期刊论文详细信息
Reproductive Biology and Endocrinology
The effects of male age on sperm analysis by motile sperm organelle morphology examination (MSOME)
José G Franco1  Ricardo LR Baruffi1  Mario Cavagna2  Fabiana C Massaro1  Ana L Mauri1  Claudia G Petersen1  Joao Batista A Oliveira1  Liliane FI Silva1 
[1] Paulista Centre for Diagnosis, Research and Training, Ribeirao Preto, Brazil;Women's Health Reference Center, Perola Byington Hospital, Sao Paulo, Brazil
关键词: DNA damage;    Sperm morphology;    IMSI;    MSOME;    Male age;   
Others  :  1150901
DOI  :  10.1186/1477-7827-10-19
 received in 2012-01-11, accepted in 2012-03-19,  发布年份 2012
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【 摘 要 】

Background

This study aimed to investigate the influence of age on sperm quality, as analysed by motile sperm organelle morphology examination (MSOME).

Methods

Semen samples were collected from 975 men undergoing evaluation or treatment for infertility. Sperm cells were evaluated at 8400× magnification using an inverted microscope equipped with Nomarski (differential interference contrast) optics. Two forms of spermatozoa were considered: normal spermatozoa and spermatozoa with large nuclear vacuoles (LNV, defined as vacuoles occupying > 50% of the sperm nuclear area). At least 200 spermatozoa per sample were evaluated, and the percentages of normal and LNV spermatozoa were determined. The subjects were divided into three groups according to age: Group I, less than or equal to 35 years; Group II, 36-40 years; and Group III, greater than or equal to 41 years.

Results

There was no difference in the percentages of normal sperm between the two younger (I and II) groups (P > 0.05). The percentage of normal sperm in the older group (III) was significantly lower than that in the younger (I and II) groups (P < 0.05). There was no difference in the percentage of LNV spermatozoa between the younger (I and II) groups (P > 0.05). The percentage of LNV spermatozoa was significantly higher in the older group (III) than in the younger (I and II) groups (P < 0.05). Regression analysis demonstrated a significant decrease in the incidence of normal sperm with increasing age (P < 0.05; r = -0.10). However, there was a significant positive correlation between the percentage of spermatozoa with LNV and male age (P < 0.05, r = 0.10).

Conclusion

The results demonstrated a consistent decline in semen quality, as reflected by morphological evaluation by MSOME, with increased age. Considering the relationship between nuclear vacuoles and DNA damage, these age-related changes predict that increased paternal age should be associated with unsuccessful or abnormal pregnancy as a consequence of fertilisation with damaged spermatozoa. Given that sperm nuclear vacuoles can be evaluated more precisely at high magnification, these results support the routine use of MSOME for ICSI as a criterion for semen analysis.

