Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Anti-Müllerian Hormone Is Not Associated with Cardiometabolic Risk Factors in Adolescent Females

  • Emma L. Anderson ,

    emma.louise.anderson@bristol.ac.uk

    Affiliation MRC CAiTE Centre, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom

  • Abigail Fraser,

    Affiliation MRC CAiTE Centre, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom

  • William McNally,

    Affiliation School of Medicine, University of Glasgow, Glasgow, United Kingdom

  • Naveed Sattar,

    Affiliation BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom

  • Hany Lashen,

    Affiliation Section of Reproductive and Developmental Medicine, University of Sheffield, Sheffield, United Kingdom

  • Richard Fleming,

    Affiliation School of Medicine, University of Glasgow, Glasgow, United Kingdom

  • Scott M. Nelson ,

    Contributed equally to this work with: Scott M. Nelson, Debbie A. Lawlor

    Affiliation School of Medicine, University of Glasgow, Glasgow, United Kingdom

  • Debbie A. Lawlor

    Contributed equally to this work with: Scott M. Nelson, Debbie A. Lawlor

    Affiliation MRC CAiTE Centre, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom

Anti-Müllerian Hormone Is Not Associated with Cardiometabolic Risk Factors in Adolescent Females

  • Emma L. Anderson, 
  • Abigail Fraser, 
  • William McNally, 
  • Naveed Sattar, 
  • Hany Lashen, 
  • Richard Fleming, 
  • Scott M. Nelson, 
  • Debbie A. Lawlor
PLOS
x

Abstract

Objectives

Epidemiological evidence for associations of Anti-Müllerian hormone (AMH) with cardiometabolic risk factors is lacking. Existing evidence comes from small studies in select adult populations, and findings are conflicting. We aimed to assess whether AMH is associated with cardiometabolic risk factors in a general population of adolescent females.

Methods

AMH, fasting insulin, glucose, HDLc, LDLc, triglycerides and C-reactive protein (CRP) were measured at a mean age 15.5 years in 1,308 female participants in the Avon Longitudinal Study of Parents and Children (ALSPAC). Multivariable linear regression was used to examine associations of AMH with these cardiometabolic outcomes.

Results

AMH values ranged from 0.16–35.84 ng/ml and median AMH was 3.57 ng/ml (IQR: 2.41, 5.49). For females classified as post-pubertal (n = 848) at the time of assessment median (IQR) AMH was 3.81 ng/ml (2.55, 5.82) compared with 3.25 ng/ml (2.23, 5.05) in those classed as early pubertal (n = 460, P≤0.001). After adjusting for birth weight, gestational age, pubertal stage, age, ethnicity, socioeconomic position, adiposity and use of hormonal contraceptives, there were no associations with any of the cardiometabolic outcomes. For example fasting insulin changed by 0% per doubling of AMH (95%CI: −3%,+2%) p  = 0.70, with identical results if HOMA-IR was used. Results were similar after additional adjustment for smoking, physical activity and age at menarche, after exclusion of 3% of females with the highest AMH values, after excluding those that had not started menarche and after excluding those using hormonal contraceptives.

Conclusion

Our results suggest that in healthy adolescent females, AMH is not associated with cardiometabolic risk factors.

Introduction

Anti-Müllerian hormone (AMH) is increasingly recognised as a biomarker of the ovarian reserve in adults, due to its strong correlation with primordial follicle number, [1] follicular recruitment rates, [2] response to exogenous gonadotrophins [2] and ability to predict the duration of the reproductive lifespan. [3] In children, similar associations between AMH and the ovarian reserve have been observed. Specifically, girls with a reduced ovarian reserve and shorter reproductive lifespan due to Turners syndrome have low AMH levels, [4] in prepubertal and peripubertal girls AMH levels reflects follicular recruitment rates, [2], [5] and as observed in adults, AMH is negatively associated with follicle stimulating hormone (FSH) in girls from 5 to 15 years. [6] Collectively these studies suggest that AMH may be a useful surrogate of the ovarian reserve and follicular recruitment throughout life.

Premature ovarian insufficiency has been associated with abnormal cardiovascular risk factors and increased cardiovascular mortality [7][9]. Ovarian decline and its sequelae are however increasingly being viewed as a continuum rather than an abrupt event at the time of menopause. Investigation of the nature of the relationship between ovarian aging and cardiovascular risk in premenopausal women, has been more limited, but has demonstrated that atherosclerotic lesions predate the onset of the menopause, [10] and that women with reduced ovarian reserve as detected by an elevated FSH but normal oestrogen concentrations exhibit abnormal lipid profiles. [11] The stronger relationship between AMH and ovarian reserve than that observed of the latter with FSH, [1] has consequently led to AMH being examined in adults relative to established cardiometabolic risk factors, including lipids, insulin, C-reactive protein (CRP) and body mass index (BMI),[12][23] and in animal models, with atherosclerosis plaque size. [24] These studies have produced conflicting results; for example the association of AMH with insulin has been reported as being positive, [20], [25] negative, [26], [27] or null. [28] This discordance may potentially reflect the relatively small sample sizes studied and the use of select populations, such as women with PCOS. [20], [25], [27] Furthermore, there may be confounding by factors such as smoking and socioeconomic status, [29], [30] or bias due to reverse causality with compromised ovarian vascular function adversely impacting on AMH concentrations. [31].

