the traditional, manual-visual light microscopic methods for evaluating semen quality maintain their central role in assessment of male fertility potential, often a definitive diagnosis of male fertility cannot be made as a result of basic semen analysis (5).

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Publisher: Cambridge University Press
Print publication year: 2008

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References

Morice, P, Josset, P, Chapron, C, Dubuisson, JB. History of infertility. Hum Reprod Update 1995;1:497–504.CrossRefGoogle ScholarPubMed
Kruger, TF, Acosta, AA, Simmons, KF, Swanson, RJ, Matta, JF, Oehninger, S. Predictive value of abnormal sperm morphology in in vitro fertilization. Fertil Steril 1988;49:112–17.CrossRefGoogle ScholarPubMed
Aziz, N, Buchan, I, Taylor, C, Kingsland, CR, Lewis-Jones, I. The sperm deformity index: a reliable predictor of the outcome of oocyte fertilization in vitro. Fertil Steril 1996;66:1000–8.CrossRefGoogle ScholarPubMed
Keel, B, Webster, B. The standard semen analysis. In: Webster, B (ed.), CRC Handbook of the Laboratory Diagnosis and Treatment of Infertility. Boca Raton, FL: CRC Press, 1990:27–69.Google Scholar
Nallella, KP, Sharma, RK, Aziz, N, Agarwal, A. Significance of sperm characteristics in the evaluation of male infertility. Fertil Steril 2006;85(3):629–34.CrossRefGoogle ScholarPubMed
Zini, A, Kamal, K, Phang, D, et al. Biologic variability of sperm DNA denaturation in infertile men. Urology 2001;58:258–61.CrossRefGoogle ScholarPubMed
Evenson, D, Larson, K, Jost, L. Sperm chromatin structure assay: its clinical use for detecting sperm DNA fragmentation in male infertility and comparisons with other techniques. J Androl 2002;23:25–43.CrossRefGoogle ScholarPubMed
Aitken, RJ, Koopman, P, Lewis, SE. Seeds of concern. Nature 2004;432:48–52.CrossRefGoogle ScholarPubMed
Ward, WS, Coffey, DS. DNA packaging and organization in mammalian spermatozoa: comparison with somatic cells. Biol Reprod 1991;44:569–74.CrossRefGoogle ScholarPubMed
Brewer, LR, Corzett, M, Balhorn, R. Protamine induced condensation and decondensation of the same DNA molecule. Science 1999;286:120–3.CrossRefGoogle ScholarPubMed
Steger, K, Pauls, K, Klonisch, T, et al. Expression of protamine-1 and -2 mRNA during human spermiogenesis. Mol Hum Reprod 2000;6:219–25.CrossRefGoogle ScholarPubMed
Kosower, NS, Katayose, H, Yanagimachi, R. Thiol-disulfide status and acridine orange fluorescence of mammalian sperm nuclei. J Androl 1992;13:342–8.Google ScholarPubMed
Gatewood, JM, Cook, GR, Balhorn, R et al. Sequence-specific packaging of DNA in human sperm chromatin. Science 1987; 236:962–4.CrossRefGoogle ScholarPubMed
Gineitis, AA, Zalenskaya, IA, Yau, PM et al. Human sperm telomere-binding complex involves histone H2B and secures telomere membrane attachment. J Cell Biol 2000;151:1591–8.CrossRefGoogle ScholarPubMed
Lewis, JD, Song, Y, Jong, ME, Bagha, SM, Ausio, J. A walk through vertebrate and invertebrate protamines. Chromosoma 1999;111:473–82.CrossRefGoogle Scholar
Bench, GS, Friz, AM, Corzett, MH, Morse, DH, Balhorn, R. DNA and total protamine masses in individual sperm from fertile mammalian subjects. Cytometry 1996;23:263–71.3.0.CO;2-I>CrossRefGoogle ScholarPubMed
Oliva, R. Protamines and male infertility. Hum Reprod Update 2006;12:417–35.CrossRefGoogle ScholarPubMed
Corzett, M, Mazrimas, J, Balhorn, R. Protamine 1: protamine 2 stoichiometry in the sperm of eutherian mammals. Mol Reprod Dev 2002;61:519–27.CrossRefGoogle ScholarPubMed
Jager, S. Sperm nuclear stability and male infertility. Arch Androl 1990;25:253–9.CrossRefGoogle ScholarPubMed
Balhorn, R, Reed, S, Tanphaichitr, N. Aberrant protamine 1/protamine 2 ratio in sperm of infertile human males. Experientia 1988;44:52–5.CrossRefGoogle Scholar
Yebra, L, Ballesca, JL, Vanrell, JA, Bassas, L, Oliva, R. Complete selective absence of protamine P2 in humans. J Biol Chem 1993; 268:10553–7.Google ScholarPubMed
Bench, G, Corzett, MH, Yebra, L, Oliva, R, Balhorn, R. Protein and DNA contents in sperm from an infertile human male possessing protamine defects that vary over time. Mol Reprod Dev 1998;50:345–53.3.0.CO;2-3>CrossRefGoogle ScholarPubMed
Yebra, L, Ballesca, JL, Vanrell, JA, Corzett, M, Balhorn, R, Oliva, R. Detection of P2 precursors in the sperm cells of infertile patients who have reduced protamine P2 levels. Fertil Steril 1998; 69:755–9.CrossRefGoogle ScholarPubMed
Carrell, DT, Liu, L. Altered protamine 2 expression is uncommon in donors of known fertility, but common among men with poor fertilizing capacity, and may reflect other abnormalities of spermiogenesis. J Androl 2001;22:604–10.Google ScholarPubMed
Carrell, DT, Emery, BR, Hammoud, S. Altered protamine expression and diminished spermatogenesis: what is the link? Hum Reprod Update 2007; advance online access:1–15.Google ScholarPubMed
Mengual, L, Ballesca, JL, Ascaso, C, Oliva, R. Marked differences in protamine content and P1/P2 ratios in sperm cells from percoll fractions between patients and controls. J Androl 2003;24:438–47.CrossRefGoogle ScholarPubMed
Nasr-Esfahani, MH, Salehi, M, Razavi, S et al. Effect of protamine-2 deficiency on ICSI outcome. Reprod Biomed Online 2004;9:652–8.CrossRefGoogle ScholarPubMed
Aoki, VW, Liu, L, Carrell, DT. Identification and evaluation of a novel sperm protamine abnormality in a population of infertile males. Hum Reprod 2005;20:1298–306.CrossRefGoogle Scholar
Carrell, DT, Jonge, C, Lamb, DJ. The genetics of male infertility: a field of study whose time is now. Arch Androl 2006;52:269–74.CrossRefGoogle ScholarPubMed
Anderson, S, Bankier, AT, Barrell, BG, et al. Sequence and organization of the human mitochondrial genome. Nature 1981;290:457–65.CrossRefGoogle ScholarPubMed
Kao, SH, Chao, HT, Wei, YH. Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa. Mol Hum Reprod 1998;4:657–66.CrossRefGoogle ScholarPubMed
Schwartz, M, Vissing, J. Paternal inheritance of mitochondrial DNA. N Engl J Med 2002;347:576–80.CrossRefGoogle ScholarPubMed
