DSpace

DSpace at RU >    University Library >    Academic bibliography >

SFX Query

Files in This Item:

File Description SizeFormat
publisher's version286.15 kBAdobe PDFUnder Embargo

Title: Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriers
Author(s): Spath, M.A. (314431578)
Feuth, T. (298205858)
Allen, E.G.
Smits, A.P.T. (147137071)
Yntema, H.G. (229521649)
Geurts van Kessel, A.H.M. (069477787)
Braat, D.D.M. (092849865)
Sherman, S.L.
Thomas, C.M.G. (068366019)
Publication year: 2011
Document type: Article / Letter to editor
Journal: Human Reproduction
ISSN: 0268-1161
Volume: vol. 26
Issue: iss. 8
Start page: p. 2185
End page: p. 2191
Annotation: Spath, M A Feuth, T B Allen, E G Smits, A P T Yntema, H G van Kessel, A Geurts Braat, D D M Sherman, S L Thomas, C M G P01 HD35576/HD/NICHD NIH HHS/United States R01 HD29909/HD/NICHD NIH HHS/United States Research Support, N.I.H., Extramural England Hum Reprod. 2011 Aug;26(8):2185-91. Epub 2011 May 15.
Abstract: BACKGROUND: Carriers of a premutation (CGG repeat length 55-200) in the fragile X mental retardation (FMR1) gene are at risk for primary ovarian insufficiency (FXPOI). The anti-Mullerian hormone (AMH) level acts as a useful marker of ovarian follicle reserve and, thus, may serve to predict when this ovarian reserve becomes too low to sustain ovarian function. We investigated the intra-individual variation of AMH levels over time for premutation carriers compared with non-carriers. METHODS: We determined AMH levels in blood samples from 240 women ascertained through fragile X families, of which 127 were premutation carriers and 113 were non-carriers. Linear mixed models were used to assess the effect of age and premutation status on AMH levels and to determine a modeled AMH value. The stability over time of the deviation of observed AMH levels from modeled levels, referred to as standardized AMH values, was assessed through correlation coefficients of 41 longitudinal samples. RESULTS: At all ages, premutation carriers exhibited lower AMH levels. For all women, AMH was found to decrease by 10% per year. The added effect of having a premutation decreased AMH levels by 54%. The deviation of an individual's AMH level from the modeled value showed a reasonable intra-individual correlation. The Pearson correlation coefficient of two samples taken at different ages was 0.36 (P = 0.05) for non-carriers and 0.69 (P = 0.01) for carriers. CONCLUSIONS: We developed a unique standardized AMH value, taking FMR1 premutation status and the subject's age into account, which appears to be stable over time and may serve as a predictor for FXPOI after further longitudinal assessment.
Subject: IGMD 3: Genomic disorders and inherited multi-system disorders
IGMD 6: Hormonal regulation ONCOL 5: Aetiology, screening and detection
NCEBP 12: Human Reproduction
NCEBP 1: Molecular epidemiology
NCMLS 3A: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders
Subject: NCEBP 12: Human Reproduction
Organization: Obstetrics and Gynaecology
Epidemiology, Biostatistics & HTA
UMCN Extern
Human Genetics
Laboratory of Genetic, Endocrine and Metabolic Diseases
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/98034

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

  DSpace Software Copyright © 2002-2011  Duraspace - Feedback