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Published on: October 21, 2013
Menopausal hot flashing and endothelial function in two vascular beds: findings from a cross-sectional study of
Stamatina Iliodromiti1, Naveed Sattar2, Christian Delles2
1Women's Health Research Division, Blizard Institute, Queen Mary University London, London, United Kingdom.
Insights
Menopausal hot flashes are linked to increased insulin resistance and reduced macrovascular function in postmenopausal women. Microvascular responses were paradoxically enhanced, suggesting non-endothelial mechanisms.
Area of Science:
- Cardiovascular physiology
- Menopause research
- Vascular biology
Background:
- Menopausal hot flashes are common and may signal underlying cardiovascular disease (CVD) risk.
- Vascular reactivity assessment provides insights into endothelial function and CVD risk.
Purpose of the Study:
- To investigate the association between menopausal hot flashes and vascular reactivity in microvascular and macrovascular beds.
- To explore the relationship between hot flashing and cardiovascular disease risk profile in postmenopausal women.
Main Methods:
- Cross-sectional study of 79 postmenopausal women (23 non-flashers, 56 flashers).
- Microvascular reactivity assessed using Laser Doppler Imaging with Iontophoresis (acetylcholine and sodium-nitroprusside).
- Macrovascular endothelial function measured by Reactive Hyperemia Index (RHI); insulin sensitivity assessed.
Main Results:
- Women with hot flashes showed enhanced microvascular responses to acetylcholine (~30%) and sodium-nitroprusside (~31%).
- Hot flash group exhibited lower RHI (~13%), indicating impaired macrovascular function.
- Hot flashers were more insulin resistant (HOMAIR: 1.9 vs 1.4, P=0.03).
Conclusions:
- Hot flashing is associated with greater insulin resistance and reduced macrovascular response.
- Enhanced microvascular reactivity in flashers may involve thermoregulatory pathways, not solely endothelial integrity.
Objective:
We sought to examine the association of menopausal hot flashing with vascular reactivity in two different vascular beds in the same cohort of postmenopausal women and explore the relationship between hot flashing and cardiovascular disease (CVD) risk profile.
Methods:
A cross-sectional study of 79 healthy postmenopausal women, 23 of whom have never had menopausal hot flashes and 56 of whom have reported hot flashes. Endothelial function at a microvascular level was measured with Laser Doppler Imaging with Iontophoresis which assesses the response to both acetylcholine (Ach, endothelium dependent) and sodium-nitroprusside (SNP, endothelium independent). Reactive Hyperemia Index (RHI) was measured with peripheral arterial tonometry as a marker of endothelial function mainly at a macrovascular level. Metabolic biomarkers including insulin sensitivity were assessed.
Results:
Women with hot flashes had enhanced microvascular response to Ach by ∼30% (P = 0.04) and to SNP by ∼31% (P = 0.02), but lower RHI by ∼13% (P = 0.05) compared with women without flashes. Hot flashing was associated with enhanced response to SNP and lower RHI after adjustment for confounders and conventional CVD risk factors. Women with hot flashes were more insulin resistant than nonflashers (HOMAIR: 1.9 (1.2-2.6) vs 1.4 (0.8-1.9), P = 0.03).
Conclusions:
Our data support the association of hot flashing with greater insulin resistance and lower macrovascular response. The paradoxical enhanced microvascular response in hot flashers could be the result of the net effect of thermoregulatory and nonnitric oxide-related pathways rather than of endothelial integrity.
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