Anti-Müllerian hormone (AMH) in the Diagnosis of Menstrual Disturbance Due to Polycystic Ovarian Syndrome
Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of...
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Published in | Frontiers in endocrinology (Lausanne) Vol. 10; p. 656 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
26.09.2019
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ISSN | 1664-2392 1664-2392 |
DOI | 10.3389/fendo.2019.00656 |
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Abstract | Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of menstrual disturbance due to PCOS.
Menstrual cycle length, serum AMH, gonadotropin and sex-hormone levels, total antral follicle count (AFC), body mass index (BMI) and ovarian morphology on ultrasound were analyzed in a cohort of 187 non-obese women, aged 18-35 years, screened for participation in a clinical trial of fertility treatment between 2013 and 2016 at a tertiary reproductive endocrine center.
Serum AMH was higher in women with menstrual disturbance when compared to those with regular cycles (65.6 vs. 34.8 pmol/L;
< 0.0001). The odds of menstrual disturbance was increased 28.5-fold (95% CI 3.6-227.3) in women with serum AMH >60 pmol/L, in comparison to those with an AMH < 15 pmol/L. AMH better discriminated women with menstrual disturbance (area under ROC 0.77) from those with regular menstrual cycles than AFC (area under ROC 0.67), however the combination of the two markers increased discrimination than either measure alone (0.83; 95% CI 0.77-0.89). Serum AMH was higher in women with all three cardinal features of PCOS (menstrual disturbance, hyperandrogenism, polycystic ovarian morphology) when compared to women with none of these features (65.6 vs. 14.6 pmol/L;
< 0.0001). The odds of menstrual disturbance were increased by 10.7-fold (95% CI 2.4-47.1) in women with bilateral polycystic morphology ovaries than those with normal ovarian morphology. BMI was a stronger predictor of free androgen index (FAI) than either AMH or AFC.
Serum AMH could serve as a useful biomarker to indicate the risk of menstrual disturbance due to PCOS. Women with higher AMH levels had increased rates of menstrual disturbance and an increased number of features of PCOS. |
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AbstractList | Introduction:
Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of menstrual disturbance due to PCOS.
Method:
Menstrual cycle length, serum AMH, gonadotropin and sex-hormone levels, total antral follicle count (AFC), body mass index (BMI) and ovarian morphology on ultrasound were analyzed in a cohort of 187 non-obese women, aged 18–35 years, screened for participation in a clinical trial of fertility treatment between 2013 and 2016 at a tertiary reproductive endocrine center.
Results:
Serum AMH was higher in women with menstrual disturbance when compared to those with regular cycles (65.6 vs. 34.8 pmol/L;
P
< 0.0001). The odds of menstrual disturbance was increased 28.5-fold (95% CI 3.6–227.3) in women with serum AMH >60 pmol/L, in comparison to those with an AMH < 15 pmol/L. AMH better discriminated women with menstrual disturbance (area under ROC 0.77) from those with regular menstrual cycles than AFC (area under ROC 0.67), however the combination of the two markers increased discrimination than either measure alone (0.83; 95% CI 0.77–0.89). Serum AMH was higher in women with all three cardinal features of PCOS (menstrual disturbance, hyperandrogenism, polycystic ovarian morphology) when compared to women with none of these features (65.6 vs. 14.6 pmol/L;
P
< 0.0001). The odds of menstrual disturbance were increased by 10.7-fold (95% CI 2.4–47.1) in women with bilateral polycystic morphology ovaries than those with normal ovarian morphology. BMI was a stronger predictor of free androgen index (FAI) than either AMH or AFC.
