Oocyte maturation arrest produced by TUBB8 mutations: impact of genetic disorders in infertility treatment

Gynecol Endocrinol. 2020 Sep;36(9):829-834. doi: 10.1080/09513590.2020.1725968. Epub 2020 Feb 17.

Abstract

Oocyte maturation defect is a challenging situation in the management of infertility, the etiology may be related to endocrine causes, protocols used in ovarian stimulation, oocyte intrinsic defects or procedures in embryology laboratory. We report three Mexican females in treatment for primary infertility with non-mature oocytes after ovary stimulation and oocyte capture in whom a genetic diagnosis of TUBB8-oocyte maturation defect was revealed by exome sequencing. Two couples achieved pregnancies though oocyte donation after establishing the genetic etiology. Our results expand the role of TUBB8-disorders in patients of non-Asian ethnicity. Oocyte maturation defects of monogenic origin are a growing group of disorders that endocrinologists and reproductive medicine specialists should be aware in order to provide referral to genetics for establish a correct and opportune diagnosis.

Keywords: exome sequencing; immature oocyte; in vitro fertilization; reproductive genetics; β-tubulin.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • Female
  • Genetic Diseases, Inborn / diagnosis
  • Genetic Diseases, Inborn / epidemiology
  • Genetic Diseases, Inborn / therapy*
  • Humans
  • Infertility, Female / diagnosis*
  • Infertility, Female / epidemiology
  • Infertility, Female / genetics
  • Infertility, Female / therapy*
  • Mexico
  • Mutation
  • Oogenesis / genetics*
  • Pedigree
  • Pregnancy
  • Prognosis
  • Reproductive Techniques, Assisted / statistics & numerical data
  • Treatment Outcome
  • Tubulin / genetics*

Substances

  • TUBB8 protein, human
  • Tubulin