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Nocturnal blood pressure and progression to end-stage renal disease or death in nondiabetic chronic kidney disease stages 3 and 4
被引:45
作者:
Redon, Josep
[1
,2
]
Plancha, Eva
[3
]
Swift, Pauline A.
[1
]
Pons, Salvador
[4
]
Munoz, Jaime
[3
]
Martinez, Fernando
[1
,2
]
机构:
[1] Univ Valencia, Hypertens Clin, Dept Internal Med, Hosp Clin, Valencia 46010, Spain
[2] Inst Hlth Carlos III, CIBER Fisiopatol Obesidad & Nutr 06 03, Madrid, Spain
[3] Univ Valencia, Cardiol Unit, Hosp Clin, Valencia 46010, Spain
[4] Univ Valencia, Nephrol Unit, Hosp Clin, Valencia 46010, Spain
关键词:
chronic kidney disease;
hypertension;
nocturnal blood pressure;
nondiabetic kidney disease;
CARDIOVASCULAR-DISEASE;
REPLACEMENT THERAPY;
RISK;
EPIDEMIOLOGY;
PROTEINURIA;
ASSOCIATION;
MORTALITY;
EVENTS;
D O I:
10.1097/HJH.0b013e328333fe4d
中图分类号:
R6 [外科学];
学科分类号:
1002 ;
100210 ;
摘要:
Objective The objective was to assess the role of office and ambulatory blood pressure (BP) on the development of end-stage renal disease (ESRD) in nondiabetic chronic renal failure. Design and method Seventy-nine patients [mean age 57 (standard deviation 11) years, 47 men, BMI 28 (4), office BP 151 (25)/92 (14) mmHg, estimated glomerular filtration rate 28 (14) ml/min per 1.73 m(2)] were included. The causes of renal disease were nephrosclerosis (n = 33), glomerulonephritis (n = 19), interstitial (n = 12) and others (n = 15). The average follow-up was 44 months (range 9-72 months). The primary outcome was a composite of death, from any cause, or the development of ESRD that require initiation of renal replacement therapy. In all patients, 24-h ambulatory BP monitoring and left ventricular mass assessment were performed at the beginning of the study. Results During the follow-up period, 41 (52%) patients progressed to ESRD. In addition, nine (11%) patients died, four before reaching ESRD. Then the combined endpoint rate, 45 patients, was 6.3/100 patients per year. In a multivariate Cox proportional hazard model, which includes age, sex, angiotensin-converting enzyme inhibitor/angiotensin II receptor blocker status and the estimated glomerular filtration rate, office BP still provided no further prognostic information on risk of the primary outcome. In addition, daytime ambulatory BP and the no-dipper status did not further discriminate in terms of predicting endpoint. Nocturnal SBP more than 130 mmHg was associated with a doubling of risk [heart rate 2.07 (95% confidence interval 1.01-4.25)] on top of the other significant factors. Conclusion Glomerular filtration rate and nocturnal SBP values, but not nondipper pattern, were associated with risk to develop ESRD. J Hypertens 28:602-607 (c) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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页码:602 / 607
页数:6
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