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Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention

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Standard

Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention. / Petrykiv, Sergei I; Laverman, Gozewijn Dirk; Persson, Frederik; Vogt, Liffert; Rossing, Peter; de Borst, Martin H; Gansevoort, Ronald T; de Zeeuw, Dick; Heerspink, Hiddo J L.

I: Clinical Journal of American Society of Nephrology. , Bind 12, Nr. 11, 07.11.2017, s. 1804-1813.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Petrykiv, SI, Laverman, GD, Persson, F, Vogt, L, Rossing, P, de Borst, MH, Gansevoort, RT, de Zeeuw, D & Heerspink, HJL 2017, 'Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention', Clinical Journal of American Society of Nephrology. , bind 12, nr. 11, s. 1804-1813. https://doi.org/10.2215/CJN.00390117

APA

Petrykiv, S. I., Laverman, G. D., Persson, F., Vogt, L., Rossing, P., de Borst, M. H., Gansevoort, R. T., de Zeeuw, D., & Heerspink, H. J. L. (2017). Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention. Clinical Journal of American Society of Nephrology. , 12(11), 1804-1813. https://doi.org/10.2215/CJN.00390117

Vancouver

Petrykiv SI, Laverman GD, Persson F, Vogt L, Rossing P, de Borst MH o.a. Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention. Clinical Journal of American Society of Nephrology. . 2017 nov 7;12(11):1804-1813. https://doi.org/10.2215/CJN.00390117

Author

Petrykiv, Sergei I ; Laverman, Gozewijn Dirk ; Persson, Frederik ; Vogt, Liffert ; Rossing, Peter ; de Borst, Martin H ; Gansevoort, Ronald T ; de Zeeuw, Dick ; Heerspink, Hiddo J L. / Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention. I: Clinical Journal of American Society of Nephrology. . 2017 ; Bind 12, Nr. 11. s. 1804-1813.

Bibtex

@article{2b31c93c93d240ef8489e70065b5243b,
title = "Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention",
abstract = "BACKGROUND AND OBJECTIVES: In the treatment of CKD, individual patients show a wide variation in their response to many drugs, including renin-angiotensin-aldosterone system inhibitors (RAASi). To investigate whether therapy resistance to RAASi can be overcome by uptitrating the dose of drug, changing the mode of intervention (with drugs from similar or different classes), or lowering dietary sodium intake, we meta-analyzed individual responses to different modes of interventions.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Randomized crossover trials were analyzed to assess correlation of individual responses to RAASi and nonsteroidal anti-inflammatory drugs (NSAIDs; n=395 patients). Included studies compared the antialbuminuric effect of uptitrating the dose of RAASi (n=10 studies) and NSAIDs (n=1), changing within the same class of RAASi (e.g., angiotensin-converting enzyme inhibition to angiotensin receptor blockers; n=5) or NSAIDs (n=1), changing from RAASi to NSAIDs (n=2), and changing from high to low sodium intake (n=5). A two-stage meta-analysis was conducted: Deming regression was conducted in each study to assess correlations in response, and individual study results were then meta-analyzed.RESULTS: The albuminuria response to one dose of RAASi or NSAIDs positively correlated with the response to a higher dose of the same drug (r=0.72; 95% confidence interval [95% CI], 0.66 to 0.78), changes within the same class of RAASi or NSAIDs (r=0.54; 95% CI, 0.35 to 0.68), changes between RAASi and NSAIDs (r=0.44; 95% CI, 0.16 to 0.66), and changes from high to moderately low salt intake (r=0.36; 95% CI, 0.22 to 0.48). Results were similar when the individual systolic BP and potassium responses were analyzed, and were consistent in patients with and without diabetes.CONCLUSIONS: Individuals who show a poor response to one dose or type of RAASi also show a poor response to higher doses, other types of RAASi or NSAIDs, or a reduction in dietary salt intake. Whether other drugs or drug combinations targeting pathways beyond the renin-angiotensin-aldosterone system and prostaglandins would improve the individual poor response requires further study.",
author = "Petrykiv, {Sergei I} and Laverman, {Gozewijn Dirk} and Frederik Persson and Liffert Vogt and Peter Rossing and {de Borst}, {Martin H} and Gansevoort, {Ronald T} and {de Zeeuw}, Dick and Heerspink, {Hiddo J L}",
note = "Copyright {\textcopyright} 2017 by the American Society of Nephrology.",
year = "2017",
month = nov,
day = "7",
doi = "10.2215/CJN.00390117",
language = "English",
volume = "12",
pages = "1804--1813",
journal = "Clinical Journal of American Society of Nephrology. ",
issn = "1555-9041",
publisher = "American Society of Nephrology",
number = "11",

}

RIS

TY - JOUR

T1 - Pooled Analysis of Multiple Crossover Trials To Optimize Individual Therapy Response to Renin-Angiotensin-Aldosterone System Intervention

AU - Petrykiv, Sergei I

AU - Laverman, Gozewijn Dirk

AU - Persson, Frederik

AU - Vogt, Liffert

AU - Rossing, Peter

AU - de Borst, Martin H

AU - Gansevoort, Ronald T

AU - de Zeeuw, Dick

AU - Heerspink, Hiddo J L

N1 - Copyright © 2017 by the American Society of Nephrology.