Conclusion:
Serum AMH could serve as a useful biomarker to indicate the risk of menstrual disturbance due to PCOS. Women with higher AMH levels had increased rates of menstrual disturbance and an increased number of features of PCOS. Introduction: Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of menstrual disturbance due to PCOS. Method: Menstrual cycle length, serum AMH, gonadotropin and sex-hormone levels, total antral follicle count (AFC), body mass index (BMI) and ovarian morphology on ultrasound were analyzed in a cohort of 187 non-obese women, aged 18-35 years, screened for participation in a clinical trial of fertility treatment between 2013 and 2016 at a tertiary reproductive endocrine center. Results: Serum AMH was higher in women with menstrual disturbance when compared to those with regular cycles (65.6 vs. 34.8 pmol/L; P < 0.0001). The odds of menstrual disturbance was increased 28.5-fold (95% CI 3.6-227.3) in women with serum AMH >60 pmol/L, in comparison to those with an AMH < 15 pmol/L. AMH better discriminated women with menstrual disturbance (area under ROC 0.77) from those with regular menstrual cycles than AFC (area under ROC 0.67), however the combination of the two markers increased discrimination than either measure alone (0.83; 95% CI 0.77-0.89). Serum AMH was higher in women with all three cardinal features of PCOS (menstrual disturbance, hyperandrogenism, polycystic ovarian morphology) when compared to women with none of these features (65.6 vs. 14.6 pmol/L; P < 0.0001). The odds of menstrual disturbance were increased by 10.7-fold (95% CI 2.4-47.1) in women with bilateral polycystic morphology ovaries than those with normal ovarian morphology. BMI was a stronger predictor of free androgen index (FAI) than either AMH or AFC. Conclusion: Serum AMH could serve as a useful biomarker to indicate the risk of menstrual disturbance due to PCOS. Women with higher AMH levels had increased rates of menstrual disturbance and an increased number of features of PCOS.Introduction: Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of menstrual disturbance due to PCOS. Method: Menstrual cycle length, serum AMH, gonadotropin and sex-hormone levels, total antral follicle count (AFC), body mass index (BMI) and ovarian morphology on ultrasound were analyzed in a cohort of 187 non-obese women, aged 18-35 years, screened for participation in a clinical trial of fertility treatment between 2013 and 2016 at a tertiary reproductive endocrine center. Results: Serum AMH was higher in women with menstrual disturbance when compared to those with regular cycles (65.6 vs. 34.8 pmol/L; P < 0.0001). The odds of menstrual disturbance was increased 28.5-fold (95% CI 3.6-227.3) in women with serum AMH >60 pmol/L, in comparison to those with an AMH < 15 pmol/L. AMH better discriminated women with menstrual disturbance (area under ROC 0.77) from those with regular menstrual cycles than AFC (area under ROC 0.67), however the combination of the two markers increased discrimination than either measure alone (0.83; 95% CI 0.77-0.89). Serum AMH was higher in women with all three cardinal features of PCOS (menstrual disturbance, hyperandrogenism, polycystic ovarian morphology) when compared to women with none of these features (65.6 vs. 14.6 pmol/L; P < 0.0001). The odds of menstrual disturbance were increased by 10.7-fold (95% CI 2.4-47.1) in women with bilateral polycystic morphology ovaries than those with normal ovarian morphology. BMI was a stronger predictor of free androgen index (FAI) than either AMH or AFC. Conclusion: Serum AMH could serve as a useful biomarker to indicate the risk of menstrual disturbance due to PCOS. Women with higher AMH levels had increased rates of menstrual disturbance and an increased number of features of PCOS. Introduction: Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of menstrual disturbance due to PCOS.Method: Menstrual cycle length, serum AMH, gonadotropin and sex-hormone levels, total antral follicle count (AFC), body mass index (BMI) and ovarian morphology on ultrasound were analyzed in a cohort of 187 non-obese women, aged 18–35 years, screened for participation in a clinical trial of fertility treatment between 2013 and 2016 at a tertiary reproductive endocrine center.Results: Serum AMH was higher in women with menstrual disturbance when compared to those with regular cycles (65.6 vs. 34.8 pmol/L; P < 0.0001). The odds of menstrual disturbance was increased 28.5-fold (95% CI 3.6–227.3) in women with serum AMH >60 pmol/L, in comparison to those with an AMH < 15 pmol/L. AMH better discriminated women with menstrual disturbance (area under ROC 0.77) from those with regular menstrual cycles than AFC (area under ROC 0.67), however the combination of the two markers increased discrimination than either measure alone (0.83; 95% CI 0.77–0.89). Serum AMH was higher in women with all three cardinal features of PCOS (menstrual disturbance, hyperandrogenism, polycystic ovarian morphology) when compared to women with none of these features (65.6 vs. 14.6 pmol/L; P < 0.0001). The odds of menstrual disturbance were increased by 10.7-fold (95% CI 2.4–47.1) in women with bilateral polycystic morphology ovaries than those with normal ovarian morphology. BMI was a stronger predictor of free androgen index (FAI) than either AMH or AFC.Conclusion: Serum AMH could serve as a useful biomarker to indicate the risk of menstrual disturbance due to PCOS. Women with higher AMH levels had increased rates of menstrual disturbance and an increased number of features of PCOS. Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for diagnosis remains subject to conjecture. In the present study, we evaluate the utility of serum Anti-Müllerian hormone (AMH) in the diagnosis of menstrual disturbance due to PCOS. Menstrual cycle length, serum AMH, gonadotropin and sex-hormone levels, total antral follicle count (AFC), body mass index (BMI) and ovarian morphology on ultrasound were analyzed in a cohort of 187 non-obese women, aged 18-35 years, screened for participation in a clinical trial of fertility treatment between 2013 and 2016 at a tertiary reproductive endocrine center. Serum AMH was higher in women with menstrual disturbance when compared to those with regular cycles (65.6 vs. 34.8 pmol/L; < 0.0001). The odds of menstrual disturbance was increased 28.5-fold (95% CI 3.6-227.3) in women with serum AMH >60 pmol/L, in comparison to those with an AMH < 15 pmol/L. AMH better discriminated women with menstrual disturbance (area under ROC 0.77) from those with regular menstrual cycles than AFC (area under ROC 0.67), however the combination of the two markers increased discrimination than either measure alone (0.83; 95% CI 0.77-0.89). Serum AMH was higher in women with all three cardinal features of PCOS (menstrual disturbance, hyperandrogenism, polycystic ovarian morphology) when compared to women with none of these features (65.6 vs. 14.6 pmol/L; < 0.0001). The odds of menstrual disturbance were increased by 10.7-fold (95% CI 2.4-47.1) in women with bilateral polycystic morphology ovaries than those with normal ovarian morphology. BMI was a stronger predictor of free androgen index (FAI) than either AMH or AFC. Serum AMH could serve as a useful biomarker to indicate the risk of menstrual disturbance due to PCOS. Women with higher AMH levels had increased rates of menstrual disturbance and an increased number of features of PCOS. |
Author | Abbara, Ali Eng, Pei Chia Salim, Rehan Owens, Lisa Kelsey, Tom Clarke, Sophie A. Islam, Rumana Dhillo, Waljit S. Hramyka, Artsiom Trew, Geoffrey H. Purugganan, Kate Hunjan, Tia Vimalesvaran, Sunitha Christopoulos, George Comninos, Alexander N. Roberts, Rachel Phylactou, Maria |
AuthorAffiliation | 3 School of Computer Science, University of St. Andrews , St. Andrews , United Kingdom 4 Institute of Reproductive and Developmental Biology, Imperial College London, Hammersmith Hospital , London , United Kingdom 1 Department of Investigative Medicine, Imperial College London, Hammersmith Hospital , London , United Kingdom 2 Hammersmith In Vitro Fertilisation Unit, Imperial College Healthcare NHS Trust , London , United Kingdom |
AuthorAffiliation_xml | – name: 2 Hammersmith In Vitro Fertilisation Unit, Imperial College Healthcare NHS Trust , London , United Kingdom – name: 1 Department of Investigative Medicine, Imperial College London, Hammersmith Hospital , London , United Kingdom – name: 3 School of Computer Science, University of St. Andrews , St. Andrews , United Kingdom – name: 4 Institute of Reproductive and Developmental Biology, Imperial College London, Hammersmith Hospital , London , United Kingdom |
Author_xml | – sequence: 1 givenname: Ali surname: Abbara fullname: Abbara, Ali – sequence: 2 givenname: Pei Chia surname: Eng fullname: Eng, Pei Chia – sequence: 3 givenname: Maria surname: Phylactou fullname: Phylactou, Maria – sequence: 4 givenname: Sophie A. surname: Clarke fullname: Clarke, Sophie A. – sequence: 5 givenname: Tia surname: Hunjan fullname: Hunjan, Tia – sequence: 6 givenname: Rachel surname: Roberts fullname: Roberts, Rachel – sequence: 7 givenname: Sunitha surname: Vimalesvaran fullname: Vimalesvaran, Sunitha – sequence: 8 givenname: George surname: Christopoulos fullname: Christopoulos, George – sequence: 9 givenname: Rumana surname: Islam fullname: Islam, Rumana – sequence: 10 givenname: Kate surname: Purugganan fullname: Purugganan, Kate – sequence: 11 givenname: Alexander N. surname: Comninos fullname: Comninos, Alexander N. – sequence: 12 givenname: Geoffrey H. surname: Trew fullname: Trew, Geoffrey H. – sequence: 13 givenname: Rehan surname: Salim fullname: Salim, Rehan – sequence: 14 givenname: Artsiom surname: Hramyka fullname: Hramyka, Artsiom – sequence: 15 givenname: Lisa surname: Owens fullname: Owens, Lisa – sequence: 16 givenname: Tom surname: Kelsey fullname: Kelsey, Tom – sequence: 17 givenname: Waljit S. surname: Dhillo fullname: Dhillo, Waljit S. |
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Copyright | Copyright © 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo. Copyright © 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo. 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo |
Copyright_xml | – notice: Copyright © 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo. – notice: Copyright © 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo. 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo |
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Keywords | oligomenorrhea antral follicle count (AFC) polycystic ovarian syndrome (PCOS) Anti-Müllerian hormone (AMH) amenorrhea hyperandrogenism |
Language | English |
License | Copyright © 2019 Abbara, Eng, Phylactou, Clarke, Hunjan, Roberts, Vimalesvaran, Christopoulos, Islam, Purugganan, Comninos, Trew, Salim, Hramyka, Owens, Kelsey and Dhillo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Endocrinology of Aging, a section of the journal Frontiers in Endocrinology Reviewed by: Rosita Angela Condorelli, University of Catania, Italy; Ljiljana Marina, Clinical Center of Serbia, Serbia Edited by: William Colin Duncan, University of Edinburgh, United Kingdom Joint first authors |
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Snippet | Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the criteria for... Introduction: Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the... Introduction: Polycystic ovarian syndrome (PCOS) is a leading cause of female subfertility worldwide, however due to the heterogeneity of the disorder, the... |
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SubjectTerms | amenorrhea Anti-Müllerian hormone (AMH) antral follicle count (AFC) Endocrinology hyperandrogenism oligomenorrhea polycystic ovarian syndrome (PCOS) |
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Title | Anti-Müllerian hormone (AMH) in the Diagnosis of Menstrual Disturbance Due to Polycystic Ovarian Syndrome |
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