It would therefore be valuable to study the associations of AMH with cardiometabolic factors in a large, well phenotyped cohort of women from the general population and without established disease. Doing this in a young (adolescent) age group would be valuable because at this age associations are less likely to be confounded by behavioural lifestyle characteristics such as smoking or subject to bias, for example by reverse causality, as atherosclerosis at this age is rare. Furthermore, both mathematical modelling of cross-sectional data and prospective longitudinal data have suggested that AMH is relatively stable at this age, [4], [32], [33] and importantly these cardiometabolic risk factors in adolescence are indicators of future cardiovascular risk. In postmortem studies they have been related to extent of clinically relevant artherosclerosis. [34] Blood pressure in adolescence/early adulthood has been shown to relate to future cardiovascular disease mortality with similar magnitudes of association to those seen for blood pressure in middle age, [35] and blood pressure, markers of dysglycaemia and dyslipidaemia in childhood/adolescence are associated with carotid intima media thickness in mid-adulthood with similar magnitudes of association to the same risk factors measured at the same time as carotid intima media thickness. [36], [37].

The aim of this paper is to examine associations of AMH with fasting insulin, glucose, lipids and CRP in a general population of females with a mean age of 15.5 years.

Subjects and Methods

Ethical approval for the study was obtained from the Avon Longitudinal Study of Parents and Children Law and Ethics Committee (IRB# 00003312) and the Local Research Ethics Committees (Bristol and Weston, Southmead, and Frenchay Health Authorities). Written informed consent was obtained from all participants in the study. Parents provided written informed consent for their child.

Study Population

The Avon Longitudinal Study of Parents and Children is a population-based, prospective birth cohort, investigating factors that affect the health and development of children. Detailed methods of ALSPAC have been described previously, [38], [39] and are on the study website (www.alspac.bris.ac.uk). Briefly, 14,541 pregnant women resident in the Bristol area with an expected date of delivery between 1st April 1991 and 31st December 1992 were enrolled into the cohort, and of these, 13,988 had a live-born child who was still alive at age 1 year. Participants who attended the 15 year follow-up clinic and who had data on AMH were eligible for inclusion in our study (n = 1,781). Our study sample consists of 1,308 female adolescents (13 sets of twins) who had complete data on AMH, cardiometabolic outcomes and all potential confounders (see Figure 1). Ethical approval was obtained from the ALSPAC Law and Ethics committee and relevant local ethics committees in line with the Declaration of Helsinki, and written informed consent was provided by all participants.

thumbnail
Figure 1. Participant flow through the study.

*Participants who had withdrawn, were lost to follow-up or had died were not invited.

https://doi.org/10.1371/journal.pone.0064510.g001

Assessment of Serum AMH

For all blood measures, participants were asked to fast overnight if attending the morning clinic, or for a minimum of 6 hours if attending after lunch. All blood samples were immediately spun and frozen at −80°C. Assays were completed on serum using the commercial AMH generation II ELISA kit provided by Beckman Coulter (Beckman Coulter UK Ltd, High Wycombe, UK). [40] Inter and intra-assay CVs were both <5%.

Assessment of Outcomes

Serum insulin was measured with an enzyme linked immunosorbent assay (ELISA, Mercodia, Uppsala, Sweden) that does not cross-react with proinsulin. Plasma glucose and CRP were measured with an automated assay, the latter with excellent sensitivity down to 0.1 mg/l. Plasma triglyceride, total cholesterol and HDL-c concentrations were measured by modification of the standard Lipid Research Clinics Protocol by using enzymatic reagents for lipid determination, and LDL-c concentration was determined from these, using the Friedwald equation. [41] Inter and intra-assay CVs for lipids, glucose and CRP were all <5%. For insulin, inter-assay CV is <9.3% and intra-assay CV were <6.0%. It has been established in children and adults that fasting insulin is very highly correlated with formulae that attempt to more accurately measure insulin resistance, such as HOMA-IR or QUICKI, by combining fasting glucose and insulin. [42], [43] A recent consensus statement recommends that fasting insulin be used (rather than HOMA-IR or QUICKI) in epidemiological studies of children/adolescents. [44] In our sample fasting insulin was very highly correlated with HOMA-IR (Pearson’s correlation coefficient 0.98) and QUICKI (0.97) and all results were identical if either of these were used in place of fasting insulin. We therefore present only results with fasting insulin.

