TY - JOUR
T1 - Resting Cerebrovascular Haemodynamics and Dynamic Assessment of Cerebrovascular Function in Polycystic Ovary Syndrome
AU - Richards, Cory T.
AU - Griffiths, Thomas D.
AU - Adams, Zoe H.
AU - Wright, Melissa E.
AU - Davies, Saajan
AU - Talbot, Jack S.
AU - Broad‐Thomas, Lauren
AU - Esteban, Diego García
AU - Steventon, Jessica J.
AU - Brassard, Patrice
AU - Murphy, Kevin
AU - James, Philip E.
AU - Rees, D. Aled
AU - Lord, Rachel N.
N1 - Publisher Copyright:
© 2025 The Author(s). Clinical Endocrinology published by John Wiley & Sons Ltd.
PY - 2025/11/25
Y1 - 2025/11/25
N2 - Objective: Despite an increased cerebrovascular disease risk, the impact of Polycystic Ovary Syndrome (PCOS) on cerebrovascular haemodynamics and function is unknown. This study characterised cerebrovascular haemodynamics and function in women with PCOS versus healthy controls. Design: Case‐control study. Patients: Fifteen women with PCOS (age: 31 ± 6 years; body mass index (BMI): 31.8 ± 5.7 kg/m2) and 16 controls (age: 30 ± 7 years; BMI: 29.9 ± 5.5 kg/m2). Measurements: Resting global cerebral blood (CBF) was assessed by 3T MRI. Middle‐ and posterior cerebral artery blood velocities (MCAv, PCAv) were measured by Doppler ultrasound and pulsatility index (MCAPI, PCAPI) calculated. Neurovascular coupling (NVC), internal carotid artery cerebrovascular reactivity (CVRCO2) and dynamic cerebral autoregulation (dCA) directional sensitivity were assessed using a visual stimulus, 6% fixed‐inspired CO2 and repeated squat‐stand manoeuvres, respectively. Results: Resting CBF (PCOS: 57.2 ± 7.5 ml/100 g/min; controls: 61.6 ± 11.6 ml/100 g/min, p = 0.25) and MCAv, PCAv, MCAPI and PCAPI (all p > 0.05) were similar between groups. NVC (14 ± 4.9% vs. 13 ± 3.4%, p = 0.45), CVRCO2 (5.1 ± 1.9% vs. 6.5 ± 2.9%, p = 0.20) and dCA directional sensitivity were similar between groups. However, women with PCOS had elevated relative PCAPI during NVC (PCOS: 12.0 ± 5.6% vs. controls: 7.0 ± 3.8%, p = 0.04), and impaired vasodilation of the internal carotid artery during CVRCO2 (PCOS: −0.10 ± 0.22 mm vs. controls: 0.18 ± 0.24 mm, p < 0.01). Conclusions: Cerebrovascular function is largely preserved in women with PCOS, although elevated arterial pulsatility and impaired vasodilatory response to carbon dioxide may indicate early endothelial dysfunction in the cerebral vasculature. Larger studies are needed to confirm this in view of our limited study power.
AB - Objective: Despite an increased cerebrovascular disease risk, the impact of Polycystic Ovary Syndrome (PCOS) on cerebrovascular haemodynamics and function is unknown. This study characterised cerebrovascular haemodynamics and function in women with PCOS versus healthy controls. Design: Case‐control study. Patients: Fifteen women with PCOS (age: 31 ± 6 years; body mass index (BMI): 31.8 ± 5.7 kg/m2) and 16 controls (age: 30 ± 7 years; BMI: 29.9 ± 5.5 kg/m2). Measurements: Resting global cerebral blood (CBF) was assessed by 3T MRI. Middle‐ and posterior cerebral artery blood velocities (MCAv, PCAv) were measured by Doppler ultrasound and pulsatility index (MCAPI, PCAPI) calculated. Neurovascular coupling (NVC), internal carotid artery cerebrovascular reactivity (CVRCO2) and dynamic cerebral autoregulation (dCA) directional sensitivity were assessed using a visual stimulus, 6% fixed‐inspired CO2 and repeated squat‐stand manoeuvres, respectively. Results: Resting CBF (PCOS: 57.2 ± 7.5 ml/100 g/min; controls: 61.6 ± 11.6 ml/100 g/min, p = 0.25) and MCAv, PCAv, MCAPI and PCAPI (all p > 0.05) were similar between groups. NVC (14 ± 4.9% vs. 13 ± 3.4%, p = 0.45), CVRCO2 (5.1 ± 1.9% vs. 6.5 ± 2.9%, p = 0.20) and dCA directional sensitivity were similar between groups. However, women with PCOS had elevated relative PCAPI during NVC (PCOS: 12.0 ± 5.6% vs. controls: 7.0 ± 3.8%, p = 0.04), and impaired vasodilation of the internal carotid artery during CVRCO2 (PCOS: −0.10 ± 0.22 mm vs. controls: 0.18 ± 0.24 mm, p < 0.01). Conclusions: Cerebrovascular function is largely preserved in women with PCOS, although elevated arterial pulsatility and impaired vasodilatory response to carbon dioxide may indicate early endothelial dysfunction in the cerebral vasculature. Larger studies are needed to confirm this in view of our limited study power.
KW - Polycystic Ovary Syndrome
KW - Doppler Ultrasonography
KW - Cerebrovascular Circulation
KW - Magnetic Resonance Imaging
KW - Neurovascular Coupling
KW - Cerebral blood flow
UR - https://www.scopus.com/pages/publications/105022908450
U2 - 10.1111/cen.70061
DO - 10.1111/cen.70061
M3 - Article
SN - 0300-0664
JO - Clinical Endocrinology
JF - Clinical Endocrinology
ER -