Abstract

SummaryAimAlthough “late onset hypogonadism”, a condition that includes low testosterone and symptoms, is common in men over the age of 40 years, diagnosis is not clear cut amongst non‐specialists. It is the aim of this review to provide an up to date picture of how this state should be diagnosed and managed.MethodsWe aim to describe how primary and secondary hypogonadism should be excluded before the diagnosis of late onset hypogonadism is reached. As laboratory testosterone measurements are essential the current pitfalls such as inappropriate sample collection and the use of population derived reference ranges are expanded. We review current evidence to determine associations between late onset hypogonadism and morbidity/mortality and benefits following testosterone replacement therapy.ResultsA review of the current evidence shows that late onset hypogonadism is associated with a worse metabolic state and increased mortality. Longitudinal studies have suggested that significant reductions in both symptoms and mortality are seen, especially in patients with type 2 diabetes.DiscussionThis review highlights the importance of diagnosing late onset hypogonadism due to its association with morbidity/mortality and benefits following testosterone replacement. Thus, after making recommendations to ensure correct diagnosis we speculate whether the time has come to move away from population derived testosterone levels towards evidence based action limits.

Highlights

  • In a meta-­ analysis by Corona et al.,[47] most studies included comprised of populations of men without “classic” hypogonadism; the resulting positive results reported in those studies indicated that symptomatic testosterone-­deficient men benefited from testosterone replacement therapy (TRT) regardless of the underlying aetiology. These results provide evidence that directly contradict recommendations to limit the use of TRT only to men with classic hypogonadism.[47]

  • The focus of this review is low testosterone levels associated with HG, a common phenomenon in middle aged and older men, i.e. late onset HG

  • Clinical training emphasises the importance of approaching most chronic pathologies from the clinical presentation and working backwards towards the aetiology before deciding on the management

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Summary

SYSTEMATIC REVIEW

Mark Livingston1 | Anura Kalansooriya1 | Andrew J. Summary Aim: “late onset hypogonadism”, a condition that includes low testosterone and symptoms, is common in men over the age of 40 years, diagnosis is not clear cut amongst non-specialists It is the aim of this review to provide an up to date picture of how this state should be diagnosed and managed. The entire anterior pituitary profile should be investigated (it is perhaps best to consider the hormonal deficiencies by both region of secretion and individual axes which is not within the scope of this review), including prolactin (high with some tumours, drug treatments and stress, while low in other instances), 9 am cortisol, thyroid-­stimulating hormone, free thyroxine, insulin-like growth factor-1, LH, FSH and repeat testosterone. Diagnosing pituitary disease requires experience with knowledge of endocrine pathways as the clinical state of the patient has to be matched to the individual hormone levels followed by a cascade of dynamic function tests and imaging.

Low or normal ACTH
10 | CONCLUSION
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CONFLICTS OF INTEREST
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