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Cited by 528

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Blood Pressure in Early Autosomal Dominant Polycystic Kidney Disease

Open access
Schrier, Robert W., Abebe, Kaleab Z., Perrone, Ronald D., Torres, Vicente E., Braun, William E., Steinman, Theodore I., Winklhofer, Franz T., Brosnahan, Godela, Czarnecki, Peter G., Hogan, Marie C., Miskulin, Dana C., Rahbari-Oskoui, Frederic F., Grantham, Jared J., Harris, Peter C., Flessner, Michael F., Bae, Kyongtae T., Moore, Charity G., Chapman, Arlene B.·2014·New England Journal of Medicine

Abstract

BACKGROUND: Hypertension is common in autosomal dominant polycystic kidney disease (ADPKD) and is associated with increased total kidney volume, activation of the renin-angiotensin-aldosterone system, and progression of kidney disease. METHODS: In this double-blind, placebo-controlled trial, we randomly assigned 558 hypertensive participants with ADPKD (15 to 49 years of age, with an estimated glomerular filtration rate [GFR] >60 ml per minute per 1.73 m(2) of body-surface area) to either a standard blood-pressure target (120/70 to 130/80 mm Hg) or a low blood-pressure target (95/60 to 110/75 mm Hg) and to either an angiotensin-converting-enzyme inhibitor (lisinopril) plus an angiotensin-receptor blocker (telmisartan) or lisinopril plus placebo. The primary outcome was the annual percentage change in the total kidney volume. RESULTS: The annual percentage increase in total kidney volume was significantly lower in the low-blood-pressure group than in the standard-blood-pressure group (5.6% vs. 6.6%, P=0.006), without significant differences between the lisinopril-telmisartan group and the lisinopril-placebo group. The rate of change in estimated GFR was similar in the two medication groups, with a negative slope difference in the short term in the low-blood-pressure group as compared with the standard-blood-pressure group (P<0.001) and a marginally positive slope difference in the long term (P=0.05). The left-ventricular-mass index decreased more in the low-blood-pressure group than in the standard-blood-pressure group (-1.17 vs. -0.57 g per square meter per year, P<0.001); urinary albumin excretion was reduced by 3.77% with the low-pressure target and increased by 2.43% with the standard target (P<0.001). Dizziness and light-headedness were more common in the low-blood-pressure group than in the standard-blood-pressure group (80.7% vs. 69.4%, P=0.002). CONCLUSIONS: In early ADPKD, the combination of lisinopril and telmisartan did not significantly alter the rate of increase in total kidney volume. As compared with standard blood-pressure control, rigorous blood-pressure control was associated with a slower increase in total kidney volume, no overall change in the estimated GFR, a greater decline in the left-ventricular-mass index, and greater reduction in urinary albumin excretion. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases and others; HALT-PKD [Study A] ClinicalTrials.gov number, NCT00283686.).

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Metadata

Authors
Schrier, R. W., Abebe, K. Z., Perrone, R. D., Torres, V. E., Braun, W. E., Steinman, T. I., Winklhofer, F. T., Brosnahan, G., Czarnecki, P. G., Hogan, M. C., Miskulin, D. C., Rahbari-Oskoui, F. F., Grantham, J. J., Harris, P. C., Flessner, M. F., Bae, K. T., Moore, C. G., & Chapman, A. B.
Venue
New England Journal of Medicine
Published
2014-12-11
Volume
371
Issue
24
Pages
2255-2266
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W1997286719
Cited by
528
References
3
FWCI
33.29
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Blood Pressure in Early Autosomal Dominant Polycystic Kidney Disease. https://app.cochat.ai/papers/10.1056/nejmoa1402685
The paper
Schrier, R. W., Abebe, K. Z., Perrone, R. D., Torres, V. E., Braun, W. E., Steinman, T. I., Winklhofer, F. T., Brosnahan, G., Czarnecki, P. G., Hogan, M. C., Miskulin, D. C., Rahbari-Oskoui, F. F., Grantham, J. J., Harris, P. C., Flessner, M. F., Bae, K. T., Moore, C. G., & Chapman, A. B. (2014). Blood Pressure in Early Autosomal Dominant Polycystic Kidney Disease. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1402685

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.