Osteoporosis, bone & mineral

Associations of Anti-Müllerian Hormone (AMH) in Midreproductive Years with Bone Mineral Density and Turnover Markers in Midlife

J Clin Endocrinol MetabPublished Prospective cohort study

Authors' conclusion

Lower AMH during midreproductive years is associated with lower BMD and higher bone turnover 14 years later. Ovarian reserve during midreproductive years may be a valuable predictor of long-term bone health.

Study context

Population
Parous women (71% White) in a US longitudinal cohort; AMH measured 2003–2006 (mean age 37.0 years, SD 5.1), bone mineral density (BMD) 2017–2021 (mean age 51.0 years, SD 5.1)
Participants
450 parous women
Exposure
AMH <1.0 ng/mL vs AMH >3.5 ng/mL in midreproductive years
Outcome
BMD (spine, hip, femoral neck; DXA)
Follow-up
∼14 years
Methodological detailslongitudinal, US cohort
  • Longitudinal
  • US cohort

Main finding

As reported in the abstract

BMD (g/cm²) · follow-up (∼14 years)

Beta (spine BMD)

−.06 g/cm²

95% CI −0.10 to −0.02

AMH <1.0 ng/mL

Beta (hip BMD)

−.05 g/cm²

95% CI −0.08 to −0.02

AMH <1.0 ng/mL

Beta (femoral neck BMD)

−.03 g/cm²

95% CI −0.06 to 0.00

AMH <1.0 ng/mL

Observational data: associations, not effects.

Secondary outcomes

OutcomeEstimate
Bone turnover markers (PINP, CTX-I) · follow-upAMH <1.0 ng/mL vs AMH >3.5 ng/mL · linear regression adjusted for demographics and lifestylebeta (PINP) .36 SD (95% CI 0.10–0.63)
Bone turnover markers (PINP, CTX-I) · follow-upAMH <1.0 ng/mL vs AMH >3.5 ng/mL · linear regression adjusted for demographics and lifestylebeta (CTX-I) .34 SD (95% CI 0.07–0.60)

Effect modification by menopausal status

AMH–spine BMD association more pronounced among postmenopausal women; associations with bone turnover markers more pronounced among women not yet menopausal

Mediation

AMH–BMD associations primarily mediated by menopausal status at follow-up

Original publication

Associations of AMH in Midreproductive Years with Bone Mineral Density and Turnover Markers in Midlife. J Clin Endocrinol Metab. Published 17 October 2024. doi:10.1210/clinem/dgae694

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