IGF-I deficiency and enhanced insulin sensitivity due to a mutated growth hormone receptor gene in humans

J. Guevara-Aguirre*, C. Torres, G. Pena, M. Palacios, C. Bautista, A. Guevara, A.W.D. Gavilanes

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Web of Science)

Abstract

Human size is achieved by the coordinated expression of many genes. From conception to adulthood, a given genomic endowment is modified by highly variable environmental circumstances. During each stage of a person's life, distinct nutritional and hormonal influences continuously shape growing physical features until mature characteristics are attained. Underlying processes depend on precise provision of substrates and energy extracted by insulin action from nutrients, which allows cell proliferation, differentiation, and survival, under the concerted actions of growth hormone and insulin-like growth factor-I (IGF-I). It should be noted that growth and metabolic signaling pathways are interdependent and superimposed at multiple levels. Attainment of a fully developed human phenotype should be considered as a harmonious increment in body size rather than a simple increase in height. From this perspective we herein analyze adult features of individuals with an inactive growth hormone receptor, who consequently have severely diminished concentrations of serum insulin and endocrine IGF-I.
Original languageEnglish
Article number111044
Number of pages10
JournalMolecular and Cellular Endocrinology
Volume519
DOIs
Publication statusPublished - 1 Jan 2021

Keywords

  • acid-labile subunit
  • adults
  • binding-proteins
  • ecuadorian patients
  • factor system
  • laron-syndrome
  • mutations
  • protein-metabolism
  • resistance
  • serum
  • PROTEIN-METABOLISM
  • ECUADORIAN PATIENTS
  • ADULTS
  • SERUM
  • LARON-SYNDROME
  • BINDING-PROTEINS
  • FACTOR SYSTEM
  • RESISTANCE
  • ACID-LABILE SUBUNIT
  • MUTATIONS

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