Anti-Mullerian hormone as a predictor of ovarian reserve in ART protocols: the hidden role of thyroid autoimmunity
© Magri et al. 2015
Received: 14 June 2015
Accepted: 9 September 2015
Published: 21 September 2015
Protocols of controlled ovarian hyper-stimulation (COH) require, as a crucial step, the identification of reliable predictors of ovarian reserve. Anti-Mullerian hormone (AMH) is one of the most reliable predictors of ovarian reserve but other factors including autoimmune thyroid diseases (ATD) have been associated with reduced fertility and poor COH outcome. Aim of the present study was to evaluate the relationship between ATD and AMH, and their role on the outcome of COH.
The study group included 288 sub-fertile euthyroid women aged less than 40 years attending a single center for Reproductive Medicine. Among them, 55 were ATD-positive and 233 ATD-negative. The serum levels of AMH, FSH, LH, estradiol (E2), and TSH were measured before COH. The ratio between serum E2 concentration on the day of oocytes pick-up and the total dose of administered recombinant FSH (r-FSH) (E2/r-FSH ratio) was calculated.
The serum levels of AMH were significantly related to E2/r-FSH ratio, total dose of r-FSH and number of M II oocytes, both in ATD-positive and ATD-negative women. Within the low stratum of AMH levels, the presence of ATD did not further affect the outcome of COH. When the serum levels of AMH were in the high stratum, the presence of ATD significantly affected the E2/rFSH ratio, the total dose of r-FSH and the number of M II oocytes.
The probability of a poor response to COH is high, and independent from ATD, in women with low AMH serum levels. In women with a good ovarian reserve, as assessed by high AMH serum levels, the presence of ATD impairs the outcome of COH.
In developed countries, about 10–15 % of all couples experience difficulties to conceive (primary infertility) or to conceive the number of children they want (secondary infertility) . As a consequence, there is a continuous increase in the number of women undergoing assisted reproductive technologies (ART) in order to achieve a pregnancy. The success rate of ART is influenced not only by the woman’s age and by infertility due to male factors, but also by several biochemical and anatomical variables, which include ovarian response to gonadotropin stimulation, oocyte in vitro fertilization, embryonic development and implantation, anatomical alterations of the fallopian tubes and the uterus, endometrial receptivity, and thrombophilic status. All these factors explain the variable response to ART even among women of similar age .
Controlled ovarian hyper-stimulation (COH) is a crucial step in all ART protocols. The magnitude of the ovarian response and the number of embryos/blastocysts available for transfer is generally considered to be a function of the gonadotropin dose , the type of stimulation protocol  and the patient’s profile [2, 5], mainly in terms of age and ovarian reserve. [6, 7]. The identification of reliable predictors of a good ovarian reserve (and as consequence of a favorable outcome) remains a challenge . In the course of ART, a poor ovarian response (POR) to COH is defined by the presence of at least two of the following three features: (i) older maternal age or any other risk factor for POR; (ii) a previous POR; and (iii) an abnormal ovarian reserve test . Tests for ovarian reserve provide an indirect estimate of the cohort of recruitable antral follicles in the FSH window at the beginning of each menstrual cycle . Both the anti-Mullerian hormone (AMH) and the antral follicular count (AFC) are considered reliable and accurate indexes of ovarian reserve [10, 11]. However, as compared to AFC, the measurement of serum AMH has several advantages: a lower intra- and inter-cycle variation , the independence from observers’ biases, and the possibility to be used in any clinical setting. For these reasons, AMH is widely recognized as a reliable biomarker of ovarian response . AMH is a member of the transforming growth factor beta family being produced in the granulosa cells of the ovarian follicle . The highest levels of AMH are detected in secondary, pre-antral, and small (up to 6 mm in diameter) antral follicles , whereas the production of this hormone ceases in growing to dominance follicles [15, 16]. AMH is barely detectable at birth, peaks after puberty, then decreases progressively with age and becomes undetectable at menopause [17, 18]. In women undergoing COH, the higher the serum levels of AMH, the better is the ovarian response to r-FSH .
