Management of Hypopituitarism: a Perspective from the Brazilian Society of Endocrinology and Metabolism
Overview
Authors
Affiliations
Hypopituitarism is a disorder characterized by insufficient secretion of one or more pituitary hormones. New etiologies of hypopituitarism have been recently described, including head trauma, cerebral hemorrhage, and drug-induced hypophysitis. The investigation of patients with these new disorders, in addition to advances in diagnosis and treatment of hypopituitarism, has increased the prevalence of this condition. Pituitary hormone deficiencies can induce significant clinical changes with consequent increased morbidity and mortality rates, while hormone replacement based on current guidelines protects these patients. In this review, we will first discuss the different etiologies of hypopituitarism and then address one by one the clinical aspects, diagnostic evaluation, and therapeutic options for deficiencies of TSH, ACTH, gonadotropin, and GH. Finally, we will detail the hormonal interactions that occur during replacement of pituitary hormones.
Hypopituitarism presenting with cardiovascular manifestations: a case report.
Zhen X, Li Y, Ren C, Li M BMC Cardiovasc Disord. 2025; 25(1):117.
PMID: 39972417 PMC: 11837320. DOI: 10.1186/s12872-025-04535-9.
Altered amino acid levels in young hypopituitarism: impact of NAFLD and insulin resistance.
Zhang Y, Qiu J, Sun S, Fang X Amino Acids. 2024; 56(1):65.
PMID: 39580591 PMC: 11585508. DOI: 10.1007/s00726-024-03429-y.
Progress, challenges and perspectives in the management of hypopituitarism.
Boguszewski C, Neggers S Rev Endocr Metab Disord. 2024; 25(3):453-455.
PMID: 38801648 DOI: 10.1007/s11154-024-09889-7.
Garmes H, Castillo A, Monte Alegre S, de Souza A, Atala Y, Zantut-Wittmann D Metabolites. 2022; 12(12).
PMID: 36557289 PMC: 9782045. DOI: 10.3390/metabo12121251.
Bitencourt M, Batista R, Biscotto I, Carvalho L Arch Endocrinol Metab. 2022; 66(4):541-550.
PMID: 35758836 PMC: 10697652. DOI: 10.20945/2359-3997000000493.