Assessment of Potential Confounders

The following were considered as potential confounders: birth weight, gestational age, pubertal stage, age, age at menarche, ethnicity, socioeconomic position, adiposity, level of physical activity, smoking status and the use of hormonal contraceptives. Birth weight was recorded in the delivery room and abstracted from obstetric records and/or birth notifications. Gestational age was abstracted from clinical records. Pubertal staging was assessed by annual questionnaires which were mailed to participants from age 8 to age 17. The puberty questionnaire could be answered by the participant, a parent, a guardian, or any combination of these individuals. On each questionnaire, the respondent was asked to examine line drawings representing the five Tanner stages for breast size and for pubic hair and to record which drawing most nearly represented the participant’s current stage of development. [45], [46] In each questionnaire, the participant was also asked whether she had had her first menstrual period and, if so, the month and year in which it occurred. Pubertal stage at the time of AMH measurement was established by taking the highest self-reported Tanner rating for either breast development or pubic hair, and using whichever was available if one of these was missing. [45] Whether the participant had started menstruating and if so, at what age this occurred was reported by the participant or her mother in questionnaires administered repeatedly between age 97 and 192 months. The small number of participants who had still not started menstruating at the time of the last questionnaire (N  = 6 (0.46%)) were allocated an age of menarche of 204 months (17 years) in order to allow all participants to be included in analyses. Age was recorded at the time of clinic assessment. Ethnicity was based on the mother’s and her partner’s ethnicity as reported by the mother. Fat mass was measured using a Lunar Prodigy Dual-energy X-ray absorptiometry (DXA) scanner (GE Medical Systems Lunar, Madison, WI). Scans were visually inspected and realigned where necessary. Height was measured to the nearest 0.1 cm with a Harpenden stadiometer with the participant unshod. To assess physical activity, all participants attending the clinic were asked to wear an Actigraph accelerometer (Actigraph LLC, Fort Walton Beach, Florida) for seven days. Data from participants who had worn the Actigraph for at least ten hours per day for at least three days were considered valid. [47] Two main physical activity variables were derived; average accelerometer counts per minute (CPM) over the full period of valid recording, and average number of minutes in moderate to vigorous physical activity (MVPA), per valid measurement day. [48] Based on questionnaire responses, the highest parental occupation was used to allocate participants to family social class groups using the 1991 British Office of Population and Census Statistics (OPCS) classification. Participants were asked about their smoking habits by questionnaire at mean age 14.3 years (the questionnaire administered closest to, and before, the time of the assessment where blood samples were taken) and these data were used to generate a three-level categorical smoking variable: ‘none’ (including those who have never tried a cigarette and those who used to smoke sometimes, but never smoke now), ‘<1 cigarette per week’ or ‘>1 cigarette per week’. Information on use of the hormonal contraceptive pill in the last year was asked in a single question, administered at the same time as the assessment where blood samples were taken. This question was answered by 1,283 (98%) of our study sample. Of the 25 study participants who did not answer this question, 13 indicated in a separate question concerned with recent sexual activity that they were taking the pill, and a further 12 who did not answer either of these questions had an assay result for sex hormone binding globulin (SHBG) >100 nmol/l, which was considered to indicate use of hormonal contraceptives.

Statistical Analysis

All analyses were conducted in Stata/MP 11.2 (StataCorp, College Station, Texas). AMH, fasting insulin, triglycerides and CRP were positively skewed. In descriptive analyses medians and interquartile ranges (IQR) are presented for these variables, and their natural logs were used in regression models; residuals in these models were approximately normally distributed after these transformations. Consistent with the age of assessment, there were no participants in Tanner stages 1 and 2, and few participants in Tanner stage 3 (Table 1). Therefore we generated a binary variable categorising Tanner stage 5 as post-pubertal and stages 1–4 as early pubertal.

thumbnail
Table 1. Characteristics of participants included in the study (n = 1,308), and excluded due to missing data (n = 473).

https://doi.org/10.1371/journal.pone.0064510.t001

In order to examine whether there were non-linear associations of AMH with outcomes and to ensure correct modelling of potential confounding factors, distributions of outcomes and confounders were examined by quintiles of AMH and tests of linear associations and deviation from linearity were computed. The first was obtained from a model in which AMH quintiles were entered as a continuous variable and the latter from comparing the linear model to a model in which AMH quintiles were included as four indicator variables using a likelihood ratio test.

A series of multivariable linear regression models were used to examine associations of AMH with each outcome. The crude association is estimated in Model 1. We then adjusted for age, pubertal stage, age at menarche, ethnicity, socioeconomic position, fat mass, height, height-squared, and hormonal contraceptive use (Model 2). The inclusion of height and height-squared as covariables in the analyses that included fat mass was to ensure adjustment for greater relative adiposity, rather than greater fat mass as a result of greater height. To make coefficients from multivariable regression models more interpretable, they were multiplied by log base 2 so that results are the mean difference in outcome per doubling of AMH. For outcomes that were logged (fasting insulin, triglycerides and CRP) regression coefficients were back transformed (exponentiated) so that coefficients represent the percentage change in the outcome per doubling of AMH. Analyses were conducted on all participants in our study sample including those taking the hormonal contraceptive pill, with hormonal contraceptive use being adjusted for in the regression model (n = 1,308). Analyses were then repeated after excluding the 170 (13%) participants taking the hormonal contraceptive pill.

Sensitivity Analyses

Smoking, physical activity and age at menarche were considered as potential confounders. However, there were variable amounts of missing data for each of these confounder; for smoking data was available for 1,096 [83.8%] of those with complete data on all other variables; physical activity data available for 607 [46.4%]; and age at menarche data for 1,191 [91.1%]. To assess potential confounding by these variables we completed sensitivity analyses on the sub-samples for who these data were available. We compared models 1 and 2 in these subsets with equivalent results from the larger main sample of 1,308. We then adjusted for smoking, physical activity and age at menarche in a group of final models (Model 3a, 3b and 3c, respectively). To ensure that females with exceptionally high AMH values were not driving any of the observed associations, we repeated all analyses excluding those females within the highest 3% of the AMH distribution (i.e. over 2 standard deviations above the mean AMH level, N = 63). We also repeated analyses after excluding the 6 (0.46%) participants who had not yet started menarche, as this small group could potentially be experiencing delayed puberty.

