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Updated: Aug 21, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Visit-to-visit variability in blood pressure and kidney disease progression in IgA nephropathy
Chen Tang1,2,3, Xiao-Yan Zhang4, Ji-Cheng Lv1,2,3
1Renal Division, Peking University First Hospital, Peking University Institute of Nephrology, Beijing, China.
Insights
Visit-to-visit variability in systolic blood pressure (SBP) is a significant risk factor for kidney disease progression in patients with immunoglobulin A nephropathy (IgAN). Higher SBP variability increases the risk of adverse kidney outcomes.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Clinical Research
Background:
- Visit-to-visit variability (VVV) in blood pressure (BP) is linked to cardiovascular events and kidney damage.
- Limited data exist on the association between BP VVV and chronic kidney disease (CKD) progression in immunoglobulin A nephropathy (IgAN).
Purpose of the Study:
- To investigate the relationship between BP VVV and IgAN progression.
- To assess if BP variability predicts kidney disease progression in IgAN patients.
Main Methods:
- 1376 IgAN patients were analyzed using standard deviation (SD), coefficient of variation (CV), and average real variability (ARV) to measure BP VVV.
- Cox models were used to examine associations between BP VVV and composite kidney disease progression events (50% eGFR decline or kidney failure).
Main Results:
- Higher SD in systolic BP (SBP) was significantly associated with an increased risk of kidney disease progression (HR 1.07 per SD increase).
- Patients in the highest quartile of SD SBP had a 2.12-fold higher risk of composite kidney disease progression compared to the lowest quartile.
- Variability in diastolic BP showed a similar trend, though not statistically significant; CV and ARV yielded similar findings.
Conclusions:
- Systolic blood pressure variability is a significant predictor of kidney disease progression in patients with IgAN.
- Managing SBP variability may be crucial for improving kidney outcomes in IgAN patients.
Background:
The visit-to-visit variability (VVV) in blood pressure (BP) is an important risk factor for stroke and coronary heart disease and may also be associated with kidney damage and the development of chronic kidney disease (CKD). Data on the association between VVV in BP and the risk of CKD progression among patients with immunoglobulin A nephropathy (IgAN) are limited. We aimed to evaluate the relationships of VVV in BP with the progression of IgAN.
Methods:
We assessed 1376 patients with IgAN at Peking University First Hospital. The main VVV in BP was expressed as the standard deviation (SD), coefficient of variation (CV) and average real variability (ARV). The associations of variability in BP with composite kidney disease progression events, defined as a 50% decline in estimated glomerular filtration rate (eGFR) and kidney failure, were examined using Cox models.
Results:
During a median follow-up of 44.1 months (interquartile range 23.0-76.7), 247 (18.0%) patients experienced composite kidney disease progression events. With a higher SD in systolic BP (SBP) values, the risk of kidney disease progression events increased {hazard ratio [HR] 1.07 [95% confidence interval (CI) 1.03-1.11]; P < .001} after maximal adjustment, including baseline SBP and mean SBP during the first 12-month period. Using the first quartile of SD SBP values as the reference, the risk of composite kidney disease progression events was higher among patients with higher SD SBP values; the HR was 2.12 (95% CI 1.31-3.44) in the highest quartile (P for trend < .001). A similar trend could be observed when analysing the SD of diastolic BP, but the risk was not significantly increased. The associations were similar when analysed with the CV and ARV.
Conclusion:
SBP variability was significantly associated with kidney disease progression in IgAN.
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