- Open Access
Hypogonadotropic hypogonadism in men with hereditary hemochromatosis
Basic and Clinical Andrology volume 27, Article number: 13 (2017)
Hereditary hemochromatosis is a genetic disease that progresses silently. This disease is often diagnosed late when complications appear. Hypogonadotropic hypogonadism (HH) is one of the classical complications of hemochromatosis. Its frequency is declining probably because of earlier diagnosis and better informed physicians. Certain symptoms linked to HH can have an impact on a patient’s sexuality, such as decreased libido, erectile dysfunction, and impairment of ejaculation, as well as on his reproductive capacities.
This review is based on an online search in English, French and German language publications found in PubMed/Medline, up to 23 September 2016 using the following key word: Male infertility, Hypogonadotropic Hypogonadism, Hereditary Hemochromatosis.
Thirty-four papers met these inclusion criteria. This review describes the impact of iron overload on male fertility, resulting in hypogonadotropic hypogonadism and proposes treatment modalities.
L’Hémochromatose Héréditaire est. une maladie génétique qui évolue en silence. Son diagnostic est. souvent fait tardivement, au stade des complications. Même si son incidence diminue, l’Hypogonadisme Hypogonadotrope (HH) est. l’une des complications classiques de l’Hémochromatose. Ceci est. probablement le résultat d’un diagnostic plus précoce, d’une meilleure information des médecins. Certains symptômes en lien avec l’HH, peuvent avoir un impact sur la sexualité (diminution de la libido, dysfonction érectile ou troubles de l’éjaculation…) ainsi que sur la reproduction.
Cette revue repose sur une recherche online en langue anglaise, française et allemande de publications disponibles sur PubMed/Medline, jusqu’au 23 sept. 2016 à partir des mots clés suivants: infertilité masculine, hypogonadisme hypogonadotrope, Hémochromatose Héréditaire. Trente quatre publications ont satisfait aux critères de sélection. Cet article de revue décrit l’impact d’une surcharge en fer sur la fertilité masculine, notamment via l’Hypogonadisme Hypogonadotrope qu’elle induit et propose des modalités de traitement.
Hemochromatosis is an iron overload disease characterized by normal erythropoiesis, an increase in the saturation coefficient of transferrin (≥ 45%), an increase in the concentration of serum ferritin (≥300 μg/L in a human) and a parenchymal iron deposition caused by low levels of hepcidin . It is the most common inherited disease in France with an estimated prevalence of 0.3% . Due to its frequency, and its potentially complications, hemochromatosis has become nowadays a public health problem .
Iron overload causes endocrine dysfunction, particularly on the pituitary axis , with a potential impact on fertility. Indeed, iron overload can affect fertility through diverse mechanisms like HH, diabetes and cirrhosis. This review focuses on the reproductive dysfunction associated with iron overload-induced HH and proposes a patient management strategy which preserves the fertility of affected patients.
Materials and methods
Key words including ‘hemochromatosis’, ‘iron’, ‘male fertility’, ‘spermatogenesis’, and ‘hypogonadism’ were explored in PubMed and articles in English, French and German were included (up to 23 September 2016). The titles and abstracts of the resulting articles were evaluated by the second first author and last authors (REO, NG, and IK). Inclusion criteria were articles that focused on current knowledge in hemochromatosis, iron metabolism and human male fertility. In addition, some background articles on reproductive complications of endocrinopathies were included. Case reports which illustrated interesting elements of the disorder were also included.
The total amount of iron in the organism is approximately 4 g for men and 3 g for women . These 4 g of iron are bound to different proteins like hemoglobin or transferrin. Iron is a constituent of the respiratory chain and cytochromes; it plays the role of enzymatic cofactor, and is implicated in DNA replication or mRNA transcription .
