Journal of Andrology, Vol. 26, No. 6, November/December 2005
Copyright © American Society of Andrology
DOI: 10.2164/jandrol.05044
Severe Hypospermatogenesis in Cases of Nonobstructive Azoospermia: Should We Use Fresh or Frozen Testicular Spermatozoa?
RON HAUSER*,
LEAH YOGEV*,
AMI AMIT
,
HAIM YAVETZ*,
AMNON BOTCHAN*,
FUAD AZEM*,
JOSEPH B. LESSING* AND
DALIT BEN-YOSEF
From the * Institute for the Study of Fertility
and the
IVF Unit, Lis Maternity Hospital, Tel
Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv
University, Israel.
|
Correspondence to: Dr Ron Hauser, Institute for the Study of Fertility, Lis
Maternity Hospital, Tel Aviv Sourasky Medical Center, 6 Weizmann St, Tel Aviv
64239, Israel (e-mail:
ronh{at}tasmc.health.gov.il). |
The aim of this comparative clinical study was to examine whether the
fertilizing potential of frozen-thawed testicular sperm in the most severe
cases of hypospermatogenesis is reduced compared with fresh testicular sperm.
The results could determine the necessity of using fresh testicular sperm
cells, which mandates involving the spouse by performing simultaneous in vitro
fertilization intracytoplasmic sperm injection (IVF-ICSI) treatment in this
subgroup of nonobstructive azoospermia (NOA) patients. We studied 13 couples
in which the husband was diagnosed as having NOA and few motile testicular
sperm cells or only immotile testicular sperm cells were isolated by
testicular sperm extraction (TESE). Each couple underwent both an ICSI cycle,
in which fresh testicular sperm that were retrieved shortly beforehand were
injected, and a consecutive cycle, which used frozen-thawed sperm that were
retrieved in the original TESE procedure but were cryopreserved and stored
until use. We found that motility was lost during the freezing and thawing
process in some cases, which resulted in significantly more cycles with only
immotile sperm cells for injection in the frozen-thawed sperm group (38.5%)
than in the fresh sperm group (7.7%; P < .05). Availability of only
immotile sperm cells significantly reduced fertilization rates in both fresh
and frozen-thawed groups, but the respective overall fertilization rate (44.9%
vs 41.1%) and quality of embryos and pregnancy rate (18.2% vs 15.4%) were not
significantly different between groups. Implantation rates were more favorable
in the fresh sperm group (10.5% vs 5.9%), but not significantly so. We
conclude that, although cryopreservation does impair motility, which results
in significantly more cycles with only immotile sperm cells for ICSI in the
most severe forms of hypospermatogenesis, fertilization and pregnancy rates
are not significantly compromised.
Key words: Testicular sperm extraction, fertilization, implantation, IVF-ICSI
Copyright © 2005 by The American Society of Andrology.