Genetics of gigantism and acromegaly

Growth Horm IGF Res. 2016 Oct-Dec:30-31:37-41. doi: 10.1016/j.ghir.2016.08.002. Epub 2016 Aug 10.

Abstract

Gigantism and acromegaly are rare disorders that are caused by excessive GH secretion and/or high levels of its mediator, IGF-1. Gigantism occurs when excess GH or IGF-1 lead to increased linear growth, before the end of puberty and epiphyseal closure. The majority of cases arise from a benign GH-secreting pituitary adenoma, with an incidence of pituitary gigantism and acromegaly of approximately 8 and 11 per million person-years, respectively. Over the past two decades, our increasing understanding of the molecular and genetic etiologies of pituitary gigantism and acromegaly yielded several genetic causes, including multiple endocrine neoplasia type 1 and 4, McCune-Albright syndrome, Carney complex, familial isolated pituitary adenoma, pituitary adenoma association due to defects in familial succinate dehydrogenase genes, and the recently identified X-linked acrogigantism. The early diagnosis of these conditions helps guide early intervention, screening, and genetic counseling of patients and their family members. In this review, we provide a concise and up-to-date discussion on the genetics of gigantism and acromegaly.

Keywords: Acromegaly; GH; Genetics; Gigantism; IGF-1; Pituitary adenoma; X-LAG.

Publication types

  • Review
  • Research Support, N.I.H., Intramural

MeSH terms

  • Acromegaly / genetics*
  • Adenoma / genetics*
  • Carney Complex / genetics*
  • Genetic Diseases, X-Linked / genetics*
  • Gigantism / genetics*
  • Growth Hormone-Secreting Pituitary Adenoma / genetics*
  • Humans
  • Multiple Endocrine Neoplasia / genetics*
  • Multiple Endocrine Neoplasia Type 1 / genetics*
  • Succinate Dehydrogenase / genetics

Substances

  • Succinate Dehydrogenase

Supplementary concepts

  • Multiple Endocrine Neoplasia, Type IV
  • Pituitary Adenoma, Familial Isolated