In addition to the ovarian reserve, which is the main determinant for a good response to COH and for the subsequent ART outcome, autoimmune thyroid diseases (ATD), which are highly prevalent in women during the childbearing age (5–15 %), and hypothyroidism are also associated with reduced fertility and ART failure [20–22]. The relationship between ATD and reduced ovarian reserve has been widely investigated [23–26]. In a previous study, we found that ATD-positive women, as compared to the ATD-negative ones, have a poorer ovarian response to gonadotropins, but data regarding ovarian reserve in these two groups of patients were not investigated . Recently, Kuroda et al. reported that the presence of ATD and the occurrence of a raised TSH (the latter indicating hypothyroidism) were associated with low serum levels of AMH . In another study, a significant association was found between ATD and low serum levels of AMH, which was independent from age . At variance with these reports, other authors found that serum AMH levels were significantly higher in women with ATD compared with a control group . Moreover, in a large cross-sectional analysis, Polyzos et al. reported that ATD and hypothyroidism were not associated with a reduced ovarian reserve, as assessed by low age-specific AMH values .
Aim of the present study was to investigate the relationship between thyroid autoimmunity and ovarian reserve, as assessed by serum AMH concentrations, and to evaluate their respective role on the outcome of COH, being defined as ovarian response to recombinant gonadotropins.
In a retrospective, single-center study, we evaluated a cohort of patients undergoing their first ART procedure from January 2011 and April 2014. The study group included 288 euthyroid (serum TSH level < 2.5mIU/L according to the current guidelines [32–35]) women aged less than 40 years with no history of previous POR and no evidence of other risk factors, both genetic and acquired. Among them, clinical and/or biochemical evidence of ATD, as assessed by positive tests for anti-thyroglobulin and/or anti-thyroid-peroxidase antibodies (serum levels at least two times higher than the reference range), was present in 55 patients (the ATD-positive group) and absent in the remaining 233 (the ATD-negative group). In the former group, 28 (50.9 %) women were euthyroid on L-Thyroxine (LT4) substitution treatment. All subjects were Caucasian women resident in a Northern Italy area, which is characterized by mild iodine deficiency. The following inclusion criteria were used: i) sub-fertility of various cause; ii) indication for an ART cycle through a long GnRH agonist protocol with r-FSH; iii) a euthyroid state at the time of COH, either spontaneous or resulting from LT4 substitution treatment; iv) information about tests for thyroid autoimmunity. Before starting COH, serum TSH, AMH, FSH, LH, estradiol (E2) and PRL at cycle day 3, and serum progesterone (P) at cycle day 21 were measured.
The study was approved by the local Institutional Board and all patients gave their written informed consent concerning the future use of clinical and hormone data for research purposes according to the local Ethics Committee and the guidelines of the Declaration of Helsinki.
Ovarian suppression was achieved by administering subcutaneously a daily dose (1 mg) of leuprorelin acetate (Enantone, Takeda Italia Farmaceutici S.p.A, Italy) started on day 21 of the previous cycle. Both ultrasound scan (absence of ovarian activity, ovarian cyst formation and endometrial proliferation) and serum E2 levels (≤40 pg/mL) confirmed ovarian suppression before starting exogenous gonadotropin administration for COH. A fixed daily dose (150 IU) of r-FSH (Gonal-F; Merck-Serono, Rome, Italy) was used for 5 days, until the ovarian response was evaluated, and then adjusted accordingly. Starting from day 9, women were observed daily until criteria were fulfilled for discontinuing the GnRH agonist and for administering hCG at a dose of 10,000 IU i.m.. Ovulation was triggered by hCG treatment when at least two leading follicles, with a mean diameter >18 mm, were detected. An adequate rise of serum E2 concentration was observed during COH. No longer than 24 h elapsed from the last injection of r-FSH and the administration of hCG. Thirty-five to 36 h after hCG administration, ovum pick-up was performed by trans-vaginal ultrasound-guided ovarian puncture. After stripping, oocytes were assessed for their maturation; only oocytes having resumed their first meiotic division and reaching metaphase II were used for IVF. On the day of transfer, embryos were graded according to their morphologic appearance under a light microscope and then transferred.
