4.7 Article

The association of CGG repeats in the FMR1 gene and timing of natural menopause

Journal

HUMAN REPRODUCTION
Volume 28, Issue 2, Pages 496-501

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/humrep/des392

Keywords

age at menopause; FMR1 gene; CGG repeats; fragile X; ovarian ageing

Funding

  1. Dutch Organisation for Scientific Research (NWO) [92003575]
  2. Andromed
  3. Ardana
  4. Ferring
  5. Genovum
  6. Merck Serono
  7. MSD
  8. Organon
  9. Pantharei Bioscience
  10. PregLem
  11. Schering
  12. Schering Plough
  13. Serono
  14. Wyeth

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Is there an association between the number of CGG repeats in the FMR1 gene in the normal and intermediate range and age at natural menopause? The number of CGG repeats in the normal and intermediate range in the FMR1 gene was not associated with age at natural menopause. Excessive triple CGG repeats in the FMR1 gene have been widely associated with primary ovarian insufficiency. Recently, the number of CGG repeats in the normal and intermediate range (up to 55 repeats) was found to be associated with serum levels of anti-Mllerian hormone and follicle-stimulating hormone, as markers for ovarian ageing. This suggests that repeats in the normal and intermediate range could be involved in the rate of exhaustion of the ovarian primordial follicle pool and ultimately the timing of menopause. Cross-sectional study in a population-based sample of 3611 Caucasian women with natural menopause. The FMR1 CGG repeat number was determined by PCR amplification in 3611 women with a known age at natural menopause. A possible relation between CGG repeats in the normal and intermediate range (up to 55 repeats) and menopausal age were analysed in various ways, including linear regression analysis and analysis of variance. The number of CGG repeats in the normal and intermediate range in the FMR1 gene was not associated with age at natural menopause. The mean age at menopause was 50.30 (4.2) years for women with 45 repeats and 50.64 (3.4) years for women with intermediate-sized repeats (P 0.37). Linear regression analysis of the number of CGG repeats showed no association with menopausal age ( 0.019, P 0.16). In our cohort, age at menopause was self-reported and determined retrospectively. Earlier observations suggesting that the number of CGG repeats in the normal and intermediate range is associated with the individual variation of the ovarian ageing process could not be confirmed in the current, large sample size study. A relation between the number of CGG repeats in the normal and intermediate range and age at natural menopause appeared to be absent. This finding questions the role of CGG repeat sizes in the ovarian ageing process. N.C.O.-M., Y.T.S. and H.K.P.A. have nothing to declare. M.V. is financially supported by a grant from the Dutch Organisation for Scientific Research (NWO). F.J.B. is a member of the external advisory board for Merck Serono, The Netherlands, and does consultancy work for MSD. B.C.J.M.F. has received fees and grant support from the following companies (in alphabetic order); Andromed, Ardana, Ferring, Genovum, Merck Serono, MSD, Organon, Pantharei Bioscience, PregLem, Schering, Schering Plough, Serono and Wyeth. Not applicable.

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