PY - 2017/11/7

Y1 - 2017/11/7

N2 - BACKGROUND AND OBJECTIVES: In the treatment of CKD, individual patients show a wide variation in their response to many drugs, including renin-angiotensin-aldosterone system inhibitors (RAASi). To investigate whether therapy resistance to RAASi can be overcome by uptitrating the dose of drug, changing the mode of intervention (with drugs from similar or different classes), or lowering dietary sodium intake, we meta-analyzed individual responses to different modes of interventions.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Randomized crossover trials were analyzed to assess correlation of individual responses to RAASi and nonsteroidal anti-inflammatory drugs (NSAIDs; n=395 patients). Included studies compared the antialbuminuric effect of uptitrating the dose of RAASi (n=10 studies) and NSAIDs (n=1), changing within the same class of RAASi (e.g., angiotensin-converting enzyme inhibition to angiotensin receptor blockers; n=5) or NSAIDs (n=1), changing from RAASi to NSAIDs (n=2), and changing from high to low sodium intake (n=5). A two-stage meta-analysis was conducted: Deming regression was conducted in each study to assess correlations in response, and individual study results were then meta-analyzed.RESULTS: The albuminuria response to one dose of RAASi or NSAIDs positively correlated with the response to a higher dose of the same drug (r=0.72; 95% confidence interval [95% CI], 0.66 to 0.78), changes within the same class of RAASi or NSAIDs (r=0.54; 95% CI, 0.35 to 0.68), changes between RAASi and NSAIDs (r=0.44; 95% CI, 0.16 to 0.66), and changes from high to moderately low salt intake (r=0.36; 95% CI, 0.22 to 0.48). Results were similar when the individual systolic BP and potassium responses were analyzed, and were consistent in patients with and without diabetes.CONCLUSIONS: Individuals who show a poor response to one dose or type of RAASi also show a poor response to higher doses, other types of RAASi or NSAIDs, or a reduction in dietary salt intake. Whether other drugs or drug combinations targeting pathways beyond the renin-angiotensin-aldosterone system and prostaglandins would improve the individual poor response requires further study.

AB - BACKGROUND AND OBJECTIVES: In the treatment of CKD, individual patients show a wide variation in their response to many drugs, including renin-angiotensin-aldosterone system inhibitors (RAASi). To investigate whether therapy resistance to RAASi can be overcome by uptitrating the dose of drug, changing the mode of intervention (with drugs from similar or different classes), or lowering dietary sodium intake, we meta-analyzed individual responses to different modes of interventions.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Randomized crossover trials were analyzed to assess correlation of individual responses to RAASi and nonsteroidal anti-inflammatory drugs (NSAIDs; n=395 patients). Included studies compared the antialbuminuric effect of uptitrating the dose of RAASi (n=10 studies) and NSAIDs (n=1), changing within the same class of RAASi (e.g., angiotensin-converting enzyme inhibition to angiotensin receptor blockers; n=5) or NSAIDs (n=1), changing from RAASi to NSAIDs (n=2), and changing from high to low sodium intake (n=5). A two-stage meta-analysis was conducted: Deming regression was conducted in each study to assess correlations in response, and individual study results were then meta-analyzed.RESULTS: The albuminuria response to one dose of RAASi or NSAIDs positively correlated with the response to a higher dose of the same drug (r=0.72; 95% confidence interval [95% CI], 0.66 to 0.78), changes within the same class of RAASi or NSAIDs (r=0.54; 95% CI, 0.35 to 0.68), changes between RAASi and NSAIDs (r=0.44; 95% CI, 0.16 to 0.66), and changes from high to moderately low salt intake (r=0.36; 95% CI, 0.22 to 0.48). Results were similar when the individual systolic BP and potassium responses were analyzed, and were consistent in patients with and without diabetes.CONCLUSIONS: Individuals who show a poor response to one dose or type of RAASi also show a poor response to higher doses, other types of RAASi or NSAIDs, or a reduction in dietary salt intake. Whether other drugs or drug combinations targeting pathways beyond the renin-angiotensin-aldosterone system and prostaglandins would improve the individual poor response requires further study.

U2 - 10.2215/CJN.00390117

DO - 10.2215/CJN.00390117

M3 - Journal article

C2 - 29021336

VL - 12

SP - 1804

EP - 1813

JO - Clinical Journal of American Society of Nephrology.

JF - Clinical Journal of American Society of Nephrology.

SN - 1555-9041

IS - 11

ER -

ID: 195158884