# Sickle Cell Disease and Male Infertility: Pathophysiological Mechanisms, Clinical Manifestations, and Fertility Preservation Strategies—A Narrative Review

**Authors:** Christos Roidos, Aris Kaltsas, Evangelos N. Symeonidis, Vasileios Tzikoulis, Nikolaos Pantazis, Chara Tsiampali, Natalia Palapela, Athanasios Zachariou, Nikolaos Sofikitis, Fotios Dimitriadis

PMC · DOI: 10.3390/life16020192 · 2026-01-23

## TL;DR

This review explores how sickle cell disease affects male fertility, the underlying mechanisms, and options for preserving fertility in affected men.

## Contribution

The paper provides a comprehensive narrative review on the pathophysiology and fertility preservation strategies for male infertility in sickle cell disease.

## Key findings

- Recurrent vaso-occlusion and chronic hypoxia can damage the seminiferous epithelium and impair Leydig cell function.
- Oxidative stress and inflammation contribute to sperm DNA and membrane damage in men with SCD.
- Fertility preservation methods like semen cryopreservation and TESE are recommended before treatments like hydroxyurea or transplantation.

## Abstract

Sickle cell disease (SCD) is an inherited hemoglobinopathy in which hemoglobin S polymerization drives hemolysis and vaso-occlusion with progressive organ morbidity. Male reproductive impairment is increasingly recognized but remains underreported. This narrative review summarizes mechanistic pathways, clinical manifestations, and fertility preservation options relevant to men with SCD. PubMed, the Cochrane Library, and Medscape were searched through 31 December 2025 for human studies addressing endocrine changes, semen quality, priapism and erectile dysfunction, oxidative stress, and treatment-related gonadotoxicity. Evidence supports converging mechanisms: recurrent vaso-occlusion and chronic hypoxia may injure the seminiferous epithelium and impair Leydig cell steroidogenesis; oxidative stress and inflammation contribute to sperm DNA and membrane damage; and disease-modifying or curative therapies such as hydroxyurea and hematopoietic stem cell transplantation can further compromise spermatogenesis. Clinically, men with SCD may present with oligozoospermia, azoospermia, hypogonadism, and sexual dysfunction, particularly after recurrent ischemic priapism. Fertility preservation should be discussed early, ideally before prolonged hydroxyurea exposure or transplantation, and may include semen cryopreservation and testicular sperm extraction (TESE) with assisted reproduction when needed. Prospective longitudinal studies are required to define reproductive trajectories and optimize counseling and management.

## Linked entities

- **Chemicals:** hydroxyurea (PubChem CID 3657)
- **Diseases:** Sickle Cell Disease (MONDO:0011382), hypogonadism (MONDO:0002146), priapism (MONDO:0004745), azoospermia (MONDO:0100459)

## Full-text entities

- **Genes:** SCD (stearoyl-CoA desaturase) [NCBI Gene 6319] {aka FADS5, MSTP008, SCD1, SCDOS, hSCD1}, GNRH1 (gonadotropin releasing hormone 1) [NCBI Gene 2796] {aka GNRH, GRH, LHRH, LNRH}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, Rhoa (ras homolog family member A) [NCBI Gene 11848] {aka Arha, Arha1, Arha2}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, HBB (hemoglobin subunit beta) [NCBI Gene 3043] {aka CD113t-C, ECYT6, beta-globin}, Rock2 (Rho-associated coiled-coil containing protein kinase 2) [NCBI Gene 19878] {aka B230113H15Rik, ROKalpha, Rho-kinase, Rock-II, Rock2m, mKIAA0619}
- **Diseases:** ischemic injury (MESH:D017202), infertility (MESH:D007246), Endocrine abnormalities (MESH:D004700), endocrinopathies (MESH:C567425), Erectile Dysfunction (MESH:D007172), acidosis (MESH:D000138), Male reproductive abnormalities (MESH:D005058), urinary infections (MESH:D014552), reperfusion injury (MESH:D015427), thrombosis (MESH:D013927), testicular atrophy and failure (MESH:C543092), anemia (MESH:D000740), azoospermia (MESH:D053713), disordered spermatogenesis (MESH:C536875), parenchymal loss (MESH:D002543), -occlusive (MESH:D001157), nutritional deficiencies (MESH:D044342), semen abnormalities (MESH:C000711649), testosterone deficiency (MESH:D007153), acute chest syndrome (MESH:D056586), hormonal dysfunction (MESH:C562704), intimal hyperplasia (MESH:D006965), necrosis (MESH:D009336), malaria (MESH:D008288), pulmonary hypertension (MESH:D006976), penile tissue injury (MESH:D017695), gonadal dysfunction (MESH:D006058), infarct (MESH:D007238), androgen (MESH:D014770), organ damage (MESH:D000092124), penile injury (MESH:D010409), Oligozoospermia (MESH:D009845), SCD (MESH:D000755), sickle hemoglobin (MESH:D006450), delayed puberty (MESH:D011628), Sexual Dysfunction (MESH:D012735), ischemic (MESH:D002545), endothelial dysfunction (MESH:D014652), autosomal recessive hemoglobinopathies (MESH:D006453), vascular insufficiency (MESH:D065666), ischemic necrosis (MESH:D005271), Iron overload (MESH:D019190), fibrosis (MESH:D005355), Testicular Injury (MESH:D013733), Zinc deficiency (MESH:C564286), Male reproductive impairment (MESH:D005832), injury to (MESH:D014947), inflammation (MESH:D007249), hypoventilation (MESH:D007040), growth delay (MESH:D006130), mitochondrial dysfunction (MESH:D028361), pain (MESH:D010146), hematuria (MESH:D006417), vaso-occlusive crises (MESH:D013224), Male infertility (MESH:D007248), hypogonadism (MESH:D007006), Testicular ischemia (MESH:D007511), compensated (MESH:D005902), impaired reproductive status (MESH:D060737), vaso-occlusive injury (MESH:D003769)
- **Chemicals:** busulfan (MESH:D002066), malondialdehyde (MESH:D008315), LH (MESH:D007986), DHT (MESH:D013196), HU (MESH:D006918), ROS (MESH:D017382), lipid (MESH:D008055), cortisol (MESH:D006854), MDA (MESH:D015104), carbon monoxide (MESH:D002248), oxygen (MESH:D010100), Zinc (MESH:D015032), hexavalent chromium (MESH:C074702), opiate (MESH:D053610), cyclophosphamide (MESH:D003520), 8-OHdG (MESH:D000080242), nitric oxide (MESH:D009569), testosterone (MESH:D013739), iron (MESH:D007501)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** valine for glutamic acid at position 6

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942092/full.md

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Source: https://tomesphere.com/paper/PMC12942092