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From the * Reproductive Medicine Center, Scanian
Andrology Center, and the
Department of
Clinical Chemistry, Lund University, Malmö University Hospital,
Malmö, Sweden
| Correspondence to: Dr Saad Elzanaty, Reproductive Medicine Center, Scanian Andrology Center, Lund University, Malmö University Hospital, SE 205 02 Malmö, Sweden (e-mail: saad.elzanaty{at}med.lu.se). |
-glucosidase [NAG]), prostate (prostate-specific antigen [PSA]
and zinc), and seminal vesicles (fructose). Three groups were defined
according to time from ejaculation to analysis: G
30
(24–30 minutes), G31–60 (31–60 minutes), and
G>60 (63–180 minutes). The proportion of progressively
motile sperm was significantly lower in G>60 than in
G
30 (mean difference, 8.0%; 95% confidence interval [CI],
2.0%–13%) or G31–60 (mean difference, 6.0%; 95% CI,
1.0%–12%). The proportion of rapid progressive sperm motility was
significantly higher in G
30 compared with
G31–60 (mean difference, 3.0%; 95% CI, 1.0%–5.0%) and
G>60 (mean difference, 6.0%; 95% CI, 1.0%–10%). Sperm
morphology and viability did not vary significantly between the groups.
However, PSA levels in G>60 were 29% and 31% significantly lower
than in G
30 (95% CI, 3.0%–54%) and
G31–60 (95% CI, 7.0%–58%), respectively. Moreover, men
in G>60 had 29% and 17% significantly lower zinc compared with
those in G
30 (95% CI, 4.0%–69%) and
G31–60 (95% CI, 4.0%–64%), respectively. Levels of NAG
and fructose did not differ significantly between the groups. There were
negative associations between the ejaculation-to-analysis interval and sperm
motility and levels of PSA and zinc. In male infertility assessments, semen
analysis should be performed within 60 minutes of ejaculation.
Key words: Biochemical markers, morphology, semen analysis, viability
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