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. 2012 Dec;19(12):1353-9.
doi: 10.1097/gme.0b013e31825b4fe2.

Premenopausal antimüllerian hormone concentration is associated with subsequent atherosclerosis

Affiliations

Premenopausal antimüllerian hormone concentration is associated with subsequent atherosclerosis

Susan E Appt et al. Menopause. 2012 Dec.

Abstract

Objective: The aim of this study was to determine if premenopausal ovarian reserve is associated with susceptibility for atherosclerosis.

Methods: Female cynomolgus macaques (n = 66, women's equivalent age = 45 y) consumed an atherogenic diet for ∼5 months before the measurement of a marker of ovarian reserve (antimüllerian hormone [AMH]), plasma lipids, follicular phase estradiol, and body weight (BW). Monkeys were then ovariectomized (OVX; n = 17), remained premenopausal (n = 20), or were induced to have reduced ovarian reserve (ROR, n = 29). After 26 additional months consuming the diet, atherosclerosis measurements and risk variables were reassessed.

Results: No differences in baseline AMH, plasma lipids, BW, and estradiol or postdiet lipids and BW were observed among the groups subsequently assigned to the OVX, premenopausal control, or reduced ovarian reserve conditions. Postdiet measurements of atherosclerosis extent did not differ among the groups. However, analysis of plaque size by tertile of baseline AMH revealed that plaques were largest in monkeys that began the experiment with the lowest baseline AMH, followed by those in the middle and high tertiles (plaque extent: low AMH, 0.76 ± 0.12 mm; mid AMH, 0.46 ± 0.1 mm; high AMH, 0.34 ± 0.08 mm; P = 0.02). Baseline AMH and plaque size were also correlated negatively (r = -0.31, P = 0.01). Plasma lipids were also correlated significantly with plaque extent (all P < 0.01) but not with AMH.

Conclusions: We report for the first time an inverse relationship between a marker of ovarian reserve (AMH) and subsequent atherosclerosis risk.

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Conflict of interest statement

Conflict of Interest: None

Figures

FIG. 1
FIG. 1
A: Iliac artery atherosclerosis plaque area (mm2) among OVX (n = 17), ROR (n = 29), and PRE (n = 20) cynomolgus monkeys after ~2 years of diet consumption. B: Plaque area depicted according to tertiles of baseline plasma antimullerian hormone (AMH), all treatment groups combined. C: Plaque area depicted according to median baseline AMH for each individual treatment group. D: Correlation between baseline AMH and atherosclerosis, all treatment groups combined: OVX (○), PREMENOP (□), and ROR subset (diamond shape). Data are presented as mean ± SE plaque area (back transformed from SQRT) (A–C) and as the association between the SQRT of plaque size ± SE and SQRT of AMH (r = −0.31, P < 0.01) (D). OVX, ovariectomized; ROR, reduced ovarian reserve; PRE, premenopausal control; AMH, antimüllerian hormone; PREMENOP, premenopausal; SQRT, square root.

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References

    1. Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, Borden WB, Bravata DM, et al. Writing Group Members, On behalf of the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation. 2012;125(1):188–197. - PubMed
    1. Deo R, Vittinghoff E, Lin F, Tseng ZH, Hulley SB, Shlipak MG. Risk factor and prediction modeling for sudden cardiac death in women with coronary artery disease. Arch Intern Med. 2011;171:1703–9. - PMC - PubMed
    1. Michos ED, Nasir K, Braunstein JB, Rumberger JA, Budoff MJ, Post WS, Blumenthal RS. Framingham risk equation underestimates subclinical atherosclerosis risk in asymptomatic women. Atherosclerosis. 2006;184:201–6. - PubMed
    1. Hodis HN, Mack WJ. A “window of opportunity:” the reduction of coronary heart disease and total mortality with menopausal therapies is age- and time-dependent. Brain Res. 2011;1379:244–52. - PMC - PubMed
    1. Atsma F, Bartelink MEL, Grobbee DE, van der Schow YT. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause. 2006:265–279. - PubMed

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