Samir S Patel, Venkatesh K Raman, Sijian Zhang, Helen M Sheriff, Gregg C Fonarow, Paul A Heidenreich, Charles Faselis, Phillip H Lam, Charity J Morgan, Hans Moore, David Atkins, Yan Cheng, Yijun Shao, Prakash Deedwania, Carlos E Palant, Brian C Sauer, Ravindra L Mehta, Thomas E Love, Richard M Allman, Michael S Heimall, Wen-Chih Wu, Qing Zeng-Treitler, Ali Ahmed
{"title":"肾素血管紧张素抑制与心力衰竭患者肾衰竭风险降低:副标题:RAS抑制与心力衰竭患者肾衰竭。","authors":"Samir S Patel, Venkatesh K Raman, Sijian Zhang, Helen M Sheriff, Gregg C Fonarow, Paul A Heidenreich, Charles Faselis, Phillip H Lam, Charity J Morgan, Hans Moore, David Atkins, Yan Cheng, Yijun Shao, Prakash Deedwania, Carlos E Palant, Brian C Sauer, Ravindra L Mehta, Thomas E Love, Richard M Allman, Michael S Heimall, Wen-Chih Wu, Qing Zeng-Treitler, Ali Ahmed","doi":"10.1016/j.amjmed.2025.04.038","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Renin-angiotensin system (RAS) inhibitors reduce risk of kidney failure in patients with chronic kidney disease, but worsen kidney function in heart failure patients, especially in those with chronic kidney disease. Less is known about risk of kidney failure in heart failure patients receiving RAS inhibitors.</p><p><strong>Methods: </strong>We used propensity score matching for outcome-blinded assembly of 168,860 Veterans with heart failure phenotyped by artificial intelligence who were balanced on 77 baseline characteristics and initiated on RAS inhibitors. Hazard ratio (95% confidence interval [CI]) for 5-year kidney failure in high-dose (vs low-dose) RAS inhibitor group was estimated, accounting for competing risk of death. Kidney failure was defined as kidney replacement therapy or estimated glomerular filtration rate (eGFR) rate <15 mL/min/1.73 m<sup>2</sup>.</p><p><strong>Results: </strong>New-onset kidney failure occurred in 4.1% (3455/84,430) and 3.5% (2966/84,430) of patients in low-dose and high-dose RAS inhibitor groups, respectively (hazard ratio, 0.85; 95% CI, 0.81-0.89). Respective hazard ratios (95% CIs) in eGFR rate subgroups ≥60, 45-59, and 15-44 mL/min/1.73 m<sup>2</sup> were 1.21 (1.08-1.36), 0.93 (0.82-1.05), and 0.82 (0.77-0.87). The association was similar across ejection fraction subgroups. There was a lower risk of death in the subgroup with ejection fraction ≤40%.</p><p><strong>Conclusions: </strong>Patients with heart failure receiving high-dose (vs low-dose) RAS inhibitors had a lower associated risk of kidney failure, which was driven by the subgroup with chronic kidney disease. This new information may help to inform future guideline recommendations and clinical practice regarding RAS inhibitor use in these patients. Future studies need to examine this association in those with normal kidney function.</p>","PeriodicalId":50807,"journal":{"name":"American Journal of Medicine","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Renin Angiotensin Inhibition and Lower Risk of Kidney Failure in Patients with Heart Failure.\",\"authors\":\"Samir S Patel, Venkatesh K Raman, Sijian Zhang, Helen M Sheriff, Gregg C Fonarow, Paul A Heidenreich, Charles Faselis, Phillip H Lam, Charity J Morgan, Hans Moore, David Atkins, Yan Cheng, Yijun Shao, Prakash Deedwania, Carlos E Palant, Brian C Sauer, Ravindra L Mehta, Thomas E Love, Richard M Allman, Michael S Heimall, Wen-Chih Wu, Qing Zeng-Treitler, Ali Ahmed\",\"doi\":\"10.1016/j.amjmed.2025.04.038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Renin-angiotensin system (RAS) inhibitors reduce risk of kidney failure in patients with chronic kidney disease, but worsen kidney function in heart failure patients, especially in those with chronic kidney disease. Less is known about risk of kidney failure in heart failure patients receiving RAS inhibitors.</p><p><strong>Methods: </strong>We used propensity score matching for outcome-blinded assembly of 168,860 Veterans with heart failure phenotyped by artificial intelligence who were balanced on 77 baseline characteristics and initiated on RAS inhibitors. Hazard ratio (95% confidence interval [CI]) for 5-year kidney failure in high-dose (vs low-dose) RAS inhibitor group was estimated, accounting for competing risk of death. Kidney failure was defined as kidney replacement therapy or estimated glomerular filtration rate (eGFR) rate <15 mL/min/1.73 m<sup>2</sup>.