The ratio between serum E2 concentration on the day of pick-up and the total number of r-FSH units administered during the CHO procedure (E2/r-FSH ratio) was calculated. This allowed measuring the performance of r-FSH in producing an adequate ovarian stimulation in ATD-positive as opposed to ATD-negative women
The serum concentrations of TSH (third generation TSH assay; normal range 0.4–4 mIU/L) were measured using an immune-chemiluminescent assay run by an automated analyzer ((Immulite 2000, DPC Cirrus, Los Angeles, CA, USA) employing commercial kits (Diagnostic Products Corporation, Los Angeles, CA, USA). The sensitivity of the assay was 0.004 mIU/L and the intra- and inter-assay coefficients of variation were 3.5 and 5.4 %, respectively. The serum concentrations of anti-thyroglobulin antibody (Tg-Ab; normal range <60 U/mL) and anti-thyroid peroxidase antibody (TPO-Ab; normal range < 60 U/mL) were measured using immune-chemiluminescent assays employing commercial kits (Brahams, Hennigsdorf, Germany). The sensitivity of the assay was 33 U/mL for TG-Ab and 50 U/mL for TPO-Ab. The intra- and inter-assay coefficients of variation were 2.6 and 13 % respectively, for TG-Ab and 3.9 and 8 %, respectively, for TPO-Ab.
The serum levels of estradiol (E2) and progesterone (P) were measured using a commercial RIA kit (Diagnostic Systems Laboratories, Inc.). The sensitivity of the assay was 2.2 pg/mL and 0.12 ng/mL, respectively; the intra- and inter-assay coefficients of variation were 7.5 and 9.3 %, for serum E2 and 6.8 and 8.8 %, for P respectively. FSH and LH, as well as PRL, were measured by immune-enzymatic assays (FSH and PRL, Abbott Laboratories, Rome, Italy; LH, Dade Behring, Milan, Italy). The sensitivity of the assay was 0.2 U/L for FSH and LH; the intra- and inter-assay coefficients of variation were: FSH, 4.7 and 8.9 %, respectively; LH, 3.1 and 4.0 %, respectively. The sensitivity of the assay was 0.6 ng/mL for PRL; the intra- and inter-assay coefficients of variation were 5.3 and 7.1 %, respectively.
During the study period, the serum concentrations of AMH were measured by an enzymatically amplified two-site immunoassay (AMH Gen II ELISA, Beckman Coulter, Brea, CA, USA) [36, 37]. Normal values for AMH were < = 12.6 ng/mL. The analytical sensitivity of the assay was 0.08 ng/mL and the intra- and inter-assay coefficients of variation were 5.4 and 5.6 %, respectively, according to the products’ inserts. The lowest amount of AMH in a sample that could be detected with a 95 % probability was 0.08 ng/mL. The estimated minimum dose achieved at 20 % total imprecision was 0.16 ng/mL.
Quantitative values were expressed as mean and 95 % confidence interval or as median and interquartile range, as appropriate. Between-group comparisons were performed by Student’s t-test for unpaired data and by the Mann–Whitney U test according to a normal or a non-parametric distribution of data. When more than two groups were compared, the analysis of variance (Kruskal-Wallis ANOVA) was performed. The coefficient of correlation was calculated with the Spearman Rank Order Correlations. A p value <0.05 was considered statistically significant. Statistical analysis was performed using the SPSS software (SPSS, Inc., Evanston, IL, USA).
Clinical and hormonal features of sub-fertile women divided according to their autoimmune thyroid (ATD) status. Results are expressed as mean (95 % confidence interval) or percent of the corresponding group
N = 233
N = 55
35.8 ± 3.62 (34.9–36.8)
Male factor (%)
The mean total dose of administered r-FSH did not significantly differ between ATD-negative and ATD-positive women (2273.8 IU, 95 % CI 2082–2465 and 2298.4 IU, 95 % CI 2034–2562, respectively). The E2/r-FSH ratio at oocyte pick-up was significantly lower in ATD-positive women compared with the ATD-negative ones (0.57, 95 % CI 0.44-0.70 and 1.05, 95 % CI 0.82-1.22, respectively, p = 0.026). This finding indicates a poorer performance of r-FSH in producing ovarian stimulation in ATD-positive women.
