Acute kidney injury (AKI) has been on the rise, attributed to multiple factors, such as an aging society, the increasing complexity of medical technology, and the increase in lifestyle-related diseases [1]. AKI causes deterioration in renal function and is associated with increased mortality in the short and long term [2]. Currently, the Kidney Disease: Improving Global Outcomes (KDIGO) criteria has widely been used to define AKI, which combined the RIFLE criteria by the Acute Dialysis Quality Initiative (ADQI) and the Acute Kidney Injury Network (AKIN) criteria [3]. In the KDIGO criteria, AKI is defined by the degrees of absolute serum creatinine increase, of percent serum creatinine increase, or decrease in urine output, and is further classified into three stages. Accumulating data have shown that the patients with AKI defined using this criteria show increased in-hospital mortality compared to non-AKI patients [4]. In addition to the short-term outcomes, AKI influences long-term effects; several studies have shown that AKI is associated with chronic kidney disease progression, cardiovascular events, and mortality in the long term [5]. Therefore, prediction, prevention, and early diagnosis of AKI are important challenges to overcome.
Previous studies have identified various risk factors to predict the occurrence of AKI in different clinical settings. These include reduced renal function, heart failure, diabetes mellitus, number of blood products infused during operation, and older age [6,7,8]. Among the antihypertensive medications, several lines of evidence indicate that using angiotensin-converting enzymes or angiotensin II receptor blockers is associated with increased frequency of AKI [9, 10]. However, the association between anti-adrenergic drugs and postoperative AKI remained undetermined.
In the NARA-AKI Cohort Study, Nishimoto et al. [11] addressed whether the use of anti-adrenergic agents (α-blockers, β-blockers, or both) is associated with AKI in patients undergoing non-cardiac surgery. The NARA-AKI Cohort study was a single-center, retrospective cohort study that included patients who ≥ 18 years old and receiving non-cardiac surgery under general anesthesia from 2007 to 2011 at Nara Medical University. Patients with preoperative dialysis, obstetric, or urological surgery were excluded. The exposure of interest was the regular use of α-blockers and β-blockers before operation. The definition of AKI was in accordance with the KDIGO criteria, and postoperative AKI within 1 week as well as trajectories of eGFR were analyzed.
Among 5168 patients who were eligible for analysis, 245 patients (4.7%) were regularly taking anti-adrenergic agents before surgery. Patients who were taking anti-adrenergic agents were older, had lower eGFR, and higher blood pressure (BP) levels at baseline. Overall, AKI after the surgery occurred in 309 patients (6.0%). The study found that the use of anti-adrenergic agents was significantly associated with postoperative AKI (unadjusted odds ratio, 2.83 [interquartile ranges, 1.94−4.13]), and that this association was significant after adjustment of potential confounders, including age, eGFR, pre-existing cardiovascular diseases, intraoperative vasopressors, and other antihypertensive medications [11]. Among the 309 patients who had postoperative AKI, 35 patients were taking anti-adrenergic agents, whereas 274 patients were not. The authors further compared the trajectories of eGFR levels after AKI and found that the recovery of kidney function after AKI was delayed in patients with anti-adrenergic agents [11]. Thus, the use of anti-adrenergic agents is considered an additional risk factor after non-cardiac surgery in this cohort, independently of other conditions.
As a possible explanation for the association of anti-adrenergic drugs with postoperative AKI, the authors speculated the role of β2 adrenergic receptor (Adrb2), a G protein-coupled receptor. Upon binding catecholamines, Adrb2 mainly signals through stimulatory G protein (Gs), which activates adenylyl cyclase and cyclic-AMP-dependent pathway and also induces inhibitory G protein (Gi) signaling [12]. Although the precise distribution of Adrb2 within the kidney is not entirely solved, studies have shown that it is present in various cells, including vascular smooth muscle cells, glomerular cells, proximal tubule cells, and immune cells [13, 14]. It has also been reported that several pathological conditions, such as sepsis and heart failure, can impair β-adrenergic receptor signaling [15, 16].
Experimental studies indicate that Adrb2 signaling has a protective effect in rodent models of AKI. In a lipopolysaccharide (LPS)-induced AKI model, Nakamura et al. showed that renal function decline and leukocyte infiltration were significantly reduced by the adenoviral delivery of human ADRB2 to the kidney [17]. Conversely, renal injury induced by acute renal infection was aggravated by a β2 adrenergic receptor antagonist [18]. Of further note, intraperitoneal injection of formoterol, a specific long-acting β2 adrenergic receptor agonist, has also been shown to rescue renal tubules from ischemia/reperfusion-induced injury [19]. Formoterol has also been shown to promote mitochondrial biogenesis [20], likely contributing to renal function recovery after AKI induced by ischemia/reperfusion [19]. These data can be relevant to the clinical study by Nishimoto et al. [11], providing possible mechanisms for the observed association.
The study by Nishimoto et al. also showed that the recovery of renal function was slower in patients taking anti-adrenergic agents [11]. Currently, time from onset to recovery is not included in the grade severity of AKI in the KDIGO classification. However, it is plausible that the duration of AKI has an additional predictive value. Indeed, a meta-analysis indicated that the period of AKI was independently associated with long-term outcomes. In that study, long-term mortality was higher for longer AKI duration in each stage of AKI [21]. In addition to this study, recent research on AKI in patients with coronavirus disease 19 [22] and those receiving vascular surgery [23] showed that persistent AKI predicts mortality, supporting the prognostic importance of AKI duration.
In summary, the study by Nishimoto et al. showed that the use of anti-adrenergic agents was significantly associated with postoperative AKI and the delayed recovery of renal function, unveiling an additional risk factor of postoperative AKI. As a future study, it would be informative to evaluate whether the types and dosages of anti-adrenergic agents alter the risk. Also, given the experimental evidence that Adrb2 is involved in sepsis and ischemia/reperfusion injury, it may be worth evaluating whether the use of anti-adrenergic agents is associated with AKI in these conditions, in addition to the post-operative AKI.