</p><p><strong>Results: </strong>New-onset kidney failure occurred in 4.1% (3455/84,430) and 3.5% (2966/84,430) of patients in low-dose and high-dose RAS inhibitor groups, respectively (hazard ratio, 0.85; 95% CI, 0.81-0.89). Respective hazard ratios (95% CIs) in eGFR rate subgroups ≥60, 45-59, and 15-44 mL/min/1.73 m<sup>2</sup> were 1.21 (1.08-1.36), 0.93 (0.82-1.05), and 0.82 (0.77-0.87). The association was similar across ejection fraction subgroups. There was a lower risk of death in the subgroup with ejection fraction ≤40%.</p><p><strong>Conclusions: </strong>Patients with heart failure receiving high-dose (vs low-dose) RAS inhibitors had a lower associated risk of kidney failure, which was driven by the subgroup with chronic kidney disease. This new information may help to inform future guideline recommendations and clinical practice regarding RAS inhibitor use in these patients. Future studies need to examine this association in those with normal kidney function.</p>\",\"PeriodicalId\":50807,\"journal\":{\"name\":\"American Journal of Medicine\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.amjmed.2025.04.038\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.amjmed.2025.04.038","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Renin Angiotensin Inhibition and Lower Risk of Kidney Failure in Patients with Heart Failure.
Background: Renin-angiotensin system (RAS) inhibitors reduce risk of kidney failure in patients with chronic kidney disease, but worsen kidney function in heart failure patients, especially in those with chronic kidney disease. Less is known about risk of kidney failure in heart failure patients receiving RAS inhibitors.
Methods: We used propensity score matching for outcome-blinded assembly of 168,860 Veterans with heart failure phenotyped by artificial intelligence who were balanced on 77 baseline characteristics and initiated on RAS inhibitors. Hazard ratio (95% confidence interval [CI]) for 5-year kidney failure in high-dose (vs low-dose) RAS inhibitor group was estimated, accounting for competing risk of death. Kidney failure was defined as kidney replacement therapy or estimated glomerular filtration rate (eGFR) rate <15 mL/min/1.73 m2.
Results: New-onset kidney failure occurred in 4.1% (3455/84,430) and 3.5% (2966/84,430) of patients in low-dose and high-dose RAS inhibitor groups, respectively (hazard ratio, 0.85; 95% CI, 0.81-0.89). Respective hazard ratios (95% CIs) in eGFR rate subgroups ≥60, 45-59, and 15-44 mL/min/1.73 m2 were 1.21 (1.08-1.36), 0.93 (0.82-1.05), and 0.82 (0.77-0.87). The association was similar across ejection fraction subgroups. There was a lower risk of death in the subgroup with ejection fraction ≤40%.
Conclusions: Patients with heart failure receiving high-dose (vs low-dose) RAS inhibitors had a lower associated risk of kidney failure, which was driven by the subgroup with chronic kidney disease. This new information may help to inform future guideline recommendations and clinical practice regarding RAS inhibitor use in these patients. Future studies need to examine this association in those with normal kidney function.
期刊介绍:
The American Journal of Medicine - "The Green Journal" - publishes original clinical research of interest to physicians in internal medicine, both in academia and community-based practice. AJM is the official journal of the Alliance for Academic Internal Medicine, a prestigious group comprising internal medicine department chairs at more than 125 medical schools across the U.S. Each issue carries useful reviews as well as seminal articles of immediate interest to the practicing physician, including peer-reviewed, original scientific studies that have direct clinical significance and position papers on health care issues, medical education, and public policy.