AMH and COH outcome
Linear regression analysis relating the serum levels of AMH and age or COH outcomes (E2/r-FSH ratio, total dose of r-FSH and number of M II oocytes) in ATD-positive and ATD-negative women
M II oocytes
R = −0.236
R = 0.628
R = −0.582
R = 0.388
P = 0.001
P = 0.0000
P = 0.0000
P = 0.0000
R = −0.403
R = 0.381
R = −0.371
R = 0.554
P = 0.005
P = 0.009
P = 0.008
P = 0.0000
ATD, AMH, and COH
Clinical and hormonal features, and outcome of COH in sub-fertile women divided according to the median level of serum AMH (low AMH stratum < 1.32 ng/mL and high AMH stratum > 1.32 ng/mL). Results are expressed as mean (95 % confidence interval)
Low AMH stratum
High AMH stratum
Estradiol at oocyte pick-up (pg/mL)
Number of MII oocytes
Clinical and hormonal data, and outcome of CHO, in sub-fertile women within the low AMH stratum (AMH < 1.32 ng/mL) divided according their autoimmune thyroid status (ATD) Results are expressed as mean (95 % confidence interval)
Low AMH stratum
Low AMH stratum
E2 pick (pg/mL)
N^ MII oocytes
Both a reduced ovarian reserve (expressed by low serum levels of AMH) and the occurrence of ATD exert a negative influence on the outcome of COH, which represents a crucial step of ART. Our results confirm that ovarian reserve is the major determinant of ovarian response to COH. Indeed, when serum AMH levels were low, the outcome of COH was poor. The relationship between ATD and ovarian reserve, and the role of ATD by itself on the success of COH, are more intriguing. In the present study, we found significantly lower serum levels of AMH in ATD-positive women compared with the ATD-negative ones. This is in line with some previous findings , but in contrast with data from a recent large cross-sectional analysis, in which neither ATD nor hypothyroidism were found to be associated with a poor ovarian reserve, as assessed by low age-specific AMH values . A possible explanation for this discrepancy might be the lack of an age-specific stratification of AMH levels.
ATD represents the main cause of thyroid failure in women of childbearing age  and, even when subclinical, it can impair fertility and increase pregnancy-related morbidities [32, 38]. For this reason, current guidelines for thyroid dysfunction in pregnancy [32–35] emphasize the crucial role of preconception serum TSH measurement, and recommend LT4 therapy in women with ATD and associated subclinical hypothyroidism in order to maintain a serum TSH concentration < 2.5 mIU/L [33, 34]. These Guidelines are nowadays widely followed in the clinical management of spontaneous pregnancies, but their application in ART pregnancies is still debated. In this context, we recently demonstrated that the outcome of COH was poorer in ATD-positive compared with ATD-negative women, but it significantly improved when the pre-stimulation TSH was lower than 2.5 mIU/L . Moreover, among ATD positive women, a trend toward a better ovarian response was found in those belonging to the lower quartiles of TSH .
In order to investigate the respective role of ovarian reserve and ATD on the outcome of COH, we enrolled euthyroid women (TSH <2.5mIU/L) with no previous POR or any other risk factor, both genetic and acquired. All other conditions possibly affecting COH, such as BMI, PCOS and endometriosis [39, 40], were equally distributed in the different groups of sub-fertile women. To assess the outcome of COH, we evaluated the total dose of administered r-FSH, the r-FSH performance (i.e. the E2/r-FSH ratio) , and the number of retrieved MII oocytes . ATD-positive women showed a lower E2/r-FSH ratio, confirming a negative role of ATD on the outcome of COH . However, this negative influence of ATD was observed only in women with a preserved ovarian follicle reserve, as assessed by their high serum levels of AMH. In women with low serum levels of AMH, the outcome of COH was invariably poor and independent from their ATD status. As expected, higher basal serum levels of FSH were found in women belonging to the low AMH stratum. Similar findings were observed in ATD-positive women. These data confirm the negative predictive value of high serum FSH levels on the outcome of ART .
FSH receptor polymorphisms were not evaluated in the present study. This represents a possible limitation because previous data suggest that FSH receptor variants might influence the ovarian response to r-FSH during COH .
The present data further support the recommendation of assessing both ovarian reserve and thyroid autoimmunity when planning an ART procedure. In women with low serum AMH levels the probability of a successful outcome is low, independently from thyroid autoimmunity. In women with a preserved ovarian reserve, the presence of ATD impairs the outcome of CHO, at least when standard doses of recombinant gonadotropins are used. In this view, a pre-stimulation screening for thyroid autoimmunity appears mandatory even in euthyroid women.