Perreault, SD, Aitken, RJ, Baker, HW et al. Integrating new tests of sperm genetic integrity into semen analysis: breakout group discussion. Adv Exp Med Biol 2003;518:253–68.CrossRefGoogle ScholarPubMed
Jung, A, Schill, WB, Schuppe, HC. Genital heat stress in men of barren couples: a prospective evaluation by means of a questionnaire. Andrologia 2002;34:349–55.CrossRefGoogle ScholarPubMed
Zini, A, Libman, J. Sperm DNA damage: clinical significance in the era of assisted reproduction. Can Med Assoc J 2006;175:495–500.CrossRefGoogle ScholarPubMed
Erenpreiss, J, Spano, M, Erenpreisa, J, Bungum, M, Giwercman, A. Sperm chromatin structure and male fertility: biological and clinical aspects. Asian J Androl 2006;8:11–29.CrossRefGoogle ScholarPubMed
Agarwal, A, Allamaneni, SS. Sperm DNA damage assessment: a test whose time has come. Fertil Steril 2005;84:850–3.CrossRefGoogle ScholarPubMed
Sakkas, D, Mariethoz, E, Manicardi, G, Bizzaro, D, Bianchi, PG, Bianchi, U. Origin of DNA damage in ejaculated human spermatozoa. Rev Reprod 1999;4:31–7.CrossRefGoogle ScholarPubMed
Shen, H, Ong, C. Detection of oxidative DNA damage in human sperm and its association with sperm function and male infertility. Free Radic Biol Med 2000;28:529–36.CrossRefGoogle ScholarPubMed
Agarwal, A, Saleh, RA, Bedaiwy, MA. Role of reactive oxygen species in the pathophysiology of human reproduction. Fertil Steril 2003;79:829–43.CrossRefGoogle ScholarPubMed
Said, TM, Aziz, N, Sharma, RK, Lewis-Jones, I, Thomas, AJ Jr., Agarwal, A. Novel association between sperm deformity index and oxidative stress-induced DNA damage in infertile male patients. Asian J Androl 2005;7, 121–6.CrossRefGoogle ScholarPubMed
McPherson, SM, Longo, FJ. Nicking of rat spermatid and spermatozoa DNA: possible involvement of DNA topoisomerase II. Dev Biol 1993;158:122–30.CrossRefGoogle ScholarPubMed
Sharma, RK, Said, T, Agarwal, A. Sperm DNA damage and its clinical relevance in assessing reproductive outcome. Asian J Androl 2004;6:139–48.Google ScholarPubMed
Lewis, SEM, Aitken, RJ. DNA damage to spermatozoa has impacts on fertilization and pregnancy. Cell Tissue Res 2005;322:33–41.CrossRefGoogle Scholar
Agarwal, A, Said, TM. Role of sperm chromatin abnormalities and DNA damage in male infertility. Hum Reprod Update 2003;9:331–45.CrossRefGoogle ScholarPubMed
Irvine, DS, Twigg, JP, Gordon, EL, Fulton, N, Milne, PA, Aitken, RJ. DNA integrity in human spermatozoa: relationships with semen quality. J Androl 2000;21:33–44.Google ScholarPubMed
Darzynkiewicz, Z, Juan, G, Li, X, Gorczyca, W, Murakami, T, Traganos, F. Cytometry in cell necrobiology: analysis of apoptosis and accidental cell death (necrosis). Cytometry 1997;27:1–20.3.0.CO;2-L>CrossRefGoogle Scholar
Roca, J, Mezquita, C. DNA topoisomerase II activity in nonreplicating, transcriptionally inactive, chicken late spermatids. Embo J 1989;8:1855–60.Google ScholarPubMed
Balhorn, R. A model for the structure of chromatin in mammalian sperm. J Cell Biol 1982;93:298–305.CrossRefGoogle ScholarPubMed
Risley, MS, Einheber, S, Bumcrot, DA. Changes in DNA topology during spermatogenesis. Chromosoma 1986;94:217–27.CrossRefGoogle ScholarPubMed
Morse-Gaudio, M, Risley, MS. Topoisomerase II expression and VM-26 induction of DNA breaks during spermatogenesis in Xenopus laevis. J Cell Sci 1994;107:2887–98.Google ScholarPubMed
Genesca, A, Caballin, MR, Miro, R, Benet, J, Germa, JR, Egozcue, J. Repair of human sperm chromosome aberrations in the hamster egg. Hum Genet 1992;89:181–6.CrossRefGoogle ScholarPubMed
Marchesi, , Feng, HL. Sperm DNA integrity from sperm to egg. J Androl. Published ahead of print.
Vogt, PH. Molecular genetic of human male infertility: from genes to new therapeutic perspectives. Curr Pharm Design 2004; 10:471–500.CrossRefGoogle ScholarPubMed
Martin, RH, Ko, E, Chan, K, Rademaker, AW. Detection of aneuploidy in human interphase spermatozoa by fluorescence in situ hybridization (FISH). Cytogenet Cell Genet 1993;64:23–6.CrossRefGoogle Scholar
Griffin, DK. The incidence, origin, and etiology of aneuploidy. Int Rev Cytol 1996;167:263–96.CrossRefGoogle ScholarPubMed
Spriggs, EL, Rademaker, AW, Martin, RH. Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction. Am J Hum Genet 1996;58:356–62.Google Scholar
Hassold, TJ. Nondisjunction in the human male. Curr Top Dev Biol 1998;37:383–406.CrossRefGoogle ScholarPubMed
Martin, RH, Rademaker, AW. Nondisjunction in human sperm: comparison of frequencies in acrocentric chromosomes. Cytogenet Cell Genet 1999;86:43–5.CrossRefGoogle ScholarPubMed
Lamb, NE, Hassold, TJ. Nondisjunction: a view from ringside. N Engl J Med 2004;351:1931–4.CrossRefGoogle ScholarPubMed
Lewis-Jones, I, Aziz, N, Seshadri, S, Douglas, A, Howard, P. Sperm chromosomal abnormalities are linked to sperm morphologic deformities. Fertil Steril 2003;79:212–15.CrossRefGoogle ScholarPubMed
Martin, RH, Rademaker, AW, Greene, C, Ko, E, Hoang, T, Barclay, L, Chernos, J. A comparison of the frequency of sperm chromosome abnormalities in men with mild, moderate, and severe oligozoospermia. Biol Reprod 2003;69:535–9.CrossRefGoogle ScholarPubMed
Calogero, AE, Palma, A, Grazioso, C et al. Aneuploidy rate in spermatozoa of selected men with abnormal semen parameters. Hum Reprod 2001;16:1172–9.CrossRefGoogle ScholarPubMed
Burrello, N, Vicari, E, Shin, P et al. Lower sperm aneuploidy frequency is associated with high pregnancy rates in ICSI programmes. Hum Reprod 2003;18:1371–6.CrossRefGoogle ScholarPubMed
Carrell, DT, Wilcox, AL, Lowy, L et al. Elevated sperm chromosome aneuploidy and apoptosis in patients with unexplained recurrent pregnancy loss. Obstet Gynecol 2003;101:1229–35.Google ScholarPubMed
Benjamin, R, Emery, BR, Carrell, DT. The effect of epigenetic sperm abnormalities on early embryogenesis. Asian J Androl 2006;8:131–42.Google Scholar
Escudero, T, Abdelhadi, I, Sandalinas, M, Munne, S. Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations. Fertil Steril 2003;79 (Suppl. 3):1528–34.CrossRefGoogle ScholarPubMed