Almost all iron is recycled. Digestive absorption balances out physiological loss, which is significant for women contrary to men because of menstruation. Fe2+ is transported from the intestinal lumen into the cytoplasm of the epithelial duodenal and jejune cells by the transporter Divalent Metal Transporter 1 (DMT1). Here, iron can be stored as ferritin or can be transported through the basal epithelial membrane by ferroportin and be exported into the lymphatic system. Iron is distributed to target tissues via transferrin which is synthetized by the liver. The iron-transferrin complex binds to the ubiquitous Transferrin Receptor (TfR-) 1 and to TfR-2, which is mainly expressed in the liver. One of the regulation mechanisms of the seric transfer of iron involves the peptide hormone hepcidin, a hormone synthezised in the liver. In physiological conditions, hepcidin synthesis is regulated by some proteins expressed in hepatocytes: Hereditary hemochromatosis Protein (HFE), transferring receptor 2 (TfR-2), hemojuvelin and transferrin. Hepcidin expression is also regulated by pathologic processes such as hypoxy or inflammation [6, 7].
HFE-TfR-1 complexes on the surface of hepatocytes sense the saturation of iron-bound transferrin in the serum. At low transferrin saturation, HFE is sequestered by TfR-1. As serum iron saturation increases, HFE is dislodged from its overlapping binding site on TfR-1 by the complex iron-transferrin. HFE is then free to interact with TfR-2 and signal the up-regulation of hepcidin. Increased levels of circulating hepcidin lead to a reduction in intestinal iron absorption and macrophage iron release, possibly through interaction with iron-export proteins such as ferroportin . This binding allows the internalization of the ferroportin-hepcidin complex. In healthy humans, the peptide hormone hepcidin plays a key role in iron homeostasis like insulin in glucose metabolism . If either HFE is mutated or absent, the complex is unable to sense increased serum transferring saturation, and dysregulation or iron homeostasis occurs. The most frequent mutation of HFE is C282Y .
Iron and spermatogenesis
Spermatogenesis requires iron both for the synthesis of DNA and for germ cell growth. In addition, spermatids and mature spermatozoa are very sensitive to oxidative stress . Thus, some evidence indicates that iron supply to germ cells may be tightly regulated by the blood testis barrier . Within the seminiferous tubules, spermatogonia and spermatocytes I acquire loaded ferritin iron from the nearby Sertoli cells. At the spermatid stage, iron is discharged to Sertoli cells which redistribute it to a new generation of spermatocytes. During spermatogenic development, iron is carried along from primary spermatocytes to spermatids; and from spermatids iron is recycled to the apical compartment of Sertoli cells, which traffic it back to a new generation of spermatocytes [11, 12].
A study of a mouse model carried out in 2012 highlighted the importance of the basal membrane of the seminiferous tubules as a protective barrier . Indeed, in case of iron overload, a large accumulation of iron is found in peripheral tissues and in the interstitial tissue of the testis and a much smaller iron accumulation can be found in the seminiferous tubules (see Fig. 1). Furthermore, this study highlights the recycling of iron within the seminiferous tubules (see Fig. 2) .
The transport of iron through the basal membrane of the seminiferous tubules is limited and indicates a largely autonomous iron cycle to provide effective protection against body overload.
It is possible to differentiate the direct effects of iron overload on fertility such as hypogonadotropic hypogonadism (HH) from the indirect damage it causes, such as diabetes or liver cirrhosis. This review focuses on HH.
Hypogonadotropic hypogonadism in iron overload
In iron overload, hypogonadism is the second most common endocrine abnormality after diabetes. Its frequency in the literature ranges from 10 to 100% . Indeed, older studies reported cases of patients at an advanced stage of hemochromatosis . Hypogonadism was reported in 6.4% of patients with hemochromatosis in the largest cohort . The study by Mc Dermott et al. that followed up 191 patients with hemochromatosis over 20 years, reported hypogonadism in 89% of patients with liver cirrhosis and 33% in patients with diabetes, both representing a complication of iron overload . In that study, the rate of hypogonadism decreased between the beginning (14.6%) and the end of the study (3%) , suggesting a potential influence of early detection and management of iron overload as potential disease modifiers of the natural history of the disease.
