Serum creatinine elevation after renin-angiotensin system blockade and long term cardiorenal risks: cohort study
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Objective To examine long term cardiorenal outcomes associated with increased concentrations of creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment. Design Population based cohort study using electronic health records from the Clinical Practice Research Datalink and Hospital Episode Statistics. Setting UK primary care, 1997-2014. Participants Patients starting treatment with angiotensin converting enzyme inhibitors or angiotensin receptor blockers (n=122 363). Main outcome measures Poisson regression was used to compare rates of end stage renal disease, myocardial infarction, heart failure, and death among patients with creatinine increases of 30% or more after starting treatment against those without such increases, and for each 10% increase in creatinine. Analyses were adjusted for age, sex, calendar period, socioeconomic status, lifestyle factors, chronic kidney disease, diabetes, cardiovascular comorbidities, and use of other antihypertensive drugs and non-steroidal anti-inflammatory drugs. Results Among the 2078 (1.7%) patients with creatinine increases of 30% or more, a higher proportion were female, were elderly, had cardiorenal comorbidity, and used non-steroidal anti-inflammatory drugs, loop diuretics, or potassium sparing diuretics. Creatinine increases of 30% or more were associated with an increased adjusted incidence rate ratio for all outcomes, compared with increases of less than 30%: 3.43 (95% confidence interval 2.40 to 4.91) for end stage renal disease, 1.46 (1.16 to 1.84) for myocardial infarction, 1.37 (1.14 to 1.65) for heart failure, and 1.84 (1.65 to 2.05) for death. The detailed categorisation of increases in creatinine concentrations (<10%, 10-19%, 20-29%, 30-39%, and ≥40%) showed a graduated relation for all outcomes (all P values for trends <0.001). Notably, creatinine increases of less than 30% were also associated with increased incidence rate ratios for all outcomes, including death (1.15 (1.09 to 1.22) for increases of 10-19% and 1.35 (1.23 to 1.49) for increases of 20-29%, using <10% as reference). Results were consistent across calendar periods, across subgroups of patients, and among continuing users. Conclusions Increases in creatinine after the start of angiotensin converting enzyme inhibitor/angiotensin receptor blocker treatment were associated with adverse cardiorenal outcomes in a graduated relation, even below the guideline recommended threshold of a 30% increase for stopping treatment.
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The most common cause of an acute rise in serum creatinine following use of a RAS blockade agent results from a decreased effective arterial blood volume.
“The most common cause of an acute rise in serum creatinine following the use of a RAS blockade agent results from a decreased effective arterial blood volume”
From KDIGO 2022 Clinical Practice Guideline for Diabetes Management in Chronic Kidney Disease (2022) · cites this paper as [63]
The Introduction says kidney function can decline suddenly after ACEI/ARB initiation and attributes this to antagonism of angiotensin II–mediated efferent arteriolar constriction. The paper does not identify decreased effective arterial blood volume as the most common cause of an acute creatinine rise. (LLM, conf=0.83)
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- Authors
- Schmidt, M., Mansfield, K. E., Bhaskaran, K., Nitsch, D., Sørensen, H. T., Smeeth, L., & Tomlinson, L. A.
- Affiliations
- Aarhus University Hospital (DK)
- London School of Hygiene & Tropical Medicine (GB)
- Corresponding author
- Schmidt, Morten
- ORCID
- Venue
- BMJ
- Publisher
- BMJ
- Published
- 2017-03-09
- Volume
- 356
- Pages
- j791
- ISSN
- 1756-1833 (ISSN-L)
- 0959-8138
- PMC
- PMC5421447
- OpenAlex
- W2592164257
- Cited by
- 157
- References
- 4
- Citations by year
- 2026: 8 · 2025: 10 · 2024: 11 · 2023: 16 · 2022: 13 · 2021: 18 · 2020: 23 · 2019: 34 · 2018: 17 · 2017: 7
- FWCI
- 19.83
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- BMJ (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
- Figshare (submittedVersion, cc-by)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Aarhus Universitet
- Aarhus Universitetshospital
- Wellcome Trust (107731/Z/15/Z, /Z/15/Z, 101143/Z/13/Z, 107731)
- Royal Society (107731/Z/15/Z)
- Lundbeckfonden (R155-2014-2647)
- Novo Nordisk
- A.P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til almene Formaal
- Novo Nordisk Fonden (NNF14SA0015794)
- H. Lundbeck A/S
- Fonden til Lægevidenskabens Fremme
- Topics
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
- Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
- Keywords
- creatinine elevation, renin-angiotensin system blockade, ACE inhibitors, angiotensin receptor blockers, cardiorenal outcomes, end-stage renal disease, myocardial infarction, heart failure, mortality, nonsteroidal anti-inflammatory drugs, loop diuretics, potassium-sparing diuretics, dose-response relationship, antihypertensive therapy
- MeSH terms
- Aged, Aged, 80 and over, Angiotensin-Converting Enzyme Inhibitors, Creatinine, Female, United Kingdom, Heart Diseases, Humans, Kidney Diseases, Male, Middle Aged, Primary Health Care, Regression Analysis, Renin-Angiotensin System, Risk Factors, Cohort Studies, Treatment Outcome, Electronic Health Records
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