Tejada, RI, Mitchell, JC, Norman, A, Marik, JJ, Friedman, S. A test for the practical evaluation of male fertility by acridine orange (AO) fluorescence. Fertil Steril 1984;42:87–91.CrossRefGoogle ScholarPubMed
Darzynkiewicz, Z. Acid-induced denaturation of DNA in situ as a probe of chromatin structure. Methods Cell Biol 1994;41:527–41.CrossRefGoogle ScholarPubMed
Erenpreisa, J, Freivalds, T, Slaidina, M et al. Toluidine blue test for sperm DNA integrity and elaboration of image cytometry algorithm. Cytometry 2003;52:19–27.CrossRefGoogle ScholarPubMed
Baker, H, Liu, D. Assessment of nuclear maturity. In: Acosta, A, Kruger, T, eds. Human Spermatozoa in Assisted Reproduction. London: CRC Press, 1996:93–203.Google Scholar
Manicardi, G, Bianchi, P, Pantano, S et al. Presence of endogenous nicks in DNA of ejaculated human spermatozoa and its relationship to chromomycin A3 accessibility. Biol Reprod 1995; 52:864–7.CrossRefGoogle ScholarPubMed
Fernandez, J, Muriel, L, Rivero, M et al. The sperm chromatin dispersion test: a simple method for the determination of sperm DNA fragmentation. J Androl 2003;24:59–66.Google ScholarPubMed
Fernandez, J, Vazquez-Gundin, F, Delgado, A et al. DNA breakage detection–FISH (DBD–FISH) in human spermatozoa: technical variants evidence different structural features. Mutat Res 2000;253:77–82.CrossRefGoogle Scholar
Gorczyza, W, Gong, J, Darzynkiewics, Z. Detection of DNA strand breaks in individual apoptotic cells by the in situ terminal deoxynucleotidyl transferase and nick translation assays. Cancer Res 1993;53:1945–51.Google Scholar
Barroso, G, Morshedi, M, Oehninger, S. Analysis of DNA fragmentation, plasma membrane translocation of phosphatidylserine and oxidative stress in human spermatozoa. Hum Reprod 2000;15:1338–44.CrossRefGoogle ScholarPubMed
Singh, N, McCoy, M, Tice, R et al. A simple technique for quantification of low levels of DNA damage in individual cells. Exp Cell Res 1988;175:184–91.CrossRefGoogle Scholar
Singh, N, Danner, D, Tice, R, McCoy, MT, Collins, GD, Schneider, EL. Abundant alkali-sensitive sites in DNA of human and mouse sperm. Exp Cell Res 1989;184:461–70.CrossRefGoogle ScholarPubMed
Evenson, D, Jost, L, Baer, R, Turner, TW, Schrader, SM. Individuality of DNA denaturation patterns in human sperm as measured by the sperm chromatin structure assay. Reprod Toxicol 1991;5:115–25.CrossRefGoogle ScholarPubMed
Erenpreisa, EA, Zirne, RA, Zaleskaia, ND, S'iakste, TG. Effect of single-stranded breaks on the ultrastructural organization and cytochemistry of the chromatin in tumor cells. Biull Eksp Biol Med 1988;106:591–3.CrossRefGoogle ScholarPubMed
Erenpreisa, EA, Sondore OIu, Zirne, RA. Conformational changes in the chromatin of tumor cells and the phenomenon of nuclear achromasia. Eksp Onkol 1988;10:54–7.Google ScholarPubMed
Rigler, R, Killander, D, Bolund, L, Ringertz, NR. Cytochemical characterization of deoxyribonucleoprotein in individual cell nuclei. Techniques for obtaining heat denaturation curves with the aid of acridine orange microfluorimetry and ultraviolet microspectrophotometry. Exp Cell Res 1969;55:215–24.CrossRefGoogle ScholarPubMed
Darzynkiewicz, Z, Traganos, F, Sharpless, T, Melamed, MR. Thermal denaturation of DNA in situ as studied by acridine orange staining and automated cytofluorometry. Exp Cell Res 1975;90:411–28.CrossRefGoogle ScholarPubMed
Evenson, D, Jost, L, Marshall, D et al. Utility of the sperm chromatin structure assay as a diagnostic tool in the human fertility clinic. Hum Reprod 1999;14:1039–49.CrossRefGoogle ScholarPubMed
Zini, A, Fischer, M, Sharir, S, Shayegan, B, Phang, D, Jarvi, K. Prevalence of abnormal sperm DNA denaturation in fertile and infertile men. Urology 2002;60:1069–72.CrossRefGoogle ScholarPubMed
Variant-Klun, I, Tomazevic, T, Meden-Vrtovec, H. Sperm single-stranded DNA, detected by acridine orange staining, reduces fertilization and quality of ICSI-derived embryos. J Assist Reprod Genet 2002;19:319–28.CrossRefGoogle Scholar
Erenpreiss, J, Bars, J, Lipatnikova, V, Erenpreisa, J, Zalkalns, J. Comparative study of cytochemical tests for sperm chromatin integrity. J Androl 2001;22:45–53.Google ScholarPubMed
Auger, J, Mesbah, M, Huber, C, Dadoune, JP. Aniline blue staining as a marker of sperm chromatin defects associated with different semen characteristics discriminates between proven fertile and suspected infertile men. Int J Androl 1990;13:452–62.CrossRefGoogle ScholarPubMed
Terquem, T, Dadoune, JP. Aniline blue staining of human spermatozoa chromatin. Evaluation of nuclear maturation. In: Adre, J, ed. The Sperm Cell. The Hague: Martinus Nijhoff Publishers; 1983.Google Scholar
Liu, DY, Baker, HW. Sperm nuclear chromatin normality: relationship with sperm morphology, sperm-zona pellucida binding, and fertilization rates in vitro. Fertil Steril 1992;58:1178–84.CrossRefGoogle ScholarPubMed
Foresta, C, Zorzi, M, Rossato, M, Varotto, A. Sperm nuclear instability and staining with aniline blue: abnormal persistence of histones in spermatozoa in infertile men. Int J Androl 1992; 15:330–7.CrossRefGoogle ScholarPubMed
Hammadeh, M, Zeginiadov, T, Rosenbaum, P et al. Predictive value of sperm chromatin condensation (aniline blue staining) in the assessment of male fertility. Arch Androl 2001;46:99–104.CrossRefGoogle ScholarPubMed
Hammadeh, M, Stieber, M, Haidl, G, Schmidt, W. Association between sperm cell chromatin condensation, morphology based on strict criteria, and fertilization, cleavage and pregnancy rates in an IVF program. Andrologia 1998;30:29–35.CrossRefGoogle Scholar
Evenson, DP, Darzynkiewicz, Z, Melamed, MR. Relation of mammalian sperm chromatin heterogeneity to fertility. Science 1980;210:1131–3.CrossRefGoogle ScholarPubMed
Evenson, DP, Jost, LK, Marshall, D, Zinaman, MJ, Clegg, E, Purvis, K et al. Utility of the sperm chromatin structure assay as a diagnostic and prognostic tool in the human fertility clinic. Hum Reprod 1999;14:1039–49.CrossRefGoogle ScholarPubMed
Spano, M, Bonde, JP, Hjollund, HI, Kolstad, HA, Cordelli, E, Leter, G. Sperm chromatin damage impairs human fertility. The Danish First Pregnancy Planner Study Team. Fertil Steril 2000;73:43–50.Google ScholarPubMed