Results

Table 1 summarises the characteristics of our analysis sample (n = 1,308) and also of those female participants who were eligible but were excluded from the analysis due to missing data for potential confounders or cardiometabolic outcomes. Excluded participants had, on average, higher insulin, glucose and LDLc than those who were included. Participants who were excluded were also more likely to be older, have a later age at menarche, of non-white ethnicity, taking hormonal contraceptives, and less likely to be post-pubertal. However, for most of these characteristics the magnitude of the differences was small.

AMH values ranged from 0.16–35.84 ng/ml and median AMH was 3.57 ng/ml (IQR: 2.41, 5.49). For females classified as post-pubertal, median (IQR) AMH was 3.81 ng/ml (2.55, 5.82) compared with 3.25 ng/ml (2.23, 5.05) in those classed as in early puberty (P value from a Mann-Whitney U-test of the difference between median AMH levels in the two puberty categories ≤0.001).

Table 2 shows the distributions of cardiometabolic outcomes and confounders by quintiles of AMH. There was some evidence of an inverse linear association of AMH with CRP and age at menarche, and that the association with DXA determined fat mass deviated from linearity; however, BMI and percentages of overweight and obese did not differ relative to quintiles of AMH. There was no strong evidence that the distribution of other outcomes or confounders varied across quintiles of AMH.

thumbnail
Table 2. Characteristics of females by quintiles of AMH (n = 1,308).

https://doi.org/10.1371/journal.pone.0064510.t002

Multivariable associations of AMH with all outcomes are displayed in Table 3. After adjustment for confounders, AMH was not associated with any of the cardiometabolic outcomes. Results did not change substantially after the 170 (13%) participants taking hormonal contraceptives were removed from the analyses (Table 4). The percentage change coefficient for the association between AMH and CRP changed direction (−3%, 95%CI −8% to+2% in the analysis including those that were taking hormonal contraceptives compared to+1%, 95% CI −5% to+7% when participants taking hormonal contraceptives were excluded). However, neither of these associations reached the conventional 5% significance level.

thumbnail
Table 3. Multivariable associations of AMH with cardiometabolic risk factors (n = 1,308).

https://doi.org/10.1371/journal.pone.0064510.t003

thumbnail
Table 4. Multivariable associations of AMH with cardiometabolic risk after excluding 170 (13%) participants taking the hormonal contraceptive pill (n = 1,138).

https://doi.org/10.1371/journal.pone.0064510.t004

Sensitivity Analyses

Table S1S3 show the multivariable analyses of AMH with cardiometabolic outcomes in the subgroup of participants who additionally had complete data on smoking, physical activity and age at menarche, respectively. Results did not differ substantially in the subgroups with smoking, physical activity and age at menarche data to those in the main analysis shown in Table 2. This suggests that missing data for these potential confounding factors did not result in selection bias. Additional adjustment for smoking, physical activity or age at menarche did not alter results. Results were largely unchanged when females in the highest 3% of the AMH distribution were excluded (Table S4) or when those that had not started menarche were excluded (Table S5).

Discussion

In this study we demonstrated that AMH was not associated with a range of cardiometabolic risk factors including lipids and insulin in a large general population of adolescent females. In accordance with recent longitudinal and cross-sectional studies, [32], [33], [49] we identified that AMH levels were slightly higher in females assessed post-puberty, compared with those assessed during early puberty, however adjusting for pubertal status did not alter the lack of association of AMH with cardiometabolic risk factors.

Although we have modelled AMH as the exposure and the cardiometabolic risk factors as the outcomes, given that they are measured at the same time their respective classification as exposure and outcome are interchangeable. Whilst studies of this association to date (see introduction) have been interpreted as examining the hypothesis that more rapid ovarian ageing (that AMH proxies for) may be associated with more adverse cardiometabolic outcomes, the opposite has also been proposed. Hyperinsulinaemia has been proposed as a possible mechanism that may disrupt normal follicular development, [50] with polycystic ovary syndrome associated with both hyperinsulinaemia and marked increases in AMH, [20], [25] however in the current study we did not see an association between AMH and insulin, and there was also no evidence of a non-linear association suggestive of a threshold effect.

We are aware of only one other study that has examined the association of AMH with CRP, in adult Asian women (n  = 290). [51] In that study of a mixed population of women with and without PCOS, consistent with our own findings, no overall association across the distributions of both AMH and CRP was observed. Lin et al reported AMH to be positively associated with total cholesterol, both HDL-C and LDL-C in a mixed population of women with and without PCOS, but this finding was not replicated in an analysis of adult ovulatory women. [52] Furthermore in an animal model of atherosclerosis, AMH was not associated with lipid concentrations. [24] Further large studies are required to ascertain whether AMH is associated with an adverse lipid profile in adolescents.

