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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Ambulatory blood pressure and endothelial dysfunction in patients with autosomal dominant polycystic kidney disease
Faruk Turgut1, Hüseyin Oflaz, Sule Namli
1School of Medicine, Department of Internal Medicine, Division of Nephrology, Istanbul University, Capa, Istanbul, Turkey. farukturgut@yahoo.com
Insights
Autosomal dominant polycystic kidney disease (ADPKD) patients who do not experience a nocturnal blood pressure dip have significantly impaired endothelial function. This endothelial dysfunction is linked to increased cardiovascular risks in ADPKD.
Area of Science:
- Nephrology
- Cardiology
- Vascular Biology
Background:
- Cardiovascular disease is a leading cause of death in autosomal dominant polycystic kidney disease (ADPKD) patients.
- Endothelial dysfunction (ED), an early sign of vascular damage, is observed in ADPKD.
- The relationship between ambulatory blood pressure patterns and ED in ADPKD remains understudied.
Purpose of the Study:
- To investigate the association between ambulatory blood pressure monitoring (ABPM) patterns and endothelial function in ADPKD patients.
- To determine if non-dipper status in ADPKD is linked to endothelial dysfunction.
Main Methods:
- Forty-one ADPKD patients with preserved renal function underwent 24-hour ABPM.
- Patients were categorized into dipper and non-dipper groups based on nocturnal blood pressure decline.
- Brachial artery endothelial function was assessed using high-resolution vascular ultrasound, measuring endothelial-dependent dilatation.
Main Results:
- No significant differences in mean 24-hour systolic or diastolic blood pressure were found between dipper and non-dipper groups.
- Non-dipper patients exhibited a significantly lower nocturnal fall rate in both systolic (0.98% vs. 11.1%) and diastolic (3.8% vs. 14.0%) blood pressure compared to dippers (p=0.001 for both).
- Endothelial-dependent dilatation was significantly impaired in non-dippers (3.57%) compared to dippers (6.22%) (p=0.025).
Conclusions:
- Non-dipper status in ADPKD is associated with significant endothelial dysfunction.
- Impaired endothelial function in non-dipper ADPKD patients may contribute to increased cardiovascular morbidity and mortality.
- ABPM and endothelial function assessment are crucial for cardiovascular risk stratification in ADPKD.
Abstract:
Cardiovascular problems are a major cause of morbidity and mortality in patients with autosomal dominant polycystic kidney disease (ADPKD). Endothelial dysfunction (ED), which is an early manifestation of vascular injury, has been shown in patients with ADPKD. However, the association between ambulatory blood pressure and ED has not been investigated in these patients. Forty-one patients with ADPKD having well-preserved renal function were included in the study. Ambulatory blood pressure monitoring was performed in all patients. Patients were divided into dipper and non-dipper groups. Endothelial function of the brachial artery was evaluated by using high-resolution vascular ultrasound. Endothelial-dependent dilatation was expressed as the percentage change in the brachial artery diameter from baseline to reactive hyperemia. The mean 24-hour systolic blood pressure was similar in both groups (125.5 +/- 10.7 mmHg in dippers and 121.2 +/- 14.3 in non-dippers, p > 0.05). There was also no significant difference between the mean 24-hour diastolic blood pressures in both groups (82.3 +/- 9.6 mmHg in dippers and 77.1 +/- 8.6 mmHg in non-dippers, p > 0.05). The nocturnal fall rate in systolic blood pressure was 11.1 +/- 1.2% in dippers and 0.98 +/- 0.9% in non-dippers (p = 0.001). The nocturnal fall rate in diastolic blood pressure was 14.0 +/- 0.9% in dippers and 3.8 +/- 0.8% in non-dippers (p = 0.001). Endothelial-dependent dilatation was significantly higher in dippers compared to non-dippers (6.22 +/- 4.14% versus 3.57 +/- 2.52%, p = 0.025). Non-dipper patients with ADPKD show significant ED, which has an important impact on cardiovascular morbidity and mortality.
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