【 授权许可】

   
2012 Silva et al; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Schwartz D, Mayaux MJ, Spira A, Moscato ML, Jouannet P, Czyglik F, David G: Semen characteristics as a function of age in 833 fertile men. Fertil Steril 1983, 39:530-535.
  • [2]Andolz P, Bielsa MA, Vila J: Evolution of semen quality in North-eastern Spain: a study in 22,759 infertile men over a 36 year period. Hum Reprod 1999, 14:731-735.
  • [3]Auger J, Kunstmann JM, Czyglik F, Jouannet P: Decline in semen quality among fertile men in Paris during the past 20 years. N Engl J Med 1995, 332:281-285.
  • [4]Centola GM, Eberly S: Seasonal variations and age-related changes in human sperm count, motility, motion parameters, morphology, and white blood cell concentration. Fertil Steril 1999, 72:803-808.
  • [5]de la Rochebrochard E, Thonneau P: Paternal age and maternal age are risk factors for miscarriage; results of a multicentre European study. Hum Reprod 2002, 17:1649-1656.
  • [6]Jung A, Schuppe HC, Schill WB: Comparison of semen quality in older and younger men attending an andrology clinic. Andrologia 2002, 34:116-122.
  • [7]Girsh E, Katz N, Genkin L, Girtler O, Bocker J, Bezdin S, Barr I: Male age influences oocyte-donor program results. J Assist Reprod Genet 2008, 25:137-143.
  • [8]Klonoff-Cohen HS, Natarajan L: The effect of advancing paternal age on pregnancy and live birth rates in couples undergoing in vitro fertilization or gamete intrafallopian transfer. Am J Obstet Gynecol 2004, 191:507-514.
  • [9]Zhu QX, Meads C, Lu ML, Wu JQ, Zhou WJ, Gao ES: Turning point of age for semen quality: a population-based study in Chinese men. Fertil Steril 2011, 96:572-576.
  • [10]de Almeida Ferreira Braga DP, Setti AS, Figueira RC, Nichi M, Martinhago CD, Iaconelli A Jr, Borges E Jr: Sperm organelle morphologic abnormalities: contributing factors and effects on intracytoplasmic sperm injection cycles outcomes. Urology 2011, 78:786-791.
  • [11]Mladenovic I, Micic S, Papic N, Genbacev O, Marinkovic B: Sperm morphology and motility in different age populations. Arch Androl 1994, 32:197-205.
  • [12]Bujan L, Mieusset R, Mondinat C, Mansat A, Pontonnier F: Sperm morphology in fertile men and its age related variation. Andrologia 1988, 20:121-128.
  • [13]Slama R, Bouyer J, Windham G, Fenster L, Werwatz A, Swan SH: Influence of paternal age on the risk of spontaneous abortion. Am J Epidemiol 2005, 161:816-823.
  • [14]Kleinhaus K, Perrin M, Friedlander Y, Paltiel O, Malaspina D, Harlap S: Paternal age and spontaneous abortion. Obstet Gynecol 2006, 108:369-377.
  • [15]Glaser RL, Broman KW, Schulman RL, Eskenazi B, Wyrobek AJ, Jabs EW: The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. Am J Hum Genet 2003, 73:939-947.
  • [16]Lambert SM, Masson P, Fisch H: The male biological clock. World J Urol 2006, 24:611-617.
  • [17]Wyrobek AJ, Eskenazi B, Young S, Arnheim N, Tiemann-Boege I, Jabs EW, Glaser RL, Pearson FS, Evenson D: Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm. Proc Natl Acad Sci USA 2006, 103:9601-9606.
  • [18]Schmid TE, Eskenazi B, Baumgartner A, Marchetti F, Young S, Weldon R, Anderson D, Wyrobek AJ: The effects of male age on sperm DNA damage in healthy non-smokers. Hum Reprod 2007, 22:180-187.
  • [19]van der Merwe FH, Kruger TF, Oehninger SC, Lombard CJ: The use of semen parameters to identify the subfertile male in the general population. Gynecol Obstet Invest 2005, 59:86-91.
  • [20]Bartoov B, Berkovitz A, Eltes F, Kogosowski A, Menezo Y, Barak Y: Real-time fine morphology of motile human sperm cells is associated with IVF-ICSI outcome. J Androl 2002, 23:1-8.
  • [21]Bartoov B, Berkovitz A, Eltes F, Kogosovsky A, Yagoda A, Lederman H, Artzi S, Gross M, Barak Y: Pregnancy rates are higher with intracytoplasmic morphologically selected sperm injection than with conventional intracytoplasmic injection. Fertil Steril 2003, 80:1413-1419.
  • [22]Antinori M, Licata E, Dani G, Cerusico F, Versaci C: d'Angelo D, Antinori S: Intracytoplasmic morphologically selected sperm injection: a prospective randomized trial. Reproductive biomedicine online 2008, 16:835-841.
  • [23]Oliveira JB, Massaro FC, Baruffi RL, Mauri AL, Petersen CG, Silva LF, Vagnini LD, Franco JG Jr: Correlation between semen analysis by motile sperm organelle morphology examination and sperm DNA damage. Fertil Steril 2010, 94:1937-1940.
  • [24]Franco JG Jr: Baruffi RL, Mauri AL, Petersen CG, Oliveira JB, Vagnini L: Significance of large nuclear vacuoles in human spermatozoa: implications for ICSI. Reproductive biomedicine online 2008, 17:42-45.
  • [25]Garolla A, Fortini D, Menegazzo M, De Toni L, Nicoletti V, Moretti A, Selice R, Engl B, Foresta C: High-power microscopy for selecting spermatozoa for ICSI by physiological status. Reproductive biomedicine online 2008, 17:610-616.
  • [26]Knez K, Zorn B, Tomazevic T, Vrtacnik-Bokal E, Virant-Klun I: The IMSI procedure improves poor embryo development in the same infertile couples with poor semen quality: a comparative prospective randomized study. Reproductive biology and endocrinology: RB&E 2011, 9:123. BioMed Central Full Text
