Replacement with sex steroids in hypopituitary men and women: implications for gender differences in morbidities and mortality

• Published in: Reviews in endocrine & metabolic disorders 2024-10, Vol.25 (5), p.839-854
• Main Authors: Donald, Darran Mc, McDonnell, Tara, O’Reilly, Michael W., Sherlock, Mark
• Format: Article
• Language: English
• Subjects: Body composition; Bone composition; Bone mineral density; Cardiovascular diseases; Cerebral infarction; Diabetes; Diabetes mellitus (non-insulin dependent); Endocrine disorders; Endocrinology; Estrogens; Fertility; Follicle-stimulating hormone; Gender; Gender differences; Gonadotropin-releasing hormone; Gonadotropins; Hormones; Hypopituitarism; Hypothalamic-pituitary-gonadal axis; Hypothalamus; Internal Medicine; Medicine; Medicine & Public Health; Morbidity; Mortality; Myocardial infarction; Pituitary (anterior); Risk factors; Sex differences; Sex hormones; Sexual dimorphism; Steroid hormones; Testosterone; Women
• ISSN: 1389-9155; 1573-2606; 1573-2606
• DOI: 10.1007/s11154-024-09897-7

Hypopituitarism is a heterogenous disorder characterised by a deficiency in one or more anterior pituitary hormones. There are marked sex disparities in the morbidity and mortality experienced by patients with hypopituitarism. In women with hypopituitarism, the prevalence of many cardiovascular risk factors, myocardial infarction, stroke and mortality are significantly elevated compared to the general population, however in men, they approach that of the general population. The hypothalamic-pituitary-gonadal axis (HPG) is the most sexually dimorphic pituitary hormone axis. Gonadotropin deficiency is caused by a deficiency of either hypothalamic gonadotropin-releasing hormone (GnRH) or pituitary gonadotropins, namely follicle-stimulating hormone (FSH) and luteinising hormone (LH). HPG axis dysfunction results in oestrogen and testosterone deficiency in women and men, respectively. Replacement of deficient sex hormones is the mainstay of treatment in individuals not seeking fertility. Oestrogen and testosterone replacement in women and men, respectively, have numerous beneficial health impacts. These benefits include improved body composition, enhanced insulin sensitivity, improved atherogenic lipid profiles and increased bone mineral density. Oestrogen replacement in women also reduces the risk of developing type 2 diabetes mellitus. When women and men are considered together, untreated gonadotropin deficiency is independently associated with an increased mortality risk. However, treatment with sex hormone replacement reduces the mortality risk comparable to those with an intact gonadal axis. The reasons for the sex disparities in mortality remain poorly understood. Potential explanations include the reversal of women’s natural survival advantage over men, premature loss of oestrogen’s cardioprotective effect, less aggressive cardiovascular risk factor modification and inadequate oestrogen replacement in women with gonadotropin deficiency. Regrettably, historical inertia and unfounded concerns about the safety of oestrogen replacement in women of reproductive age have impeded the treatment of gonadotropin deficiency.