Related reproductive issues on male autosomal dominant polycystic kidney disease.
- Author:
Hong-cai CAI
;
Xue-jun SHANG
;
Yu-feng HUANG
- Publication Type:Journal Article
- MeSH:
Cysts;
pathology;
Ejaculatory Ducts;
pathology;
Female;
Humans;
Infertility, Male;
physiopathology;
Kidney;
pathology;
Male;
Mutation;
Polycystic Kidney, Autosomal Dominant;
physiopathology;
Pregnancy;
Reproductive Techniques, Assisted;
Semen Analysis;
Spermatozoa;
pathology
- From:
National Journal of Andrology
2015;21(11):1020-1025
- CountryChina
- Language:Chinese
-
Abstract:
Autosomal dominant polycystic kidney disease (ADPKD) is a most common inherited renal disease, about 50% with a family history, although the exact etiology not yet clear. To date, ADPKD, a multisystem disorder without effective preventive and therapeutic means, has been shown to be detrimental to human health. Recent studies show that severe oligoasthenozoospermia, necrospermia, immotile sperm, azoospermia, epididymal cyst, seminal vesicle cyst, and ejaculatory duct cyst found in male ADPKD patients may lead to male infertility, though the specific mechanisms remain unknown. Structural anomaly of spermatozoa, defect of polycystin, mutation of PKD genes, and micro-deletion of the AZF gene could be the reasons for the higher incidence of abnormal semen quality in male ADPKD patients. Assisted reproductive techniques can increase the chances of pregnancy, whereas the health of the offspring should be taken into consideration. This article presents an overview of reproductive issues concerning infertile male ADPKD patients from the perspective of the morbidity, pathophysiological mechanism, diagnosis, and management of the disease.