According to McDermott and Walsh, hypogonadism occurs at a relatively advanced stage of iron overload. Even if hypogonadism is generally diagnosed in patients with known iron overload, it could in some cases represent the main reason to consult a physician with a secondary diagnosis of iron overload . Due to social changes in the reasons for consulting a physician, notably the desire for children in men above 50, and the epidemiological landscape of iron overload-related complications in the elderly, hypogonadism could be more frequently diagnosed in Reproduction facilities.
Since the first description by Althausen and Kerr in 1933 , endocrine disorders related to iron-overload are better recognized [15, 16]. Some authors have suggested a testicular origin of hypogonadism [11, 17] but a pituitary origin is more commonly accepted ; however, regarding the hypothesis of a gonadic origin of hypogonadism, Lucesoli et al. reported in vivo experiments on rat testis response to acute iron overload: histopathology showed an iron deposition in the interstitial tissue at the periphery of seminiferous tubules and a rarefication of germ cells in them . Authors also highlighted an association between a moderate iron increase in the testis and an increase in oxidative stress in the testis with oxidative damage to lipids, proteins, and DNA. These observations confirmed the importance of the blood-testis barrier in the protection of germ cells against iron overload [17, 18]. In addition, the study by Lucesoli et al. emphasized the possibility of testicular damage directly related to iron deposition. Indeed, the iron deposition found in the testis suggested the potential involvement of testicular participation in the pathogenesis of hypogonadism associated with iron overload. These animal experimentations are in concordance with the case reported by Vogt et al. . They reported a case of a 45-year-old man presenting with hemochromatosis diagnosed 4 years earlier and consulting for a decreased libido and an erectile dysfunction suggesting hypogonadism. Gonadotrophin and testosterone levels were lower. The response of Leydig cells to human Chorionic Gonadotropin (hCG) injections was abnormally weak. The testicular histology was abnormal: maturation arrest at the spermatocyte stage was associated with an iron deposit in endothelial cells and perivascular spaces. Sertoli cells and Leydig cells contained no siderosomes but some lipofuscin, which is a pigment resulting from cell debris related to lysosomes aging in cases of cell sufferance . However these testicular deposits appeared to be variable [20,21,22].
Concerning the hypothesis of a pituitary origin of HH, the literature suggests that only the gonadotropic axis is disturbed. A review provided in 1996 reported hypogonadism in 46% of cases and only a subclinical deficiency of other axes (15% somatotropic, 8% lactotropic, 4% thyreotropic and 1.5% corticotropic) . The mechanism seemed to be the same whatever the etiology of the hemochromatosis (congenital or secondary). An iron deposit in gonadotropic cells of the anterior part of pituitary led to a decreased production of Follicle Stimulating Hormone (FSH) and Luteinizing Hormone (LH) by these cells .
In 1997, Oehninger et al. illustrated the unusual presentation of infertility linked to HH and due to retrograde ejaculation in a 44-year-old patient with hemochromatosis (homozygosity C282Y). They also showed that treatment with gonadotropin (hCG 2500 U twice a week and FSH 75 IU three times per week) associated with phlebotomy allows an improvement in the fertility of these patients  while dietary precautions, chelator administration and phlebotomy alone were not sufficient.
