Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep568 | Pituitary and Neuroendocrinology | ECE2024

Diagnostic discordance of osteoporosis in acromegaly: a comparison of quantitative computed tomography and dual-energy X-ray absorptiometry

Shuaiming Chen , Jing Li , Yerong Yu , Jianwei Li

Background: Patients with acromegaly have an increased risk of vertebral fractures, yet normal or elevated bone mineral density (BMD) by dual-energy X-ray absorptiometry (DXA). This suggests that DXA may not be a reliable tool for assessing BMD in acromegalic patients. Multiple studies have suggested that patients with acromegaly have compromised trabecular bone but not cortical bone. Quantitative computed tomography (QCT) represents a three-dimensional technique for quantifyi...

ea0099p327 | Pituitary and Neuroendocrinology | ECE2024

High prevalence of vertebral fractures associated with age, GH, and bone mineral density in patients with acromegaly

Shuaiming Chen , Jing Li , Chun Wang , Huiwen Tan , Zhenmei An , Yerong Yu , Jianwei Li

Objective: Studies have demonstrated that patients with acromegaly have compromised bone health and an increased risk of vertebral fractures (VFs). However, the prevalence of VFs in Chinese patients with acromegaly has not been investigated by far. This study aimed to evaluate the prevalence and determinants of VFs in patients with acromegaly in a tertiary hospital in China.Methods: We enrolled patients diagnosed with acromegaly consecutively at West Chi...

ea0092ps3-30-08 | Thyroid Physiology in Periphery & Development Basic | ETA2023

Identification of FOXE1 promoter variants in families with cleft palate, struma ovarii and thyroid lesions

Pires Carolina , Saramago Ana , M. Moura Margarida , Li Jing , Marques Ines , Cabrera Rafael , Machado Ana , Grunewald Thomas , Leite Valeriano , Cavaco Branca

Introduction: Forkhead box E1 (FOXE1) gene encodes a transcription factor crucial for thyroid morphogenesis, differentiation, and function. We previously found evidence of the involvement of a rare germline FOXE1 variant in familial non-medullary thyroid carcinoma (FNMTC) etiology. FNMTC most common subtype is papillary thyroid carcinoma (PTC), and family members frequently present thyroid follicular nodular disease (FND). Germline FOXE1 mu...