Dr. Giovanni Adami, a researcher studying bone loss in patients treated with low-dose glucocorticoids, discusses the potential benefits of low doses in inflammatory diseases and the limitations of measuring bone mineral density in glucocorticoid-induced osteoporosis. The podcast also explores the findings of a study on osteoporosis therapy for rheumatic disease patients receiving lower glucocorticoid doses, suggesting a change in practice compared to current guidelines.
Low doses of glucocorticoids combined with anti-osteoporosis medications can halt or reverse bone loss in patients with inflammatory rheumatic musculoskeletal diseases.
Risk of fractures increases with longer glucocorticoid exposure, emphasizing the need for anti-osteoporosis treatment.
Deep dives
The Effectiveness of Low Dose Glucocorticoids in Reducing Fracture Risk
In this podcast episode, the speaker discusses the potential trade-off between low doses of glucocorticoids and reduced fracture risk in patients with inflammatory rheumatic musculoskeletal diseases. While high doses of glucocorticoids have long been known to be detrimental to bone health, recent studies have suggested that low doses may have some benefits. The speaker references the Gloria trial, which found that five milligrams of prednisone may be beneficial with few adverse effects. However, it is important to note that the use of dual x-ray absorbitometry (DEXA) to measure bone mineral density can sometimes be misleading in patients with glucocorticoid-induced osteoporosis. This is because glucocorticoids not only affect bone density but also the microarchitecture of the bone. The speaker also introduces the derived fracture risk assessment tool (DFRO), which is similar to the FRAX but incorporates additional factors tailored to the Italian population. The speaker presents data from a longitudinal study using the DFRO database, revealing that patients on low doses of glucocorticoids combined with anti-osteoporosis medications can halt or even reverse bone loss. However, patients on higher doses of glucocorticoids continue to experience bone loss. The speaker highlights the importance of considering fracture risk beyond bone mineral density, particularly in patients on glucocorticoids. The study also explores bone turnover markers and discusses the limitations of real-world data and potential confounding factors in interpreting the results.
Methodology and Cohort Characteristics
The speaker provides insights into the study's methodology and cohort characteristics. The study utilized a longitudinal design, analyzing patients with inflammatory rheumatic musculoskeletal diseases and controls through the DFRO database. The cohort consisted predominantly of patients with rheumatoid arthritis, along with smaller proportions of other conditions such as psoriatic arthritis and systemic lupus erythematosus. The participants were primarily postmenopausal women, above the age of 50. The speaker also mentions the inclusion of bone turnover markers in the analysis, emphasizing that the availability of this data depended on its inclusion by the physicians. The speaker acknowledges the strengths of real-world data in providing a larger sample size but also highlights certain limitations, such as the potential for misclassification bias and the absence of data on disease activity in the rheumatic disease cohort.
Fracture Risk and Clinical Implications
The speaker discusses the key findings of the study related to fracture risk and their clinical implications. The analysis revealed that the risk of fractures increases with longer glucocorticoid exposure, particularly beyond two years of treatment. Patients on very low doses of glucocorticoids showed increased fracture risk even with a small loss in bone mineral density. The study highlights the importance of considering factors beyond bone mineral density alone, as glucocorticoids may affect bone microarchitecture and lead to a low bone turnover state. The speaker acknowledges the need for further research and confirms that these findings align with recent guidelines that recommend initiating anti-osteoporosis treatment for patients receiving low doses of glucocorticoids. Finally, the speaker shares personal insights, expressing gratitude for the support of colleagues and a supportive home environment, which have contributed to their productivity as a researcher and author.
Knowing that glucocorticoids significantly increase the risk of fractures and is the most common cause of secondary osteoporosis, the use of the steroid has always been viewed as a doubled edged sword and “Bad for the Bones”. This week, we welcome Dr. Giovanni Adami, first author of Bone Loss in Inflammatory Rheumatic Musculoskeletal Disease Patients Treated with Low-Dose Glucocorticoids and Prevention by Anti-Osteoporosis Medications , whose goal for this study was to assess if a “safe” dose of glucocorticoids exists, with an attention focus on those with inflammatory rheumatic musculoskeletal diseases (iRMDs) to determine if a low enough dose of glucocorticoids can still reduce inflammatory burden and yet significantly reduce expected risk of fracture.
Get the Snipd podcast app
Unlock the knowledge in podcasts with the podcast player of the future.
AI-powered podcast player
Listen to all your favourite podcasts with AI-powered features
Discover highlights
Listen to the best highlights from the podcasts you love and dive into the full episode
Save any moment
Hear something you like? Tap your headphones to save it with AI-generated key takeaways
Share & Export
Send highlights to Twitter, WhatsApp or export them to Notion, Readwise & more
AI-powered podcast player
Listen to all your favourite podcasts with AI-powered features
Discover highlights
Listen to the best highlights from the podcasts you love and dive into the full episode