Long-term Pegvisomant Therapy of Acromegaly: Effects on Bone Density, Turnover and Microstructure Using HRpQCT.

HRpQCT acromegaly bone

Journal

Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997

Informations de publication

Date de publication:
06 Apr 2024
Historique:
received: 06 02 2024
medline: 8 5 2024
pubmed: 8 5 2024
entrez: 8 5 2024
Statut: epublish

Résumé

Fracture rate is increased in patients with active acromegaly and those in remission. Abnormalities of bone microstructure are present in patients with active disease and persist despite biochemical control after surgery. Effects of treatment with the GH receptor antagonist pegvisomant on bone microstructure were unknown. We studied 25 patients with acromegaly (15 men, 10 women). In 20, we evaluated areal bone mineral density (BMD) by dual-energy X-ray absorptiometry and bone turnover markers (BTMs) longitudinally, before and during pegvisomant treatment. After long-term pegvisomant in 17, we cross-sectionally assessed volumetric BMD, microarchitecture, stiffness, and failure load of the distal radius and tibia using high-resolution peripheral quantitative computed tomography (HRpQCT) and compared these results to those of healthy controls and 2 comparison groups of nonpegvisomant-treated acromegaly patients, remission, and active disease, matched for other therapies and characteristics. In the longitudinal study, areal BMD improved at the lumbar spine but decreased at the hip in men after a median ∼7 years of pegvisomant. In the cross-sectional study, patients on a median ∼9 years of pegvisomant had significantly larger bones, lower trabecular and cortical volumetric density, and disrupted trabecular microarchitecture compared to healthy controls. Microstructure was similar in the pegvisomant and acromegaly comparison groups. BTMs were lowered, then stable over time. In this, the first study to examine bone microstructure in pegvisomant-treated acromegaly, we found deficits in volumetric BMD and microarchitecture of the peripheral skeleton. BTM levels remained stable with long-term therapy. Deficits in bone quality identified by HRpQCT may play a role in the pathogenesis of fragility in treated acromegaly.

Identifiants

pubmed: 38715589
doi: 10.1210/jendso/bvae079
pii: bvae079
pmc: PMC11074588
doi:

Types de publication

Journal Article

Langues

eng

Pagination

bvae079

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society.

Auteurs

Adriana P Kuker (AP)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Sanchita Agarwal (S)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Elizabeth Shane (E)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Juliana Bicca (J)

Plenicca Clinic, Sao Paolo 05688-021, Brazil.

Eliza B Geer (EB)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.

Serge Cremers (S)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.
Department of Pathology and Cell Biology, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Elzbieta Dworakowski (E)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Adi Cohen (A)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Thomas L Nickolas (TL)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Emily M Stein (EM)

Endocrinology and Metabolic Bone Diseases, Hospital for Special Surgery, New York, NY 10021, USA.

Pamela U Freda (PU)

Department of Medicine, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

Classifications MeSH