Another treatment consisted of testosterone hormonal replacement therapy in combination with phlebotomy. Indeed, patients with hemochromatosis have chronic liver disease and low testosterone blood levels with repercussions on erectile function and libido. Kley et al. showed the benefit of treatment with testosterone enanthate on the quality of life, libido and erectile function . These results agreed with the publication of Gama et al. which presented the case of a 44-years-old man with hemochromatosis C282Y/C282Y and suffering from HH . A replacement therapy with testosterone esters (Sustanon® then Proviron®) was administered for 6 years associated with regular phlebotomy (once a week for 4 years). The patient’s condition improved considerably. The substitution was stopped after 6 years. A complete restoration of pituitary function was obtained after treatment by the association of phlebotomy and hormonal replacement therapy . In 2001, Hamer et al. confirmed this result with another case . This patient was 36 years old, and presented also the homozygous mutation of the hemochromatosis allele C282Y/C282Y. He had been diagnosed at the stage of a prefibrotic liver without cirrhosis associated with HH. The history revealed 2 years of erectile dysfunction, decreased libido and infertility. Physical examination revealed symptoms of hypogonadism (a decrease of androgen-dependent hairiness, testicular atrophy and azoospermia). Because of the couple’s desire for a child, the initial phlebotomy (every 14 days, volume not indicated in the publication) was increased to a total of 700 mL per week. Testosterone intake was likewise increased from 100 mg every 3 weeks to 250 mg every 3 weeks. A year after the start of replacement therapy, the patient’s wife was pregnant and the patient’s sexual disorders vanished. After a few months, phlebotomy was carried out again only once a month. The replacement therapy was continued for another year. A yearly control showed no disorder related to hypogonadism and sexual behavior. The patient continued phlebotomy but no longer required replacement therapy. Thus, although testosterone was necessary for a rapid correction of sexual problems, only intensive phlebotomies allowed the normalization of endocrine function . Moreover, the age of the patient on diagnosis also appeared to be key in the reversibility of gonadotropic disorders: in another study, Cundy et al. reported the follow-up of six men suffering from hemochromatosis and treated by venesection therapy: only the youngest patient under 40 presented a complete reversal of his hypogonadotropic hypogonadism .
Firstly, regarding pituitary damage, the literature data suggest that it concerns only the gonadal axis. This may result from the exclusive iron deposition in the gonadotropic cells of the anterior pituitary gland leading to a defect of FSH and LH production that explains hypogonadism .
Secondly, hypogonadism in hemochromatosis has been long considered irreversible [30,31,32,33]. However, some examples of secondary hypogonadism in hemochromatosis with a recovered endocrine function prove that this is not always the case. The combination of iron depletion and hormonal replacement therapy appears to be the best strategy for a rapid improvement in a patient’s health status and quality of life. Replacement therapy helps to maintain a physiological level of testosterone and its metabolites (including dihydrotestosterone and estradiol) to optimize the maintenance of libido and sexual function . In addition, the correction of iron overload by phlebotomy is not always sufficient to normalize pituitary function .
These data emphasize that the age at diagnosis and the stage of the disease - especially liver complications - are determining factors for the success of phlebotomy, perhaps because of other indirect effects of Idiopathic Hereditary Hemochromatosis (IHH) (e.g. diabetes and cirrhosis). It is crucial to establish the diagnosis and to start treatment at an early stage of the disease. Thus, patients diagnosed for hereditary hemochromatosis and suffering from infertility or other reproductive disorders should have a brain Magnetic Resonance Imaging (MRI) and a Gonadotropin Releasing Hormone (GnRH) test in order to detect pituitary iron deposits. They could thus be treated by a combined therapy of hCG and phlebotomy. Figure 3 summarizes a suggestion of management optimization of a male patient with hereditary hemochromatosis including a hormonal check-up once Ferritin is ≥300 μg/L, whatever the clinical manifestation of the patient. In case of abnormal sex hormone concentrations, phlebotomy weekly should be proposed alone if patients are younger than 40, systematically associated with gonadotrophin treatment if 40 or older. According to cases reported in the literature, we recommend a systematic replacement therapy with gonadotropin associated with phlebotomy in hereditary hemochromatosis patients with infertility until they obtain the desired child.
Finally, before stopping the replacement therapy and returning to a less intense rhythm of phlebotomy, cryopreservation of spermatozoa may be offered to them.