  • [27]Franco JG Jr, Mauri AL, Petersen CG, Massaro FC, Silva LF, Felipe V, Cavagna M, Pontes A, Baruffi RL, Oliveira JB, Vagnini LD: Large nuclear vacuoles are indicative of abnormal chromatin packaging in human spermatozoa. Int J Androl 2011.
  • [28]Wilding M, Coppola G, di Matteo L, Palagiano A, Fusco E, Dale B: Intracytoplasmic injection of morphologically selected spermatozoa (IMSI) improves outcome after assisted reproduction by deselecting physiologically poor quality spermatozoa. J Assist Reprod Genet 2011, 28:253-262.
  • [29]Cassuto NG, Bouret D, Plouchart JM, Jellad S, Vanderzwalmen P, Balet R, Larue L, Barak Y: A new real-time morphology classification for human spermatozoa: a link for fertilization and improved embryo quality. Fertil Steril 2009, 92:1616-1625.
  • [30]Berkovitz A, Eltes F, Ellenbogen A, Peer S, Feldberg D, Bartoov B: Does the presence of nuclear vacuoles in human sperm selected for ICSI affect pregnancy outcome? Hum Reprod 2006, 21:1787-1790.
  • [31]Balaban B, Yakin K, Alatas C, Oktem O, Isiklar A, Urman B: Clinical outcome of intracytoplasmic injection of spermatozoa morphologically selected under high magnification: a prospective randomized study. Reproductive biomedicine online 2011.
  • [32]Oliveira JB, Cavagna M, Petersen CG, Mauri AL, Massaro FC, Silva LF, Baruffi RL, Franco JG Jr: Pregnancy outcomes in women with repeated implantation failures after intracytoplasmic morphologically selected sperm injection (IMSI). Reproductive biology and endocrinology: RB&E 2011, 9:99. BioMed Central Full Text
  • [33]Sermondade N, Hafhouf E, Dupont C, Bechoua S, Palacios C, Eustache F, Poncelet C, Benzacken B, Levy R, Sifer C: Successful childbirth after intracytoplasmic morphologically selected sperm injection without assisted oocyte activation in a patient with globozoospermia. Hum Reprod 2011, 26:2944-2949.
  • [34]Berkovitz A, Eltes F, Yaari S, Katz N, Barr I, Fishman A, Bartoov B: The morphological normalcy of the sperm nucleus and pregnancy rate of intracytoplasmic injection with morphologically selected sperm. Hum Reprod 2005, 20:185-190.
  • [35]Cassuto NG, Hazout A, Benifla JL, Balet R, Larue L, Viot G: Decreasing birth defect in children by using high magnification selected spermatozoon injection. Fertil Steril 2011, 96:S85.
  • [36]WHO laboratory manual for the examination and processing of human semen. 5th edition. [Geneva]: World Health Organization; 2010.
  • [37]ASTM: Standart E1951-02 Physical and mechanical testing standards [http://www.astm.org] webciteWest Conshohocken, PA; 2007. doi: 10.1520/E1951-02R07
  • [38]Auger J, Eustache F, Ducot B, Blandin T, Daudin M, Diaz I, Matribi SE, Gony B, Keskes L, Kolbezen M, et al.: Intra- and inter-individual variability in human sperm concentration, motility and vitality assessment during a workshop involving ten laboratories. Hum Reprod 2000, 15:2360-2368.
  • [39]Brahem S, Mehdi M, Elghezal H, Saad A: The effects of male aging on semen quality, sperm DNA fragmentation and chromosomal abnormalities in an infertile population. Journal of assisted reproduction and genetics 2011, 28:425-432.
  • [40]Nijs M, De Jonge C, Cox A, Janssen M, Bosmans E, Ombelet W: Correlation between male age, WHO sperm parameters, DNA fragmentation, chromatin packaging and outcome in assisted reproduction technology. Andrologia 2011, 43:174-179.
  • [41]Kidd SA, Eskenazi B, Wyrobek AJ: Effects of male age on semen quality and fertility: a review of the literature. Fertil Steril 2001, 75:237-248.
  • [42]Vagnini L, Baruffi RL, Mauri AL, Petersen CG, Massaro FC, Pontes A, Oliveira JB, Franco JG Jr: The effects of male age on sperm DNA damage in an infertile population. Reproductive biomedicine online 2007, 15:514-519.
  • [43]Borini A, Tarozzi N, Bizzaro D, Bonu MA, Fava L, Flamigni C, Coticchio G: Sperm DNA fragmentation: paternal effect on early post-implantation embryo development in ART. Hum Reprod 2006, 21:2876-2881.
  • [44]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.
  • [45]Zini A, Libman J: Sperm DNA damage: importance in the era of assisted reproduction. Curr Opin Urol 2006, 16:428-434.
  • [46]Bungum M, Humaidan P, Axmon A, Spano M, Bungum L, Erenpreiss J, Giwercman A: Sperm DNA integrity assessment in prediction of assisted reproduction technology outcome. Hum Reprod 2007, 22:174-179.
  • [47]Menezo YJ, Hazout A, Panteix G, Robert F, Rollet J, Cohen-Bacrie P, Chapuis F, Clement P, Benkhalifa M: Antioxidants to reduce sperm DNA fragmentation: an unexpected adverse effect. Reproductive biomedicine online 2007, 14:418-421.
  • [48]Bar-Chama N, Schiff J, Luna M, Dann B, Copperman A, Barritt J: The level of sperm vacuoles in the fresh post-processed sperm sample significantly affects IVF cycle outcomes. Fertil Steril 2007, 88:S18.
  • [49]Carrell DT: Contributions of spermatozoa to embryogenesis: assays to evaluate their genetic and epigenetic fitness. Reproductive biomedicine online 2008, 16:474-484.
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