Why the study?
To evaluate the impact of visit-to-visit variability of blood pressure on diabetic nephropathy risk and assess whether it provides additional predictive information in patients with type 2 diabetes in China.
Does high visit-to-visit systolic blood pressure variability increase the risk of diabetic kidney disease in patients with type 2 diabetes?
Does high visit-to-visit systolic blood pressure variability increase the risk of diabetic kidney disease in patients with type 2 diabetes?
Answers are grounded in this paper and cite their sources.
Visit-to-visit systolic blood pressure variability is an independent risk factor for diabetic kidney disease in patients with type 2 diabetes, improving risk prediction beyond mean and maximum blood pressure values.
BACKGROUND: This study aimed to evaluate the impact of visit-to-visit variability (VVV) of blood pressure on the risk of diabetic nephropathy and whether it provides additional predictive information among patients with type 2 diabetes mellitus (T2DM) in China. METHODS: We included 12 630 T2DM patients during January 2008-December 2012 using a retrospective cohort design. VVV of SBP was assessed as standard deviation, coefficient of variation and variation independent of mean of the blood pressure readings during the measurement period. Hazard ratios and 95% confidence intervals were estimated for the associations of variability in SBP with risk of diabetes nephropathy by using Cox proportional hazards regression models. Risk prediction ability was assessed using C statistic, integrated discrimination improvement (IDI) and net reclassification index (NRI). RESULTS: We found a dose-response relationship across quartiles of VVV SBP (P trend < 0.001). Hazard ratio in the highest quartile of SD SBP (≥9.2 mmHg) was 1.49 (1.16-1.93) as compared with the lowest quartile (<4.8 mmHg) after adjusted for mean SBP values, max SBP values and other covariates. Addition of SD SBP significantly improved risk prediction for diabetic kidney disease (DKD) [C statistic (from 0.664 to 0.673), IDI (0.0011, 95% CI: 0.0003-0.0104) and NRI (0.053, 95% CI: 0.0017-0.113)]. Results remained similar across different subgroups, sensitivity analyses or using coefficient of variation and variance independent of mean. CONCLUSION: VVV of SBP is a significant risk factor of DKD among T2DM patients on top of mean and max BP values, which provides additional significant predictive information.
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Yu et al. (2019) studied this question.
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