Low-dose lisinopril in normotensive men with idiopathic oligospermia and infertility: a 5-year randomized, controlled, crossover pilot study

Clinical pharmacology and therapeutics, 91(4), 582-589

DOI 10.1038/clpt.2011.265 PMID 22378155

Abstract

The outcomes of drug treatment for male infertility remain conjectural, with controversial study results. Our pilot study employed a randomized, placebo-controlled, crossover methodology with intention-to-treat analysis. Thirty-three men with idiopathic oligospermia were randomized to start either daily oral lisinopril 2.5 mg (n = 17) or daily oral placebo (n = 16). Lisinopril was found to cause a normalization of seminal parameters in 53.6% of the participants. Although the mean ejaculate volume was unchanged (P ≥ 0.093), the total sperm cell count and the percentage of motile sperm cells increased (P ≤ 0.03 and P < 0.001, respectively), whereas the percentage of sperm cells with abnormal morphology decreased (P ≤ 0.04). The pregnancy rate was 48.5%, and there was no serious adverse drug event. It is concluded, albeit cautiously, that prolonged treatment with 2.5 mg/day of oral lisinopril may be well tolerated in normotensive men with idiopathic oligospermia, may improve sperm quantity and quality, and may enhance fertility in approximately half of those treated.

Topics

male factor infertility treatment, oligospermia lisinopril, idiopathic oligospermia pharmacological treatment, sperm count improvement medication, male infertility drug therapy, ace inhibitor fertility, sperm motility improvement, normotensive men oligospermia treatment, pregnancy rate male infertility

Cite this article

Mbah, A. U., Ndukwu, G. O., Ghasi, S. I., Shu, E. N., Ozoemena, F. N., Mbah, J. O., Onodugo, O. D., Ejim, E. C., Eze, M. I., Nkwo, P. O., & Okonkwo, P. O. (2012). Low-dose lisinopril in normotensive men with idiopathic oligospermia and infertility: a 5-year randomized, controlled, crossover pilot study. *Clinical pharmacology and therapeutics*, *91*(4), 582-589. https://doi.org/10.1038/clpt.2011.265

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