The authors wish to thank Giorgia Testa and Sabrina Nigrisoli (Fondazione IRCCS Policlinico S. Matteo, Pavia) for their technical support.
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- Evers JLH. Female subfertility. Lancet. 2002;360:151–9.View ArticlePubMedGoogle Scholar
- Fauser BCJM, Diedrich K, Devroey P. Predictors of ovarian response: progress towards individualized treatment in ovulation induction and ovarian stimulation. Hum Reprod Update. 2008;14:1–14.View ArticlePubMedGoogle Scholar
- Sterrenburg MD, Veltman-Verhulst SM, Eijkemans MJC, Hughes EG, Macklon NS, Broekmans FJ, et al. Clinical outcomes in relation to the daily dose of recombinant follicle-stimulating hormone for ovarian stimulation in in vitro fertilization in presumed normal responders younger than 39 years: a meta-analysis. Hum Reprod Update. 2011;17:184–96.View ArticlePubMedGoogle Scholar
- Arslan M, Bocca S, Mirkin S, Barroso G, Stadtmauer L, Oehninger S. Controlled ovarian hyperstimulation protocols for in vitro fertilization: two decades of experience after the birth of Elizabeth Carr. Fertil Steril. 2005;84:555–69.View ArticlePubMedGoogle Scholar
- Kwee J, Schats R, McDonnell J, Themmen A, de Jong F, Lambalk C. Evaluation of anti-Müllerian hormone as a test for the prediction of ovarian reserve. Fertil Steril. 2008;90:737–43.View ArticlePubMedGoogle Scholar
- Broer SL, van Disseldorp J, Broeze KA, Dolleman M, Opmeer BC, Bossuyt P, et al. Added value of ovarian reserve testing on patient characteristics in the prediction of ovarian response and ongoing pregnancy: an individual patient data approach. Hum Reprod Update. 2013;19:26–36.View ArticlePubMedGoogle Scholar
- Van Loendersloot LL, van Wely M, Limpens J, Bossuyt PMM, Repping S, van der Veen F. Predictive factors in in vitro fertilization (IVF): a systematic review and meta-analysis. Hum Reprod Update. 2010;16:577–89.View ArticlePubMedGoogle Scholar
- Ferraretti AP, La Marca A, Fauser BCJM, Tarlatzis B, Nargund G, Gianaroli L. ESHRE consensus on the definition of “poor response” to ovarian stimulation for in vitro fertilization: the Bologna criteria. Hum Reprod. 2011;26:1616–24.View ArticlePubMedGoogle Scholar
- McGee EA, Hsueh AJ. Initial and cyclic recruitment of ovarian follicles. Endocr Rev. 2000;21:200–14.PubMedGoogle Scholar
- Broer SL, Mol BWJ, Hendriks D, Broekmans FJM. The role of antimullerian hormone in prediction of outcome after IVF: comparison with the antral follicle count. Fertil Steril. 2009;91:705–14.View ArticlePubMedGoogle Scholar
- La Marca A, Sighinolfi G, Radi D, Argento C, Baraldi E, Artenisio AC, et al. Anti-Mullerian hormone (AMH) as a predictive marker in assisted reproductive technology (ART). Hum Reprod Update. 2010;16:113–30.View ArticlePubMedGoogle Scholar
- Arce J-C, Nyboe Andersen A, Fernández-Sánchez M, Visnova H, Bosch E, García-Velasco JA, et al. Ovarian response to recombinant human follicle-stimulating hormone: a randomized, antimüllerian hormone-stratified, dose-response trial in women undergoing in vitro fertilization/intracytoplasmic sperm injection. Fertil Steril. 2014;102:1633–40.View ArticlePubMedGoogle Scholar
- Lee MM, Donahoe PK, Hasegawa T, Silverman B, Crist GB, Best S, et al. Mullerian inhibiting substance in humans: normal levels from infancy to adulthood. J Clin Endocrinol Metab. 1996;81:571–6.PubMedGoogle Scholar