Larson-Cook, KL, Brannian, JD, Hansen, KA, Kasperson, KM, Aamold, ET, Evenson, DP. Relationship between the outcomes of assisted reproductive techniques and sperm DNA fragmentation as measured by the sperm chromatin structure assay. Fertil Steril 2003;80:895–902.CrossRefGoogle ScholarPubMed
Evenson, D, Wixon, R. Meta-analysis of sperm DNA fragmentation using the sperm chromatin structure assay. Reprod Biomed Online 2006;12:466–72.CrossRefGoogle ScholarPubMed
Spano, M, Kolstad, A, Larsen, S et al. The applicability of the flow cytometric sperm chromatin structure assay in epidemiological studies. Hum Reprod 1998;13:2495–505.CrossRefGoogle ScholarPubMed
Perreault, SD, Aitken, HW, Baker, DP et al. Integrating new tests of sperm genetic integrity into semen analysis: breakout group discussion. In: Robaire, B, Hales, BF, eds. Male-Mediated Developmental Toxicity. Kluwer Academic/Plenum Publisher; 2003:256–66.Google Scholar
Bianchi, PG, Manicardi, GC, Bizzaro, D, Bianchi, U, Sakkas, D. Effect of deoxyribonucleic acid protamination on fluorochrome staining and in situ nick-translation of murine and human mature spermatozoa. Biol Reprod 1993;49:1083–8.CrossRefGoogle ScholarPubMed
Sakkas, D, Urner, F, Bizzaro, D, Manicardi, G, Bianchi, PG, Shoukir, Y et al. Sperm nuclear DNA damage and altered chromatin structure: effect on fertilization and embryo development. Hum Reprod 1998;13 (Suppl. 4):11–19.CrossRefGoogle ScholarPubMed
Lopes, S, Sun, JG, Jurisicova, A, Meriano, J, Casper, RF. Sperm deoxyribonucleic acid fragmentation is increased in poor- quality semen samples and correlates with failed fertilization in intracytoplasmic sperm injection. Fertil Steril 1998;69: 528–32.CrossRefGoogle ScholarPubMed
Gorczyca, W, Traganos, F, Jesionowska, H, Darzynkiewicz, Z. Presence of DNA strand breaks and increased sensitivity of DNA in situ to denaturation in abnormal human sperm cells: analogy to apoptosis of somatic cells. Exp Cell Res 1993;207:202–5.CrossRefGoogle ScholarPubMed
Aravindan, GR, Bjordahl, J, Jost, LK, Evenson, DP. Susceptibility of human sperm to in situ DNA denaturation is strongly correlated with DNA strand breaks identified by single cell electrophoresis. Exp Cell Res 1997;236:231–7.CrossRefGoogle ScholarPubMed
Chan, PJ, Corselli, JU, Patton, WC, Jacobson, JD, Chan, SR, King, A. Simple comet assay for archived sperm correlates DNA fragmentation. Reduced hyperactivation and penetration of zona-free hamster ocytes. Fertil Steril 2001;75:186–92.CrossRefGoogle Scholar
Duty, S, Singh, N, Ryan, L et al. Reliability of the comet assay in cryopreserved human sperm. Hum Reprod 2002;17:1274–80.CrossRefGoogle ScholarPubMed
Morris, I, Ilott, S, Dixon, L, Brison, DR. The spectrum of DNA damage in human sperm assessed by single cell gel electrophoresis (comet assay) and its relationship to fertilization. Hum Reprod 2002;17:990–8.CrossRefGoogle Scholar
Tomsu, M, Sharma, V, Miller, D. Embryo quality and IVF treatment outcomes may correlate with different sperm comet assay parameters. Hum Reprod 2002;17:1856–62.CrossRefGoogle ScholarPubMed
Hughes, CM, Lewis, SE, McKelvey-Martin, VJ, Thompson, W. A comparison of baseline and induced DNA damage in human spermatozoa from fertile and infertile men, using a modified comet assay. Mol Hum Reprod 1996;2:613–19.CrossRefGoogle ScholarPubMed
Ankem, MK, Mayer, E, Ward, WS, Cummings, KB, Barone, JG. Novel assay for determining DNA organization in human spermatozoa: implications for male factor infertility. Urology 2002; 59:575–8.CrossRefGoogle ScholarPubMed
Ward, WS, Kimura, Y, Yanagimachi, R. An intact sperm nuclear matrix may be necessary for the mouse paternal genome to participate in embryonic development. Biol Reprod 1999;60:702–6.CrossRefGoogle ScholarPubMed
Sjakste, N, Sjakste, T. Nuclear matrix proteins and hereditary diseases. Genetika 2005;41:293–8.Google ScholarPubMed
Iwasaki, A, Gagnon, C. Formation of reactive oxygen species of spermatozoa of infertile patients. Fertil Steril 1992;57:409.CrossRefGoogle ScholarPubMed
Sharma, RK, Agarwal, A. Role of reactive oxygen species in male infertility. J Urol 1996;48:835–50.CrossRefGoogle ScholarPubMed
Aitken, RJ, Fisher, H. Reactive oxygen species generation and human spermatozoa: the balance of benefit and risk. Bioassays 1994;16:259–67.CrossRefGoogle ScholarPubMed
Aitken, RJ, Irvine, DS, Wu, FC. Prospective analysis of sperm-oocyte fusion and reactive oxygen species generation as criteria for the diagnosis of infertility. Am J Obstet Gynecol 1991;64: 542–51.CrossRefGoogle Scholar
Agarwal, A, Ftabakaran, SA. Mechanism, measurement, and prevention of oxidative stress in male reproductive physiology. Indian J Exp Biol 2003;43:963–74.Google Scholar
Darley-Usmar, V, Wiseman, H, Halliwell, B. Nitric oxide and oxygen radicals: a question of balance. FEBS Lett 1995;369: 131–5.CrossRefGoogle Scholar
Gutierrez, J, Ballinger, SW, Darley-Usmar, VM, Landar, A. Free radicals, mitochondria, and oxidized lipids: the emerging role in signal transduction in vascular cells. Circ Res 2006;27;99:924–32.CrossRefGoogle Scholar
Gomez, E, Buckingham, DW, Brindle, J, Lanzafame, F, Irvine, DS, Aitken, RJ. Development of an image analysis system to monitor the retention of residual cytoplasma by human spermatozoa: correlation with biochemical markers of the cytoplasmic space, oxidative stress, and sperm function. J Androl 1996;17:276–87.Google ScholarPubMed
Gil-Guzman, E, Ollero, M, Lopez, MC, Sharma, RK, Alvarez, JG, Thomas, AJ Jr., Agarwal, A. Differential production of reactive oxygen species by subsets of human spermatozoa at different stages of maturation. Hum Reprod 2001;16:1922–30.CrossRefGoogle ScholarPubMed
Aziz, N, Saleh, RA, Sharma, RK, Lewis-Jones, I, Esfandiari, N, Thomas, AJ Jr., Agarwal, A. Novel association between sperm reactive oxygen species production, sperm morphological defects, and the sperm deformity index. Fertil Steril 2004; 81:349–54.CrossRefGoogle ScholarPubMed
