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. 2017 Nov 22;6(Suppl):S49–S56. doi: 10.1016/j.ijvsm.2017.11.001

Table 2.

The effect of different processing steps of semen cryopreservation on sperm plasma membrane (PM) and acrosome reaction (AR) examined by transmission electron microscopy.

Sample Slightly swollen PM
Swollen PM
Lost PM
P% OR CI (95%) P% OR CI (95%) P% OR CI (95%)
Diluted (37°C) 16a 2a 2a
Cooled (4°C, 2 h) 21a 1.40 0.68–2.87 2a 1.00 0.14–7.24 2a 1.00 0.14–7.24
Equilibrated (4°C, 4 h) 22a 1.48 0.73–3.02 15b 8.65 1.92–38.90 3a 1.52 0.25–9.27
Frozen-thawed (37°C) 10 a 0.58 0.25–1.36 40c 32.67 7.62–140.1 10b 5.44 1.16–25.52



Sample Typical AR Atypical AR Lost acrosome

P% Exact Sig.* P% OR CI (95%) P% OR CI (95%)

Diluted (37°C) 0a 9a 1a
Cooled (4°C, 2 h) 0a 1.000 14a 1.64 0.67–3.99 1a 1.00 0.62–16.2
Equilibrated (4°C, 4 h) 3a 0.246 16a 1.93 0.81–4.59 1a 1.00 0.62–16.2
Frozen-thawed (37°C) 10b 0.002 19b 2.37 1.06–5.54 6a 6.32 0.74–53.5

Data are shown as the “P” proportions of each parameter per 100 sperm counted in each sample. OR: Odds ratio and CI (95%): confidence interval are shown in comparison to freshly diluted semen at 37°C. Different alphabet superscripts within each column indicate significant different at P < .05 as analyzed by logistic regression (Wald test).

*

Typical AR was analyzed using 2-tailed Fisher exact test because the probability of 2 groups equals zero.