Our null results could be because there is, in fact, no association of AMH with cardiometabolic outcomes, and the contradictory results in select adult women to date represent the expected variation around a true null association. It is also possible that associations observed in previous studies are explained by confounding, either because they did not appropriately adjust for confounders such as socioeconomic position or fat mass, or because they had inadequate measurements of potential confounders. It is notable that in our study of adolescent females, where confounding by characteristics such as smoking or an effect of existing undiagnosed atherosclerosis on AMH is highly unlikely, we did not observe an association even before multivariable adjustment for potential confounders. In previous publications we have shown expected associations with fasting insulin, glucose and the other cardiovascular risk factors examined here, for example we have shown a dose response association of BMI, waist circumference and total body fat mass with these outcomes, [53] illustrating that the null results presented here are highly unlikely to be due to error in the outcome measurements. It is possible that associations of AMH with cardiometabolic outcomes emerge only at a later age and/or exist only in sub-groups of the population such as those with PCOS. Future prospective studies with AMH and cardiovascular risk factors in adult premenopausal women are needed to ascertain whether ovarian reserve is independently associated with cardiovascular risk over the established associations with oestrogen production. Overall our findings raise the possibility that functional ovarian reserve as assessed by AMH is not a direct determinant of the lipid and insulin cardiometabolic risk profile during the early reproductive years in healthy women.

Strengths and Limitations

To our knowledge, this is the largest study to date to examine associations of AMH with a range cardiometabolic factors in a general adolescent female population. The cross-sectional design does not allow us to establish causality or the direction of association. Some potential confounders (smoking, physical activity and age at menarche) were only available in subgroups of participants, but analyses in these subgroups did not suggest they were importantly different from the main analysis sample or that these characteristics were important confounders. As is common in birth cohort studies there has been loss to follow-up over time (Figure 1) and participants who were excluded from our study because of missing data differed slightly for some characteristics compared to those who were included (Table 1). Our results would only be biased if associations were markedly different in those lost to follow-up or with missing data compared to those included in our analyses, and whilst we cannot test this, we cannot think of any reason as to why this would be the case. Consistent with other large epidemiological studies conducted in general population samples; we are not able to directly measure insulin resistance using the gold standard euglycaemic hyperinsulinemic clamp. Fasting insulin has been shown to have modest to strong correlations with clamp assessed insulin resistance (correlation coefficients 0.5 to 0.9) in children and adolescents. [42] Any measurement error is likely to be non-differential and therefore would be expected to bias results towards the null. However, even if non-differential measurement error resulted in our associations being weaker than they would be with a direct measure of insulin resistance, with correlations of 0.5 to 0.9 we would have expected some association of AMH with fasting insulin if this were an important determinant and/or predictor. For this study we were unable to conduct physical assessments of pubertal development by trained clinical personnel. In the absence of a direct visual assessment by a clinician, self-assessment of Tanner stage is considered a practical and valid choice, particularly for longitudinal studies with repeat assessments. [54] Kappa coefficients comparing clinician to self-assessments range from 0.3 to 0.9 for breast and from 0.4 to 0.9 for pubic-hair development in different studies. [55] Our study used the drawings of pubertal stages developed by Morris and Udry, [46] which had been successfully used in previous cohort studies. [56], [57] We do not have diagnostic information on whether female participants had PCOS; however removing participants with an AMH >2 standard deviations from the mean (the highest 3% of the AMH distribution) did not change any associations. We adopted this approach as the adult diagnostic criteria for PCOS has recently been recognised as not appropriate for adolescent girls, [58] although AMH is elevated in adolescents with polycystic ovarian morphology and in PCOS. [59] We also do not have measures of testosterone and could therefore not investigate the association between androgens and AMH. Lastly our population are largely of European, white ethnic origin and we cannot assume that results would generalise to other ethnicities.

In conclusion, we have found that in a general population of adolescent females, AMH is not associated with fasting insulin or other cardiometabolic outcomes. There is a need for further large prospective studies of these associations that include repeat measurements with increasing age in order to understand whether AMH, a marker of ovarian reserve, is importantly related to cardiometabolic health in healthy women as they age from early adolescence to peak reproductive age and beyond.

Supporting Information

Table S1.

Multivariable associations of AMH with cardiometabolic outcomes in participants with complete data on all variables including smoking.

https://doi.org/10.1371/journal.pone.0064510.s001

(DOCX)

Table S2.

Multivariable associations of AMH with cardiometabolic outcomes in participants with complete data on all variables including minutes spent in moderate to vigorous activity and counts per minute (n = 607).

https://doi.org/10.1371/journal.pone.0064510.s002

(DOCX)

Table S3.

Multivariable associations of AMH with cardiometabolic outcomes in participants with complete data on all variables including age at menarche (n = 1,191).

https://doi.org/10.1371/journal.pone.0064510.s003

(DOCX)

Table S4.

Multivariable associations of AMH with cardiometabolic risk factors, excluding females with the top 3% of AMH values.

https://doi.org/10.1371/journal.pone.0064510.s004

(DOCX)

Table S5.

