reviewJournal of Clinical InvestigationNov 2, 2009GREEN OA

Acromegaly pathogenesis and treatment

Cedars-Sinai Medical Center

PubMed
Indexed incrossrefdoajpubmed

Abstract

Dysregulated growth hormone (GH) hypersecretion is usually caused by a GH-secreting pituitary adenoma and leads to acromegaly - a disorder of disproportionate skeletal, tissue, and organ growth. High GH and IGF1 levels lead to comorbidities including arthritis, facial changes, prognathism, and glucose intolerance. If the condition is untreated, enhanced mortality due to cardiovascular, cerebrovascular, and pulmonary dysfunction is associated with a 30% decrease in life span. This Review discusses acromegaly pathogenesis and management options. The latter include surgery, radiation, and use of novel medications. Somatostatin receptor (SSTR) ligands inhibit GH release, control tumor growth, and attenuate…

Citation impact

684
total citations
FWCI
20.83
Percentile
100%
References
141
Citations per year

Authors

1

Topics & keywords

Keywords
  • Acromegaly
  • Medicine
  • Somatostatin
  • Endocrinology
  • Internal medicine
  • Pathogenesis
  • Somatostatin receptor
  • Pegvisomant
UN Sustainable Development Goals
  • Good health and well-being
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