Iron overload causes endocrine dysfunction, particularly on the gonadotropic axis, which is responsible for subfertility or infertility. However, the impact of hemochromatosis on reproductive function is multifactorial and depends mainly on pituitary and testicular damage despite the fact that liver or pancreatic damage can also play a role. A decrease in serum testosterone level in hypogonadal patients causes a decline in sexual desire and reduces ejaculation frequency impacting on the quality and quantity of semen. Nearly half of the men affected by hemochromatosis suffer from sexual disorders: erectile and ejaculation dysfunction and libido disorders. Knowledge of the presence of hemochromatosis and its complications in an infertile patient would help the andrologist to determine the best and most rapid strategies to normalize his gonadotropic function and to optimize his fertility.
Divalent Metal Transporter 1
Follicle Stimulating Hormone
Gonadotropin Releasing Hormone
Human Chorionic Gonadotropin
Idiopathic Hereditary Hemochromatosis
Periodic Acid Schiff
Transferrin Receptor 1
Transferrin Receptor 2
Janssen MCH, Swinkels DW. Hereditary haemochromatosis. Best Pract Res Clin Gastroenterol. 2009;23:171–83.
Corberand J, Martinez PA, Vinel J-P, Dine G, Michel H. Hereditary hemochromatosis, the clinician point of view. Ann Biol Clin (Paris). 2012;70:397–403.
Pietrangelo A. Hereditary hemochromatosis--a new look at an old disease. N Engl J Med. 2004;350:2383–97.
McDermott JH, Walsh CH. Hypogonadism in hereditary hemochromatosis. J Clin Endocrinol Metab. 2005;90:2451–5.
Finch CA, Huebers HA. Iron metabolism. Clin Physiol Biochem. 1986;4:5–10.
Zhang C. Essential functions of iron-requiring proteins in DNA replication, repair and cell cycle control. Protein Cell. 2014;5:750–60.
Weinstein DA, Roy CN, Fleming MD, Loda MF, Wolfsdorf JI, Andrews NC. Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease. Blood. 2002;100:3776–81.
Nemeth E, Tuttle MS, Powelson J, Vaughn MB, Donovan A, Ward DM, et al. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science. 2004;306:2090–3.
Pietrangelo A. Hemochromatosis: an endocrine liver disease. Hepatol Baltim Md. 2007;46:1291–301.
Aitken RJ, Curry BJ. Redox regulation of human sperm function: from the physiological control of sperm capacitation to the etiology of infertility and DNA damage in the germ line. Antioxid Redox Signal. 2011;14:367–81.
Leichtmann-Bardoogo Y, Cohen LA, Weiss A, Marohn B, Schubert S, Meinhardt A, et al. Compartmentalization and regulation of iron metabolism proteins protect male germ cells from iron overload. Am J Physiol Endocrinol Metab. 2012;302:E1519–30.
Jabado N, Canonne-Hergaux F, Gruenheid S, Picard V, Gros P. Iron transporter Nramp2/DMT-1 is associated with the membrane of phagosomes in macrophages and Sertoli cells. Blood. 2002;100:2617–22.
Walsh CH, Wright AD, Williams JW, Holder G. A study of pituitary function in patients with idiopathic hemochromatosis. J Clin Endocrinol Metab. 1976;43:866–72.
Wlazlo N, Peters W, Bravenboer B. Hypogonadism in a patient with mild hereditary haemochromatosis. Neth J Med. 2012;70:318–20.
Althausen T, Kerr W. A report of three cases with endocrine disturbances and notes on a previously reported case. Discussion of etiology. Endocrinology. 1933;17:621–46.
Simon M, Franchimont P, Murie N, Ferrand B, van Cauwenberge H, Bourel M. Study of somatotropic and gonadotropic pituitary function in idiopathic haemochromatosis (31 cases). Eur J Clin Investig. 1972;2:384–9.
Leichtmann-Bardoogo Y, Cohen LA, Weiss A, Marohn B, Schubert S, Meinhardt A, et al. Compartmentalization and regulation of iron metabolism proteins protect male germ cells from iron overload. Am J Physiol Endocrinol Metab. 2012;302:1519–30.
Lucesoli F, Caligiuri M, Roberti MF, Perazzo JC, Fraga CG. Dose-dependent increase of oxidative damage in the testes of rats subjected to acute iron overload. Arch Biochem Biophys. 1999;372:37–43.
