Published online Nov 18, 2025. doi: 10.5312/wjo.v16.i11.110420
Revised: July 5, 2025
Accepted: September 28, 2025
Published online: November 18, 2025
Processing time: 161 Days and 17 Hours
Acromegaly, a disease of excess growth hormone, is known to alter bone structure and increase the risk of osteoporosis and fractures. This study aimed to assess the prevalence of vertebral, non-vertebral, and hip fragility fractures, as well as osteoporosis, in a cohort of patients with acromegaly.
To assess the prevalence of vertebral fragility fractures, non-vertebral fragility fractures, hip fragility fractures, and osteoporosis in patients diagnosed with acromegaly.
Data were collected on age, sex, body mass index (BMI), time from diagnosis of acromegaly, insulin-like growth factor (IGF-1) levels, disease control, pharmacological management, risk factors for osteoporosis, vertebral fragility fractures, non-vertebral fragility fractures, hip fragility fractures, and osteoporosis.
A total of 124 patients with acromegaly were included (67 men and 57 women). The mean age at diagnosis was 44 ± 12 years; the mean time from diagnosis was 12 ± 8 years; and the mean BMI was 27 ± 4 kg/m². Fragility fractures were found in 27 patients (21%). There were no significant differences in the presence of osteoporosis or fragility fractures according to age, sex, BMI, duration of acrom
A high prevalence of osteoporosis and fragility fractures was found in patients with acromegaly, regardless of age, sex, BMI, time from diagnosis, IGF-1 levels, and disease control. More patients with osteoporosis were treated with somatostatin analogs compared to those without osteoporosis. Taken together, our results suggest that the severity of the disease and the need for second-line therapies, may be associated with the increased risk of osteoporosis.
Core Tip: The current study found a high prevalence of osteoporosis and non-vertebral fragility fractures in patients with acromegaly, independent of age, sex, body mass index, time from diagnosis, insulin-like growth factor level, and disease control and regardless of the presence of independent risk factors. Somatostatin analog therapy in patients with acromegaly was associated with a higher risk for having osteoporosis. Taken together, our results suggest that the severity of the disease and the need for second-line therapies, rather than a specific medication for acromegaly, may be associated with the increased risk of osteoporosis. However, further studies are required to assess the effect of somatostatin analogs on bone metabolism.