Aitken, J. Molecular mechanisms regulating human sperm function. Mol Hum Reprod 1997;3:169–73.CrossRefGoogle ScholarPubMed
Huszar, G, Vigue, L. Correlation between the rate of lipid peroxidation and cellular maturity as measured by creatine kinase activity in human spermatozoa. J Androl 1994;15:71–7.Google ScholarPubMed
Clermont, Y. The cycle of the seminiferous epithelium in man. Am J Anat 1963;112:35–51.CrossRefGoogle ScholarPubMed
Vernet, P, Fulton, N, Wallace, C, Aitken, RJ. Analysis of reactive oxygen species generating systems in rat epididymal spermatozoa. Biol Reprod 2001;65:1102–13.CrossRefGoogle ScholarPubMed
Baker, MA, Aitken, RJ. Reactive oxygen species in spermatozoa: methods for monitoring and significance for the origins of genetic disease and infertility. Reprod Biol Endocrinol 2005;3: 67–75.CrossRefGoogle ScholarPubMed
Balercia, G, Moretti, S, Vignini, A, Magagnini, M, Mantero, F, Boscaro, M et al. Role of nitric oxide concentrations on human sperm motility. J Androl 2004;25:245–9.CrossRefGoogle ScholarPubMed
Lewis, SEM, Donnelly, ET, Sterling, ESL, Kennedy, MS, Thompson, W, Chakrawarthy, U. Nitric oxide synthase and nitrite production in human spermatozoa: evidence that endogenous nitric oxide is beneficial to sperm motility. Mol Hum Reprod 1996; 2:873–8.CrossRefGoogle ScholarPubMed
Herrero, MB, Chatterjee, S, Lefievre, L, Lamirande, E, Gagnon, C. Nitric oxide interacts with the cAMP pathway to modulate capacitation of human spermatozoa. Free Rad Biol Med 2000; 29:522–36.CrossRefGoogle Scholar
Aitken, RJ, Baker, HW. Seminal leukocytes: passengers, terrorists or good samaritans?Hum Reprod 1995;10:1736–9.CrossRefGoogle ScholarPubMed
Shalika, S, Duaan, K, Smith, RD. The effect of positive semen bacterial and uroplasmal cultures on in vitro fertilization success. Hum Reprod 1996;11:2789–92.CrossRefGoogle ScholarPubMed
Aitkin, RJ, Fisher, HM, Fulton, N. Reactive oxygen species generation by human spermatozoa is induced by exogenous NADPH and inhibited by the flavoprotein inhibitors diphenylene iodonium and quinacrine. Mot Reprad Dev 1997;47:468–82.3.0.CO;2-S>CrossRefGoogle Scholar
Hendin, BN, Kolettis, PN, Sharma, RK, Thomas, AJ Jr., Agarwal, A. Varicocele is associated with elevated spermatozoal reactive oxygen species production and diminished seminal plasma antioxidant capacity. J Urol 1999;161:1831–4.CrossRefGoogle ScholarPubMed
Saleh, RA, Agarwal, A, Kandirali, E, Sharma, RK, Thomas, AJ Jr., Nada, EA et al. Leukocytospermia is associated with increased reactive oxygen species production by human spermatozoa. Fertil Steril 2002;78:1215–24.CrossRefGoogle ScholarPubMed
Alvarez, JG, Sharma, RK, Ollero, M, Saleh, RA, Lopez, MC, Thomas, AJ Jr. et al. Increased DNA damage in sperm from leukocytospermic semen samples as determined by the sperm chromatin structure assay. Fertil Steril 2002;78:319–29.CrossRefGoogle ScholarPubMed
Aziz, N, Agarwal, A, Lewis-Jones, I, Sharma, RK, Thomas, AJ Jr. Novel associations between specific sperm morphological defects and leukocytospermia. Fertil Steril 2004;82:621–7.CrossRefGoogle ScholarPubMed
Garrido, N, Meseguer, M, Simon, C, Pellicer, A, Remohi, J. Pro-oxidative and anti-oxidative imbalance in human semen and its relation with male fertility. Asian J Androl 2004;6:59–65.Google ScholarPubMed
Hendin, BN, Kolettis, PN, Sharma, RK, Thomas, AJ Jr., Agarwal, A. Varicocele is associated with elevated spermatozoal reactive oxygen species production and diminished seminal plasma antioxidant capacity. J Urol 1999;161:1831–4.CrossRefGoogle ScholarPubMed
Lamirande, E, Leclerc, P, Gagnon, C. Capacitation as a regulatory event that primes spermatozoa for the acrosome reaction and fertilization. Mol Hum Reprod 1997;3:175–94.CrossRefGoogle ScholarPubMed
Sanchez-Pena, LC, Reyes, BE, Lopez-Carrillo, L, Recio, R, Moran-Martinez, J, Cebrian, ME, Quintanilla-Vega, B. Organophosphorous pesticide exposure alters sperm chromatin structure in Mexican agricultural workers. Toxicol Appl Pharm 2004;196:108–13.CrossRefGoogle ScholarPubMed
Agarwal, A, Said, TM. Oxidative stress, DNA damage and apoptosis in male infertility: a clinical approach. Brit J Urol Int 2005;95:503–7.CrossRefGoogle ScholarPubMed
Saleh, RA, Agarwal, A, Sharma, RK, Nelson, DR, Thomas, AJ Jr. Effect of cigarette smoking on levels of seminal oxidative stress in infertile men: a prospective study. Fertil Steril 2002;78:491–9.CrossRefGoogle ScholarPubMed
Love, CC, Kenney, RM. Scrotal heat stress induces altered sperm chromatin structure associated with a decrease in protamines disulfide bonding in the stallion. Biol Reprod 1999; 60:615–20.CrossRefGoogle ScholarPubMed
Ishii, T, Matsuki, S, Iuchi, Y, Okada, F, Toyosaki, S, Tomita, Y et al. Accelerated impairment of spermatogenic cells in SOD1-knockout mice under heat stress. Free Radic Res 2005;39:697–705.CrossRefGoogle ScholarPubMed
Agarwal, A, Prabakaran, S, Allamaneni, SS. Relationship between oxidative stress, varicocele and infertility: a meta-analysis. Reprod Biomed Online 2006;12:630–3.CrossRefGoogle ScholarPubMed
Sheynkin, Y, Jung, M, Yoo, P, Schulsinger, D, Komaroff, E. Increase in scrotal temperature in laptop computer users. Hum Reprod 2005;20:452–5.CrossRefGoogle ScholarPubMed
Aitken, RJ, Buckingham, DW, Harkiss, D, Paterson, M, Fisher, H, Irvine, DS. The extragenomic action of progesterone on human spermatozoa is influenced by redox regulated changes in tyrosine phosphorylation during capacitation. Mol Cell Endocrinol 1996;117:83–93.CrossRefGoogle ScholarPubMed
Lamirande, E, Tsai, C, Harakat, A, Gagnon, C. Involvement of reactive oxygen species in human sperm acrosome reaction induced by A23187, lysophosphatidylcholine, and biological fluid ultrafiltrates. J Androl 1998;19:585–94.Google ScholarPubMed
Zini, A, Lamirande, E, Gagnon, C. Low levels of nitric oxide promote human sperm capacitation in vitro. J Androl 1995;16:424–31.Google ScholarPubMed
Sengoku, K, Tamate, K, Yoshida, T, Takaoka, Y, Miyamoto, T, Ishikawa, M. Effects of low concentrations of nitric oxide on the zona pellucida binding ability of human spermatozoa. Fertil Steril 1998;69:522–7.CrossRefGoogle ScholarPubMed