Vogt HJ, Weidenbach T, Marquart KH, Vogel GE. Idiopathic hemochromatosis in a 45-year-old infertile man. Andrologia. 1987;19:532–8.
Hedinger C. Pathology of hemochromatosis; hemochromatosis as a syndrome. Helvetica Medica Acta Suppl. 1953;20:5–109.
Gilbert-Dreyfus. Testicular function in idiopathic hemochromatosis. Rev Fr Endocrinol Clin. 1969;10:191–203.
Onitilo AA, Engel JM, Sajjad SM. The possible role of hemochromatosis in testicular cancer. Med Hypotheses. 2011;77:179–81.
Pedersen-Bjergaard U, Thorsteinsson B, Kirkegaard BC. Pituitary function in hemochromatosis. Ugeskr Laeger. 1996;158:1818–22.
Bergeron C, Kovacs K. Pituitary siderosis. A histologic, immunocytologic, and ultrastructural study. Am J Pathol. 1978;93:295–309.
Oehninger S, Pike I, Slotnick N. Hemochromatosis and male infertility. Obstet Gynecol. 1998;92:652–3.
Kley HK, Stremmel W, Kley JB, Schlaghecke R. Testosterone treatment of men with idiopathic hemochromatosis. Clin Investig. 1992;70:566–72.
Gama R, Smith MJ, Wright J, Marks V. Hypopituitarism in primary haemochromatosis; recovery after iron depletion. Postgrad Med J. 1995;71:297–8.
Hamer OW, Gnad M, Schölmerich J, Palitzsch KD. Successful treatment of erectile dysfunction and infertility by venesection in a patient with primary haemochromatosis. Eur J Gastroenterol Hepatol. 2001;13:985–8.
Cundy T, Butler J, Bomford A, Williams R. Reversibility of hypogonadotrophic hypogonadism associated with genetic haemochromatosis. Clin Endocrinol. 1993;38:617–20.
Adams PC, Kertesz AE, Valberg LS. Clinical presentation of hemochromatosis: a changing scene. Am J Med. 1991;90:445–9.
Bomford A, Williams R. Long term results of venesection therapy in idiopathic haemochromatosis. Q J Med. 1976;45:611–23.
Lufkin EG, Baldus WP, Bergstralh EJ, Kao PC. Influence of phlebotomy treatment on abnormal hypothalamic-pituitary function in genetic hemochromatosis. Mayo Clin Proc. 1987;62:473–9.
McDonnell SM, Preston BL, Jewell SA, Barton JC, Edwards CQ, Adams PC, et al. A survey of 2,851 patients with hemochromatosis: symptoms and response to treatment. Am J Med. 1999;106:619–24.
Stremmel W, Niederau C, Berger M, Kley HK, Krüskemper HL, Strohmeyer G. Abnormalities in estrogen, androgen, and insulin metabolism in idiopathic hemochromatosis. Ann N Y Acad Sci. 1988;526:209–23.
Thanks to Pierre MONNIN from LORIA (CNRS, Inria Nancy-Grand Est, Université de Lorraine, Vandoeuvre-lès-Nancy, France) to Shyue-Fang HSU-BATTAGLIA and Cathy DIRIG for English language assistance.
This work has no financial support.
All studies used in this review were available on https://www-ncbi-nlm-nih-gov.gate2.inist.fr/pubmed/ except for some old studies which were available in a paper form at the Library of the Strasbourg University.
Availability of data and materials
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
El Osta, R., Grandpre, N., Monnin, N. et al. Hypogonadotropic hypogonadism in men with hereditary hemochromatosis. Basic Clin. Androl. 27, 13 (2017). https://doi.org/10.1186/s12610-017-0057-8
- Male infertility
- Hypogonadotropic Hypogonadism
- Hereditary Hemochromatosis
- infertilité masculine
- hypogonadisme hypogonadotrope
- Hémochromatose Héréditaire