Severe asthenozoospermia: a structural and functional study

Abstract

Ejaculates from 25 patients with severe asthenozoospermia (all spermatozoa immotile or only non‐progressively motile) were studied to identify individually the cause of impaired motility. Multiple tests were performed, viz. light and electron microscopic studies and sperm function tests. An objective scoring was applied to both the routine and the functional analyses. Three categories of samples were identified: (1) necrozoospermia (n=9), where sperm viability was very poor; (2) structural tail abnormality as seen by light microscopy (n=4); and (3) ultrastructural abnormality (n=12). In the last category, one case showed absence of dynein arms; this was associated with mitochondrial abnormalities. Mitochondrial abnormality with normal tail components was observed in the majority (n=7) and accessory fibre abnormality in four cases. The scoring system revealed that, functionally, all samples were abnormal whereas routine analysis showed 15 samples to be subnormal and 10 to be abnormal, which indicates the need for functional analysis. Because of the multiple defects seen in these samples, there is a need for a battery of sperm function tests. This study indicates that mitochondrial defects are one of the causes that may account for the loss of sperm motility in the patient population. Copyright © 1995, Wiley Blackwell. All rights reserved