作者
Jong Hyun Jhee,Donghwan Oh,Jiwon Seo,Chan Joo Lee,Min‐Yu Chung,Jung Tak Park,Seung Hyeok Han,Shin‐Wook Kang,Sungha Park,Tae‐Hyun Yoo
摘要
Rationale & Objective The association between short-term blood pressure variability (BPV) and kidney outcomes is poorly understood. This study evaluated the association between short-term BPV and kidney disease outcomes in people with hypertension. Study Design Prospective observational cohort study. Setting & Participants 1,173 hypertensive participants in the Cardiovascular and Metabolic Disease Etiology Research Center–High Risk (2013-2018) Study with estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73 m2. Exposure Short-term BPV assessed by average real variability (ARV). Outcome Composite kidney disease outcome (30% decline in eGFR from baseline, new occurrence of eGFR <60 mL/min/1.73 m2, or onset of UACR >300 mg/g). Analytical Approach Multivariable Cox regression analyses to evaluate the association between systolic and diastolic BP ARV (SBP-ARV and DBP-ARV) and outcomes. Results During a median follow-up of 5.4 [4.1-6.5] years, 271 events of the composite kidney disease outcome occurred (46.5 per 1,000 person-years). Multivariable Cox analysis revealed that the highest SBP-ARV and DBP-ARV tertiles were associated with a higher risk of the composite kidney disease outcome than the lowest tertiles, independent of the 24-hour SBP or DBP levels (HR, 1.64 [95% CI, 1.16-2.33], and 1.60 [95% CI, 1.15-2.24] for SBP-ARV and DBP-ARV, respectively). These associations were consistent when SBP-ARV and DBP-ARV were treated as continuous variables (HR per 1.0-unit greater SBP-ARV, 1.03 [95% CI, 1.01-1.06]; HR per 1.0-unit greater DBP-ARV, 1.04 [95% CI, 1.01-1.08]). These associations were consistent, irrespective of subgroups (age, sex, 24-hour SBP or DBP, and moderate albuminuria). However, other measures of short-term BPV including SD, coefficient of variation, and dipping patterns were not associated with the composite kidney disease outcome. Limitations Observational study design, the use of single measurement of 24-hour BP, lack of information on changes in antihypertensive medication during the follow-up. Conclusions Short-term BPV is associated with the development of a composite kidney disease outcome in hypertensive patients. The association between short-term blood pressure variability (BPV) and kidney outcomes is poorly understood. This study evaluated the association between short-term BPV and kidney disease outcomes in people with hypertension. Prospective observational cohort study. 1,173 hypertensive participants in the Cardiovascular and Metabolic Disease Etiology Research Center–High Risk (2013-2018) Study with estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73 m2. Short-term BPV assessed by average real variability (ARV). Composite kidney disease outcome (30% decline in eGFR from baseline, new occurrence of eGFR <60 mL/min/1.73 m2, or onset of UACR >300 mg/g). Multivariable Cox regression analyses to evaluate the association between systolic and diastolic BP ARV (SBP-ARV and DBP-ARV) and outcomes. During a median follow-up of 5.4 [4.1-6.5] years, 271 events of the composite kidney disease outcome occurred (46.5 per 1,000 person-years). Multivariable Cox analysis revealed that the highest SBP-ARV and DBP-ARV tertiles were associated with a higher risk of the composite kidney disease outcome than the lowest tertiles, independent of the 24-hour SBP or DBP levels (HR, 1.64 [95% CI, 1.16-2.33], and 1.60 [95% CI, 1.15-2.24] for SBP-ARV and DBP-ARV, respectively). These associations were consistent when SBP-ARV and DBP-ARV were treated as continuous variables (HR per 1.0-unit greater SBP-ARV, 1.03 [95% CI, 1.01-1.06]; HR per 1.0-unit greater DBP-ARV, 1.04 [95% CI, 1.01-1.08]). These associations were consistent, irrespective of subgroups (age, sex, 24-hour SBP or DBP, and moderate albuminuria). However, other measures of short-term BPV including SD, coefficient of variation, and dipping patterns were not associated with the composite kidney disease outcome. Observational study design, the use of single measurement of 24-hour BP, lack of information on changes in antihypertensive medication during the follow-up. Short-term BPV is associated with the development of a composite kidney disease outcome in hypertensive patients.