Multivariable associations of AMH with cardiometabolic risk factors, excluding those that have not yet started.

https://doi.org/10.1371/journal.pone.0064510.s005

(DOCX)

Acknowledgments

We thank Anne Currie and Anne Alexander based at Glasgow Royal Infirmary Department of Biochemistry for the excellent technical input to key laboratory measurements. We are grateful to all the families who took part in this study, the midwives for their help in recruiting them, and the whole ALSPAC team, which includes interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and nurses.

Author Contributions

Conceived and designed the experiments: DAL SMN. Performed the experiments: WM SMN NS. Analyzed the data: EA. Contributed reagents/materials/analysis tools: EA AF WM SMN NS. Wrote the paper: EA AF DAL SMN. Helped with the interpretation of the data and with the critical revision of the manuscript: RF HL SMN NS WM.

References

  1. 1. Hansen KR, Hodnett GM, Knowlton N, Craig LB (2011) Correlation of ovarian reserve tests with histologically determined primordial follicle number. Fertility and Sterility 95: 170–175.
  2. 2. Fleming R, Kelsey TW, Anderson RA, Wallace WH, Nelson SM (2012) Interpreting human follicular recruitment and antimullerian hormone concentrations throughout life. Fertility and Sterility 98: 1097–1102.
  3. 3. van Rooij IA, Tonkelaar I, Broekmans FJ, Looman CW, Scheffer GJ, et al. (2004) Anti-mullerian hormone is a promising predictor for the occurrence of the menopausal transition. Menopause 11: 601–606.
  4. 4. Hagen CP, Aksglaede L, Sørensen K, Main KM, Boas M, et al. (2010) Serum Levels of Anti-Mullerian Hormone as a Marker of Ovarian Function in 926 Healthy Females from Birth to Adulthood and in 172 Turner Syndrome Patients. Journal of Clinical Endocrinology & Metabolism 95: 5003–5010.
  5. 5. Kelsey T, Wright P, Nelson SM, Anderson RA, Wallace WHB (2012) Data Aggregation and Analysis for Assessment of Ovarian Reserve. Mol Cell Endocrinol 18: 79–87.
  6. 6. Aksglaede L, Sorensen K, Boas M, Mouritsen A, Hagen CP, et al. (2010) Changes in anti-Mullerian hormone (AMH) throughout the life span: a population-based study of 1027 healthy males from birth (cord blood) to the age of 69 years. J Clin Endocrinol Metab 95: 5357–5364.
  7. 7. Atsma F, Bartelink ML, Grobbee DE, van der Schouw YT (2006) Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause 13:
  8. 8. van der Schouw YT, van der Graaf Y (1996) Age at menopause as a risk factor for cardiovascular mortality. Lancet 347: 714.
  9. 9. Hu FB, Goldstein F, Hennekens CH (1999) AGe at natural menopause and risk of cardiovascular disease. Arch Intern Med 159: 1061–1066.
  10. 10. Berenson GS, Srinivasan SR, Bao W, Newman WP, Tracy RE, et al. (1998) Association between Multiple Cardiovascular Risk Factors and Atherosclerosis in Children and Young Adults. New England Journal of Medicine 338: 1650–1656.
  11. 11. Chu MC, Rath KM, Huie J, Taylor HS (2003) Elevated basal FSH in normal cycling women is associated with unfavourable lipid levels and increased cardiovascular risk. Human Reproduction 18: 1570–1573.
  12. 12. Bayrak A, Terbell H, Urwitz-Lane R, Mor E, Stanczyk FZ, et al. (2007) Acute effects of metformin therapy include improvement of insulin resistance and ovarian morphology. Fertil Steril 87: 870–875.
  13. 13. Buyuk E, Seifer DB, Illions E, Grazi RV, Lieman H (2011) Elevated body mass index is associated with lower serum anti-mullerian hormone levels in infertile women with diminished ovarian reserve but not with normal ovarian reserve. Fertil Steril 95: 2364–2368.
  14. 14. Chen MJ, Yang WS, Chen CL, Wu MY, Yang YS, et al. (2008) The relationship between anti-Mullerian hormone, androgen and insulin resistance on the number of antral follicles in women with polycystic ovary syndrome. Hum Reprod 23: 952–957.
  15. 15. Freeman EW, Gracia CR, Sammel MD, Lin H, Lim LC-L, et al. (2007) Association of anti-mullerian hormone levels with obesity in late reproductive-age women. Fertility and Sterility 87: 101–106.
  16. 16. La Marca A, Orvieto R, Giulini S, Jasonni VM, Volpe A, et al. (2004) Mullerian-inhibiting substance in women with polycystic ovary syndrome: relationship with hormonal and metabolic characteristics. Fertil Steril 82: 970–972.
  17. 17. La Marca A, Spada E, Grisendi V, Argento C, Papaleo E, et al. (2012) Normal serum anti-Mullerian hormone levels in the general female population and the relationship with reproductive history. European Journal of Obstetrics & Gynecology and Reproductive Biology 163: 180–184.
