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Updated: Oct 5, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Anti-Müllerian hormone and vascular dysfunction in women with chronic kidney disease
Sandra M Dumanski1,2,3, Todd J Anderson1,2, Kara A Nerenberg1,2,4,5
1Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
Insights
In young women with chronic kidney disease (CKD), lower anti-Müllerian hormone (AMH) levels correlate with poorer vascular function, indicating a potential marker for increased cardiovascular risk. This highlights AMH as a crucial factor for cardiovascular health in this population.
Area of Science:
- Nephrology and Cardiovascular Medicine
- Reproductive Endocrinology
- Vascular Physiology
Background:
- Young women with chronic kidney disease (CKD) face a disproportionately high risk of cardiovascular mortality.
- Reduced anti-Müllerian hormone (AMH) is linked to cardiovascular issues in the general population, but its role in CKD is unclear.
Purpose of the Study:
- To investigate the association between AMH levels and vascular function in young women with CKD.
- To explore AMH as a potential marker for cardiovascular risk in this high-risk group.
Main Methods:
- An exploratory cross-sectional study involving 47 young women with CKD (non-dialysis-dependent and dialysis-dependent).
- Measured AMH levels, endothelial function (brachial artery flow-mediated dilation), and arterial stiffness (aortic augmentation index, pulse wave velocity).
- Utilized multivariate linear regression to analyze associations between AMH and vascular health markers.
Main Results:
- AMH levels were inversely associated with age but not with estimated glomerular filtration rate (eGFR) or dialysis status.
- In non-dialysis-dependent participants, AMH correlated with impaired brachial artery flow-mediated dilation and increased aortic augmentation index.
- AMH was associated with increased aortic augmentation index in all participants, but not in dialysis-dependent individuals.
Conclusions:
- AMH levels are associated with impaired vascular function in young women with non-dialysis-dependent CKD.
- AMH may serve as an important indicator of future cardiovascular risk in young women with CKD.
- Further research on this female-specific cardiovascular risk factor in the CKD population is warranted.
Abstract:
Young women with chronic kidney disease (CKD) have disproportionately increased risk of cardiovascular mortality. Reduced anti-Müllerian hormone (AMH) is linked to poor cardiovascular outcomes in the general population, but whether AMH is associated with increased cardiovascular risk in the high-risk CKD population is unknown. This study examined the association between AMH and vascular function, validated markers of cardiovascular risk, in women with CKD. An exploratory cross-sectional study was performed in 47 young women with CKD. Laboratory measurements of AMH were collected. Using standardized protocols, endothelial function was measured with brachial artery flow-mediated dilation and hyperemic velocity time integral. Arterial stiffness was measured with aortic augmentation index and pulse wave velocity. Multivariate linear regression analyses were utilized to evaluate the association between AMH levels and each measure of vascular health. Forty women (36 ± 7 years) with non-dialysis-dependent CKD and 7 women (38 ± 6 years) with dialysis-dependent CKD participated. AMH levels were inversely associated with age (p = 0.01) but not associated with eGFR (p = 0.59) or dialysis status (p = 0.97). AMH was associated with brachial artery flow-mediated dilation (R2 = 0.21 [p = 0.03]) and aortic augmentation index (R2 = 0.20 [p = 0.04]) in the non-dialysis-dependent participants, and with aortic augmentation index in all participants (R2 = 0.18 [p = 0.03]). No association between AMH and any measure of vascular function was demonstrated in the dialysis-dependent participants. AMH levels are associated with impaired vascular function in young women with CKD and may be an important marker of future cardiovascular risk. Further investigation into this female-specific cardiovascular risk factor is warranted in this high-risk population.
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