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Quantifying the intraindividual variation of antimüllerian hormone in the ovarian cycle.
Hadlow, Narelle; Brown, Suzanne J; Habib, Afsana; Wardrop, Robert; Joseph, John; Gillett, Melissa; Maguire, Rhonda; Conradie, Johan.
Afiliação
  • Hadlow N; Department of Biochemistry, PathWest Laboratory Medicine, Nedlands, Western Australia, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Crawley, Western Australia, Australia; Western Diagnostic Pathology, Myaree, Western Australia, Australia. Electronic addres
  • Brown SJ; Department of Endocrinology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Habib A; Western Diagnostic Pathology, Myaree, Western Australia, Australia.
  • Wardrop R; Department of Biochemistry, PathWest Laboratory Medicine, Nedlands, Western Australia, Australia.
  • Joseph J; Department of Biochemistry, PathWest Laboratory Medicine, Nedlands, Western Australia, Australia.
  • Gillett M; Western Diagnostic Pathology, Myaree, Western Australia, Australia.
  • Maguire R; Department of Biochemistry, PathWest Laboratory Medicine, Nedlands, Western Australia, Australia.
  • Conradie J; Western Diagnostic Pathology, Myaree, Western Australia, Australia.
Fertil Steril ; 106(5): 1230-1237, 2016 Oct.
Article em En | MEDLINE | ID: mdl-27351446
OBJECTIVE: To quantify intraindividual variability of antimüllerian hormone (AMH) as analytical and biological coefficients of variation and assess the effects of variation on clinical classification. DESIGN: Retrospective cohort study. SETTING: Not applicable. PATIENT(S): Thirty-eight women referred by general practitioners. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Total intraindividual variability (CVW), analytical (CVA) and biological variability (CVI) for each woman and for AMH ranges: low (<5 pmol/L), reduced (5-10), moderate (>10-30) and high (>30 pmol/L), with calculation of proportion of women crossing clinical cutoffs and expected variability around each cutoff. RESULT(S): Cycling women (n = 38) contributed 238 blood samples (average 6 samples each). The average total intraindividual AMH variability was 20% (range: 2.1% to 73%). Biological variation was 19% (range: 0 to 71%) and at least twice the analytical variation of 6.9% (range: 4.5% to 16%). Reclassification rates were highest in women with low (33%) or reduced AMH (67%) levels. Expected variations around the 5, 10, and 30 pmol/L cutoffs were 3-7, 7-13, and 20-40 pmol/L, respectively. In a woman with mean AMH in the 10-30 pmol/L range, the span of results that could occur was 7-40 pmol/L. CONCLUSION(S): Total variation in AMH was 20%, and the majority of this was biological. Changes in AMH resulted in reclassification in 29% of women and occurred most frequently in those with low and reduced AMH. In cycling women, the variability in AMH should be considered by clinicians, especially if a result is close to a clinical cutoff.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hormônio Antimülleriano / Ciclo Menstrual Tipo de estudo: Observational_studies Limite: Adult / Female / Humans Idioma: En Revista: Fertil Steril Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hormônio Antimülleriano / Ciclo Menstrual Tipo de estudo: Observational_studies Limite: Adult / Female / Humans Idioma: En Revista: Fertil Steril Ano de publicação: 2016 Tipo de documento: Article