  18. 18. Piouka A, Farmakiotis D, Katsikis I, Macut D, Gerou S, et al. (2009) Anti-Mullerian hormone levels reflect severity of PCOS but are negatively influenced by obesity: relationship with increased luteinizing hormone levels. American Journal of Physiology - Endocrinology And Metabolism 296: E238–E243.
  19. 19. Sir-Petermann T, Codner E, Maliqueo M, Echiburu B, Hitschfeld C, et al. (2006) Increased anti-Mullerian hormone serum concentrations in prepubertal daughters of women with polycystic ovary syndrome. J Clin Endocrinol Metab 91: 3105–3109.
  20. 20. Skalba P, Cygal A, Pawel M, Dabkowska-Huc A, Sikora J, et al. (2011) Is the plasma anti-Mullerian hormone (AMH) level associated with body weight and metabolic, and hormonal disturbances in women with and without polycystic ovary syndrome? European Journal of Obstetrics & Gynecology and Reproductive Biology 158: 254–259.
  21. 21. Steiner AZ, Stanczyk FZ, Patel S, Edelman A (2010) Antimullerian hormone and obesity: insights in oral contraceptive users. Contraception 81: 245–248.
  22. 22. Thomson RL, Buckley JD, Moran LJ, Noakes M, Clifton PM, et al. (2009) The effect of weight loss on anti-Mullerian hormone levels in overweight and obese women with polycystic ovary syndrome and reproductive impairment. Human Reproduction 24: 1976–1981.
  23. 23. Woo HY, Kim KH, Rhee EJ, Park H, Lee MK (2012) Differences of the association of anti-Mullerian hormone with clinical or biochemical characteristics between women with and without polycystic ovary syndrome. Endocrine Journal 59: 781–790.
  24. 24. Appt SE, Chen H, Clarkson TB, Kaplan JR (2012) Premenopausal antimullerian hormone concentration is associated with subsequent atherosclerosis. Menopause [Epub ahead of print]:
  25. 25. Nardo LG, Yates AP, Roberts SA, Pemberton P, Laing I (2009) The relationships between AMH, androgens, insulin resistance and basal ovarian follicular status in non-obese subfertile women with and without polycystic ovary syndrome. Hum Reprod 24: 2917–2923.
  26. 26. Villarroel C, Merino PM, López P, Eyzaguirre FC, Van Velzen A, et al. (2011) Polycystic ovarian morphology in adolescents with regular menstrual cycles is associated with elevated anti-Mullerian hormone. Human Reproduction 26: 2861–2868.
  27. 27. Park HT, Cho GJ, Ahn KH, Shin JH, Kim YT, e al (2010) Association of insulin resistance with anti-Mullerian hormone levels in women without polycystic ovary syndrome (PCOS). Clin Endocrinol (Oxf) 72: 26–31.
  28. 28. Nelson SM, Stewart F, Fleming R, Freeman DJ (2010) Longitudinal assessment of antimullerian hormone during pregnancy-relationship with maternal adiposity, insulin, and adiponectin. Fertil Steril 93: 1356–1358.
  29. 29. Freour T, Masson D, Mirallie S, Jean M, Bach K, et al. (2008) Active smoking compromises IVF outcome and affects ovarian reserve. Reprod Biomed Online 16: 96–102.
  30. 30. Kerkhof GF, Leunissen RWJ, Willemsen RH, de Jong FH, Visser JA, et al. (2010) Influence of preterm birth and small birth size on serum anti-Mullerian hormone levels in young adult women. European Journal of Endocrinology 163: 937–944.
  31. 31. Hehenkamp WJK, Volkers NA, Broekmans FJM, de Jong FH, Themmen APN, et al. (2007) Loss of ovarian reserve after uterine artery embolization: a randomized comparison with hysterectomy. Human Reproduction 22: 1996–2005.
  32. 32. Hagen CP, Aksglaede L, Sorensen K, Mouritsen A, Andersson AM, et al. (2012) Individual serum levels of anti-Mullerian hormone in healthy girls persist through childhood and adolescence: a longitudinal cohort study. Human Reproduction 27: 861–866.
  33. 33. Kelsey TW, Wright P, Nelson SM, Anderson RA, Wallace WH (2011) A Validated Model of Serum Anti-Mullerian Hormone from Conception to Menopause. PLoS ONE 6: e22024.
  34. 34. Strong JP, Malcom GT, McMahan CA, Tracy RE, Newman WP III, et al. (1999) Prevalence and extent of atherosclerosis in adolescents and young adults: Implications for prevention from the pathobiological determinants of atherosclerosis in youth study. JAMA 281: 727–735.
  35. 35. McCarron P, Smith GD, Okasha M, McEwen J (2000) Blood pressure in young adulthood and mortality from cardiovascular disease. The Lancet 355: 1430–1431.
  36. 36. Juonala M, Magnussen CG, Venn A, Dwyer T, Burns TL, et al. (2010) Influence of Age on Associations Between Childhood Risk Factors and Carotid Intima-Media Thickness in Adulthood: The Cardiovascular Risk in Young Finns Study, the Childhood Determinants of Adult Health Study, the Bogalusa Heart Study, and the Muscatine Study for the International Childhood Cardiovascular Cohort (i3C) Consortium. Circulation 122: 2514–2520.