Saleh, RA, Agarwal, A. Oxidative stress and male infertility: from research bench to clinical practice. J Androl 2002;23: 737–52.Google ScholarPubMed
Balercia, G, Moretti, S, Vignini, A et al. Role of nitric oxide concentrations on human sperm motility. J Androl 2004;25:245–9.CrossRefGoogle ScholarPubMed
Agarwal, A, Saleh, RA. Role of oxidants in male infertility: rationale, significance, and treatment. Urol Clin North Am 2002; 29:817–27.CrossRefGoogle ScholarPubMed
Tominaga, H, Kodama, S, Matsuda, N et al. Involvement of reactive oxygen species (ROS) in the induction of genetic instability by radiation. J Radiat Res 2004;45:181–8.CrossRefGoogle ScholarPubMed
Moustafa, MH, Sharma, RK, Thornton, J et al. Relationship between ROS production, apoptosis and DNA denaturation in spermatozoa from patients examined for infertility. Hum Reprod 2004;19:129–38.CrossRefGoogle ScholarPubMed
Agarwal, A, Allamaneni, SS. The effect of sperm DNA damage on assisted reproduction outcomes. Minerva Ginecol 2004;56:235–45.Google ScholarPubMed
Agarwal, A, Said, TM. Role of sperm chromatin abnormalities and DNA damage in male infertility. Hum Reprod Update 2003;9(45):331.CrossRefGoogle ScholarPubMed
Saleh, RA, Agaswat, A, Nada, EA et al. Negative effects of increased sperm DNA damage in relation to seminal oxidative stress in men with idiopathic and male factor infertility. Fertil Steril 2003;79 (Suppl. 3):1597–605.CrossRefGoogle ScholarPubMed
Twigg, J, Fuhpa, N, Gomez, E, Irvine, DS, Aitken, RJ. Analysis of the impact of intracellular reactive oxygen species generation on the structural and functional integrity of human spermatozoa: lipid peroxidation, DNA fragmentation and effectiveness of antioxidants. Hum Reprod 1998;13(6):1429–36.CrossRefGoogle ScholarPubMed
Agarwal, A, Prabakaran, SA, Sikka, S. Clinical relevance of oxidative stress in patients with male factor infertility: evidence-based analysis. AUA Update 2007;26:1–12.Google Scholar
Aitken, RJ, Baker, MA, O'Bryan, M. Shedding light on chemiluminescence: the application of chemiluminescence in diagnostic andrology. J Androl 2004;25:455–65.CrossRefGoogle ScholarPubMed
Marchetti, C, Obert, G, Deffosez, A, Formstecher, P, Marchetti, P. Study of mitochondrial membrane potential, reactive oxygen species, DNA fragmentation and cell viability by flow cytometry in human sperm. Hum Reprod 2002;17:1257–65.CrossRefGoogle ScholarPubMed
Robinson, JP, Carter, WO, Narayanan, PK. Oxidative product formation analysis by flow cytometry. Methods Cell Biol 1994; 41:437–47.CrossRefGoogle ScholarPubMed
Cao, G, Prior, RL. Comparison of different analytical methods for assessing total antioxidant capacity of human serum. Clin Chem 1998;44:1309–15.Google ScholarPubMed
Benzie, IF, Strain, JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem 1996;239:70–6.CrossRefGoogle ScholarPubMed
Miller, NJ, Rice-Evans, C, Davies, MJ et al. A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. Clin Sci (Lond) 1993;84:407–12.CrossRefGoogle ScholarPubMed
Sharma, RK, Pasqualotto, FF, Nelson, DR et al. The reactive oxygen species-total antioxidant capacity score is a new measure of oxidative stress to predict male infertility. Hum Reprod 1999;14:2801–7.CrossRefGoogle ScholarPubMed
Wyllie, AH, Kerr, JF, Currie, AR. Cell death: the significance of apoptosis. Int Rev Cytol 1980;68:251–306.CrossRefGoogle Scholar
Spano, M, Seli, E, Bizzaro, D, Manicardi, GC, Sakkas, D. The significance of sperm nuclear DNA strand breaks on reproductive outcome. Curr Opin Obstet Gynecol 2005;17:255–60.CrossRefGoogle ScholarPubMed
Anzar, M, He, L, Buhr, MM, Kroetsch, TG, Pauls, KP. Sperm apoptosis in fresh and cryopreserved bull semen detected by flow cytometry and its relationship with fertility. Biol Reprod 2002;66:354–60.CrossRefGoogle ScholarPubMed
Gottlieb, RA. Mitochondria and apoptosis. Biol Signals Recept 2001;10:147–61.CrossRefGoogle ScholarPubMed
Scaffidi, C, Fulda, S, Srinivasan, A, Friesen, et al. Two CD95 (APO-1/Fas) signaling pathways. EMBO J 1998;7:1675–87.CrossRefGoogle Scholar
Thornberry, NA, Lazebnik, Y. Caspases: enemies within. Science 1998;281:1312–16.CrossRefGoogle Scholar
Selivanova, G, Wiman, KG. p53: a cell cycle regulator activated by DNA damage. Adv Cancer Res 1995;66:143–80.CrossRefGoogle ScholarPubMed
Fadok, VA, Cathelineau, A, Daleke, DL, Henson, PM, Bratton, DL. Loss of phospholipid asymmetry and surface exposure of phospha-tidylserine is required for phagocytosis of apoptotic cells by macrophages and fibroblasts. J Biol Chem 2001;276, 1071–7.CrossRefGoogle Scholar
Hoffmann, PR, Cathelineau, AM, Ogden, CA et al. Phosphatidylserine (PS) induces PS receptor-mediated macropinocytosis and promotes clearance of apoptotic cells. J Cell Biol (2001); 115:649–59.CrossRefGoogle Scholar
Hampton, MB, Fadeel, B, Orrenius, S. Redox regulation of the caspase during apoptosis. Am N Y Acad Sci 1999;854:328–35.CrossRefGoogle Scholar
Agarwal, A, Sharma Bedaiwy, MA. Role of reactive oxygen species in the pathophysiology of human reproduction. Fertil Steril 2003;79:829–43.CrossRefGoogle ScholarPubMed
Wang, X, Sharma, RK, Sikka, SC, Falcone, T, Agarwal, A. Oxidative sum is associated with increased apoptosis leading to spermatime DNA damage in patients with male factor infertility. Fertil Steril 2003;80:531–5.CrossRefGoogle Scholar
Halliwell, B. Antioxidant defence mechanisms: from the beginning to the end (of the beginning). Free Radic Res 1999;31:261–72.CrossRefGoogle Scholar
Muratori, M, Maggi, M, Spinelli, S, Filimberti, E, Forti, G, Baldi, E. Spontaneous DNA fragmentation in swim-up selected human spermatozoa during long term incubation. J Androl 2003;24:253–62.CrossRefGoogle ScholarPubMed
Oosterhuis, GJ, Mulder, AB, Kalsbeek-Batenburg, E, Lambalk, CB, Schoemaker, J, Vermes, I. Measuring apoptosis in human spermatozoa: a biological assay for semen quality?Fertil Steril 2000;74:245–50.CrossRefGoogle ScholarPubMed
