[Influence of the depth of the sperm counting chamber on sperm motility].

Zhonghua Nan Ke Xue

Geoffrey Laboratory for Semen Analysis, Jiangsu Jingcheng Pharmaceuticals Co., Ltd., Nanjing, Jiangsu 210036, China.

Published: September 2013

AI Article Synopsis

  • The study aimed to investigate how the depth of sperm counting chambers affects sperm motility by analyzing various semen samples using specialized measurement systems.
  • Four sperm counting chambers with different depths were tested, revealing that deeper chambers resulted in lower percentages of progressively motile sperm while non-progressively motile sperm increased.
  • The findings suggest that depth should be considered in sperm analysis to avoid misdiagnosis, indicating the need for updated reference ranges based on chamber depth.

Article Abstract

Objective: To investigate the influence of the depth of the sperm counting chamber on sperm motility.

Methods: We measured the depths of sperm counting chambers using the Filmetrics F20 Spectral Reflectance Thin-Film Measurement System. Then, according to the WHO5 manual, we analyzed 36 semen samples for the percentages of progressively motile sperm (PR) and non-progressively motile sperm (NP) and sperm motility (PR + NP) with the Ruiqi CFT-9201 computer-aided sperm analysis system, and compared the results of analysis.

Results: The depths of the 4 sperm counting chambers were 9.8, 12.7, 15.7 and 19.9 microm, respectively, and the obtained PR were (44.00 +/- 11.63), (41.96 +/- 12.62), (40.86 +/- 11.71) and (37.78 +/- 11.38)%, NP (13.54 +/- 3.01), (14.13 +/- 2.94), (14.91 +/- 3.02) and (16.53 +/- 2.77)%, and sperm motility (57.53 +/- 11.06), (56.08 +/- 11.97), (55.78 +/- 11.55) and (54.31 +/- 12.11)% from the 4 chambers, respectively. The depth of the sperm counting chamber was correlated negatively with PR (r = -0.993, P < 0.05) and sperm motility (r = -0.978, P < 0.05), but positively with NP (r = 0.989, P < 0.05). There were statistically significant differences between the 9.8 microm and 19.9 microm deep chambers in PR and NP (P < 0.05) though not in sperm motility among the 4 chambers of different depths.

Conclusion: The impact of the depth of the sperm counting chamber on sperm motility should not be ignored, for the deviation of the results from the chambers of different depths may lead clinicians to incorrect diagnosis and consequently inappropriate therapeutic approaches. Different reference ranges of sperm motility need to be normalized in correspondence to the depths of sperm counting chambers.

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