  37. 37. Raitakari OT JM (2003) Cardiovascular risk factors in childhood and carotid artery intima-media thickness in adulthood: The cardiovascular risk in young finns study. JAMA 290: 2277–2283.
  38. 38. Boyd A, Golding J, Macleod J, Lawlor DA, Fraser A, et al.. (2012) Cohort Profile: The ‘Children of the 90s’ - the index offspring of the Avon Longitudinal Study of Parents and Children. International Journal of Epidemiology.
  39. 39. Fraser A, Macdonald-Wallis C, Tilling K, Boyd A, Golding J, et al.. (2012) Cohort Profile: The Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort. International Journal of Epidemiology.
  40. 40. Wallace AM, Faye SA, Fleming R, Nelson SM (2011) A multicentre evaluation of the new Beckman Coulter anti-Mullerian hormone immunoassay (AMH Gen II). Annals of Clinical Biochemistry 48: 370–373.
  41. 41. Friedewald WT, Levy RI, Fredrickson DS (1972) Estimation of the Concentration of Low-Density Lipoprotein Cholesterol in Plasma, Without Use of the Preparative Ultracentrifuge. Clin Chem 18: 499–502.
  42. 42. Gungor N, Saad R, Janosky J, Arslanian S (2004) Validation of surrogate estimates of insulin sensitivity and insulin secretion in children and adolescents. J Pediatr 144: 47–55.
  43. 43. Schwartz B, Jacobs DR Jr, Moran A, Steinberger J, Hong CP, et al. (2008) Measurement of insulin sensitivity in children: comparison between the euglycemic-hyperinsulinemic clamp and surrogate measures. Diabetes Care 31: 783–788.
  44. 44. Levy-Marchal C, Arslanian S, Cutfield W, Sinaiko A, Druet C, et al. (2010) Insulin resistance in children: consensus, perspective, and future directions. J Clin Endocrinol Metab 95: 5189–5198.
  45. 45. Marshall WA, Tanner JM (1969) Variations in pattern of pubertal changes in girls. Arch Dis Child 44: 291–303.
  46. 46. Morris N, Udry JR (1980) Validation of a self-administered instrument to assess stage of adolescent development. J Youth Adolescence 9: 271–280.
  47. 47. Mattocks C, Ness A, Leary S, Tilling K, Blair SN, et al. (2008) Use of accelerometers in a large field-based study of children: protocols, design issues, and effects on precision. J Phys Act Health 5 Suppl 1S98–111.
  48. 48. Riddoch CJ, Mattocks C, Deere K, Saunders J, Kirkby J, et al. (2007) Objective measurement of levels and patterns of physical activity. Archives of Disease in Childhood 92: 963–969.
  49. 49. Codner E, Iniguez G, Hernandez IM, Lopez P, Rhumie HK, et al. (2011) Elevated anti-Mullerian hormone (AMH) and inhibin B levels in prepubertal girls with type 1 diabetes mellitus. Clin Endocrinol (Oxf) 74: 73–78.
  50. 50. Palomba S, Falbo A, Zullo F, Orio F (2009) Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review. Endocrine Reviews 30: 1–50.
  51. 51. Lin YH, Chiu WC, Wu CH, Tzeng CR, Hsu CS, et al. (2011) Antimullerian hormone and polycystic ovary syndrome. Fertil Steril 96: 230–235.
  52. 52. Johnstone EB, Rosen MP, Neril R, Trevithick D, Sternfeld B, et al. (2010) The polycystic ovary post-rotterdam: a common, age-dependent finding in ovulatory women without metabolic significance. J Clin Endocrinol Metab 95: 4965–4972.
  53. 53. Lawlor DA, Benfield L, Logue J, Tilling K, Howe LD, et al.. (2010) Association between general and central adiposity in childhood, and change in these, with cardiovascular risk factors in adolescence: prospective cohort study. BMJ 341:
  54. 54. Rockett JC, Lynch CD, Buck GM (2004) Biomarkers for assessing reproductive development and health: Part 1–Pubertal development. Environ Health Perspect 112: 105–112.
  55. 55. Hergenroeder AC, Hill RB, Wong WW, Sangi-Haghpeykar H, Taylor W (1999) Validity of self-assessment of pubertal maturation in African American and European American adolescents. J Adolesc Health 24: 201–205.
  56. 56. Blanck HM, Marcus M, Tolbert PE, Rubin C, Henderson AK, et al. (2000) Age at menarche and tanner stage in girls exposed in utero and postnatally to polybrominated biphenyl. Epidemiology 11: 641–647.
  57. 57. Gladen BC, Ragan NB, Rogan WJ (2000) Pubertal growth and development and prenatal and lactational exposure to polychlorinated biphenyls and dichlorodiphenyl dichloroethene. J Pediatr 136: 490–496.
  58. 58. Hickey M, Doherty DA, Atkinson H, Sloboda DM, Franks S, et al. (2011) Clinical, ultrasound and biochemical features of polycystic ovary syndrome in adolescents: implications for diagnosis. Human Reproduction 26: 1469–1477.
  59. 59. Hart R, Doherty DA, Norman RJ, Franks S, Dickinson JE, et al. (2010) Serum antimullerian hormone (AMH) levels are elevated in adolescent girls with polycystic ovaries and the polycystic ovarian syndrome (PCOS). Fertility and Sterility 94: 1118–1121.