Shen, HM, Dai, J, Chia, SE, Lim, A, Ong, CN. Detection of apoptotic alterations in sperm in subfertile patients and their correlations with sperm quality. Hum Reprod 2002;17:1266–73.CrossRefGoogle ScholarPubMed
Sun, JG, Jurisicova, A, Casper, RF. Detection of deoxyribonucleic acid fragmentation in human sperm: correlation with fertilization in vitro. Biol Reprod 1997;56:602–7.CrossRefGoogle ScholarPubMed
Weil, M, Jacobson, MD, Raff, MC. Are caspases involved in the death of cells with a transcriptionally inactive nucleus? Sperm and chicken erythrocytes. J Cell Sci 1998;111:2707–15.Google ScholarPubMed
Grunewald, S, Paasch, U, Glander, HJ, Anderegg, U. Mature human spermatozoa do not transcribe novel RNA. Andrologia 2005;37:69–71.CrossRefGoogle Scholar
Paasch, U, Sharma, RK, Gupta, AK, Grunewald, S, Mascha, EJ, Thomas, AJ Jr. et al. Cryopreservation and thawing is associated with varying extent of activation of apoptotic machinery in subsets of ejaculated human spermatozoa. Biol Reprod 2004;71:1828–37.CrossRefGoogle ScholarPubMed
Oehninger, S, Morshedi, M, Weng, SL, Taylor, S, Duran, H, Beebe, S. Presence and significance of somatic cell apoptosis markers in human ejaculated spermatozoa. Reprod Biomed Online 2003; 7:469–76.CrossRefGoogle ScholarPubMed
Taylor, SL, Weng, SL, Fox, P, Duran, EH, Morshedi, MS, Oehninger, S, Beebe, SJ. Somatic cell apoptosis markers and pathways in human ejaculated sperm: potential utility as indicators of sperm quality. Mol Hum Reprod 2004;10:825–34.CrossRefGoogle ScholarPubMed
Sakkas, D, Seli, E, Bizzaro, D, Tarozzi, N, Manicardi, GC. Abnormal spermatozoa in the ejaculate: abortive apoptosis and faulty nuclear remodelling during spermatogenesis. Reprod Biomed Online 2003;7:428–32.CrossRefGoogle ScholarPubMed
Lin, WW, Lamb, DJ, Wheeler, TM, Lipshultz, LI, Kim, ED. In situ end-labeling of human testicular tissue demonstrates increased apoptosis in conditions of abnormal spermatogenesis. Fertil Steril 1997;68:1065–9.CrossRefGoogle ScholarPubMed
Jurisicova, A, Lopes, S, Meriano, J, Oppedisano, L, Casper, RF, Varmuza, S. DNA damage in round spermatids of mice with a targeted disruption of the Pp1cgamma gene and in testicular biopsies of patients with non-obstructive azoospermia. Mol Hum Reprod 1999;5:323–30.CrossRefGoogle ScholarPubMed
Grunewald, S, Paasch, U, Wuendrich, K, Glander, HJ. Sperm caspases become more activated in infertility patients than in healthy donors during cryopreservation. Arch Androl 2005;51:449–60.CrossRefGoogle ScholarPubMed
Sakkas, D, Urner, F, Bianchi, PG, Bizzaro, D, Wagner, I, Jaquenoud, N et al. Sperm chromatin anomalies can influence decondensation after intracytoplasmic sperm injection. Hum Reprod 1996;11:837–43.CrossRefGoogle ScholarPubMed
Shoukir, Y, Chardonnens, D, Campana, A, Sakkas, D. Blastocyst development from supernumerary embryos after intracytoplasmic sperm injection: a paternal influence?Hum Reprod 1998;13:1632–7.CrossRefGoogle ScholarPubMed
Weil, M, Jacobson, MD, Raff, MC. Are caspases involved in the death of cells with a transcriptionally inactive nucleus? Sperm and chicken erythrocytes. J Cell Sci 1998;111:2707–15.Google ScholarPubMed
Pena, FJ, Johannisson, A, Wallgren, M, Rodriguez-Martinez, H. Assessment of fresh and frozen-thawed boar semen using an Annexin-V assay: a new method of evaluating sperm membrane integrity. Theriogenology 2003;60:677–89.CrossRefGoogle ScholarPubMed
Liu, CH, Tsao, HM, Cheng, TC, Wu, HM, Huang, CC, Chen, CI et al. DNA fragmentation, mitochondrial dysfunction and chromosomal aneuploidy in the spermatozoa of oligoasthenoteratozoospermic males. J Assist Reprod Genet 2004;21:119–26.CrossRefGoogle ScholarPubMed
Chen, Z, Hauser, R, Trbovich, AM, Shifren, JL, Dorer, DJ, Godfrey-Bailey, et al. The relationship between human semen characteristics and sperm apoptosis: a pilot study. J Androl 2006;27:112–20.CrossRefGoogle ScholarPubMed
Siddighi, S, Patton, WC, Jacobson, JD, King, A, Chan, PJ. Correlation of sperm parameters with apoptosis assessed by dual fluorescence DNA integrity assay. Arch Androl 2004;50:311–14.CrossRefGoogle ScholarPubMed
Said, TM, Paasch, U, Grunewald, S, Baumann, T, Li, L, Glander HJ, Agarwal, A. Advantage of combining magnetic cell separation with sperm preparation techniques. Reprod Biomed Online 2005b;10:740–6.CrossRefGoogle ScholarPubMed
Aziz, N, Said, T, Paasch, U, Agarwal, A. The relationship between human sperm apoptosis, morphology and the sperm deformity index. Hum Reprod 2007;15; [Epub ahead of print].Google ScholarPubMed
Sakkas, D, Mariethoz, E, St John, JC. Abnormal sperm parameters in humans are indicative of an abortive apoptotic mechanism linked to the Fas-mediated pathway. Exp Cell Res 1999; 15:350–5.CrossRefGoogle Scholar
Sakkas, D, Mariethoz, E, Manicardi, G, Bizzarro, D, Bianchi, PG, Bianchi, U. Origin of DNA damage in ejaculated human spermatozoa. Rev Reprod 1999;4:31–7.CrossRefGoogle ScholarPubMed
Sakkas, D, Moffat, O, Manicardi, GC, Mariethoz, E, Tarozzi, N, Bizzaro, D. Nature of DNA damage in ejaculated human spermatozoa and the possible involvement of apoptosis. Biol Reprod 2002;66:1061–7.CrossRefGoogle Scholar
Cayli, S, Sakkas, D, Vigue, L, Demir, R, Huszar, G. Cellular maturity and apoptosis in human sperm: creatine kinase, caspase-3 and Bcl-XL levels in mature and diminished maturity sperm. Mol Hum Reprod 2004;10:365–72.CrossRefGoogle ScholarPubMed
Frisch, SM, Screaton, RA. Anoikis mechanisms. Curr Opin Cell Biol 2001;13:555–62.CrossRefGoogle ScholarPubMed
Grunewald, S, Paasch, U, Glander, HJ. Enrichment of non-apoptotic human spermatozoa after cryopreservation by immunomagnetic cell sorting. Cell Tissue Bank 2001;2:127–33.CrossRefGoogle ScholarPubMed
Glander, HJ, Schiller, J, Suss, R, Paasch, U, Grunewald, S, Arnhold, J. Deterioration of spermatozoal plasma membrane is associated with an increase of sperm lyso-phosphatidylcholines. Andrologia 2002;34:360–6.CrossRefGoogle ScholarPubMed
Said, TM, Grunewald, S, Paasch, U et al. Effects of magnetic-activated cell sorting on sperm motility and cryosurvival rates. Fertil Steril 2005;83:1442–6.CrossRefGoogle ScholarPubMed