- Weenen C, Laven JSE, Von Bergh ARM, Cranfield M, Groome NP, Visser JA, et al. Anti-Müllerian hormone expression pattern in the human ovary: potential implications for initial and cyclic follicle recruitment. Mol Hum Reprod. 2004;10:77–83.View ArticlePubMedGoogle Scholar
- Fanchin R, Schonäuer LM, Righini C, Frydman N, Frydman R, Taieb J. Serum anti-Müllerian hormone dynamics during controlled ovarian hyperstimulation. Hum Reprod. 2003;18:328–32.View ArticlePubMedGoogle Scholar
- La Marca A, Malmusi S, Giulini S, Tamaro LF, Orvieto R, Levratti P, et al. Anti-Müllerian hormone plasma levels in spontaneous menstrual cycle and during treatment with FSH to induce ovulation. Hum Reprod. 2004;19:2738–41.View ArticlePubMedGoogle Scholar
- Hudson PL, Dougas I, Donahoe PK, Cate RL, Epstein J, Pepinsky RB, et al. An immunoassay to detect human müllerian inhibiting substance in males and females during normal development. J Clin Endocrinol Metab. 1990;70:16–22.View ArticlePubMedGoogle Scholar
- De Vet A, Laven JSE, de Jong FH, Themmen APN, Fauser BCJM. Antimüllerian hormone serum levels: a putative marker for ovarian aging. Fertil Steril. 2002;77:357–62.View ArticlePubMedGoogle Scholar
- Broer SL, Broekmans FJM, Laven JSE, Fauser BCJM. Anti-Müllerian hormone: ovarian reserve testing and its potential clinical implications. Hum Reprod Update. 2014;20:688–701.View ArticlePubMedGoogle Scholar
- Krassas GE, Poppe K, Glinoer D. Thyroid Function and Human Reproductive Health. Endocr Rev. 2010;31:702–55.View ArticlePubMedGoogle Scholar
- Poppe K, Glinoer D. Thyroid autoimmunity and hypothyroidism before and during pregnancy. Hum Reprod Update. 2003;9:149–61.View ArticlePubMedGoogle Scholar
- Glinoer D. Management of hypo- and hyperthyroidism during pregnancy. Growth Horm IGF Res. 2003;13(Suppl A):S45–54.View ArticlePubMedGoogle Scholar
- Muller AF, Verhoeff A, Mantel MJ, Berghout A. Thyroid autoimmunity and abortion: a prospective study in women undergoing in vitro fertilization. Fertil Steril. 1999;71:30–4.View ArticlePubMedGoogle Scholar
- Negro R, Formoso G, Mangieri T, Pezzarossa A, Dazzi D, Hassan H. Levothyroxine treatment in euthyroid pregnant women with autoimmune thyroid disease: effects on obstetrical complications. J Clin Endocrinol Metab. 2006;91:2587–91.View ArticlePubMedGoogle Scholar
- Poppe K, Glinoer D, Tournaye H, Devroey P, van Steirteghem A, Kaufman L, et al. Assisted reproduction and thyroid autoimmunity: an unfortunate combination? J Clin Endocrinol Metab. 2003;88:4149–52.View ArticlePubMedGoogle Scholar
- Kim C-H, Ahn J-W, Kang SP, Kim S-H, Chae H-D, Kang B-M. Effect of levothyroxine treatment on in vitro fertilization and pregnancy outcome in infertile women with subclinical hypothyroidism undergoing in vitro fertilization/intracytoplasmic sperm injection. Fertil Steril. 2011;95:1650–4.View ArticlePubMedGoogle Scholar
- Magri F, Capelli V, Gaiti M, Brambilla E, Montesion L, Rotondi M, et al. Impaired outcome of controlled ovarian hyperstimulation in women with thyroid autoimmune disease. Thyroid. 2013;23:1312–8.View ArticlePubMedGoogle Scholar
- Kuroda K, Uchida T, Nagai S, Ozaki R, Yamaguchi T, Sato Y, et al. Elevated serum thyroid-stimulating hormone is associated with decreased anti-Müllerian hormone in infertile women of reproductive age. J Assist Reprod Genet. 2015;32:243–7.View ArticlePubMedGoogle Scholar
- Saglam F, Onal ED, Ersoy R, Koca C, Ergin M, Erel O, et al. Anti-Müllerian hormone as a marker of premature ovarian aging in autoimmune thyroid disease. Gynecol Endocrinol. 2015;31:165–8.View ArticlePubMedGoogle Scholar
