Approach to the patient with controlled acromegaly and acromegalic arthropathy: clinical diagnosis and management

Pituitary. 2024 Dec;27(6):824-836. doi: 10.1007/s11102-024-01465-1. Epub 2024 Nov 1.

Abstract

Following the description of an illustrative case of a 70-year-old female patient with longstanding active acromegaly and invalidating, progressive joint complaints, current insights regarding diagnosis, treatment, and long-term management of acromegalic arthropathy are summarized. Since clinical trials on this topic are lacking, the reported recommendations are based on extensive clinical and research experience with this clinical entity, and on established diagnostics and interventions in patients with other rheumatic diseases. The cornerstones of the management of acromegalic arthropathy remains normalization of growth hormone and insulin growth factor-1 levels. However, patients with severe or progressive acromegalic arthropathy require a multidisciplinary approach to determine adequate diagnostics and treatment options. Because of the high prevalence and invalidating character of acromegalic arthropathy, developing evidence-based effective prevention and treatment strategies, preferably by international collaboration within rare disease networks, e.g., Endo-ERN, is a clear unmet need.

Keywords: Acromegaly; Arthropathy; Management; Osteoarthritis; Treatment.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Acromegaly* / diagnosis
  • Acromegaly* / therapy
  • Aged
  • Female
  • Human Growth Hormone / blood
  • Human Growth Hormone / metabolism
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Joint Diseases* / diagnosis
  • Joint Diseases* / etiology

Substances

  • Insulin-Like Growth Factor I
  • Human Growth Hormone