Fertility in cystinosis

Ahmed Reda*, Koenraad Veys*, Martine Besouw*

*Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    3 Citations (Scopus)
    38 Downloads (Pure)

    Abstract

    Cystinosis is a rare inheritable lysosomal storage disorder characterized by cystine accumulation throughout the body, chronic kidney disease necessitating renal replacement therapy mostly during adolescence, and multiple extra-renal complications. The majority of male cystinosis patients are infertile due to azoospermia, in contrast to female patients who are fertile. Over recent decades, the fertility status of male patients has evolved from a primary hypogonadism in the era before the systematic treatment with cysteamine to azoospermia in the majority of cysteamine-treated infantile cystinosis patients. In this review, we provide a state-of-the-art overview on the available clinical, histopathological, animal, and in vitro data. We summarize current insights on both cystinosis males and females, and their clinical implications including the potential effect of cysteamine on fertility. In addition, we identify the remaining challenges and areas for future research.

    Original languageEnglish
    Article number3539
    JournalCells
    Volume10
    Issue number12
    DOIs
    Publication statusPublished - Dec-2021

    Keywords

    • Azoospermia
    • Cysteamine
    • Cystinosis
    • Fertility
    • Histopathology
    • Hypogonadism
    • Mouse model

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