Testosterone and fracture risk in older men

By Professor Bu Yeap, Endocrinologist, UWA & Fiona Stanley Hospital

The Western Australian Health In Men Study (HIMS) recently looked at how sex hormones might influence bone fracture risk, particularly hip fractures, in men. In 3,307 community-dwelling men aged 70 years and older, men with plasma testosterone levels in the middle two quartiles experienced the lowest risk of any fracture, and of hip fracture. Men with lower and higher plasma testosterone levels had greater fracture risk. The study allowed for other variables (e.g. age, existing medical conditions, frailty) indicating that testosterone was independently associated with fracture risk. This was 30-40% lower (40-50% for hip fracture) in men with mid-range plasma testosterone, compared to men with plasma testosterone in the lowest 25%. Men with plasma testosterone in the highest 25% had similar risk of any fracture, and hip fracture, as with men in the lowest 25%. Plasma oestradiol levels were not related to fracture occurrence.

Most previous studies have linked plasma oestradiol levels to fracture risk in men. HIMS, with a 10-year follow-up and 330 fracture events, including 144 hip fractures, is the largest study of its kind. The findings indicate plasma testosterone levels, rather than oestradiol levels, are a robust hormonal indicator of fracture risk continued from Page 29 but how long do you leave them in place for, because they are inefficiencies.” Mr Jones believes business would be better placed to consider what improvements have been made to their business over the past three months. Key messages

A U-shaped association of plasma testosterone levels with fracture incidence is seen in older men Men with mid-normal range testosterone levels had lower risk of any fracture, including hip fracture Testosterone treatment is indicated for men with pituitary or testicular disease (causing androgen deficiency) to restore levels to the physiological range.

in older men. Due to the nature of HIMS, it is not possible to assess the rate at which testosterone was converted to oestradiol in tissues such as bone.

A major Australia-wide randomised controlled trial (T4DM) of testosterone treatment in men aged 50-74 years with waist circumference 95cm or greater and either impaired glucose tolerance or newly diagnosed Type 2 diabetes, completed in 2019, is about to be reported. T4DM will discover whether testosterone treatment in men who do not have pituitary or testicular disease prevents or reverts Type 2 diabetes and whether testosterone treatment improves bone mineral density, coming back, so from a financial sense we have to look at each process and make it as efficient as possible,” he said. “Is telehealth going to be an improvement to keep? What other technology can be used? How can technology be used to prevent inefficiencies but enhance cash flow. “Consider the value both professionally and financially of the work you do and match the best approach to each. Is face-to-face and bone micro-architecture. If so, a larger interventional trial would be needed to clarify the role of testosterone treatment to reduce fracture risk in men.

The T4DM results and its bone sub-study, T4Bone, will be very informative.

Testosterone treatment is currently indicated in men with pituitary or testicular disease resulting in symptoms and signs of androgen deficiency, with commensurately low testosterone levels. Careful clinical assessment should precede, and ongoing clinical and biochemical monitoring accompany, testosterone therapy, aiming to achieve physiological levels.

The HIMS findings regarding fracture risk, reinforce this concept, highlighting that very high plasma testosterone levels may not be beneficial. Certainly, misuse and abuse of testosterone, (e.g. for performance or image enhancing) should be strongly discouraged.

– References available on request Author competing interests – the author has received speaker honoraria, conference and/or research support from Bayer, Lilly, Lawley Pharmaceuticals, Besins Healthcare

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