- Tuten A, Hatipoglu E, Oncul M, Imamoglu M, Acikgoz AS, Yilmaz N, et al. Evaluation of ovarian reserve in Hashimoto’s thyroiditis. Gynecol Endocrinol. 2014;30:708–11.View ArticlePubMedGoogle Scholar
- Polyzos NP, Sakkas E, Vaiarelli A, Poppe K, Camus M, Tournaye H. Thyroid autoimmunity, hypothyroidism and ovarian reserve: a cross-sectional study of 5000 women based on age-specific AMH values. Hum Reprod. 2015;30:1690–6.View ArticlePubMedGoogle Scholar
- De Groot L, Abalovich M, Alexander EK, Amino N, Barbour L, Cobin RH, et al. Management of Thyroid Dysfunction during Pregnancy and Postpartum: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2012;97:2543–65.View ArticlePubMedGoogle Scholar
- Jonklaas J, Bianco AC, Bauer AJ, Burman KD, Cappola AR, Celi FS, et al. Guidelines for the treatment of hypothyroidism: prepared by the american thyroid association task force on thyroid hormone replacement. Thyroid. 2014;24:1670–751.View ArticlePubMedGoogle Scholar
- Stagnaro-Green A, Abalovich M, Alexander E, Azizi F, Mestman J, Negro R, et al. Guidelines of the American Thyroid Association for the diagnosis and management of thyroid disease during pregnancy and postpartum. Thyroid. 2011;21:1081–125.View ArticlePubMed CentralPubMedGoogle Scholar
- Lazarus J, Brown RS, Daumerie C, Hubalewska-Dydejczyk A, Negro R, Vaidya B. European thyroid association guidelines for the management of subclinical hypothyroidism in pregnancy and in children. Eur Thyroid J. 2014;3:76–94.View ArticlePubMed CentralPubMedGoogle Scholar
- Nelson SM, La Marca A. The journey from the old to the new AMH assay: how to avoid getting lost in the values. Reprod Biomed Online. 2011;23:411–20.View ArticlePubMedGoogle Scholar
- Nelson SM, Iliodromiti S, Fleming R, Anderson R, McConnachie A, Messow C-M. Reference range for the antimüllerian hormone Generation II assay: a population study of 10,984 women, with comparison to the established Diagnostics Systems Laboratory nomogram. Fertil Steril. 2014;101:523–9.View ArticlePubMedGoogle Scholar
- Glinoer D, Soto MF, Bourdoux P, Lejeune B, Delange F, Lemone M, et al. Pregnancy in patients with mild thyroid abnormalities: maternal and neonatal repercussions. J Clin Endocrinol Metab. 1991;73:421–7.View ArticlePubMedGoogle Scholar
- Penzias AS. Recurrent IVF, failure: other factors. Fertil Steril. 2012;97:1033–38.View ArticlePubMedGoogle Scholar
- Garrido N, Navarro J, Remohí J, Simón C, Pellicer A. Follicular hormonal environment and embryo quality in women with endometriosis. Hum Reprod Update. 2000;6:67–74.View ArticlePubMedGoogle Scholar
- Rienzi L, Ubaldi FM, Iacobelli M, Minasi MG, Romano S, Ferrero S, et al. Significance of metaphase II human oocyte morphology on ICSI outcome. Fertil Steril. 2008;90:1692–700.View ArticlePubMedGoogle Scholar
- Devine K, Mumford SL, Wu M, DeCherney AH, Hill MJ, Propst A. Diminished ovarian reserve in the United States assisted reproductive technology population: diagnostic trends among 181,536 cycles from the Society for Assisted Reproductive Technology Clinic Outcomes Reporting System. Fertil Steril. 2015; doi: 10.1016/j.fertnstert.2015.05.017.Google Scholar
- Laan M, Grigorova M, Huhtaniemi IT. Pharmacogenetics of follicle-stimulating hormone action. Curr Opin Endocrinol Diabetes Obes. 2012;19:220–7.View ArticlePubMed CentralPubMedGoogle Scholar