Said, T, Agarwal, A, Grunewald, S et al. Selection of nonapoptotic spermatozoa as a new tool for enhancing assisted reproduction outcomes: an in vitro model. Biol Reprod 2006;74:530–7.CrossRefGoogle Scholar
Ricci, G, Perticarari, S, Fragonas, E et al. Apoptosis in human sperm: its correlation with semen quality and the presence of leukocytes. Hum Reprod 2002;17:2665–72.CrossRefGoogle ScholarPubMed
Ekert, PG, Silke, J, Vaux, DL. Caspase inhibitors. Cell Death Differ 1999;6:1081–6.CrossRefGoogle ScholarPubMed
Barroso, G, Taylor, S, Morshedi, M et al. Mitochondrial membrane potential integrity and plasma membrane translocation of phosphatidylserine as early apoptotic markers: a comparison of two different sperm subpopulations. Fertil Steril 2006;85:149–54.CrossRefGoogle ScholarPubMed
Paasch, U, Grunewald, S, Fitzl, G, Glander, HJ. Deterioration of plasma membrane is associated with activation of caspases in human spermatozoa. J Androl 2003;24:246–52.CrossRefGoogle Scholar
Weng, SL, Taylor, SL, Morshedi, M et al. Caspase activity and apoptotic markers in ejaculated human sperm. Mol Hum Reprod 2002;8:984–91.CrossRefGoogle ScholarPubMed
Almeida, C, Cardoso, F, Sousa, M et al. Quantitative study of caspase-3 activity in semen and after swim-up preparation in relation to sperm quality. Hum Reprod 2005;20:1307–13.CrossRefGoogle ScholarPubMed
Benchaib, M, Braun, V, Lornage, J et al. Sperm DNA fragmentation decreases the pregnancy rate in an assisted reproductive technique. Hum Reprod 2003;18:1023–8.CrossRefGoogle Scholar
Blackwell, RP. Standards for microwave radiation. Nature 1979;282:360.CrossRefGoogle ScholarPubMed
Kandeel, FR, Swerdloff, RS. Role of temperature in regulation of spermatogenesis and the use of heating as a method for contraception. Fertil Steril 1988;49:1–23.Google Scholar
Saunders, R, Sienkiewicz, Z, Kowalczuk, C. Biological effects of electromagnetic fields and radiation. J Radiol Prot 1991;11:27–42.CrossRefGoogle Scholar
Ozguner, M, Koyu, A, Cesur, G, Ural, M, Ozguner, F, Gokcimen, A et al. Biological and morphological effects on the reproductive organ of rats after exposure to electromagnetic field. Saudi Med J 2005;26:405–10.Google ScholarPubMed
Yu, C, Yao, Y, Yang, Y, Li, D. [Changes of rat testicular germ cell apoptosis after high power microwave radiation]. Zhonghua Nan Ke Xue 2004;10:407–10.Google ScholarPubMed
Saunders, RD, Kowalczuk, CI. Effects of 2.45 GHz microwave radiation and heat on mouse spermatogenic epithelium. Int J Radiat Biol Relat Stud Phys Chem Med 1981;40:623–32.CrossRefGoogle ScholarPubMed
Lebovitz, RM, Johnson, L, Samson, WK. Effects of pulse- modulated microwave radiation and conventional heating on sperm production. J Appl Physiol 1987;62:245–52.CrossRefGoogle ScholarPubMed
Fejes, I, Zavaczki, Z, Szollosi, J, Koloszar, S, Daru, J, Kovacs, L et al. Is there a relationship between cell phone use and semen quality?Arch Androl 2005;51:385–93.CrossRefGoogle Scholar
Davoudi, M, Brossner, C, Kuber, W. The influence of electromagnetic waves on sperm motility. Urol Urogynacol 2002;19:18–22.Google Scholar
Erogul, O, Oztas, E, Yildirim, I, Kir, T, Aydur, E, Komesli, G et al. Effects of electromagnetic radiation from a cellular phone on human sperm motility: an in vitro study. Arch Med Res 2006;37:840–3.CrossRefGoogle Scholar
Agarwal, A, Deepinder, F, Sharma, RK, Ranga, G, Li, J. Effect of cell phone usage on semen analysis in men attending infertility clinic: an observational study. Fertil Steril 2007. In press.Google ScholarPubMed
Aitken, RJ. The Amoroso Lecture. The human spermatozoon—a cell in crisis?J Reprod Fertil 1999;115:1–7.CrossRefGoogle ScholarPubMed
Lai, H, Singh, NP. Single- and double-strand DNA breaks in rat brain cells after acute exposure to radiofrequency electromagnetic radiation. Int J Radiat Biol 1996;69:513–21.CrossRefGoogle ScholarPubMed
Aitken, RJ, Bennetts, , Sawyer, D, Wiklendt, AM, King, BV. Impact of radiofrequency electromagnetic radiation on DNA integrity in the male germline. Int J Androl 2005;28:171–9.CrossRefGoogle Scholar
Diem, E, Schwarz, C, Adlkofer, F, Jahn, O, Rudiger, H. Non- thermal DNA breakage by mobile-phone radiation (1800 MHz) in human fibroblasts and in transformed GFSH-R17 rat granulosa cells in vitro. Mutat Res 2005;583:178–83.CrossRefGoogle ScholarPubMed
Musaev, AV, Ismailova, LF, Gadzhiev, AM. [Influence of (460 MHz) electromagnetic fields on the induced lipid peroxidation in the structures of visual analyzer and hypothalamus in experimental animals]. Vopr Kurortol Fizioter Lech Fiz Kult 2005; 17–20.Google ScholarPubMed
Hook, GJ, Spitz, DR, Sim, JE et al. Evaluation of parameters of oxidative stress after in vitro exposure to FMCW- and CDMA-modulated radiofrequency radiation fields. Radiat Res 2004;162:497–504.CrossRefGoogle ScholarPubMed
Burch, JB, Reif, JS, Noonan, CW et al. Melatonin metabolite excretion among cellular telephone users. Int J Radiat Biol 2002;78:1029–36.CrossRefGoogle ScholarPubMed
Seze, R, Ayoub, J, Peray, P, Miro, L, Touitou, Y. Evaluation in humans of the effects of radiocellular telephones on the circadian patterns of melatonin secretion, a chronobiological rhythm marker. J Pineal Res 1999;27:237–42.CrossRefGoogle ScholarPubMed
Gavella, M, Lipovac, V. Antioxidative effect of melatonin on human spermatozoa. Arch Androl 2000;44:23–7.Google ScholarPubMed
Lantow, M, Viergutz, T, Weiss, DG, Simko, M. Comparative study of cell cycle kinetics and induction of apoptosis or necrosis after exposure of human mono mac 6 cells to radiofrequency radiation. Radiat Res 2006;166:539–43.CrossRefGoogle ScholarPubMed
Port, M, Abend, M, Romer, B, Beuningen, D. Influence of high-frequency electromagnetic fields on different modes of cell death and gene expression. Int J Radiat Biol 2003;79:701–8.CrossRefGoogle ScholarPubMed
Rizk, B. (Ed.). Ultrasonography in reproductive medicine and infertility, Cambridge: United Kingdom, Cambridge University Press 2008: (in press).Google Scholar

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