The aim of this study was the evaluation of DNA flow cytometry for the anal
ysis of male infertility, 171 ejaculates from 155 patients with fertility p
roblems were analysed by flow cytometry and by conventional microscopical p
rocedures, Using flow cytometry, it was possible to determine the relative
proportions of the various cell populations: mature haploid and abnormal di
ploid mature spermatozoa, cellular fragments, immature germ cells (haploid
round spermatids, diploid cells, S phase and 4C cells), and of leukocytes a
s indicators of infection. A linear association was observed between sperm
concentration in semen as quantified by light microscopy and by flow cytome
try, even with fewer than 20 x 10(6) spermatozoa/ml, Eight classes of histo
grams, each with differing fractions of spermatozoa and other particles, we
re obtained and correlated with the results of the spermiograms. During the
10 year follow-up, the two patient groups with a low sperm concentration o
r a high concentration of cellular debris exhibited significantly impaired
fertility. The two patient groups with greater than or equal to 5% diploid
spermatozoa and with malcondensed sperm chromatin were also subfertile, No
ovulatory disorders were revealed in the 155 female partners. DNA flow cyto
metry thus provides an additional dimension to semen analysis not easily ga
ined by other methods and has the advantage of being rapidly performed and
interpreted, We therefore recommend application of this technique in the di
agnosis of male infertility.