References
Hsu RK, McCulloch CE, Heung M, Saran R, Shahinian VB, Pavkov ME, et al. Exploring potential reasons for the temporal trend in dialysis-requiring AKI in the United States. Clin J Am Soc Nephrol. 2016;11:14–20.
Lassnigg A, Schmidlin D, Mouhieddine M, Bachmann LM, Druml W, Bauer P, et al. Minimal changes of serum creatinine predict prognosis in patients after cardiothoracic surgery: a prospective cohort study. J Am Soc Nephrol. 2004;15:1597–605.
KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int Suppl. 2012;2:1–138.
Luo X, Jiang L, Du B, Wen Y, Wang M, Xi X, et al. A comparison of different diagnostic criteria of acute kidney injury in critically ill patients. Crit Care. 2014;18:R144.
Ostermann M, Bellomo R, Burdmann EA, Doi K, Endre ZH, Goldstein SL, et al. Controversies in acute kidney injury: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Conference. Kidney Int. 2020;98:294–309.
Wang YN, Cheng H, Yue T, Chen YP. Derivation and validation of a prediction score for acute kidney injury in patients hospitalized with acute heart failure in a Chinese cohort. Nephrology. 2013;18:489–96.
Ng RR, Chew ST, Liu W, Shen L, Ti LK. Identification of modifiable risk factors for acute kidney injury after coronary artery bypass graft surgery in an Asian population. J Thorac Cardiovasc Surg. 2014;147:1356–61.
Weingarten TN, Gurrieri C, McCaffrey JM, Ricter SJ, Hilgeman ML, Schroeder DR, et al. Acute kidney injury following bariatric surgery. Obes Surg. 2013;23:64–70.
Plataki M, Kashani K, Cabello-Garza J, Maldonado F, Kashyap R, Kor DJ, et al. Predictors of acute kidney injury in septic shock patients: an observational cohort study. Clin J Am Soc Nephrol. 2011;6:1744–51.
Abdullah HR, Tan TP, Vaez M, Deb C, Farag N, Jackson TD, et al. Predictors of Perioperative Acute Kidney Injury in Obese Patients Undergoing Laparoscopic Bariatric Surgery: a Single-Centre Retrospective Cohort Study. Obes Surg. 2016;26:1493–9.
Nishimoto M, Murashima M, Kokubu M, Matsui M, Eriguchi M, Samejima KI, et al. The use of anti-adrenergic agents as a predictor of acute kidney injury and delayed recovery of kidney function: the NARA-AKI cohort study. Hypertens Res. 2023 (e-pub ahead of print; https://doi.org/10.1038/s41440-023-01352-5).
Ma X, Hu Y, Batebi H, Heng J, Xu J, Liu X, et al. Analysis of beta(2)AR-G(s) and beta(2)AR-G(i) complex formation by NMR spectroscopy. Proc Natl Acad Sci USA. 2020;117:23096–105.
Moriyama S, Brestoff JR, Flamar AL, Moeller JB, Klose CSN, Rankin LC, et al. beta(2)-adrenergic receptor-mediated negative regulation of group 2 innate lymphoid cell responses. Science. 2018;359:1056–61.
Arif E, Nihalani D. Beta2-adrenergic receptor in kidney biology: A current perspective. Nephrology. 2019;24:497–503.
Ping P, Anzai T, Gao M, Hammond HK. Adenylyl cyclase and G protein receptor kinase expression during the development of heart failure. Am J Physiol. 1997;273:H707–17.
Bernardin G, Strosberg AD, Bernard A, Mattei M, Marullo S. Beta-adrenergic receptor-dependent and -independent stimulation of adenylate cyclase is impaired during severe sepsis in humans. Intensive Care Med. 1998;24:1315–22.
Nakamura A, Imaizumi A, Yanagawa Y, Kohsaka T, Johns EJ. beta(2)-Adrenoceptor activation attenuates endotoxin-induced acute renal failure. J Am Soc Nephrol. 2004;15:316–25.
Nakamura A, Niimi R, Yanagawa Y. Renal beta2-adrenoceptor blockade worsens the outcome of an induced Escherichia coli renal infection. J Nephrol. 2010;23:341–9.
Jesinkey SR, Funk JA, Stallons LJ, Wills LP, Megyesi JK, Beeson CC, et al. Formoterol restores mitochondrial and renal function after ischemia-reperfusion injury. J Am Soc Nephrol. 2014;25:1157–62.
Wills LP, Trager RE, Beeson GC, Lindsey CC, Peterson YK, Beeson CC, et al. The beta2-adrenoceptor agonist formoterol stimulates mitochondrial biogenesis. J Pharm Exp Ther. 2012;342:106–18.
Mehta S, Chauhan K, Patel A, Patel S, Pinotti R, Nadkarni GN, et al. The prognostic importance of duration of AKI: a systematic review and meta-analysis. BMC Nephrol. 2018;19:91.
Kim SG, Han CH, Yu SB, Lee H, Kwon S, Kim Y, et al. Trajectory of AKI and hospital mortality among patients with COVID-19. Ren Fail. 2023;45:2177086.
MacGillivray RG, Jann H, Vanker E, Gemmell L, Mahomedy AE. Development of malignant hyperthermia obscured by cardiopulmonary bypass. Can Anaesth Soc J. 1986;33:509–14.
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Asakawa, S., Shibata, S. Anti-adrenergic agents and the risk of postoperative acute kidney injury. Hypertens Res 47, 796–798 (2024). https://doi.org/10.1038/s41440-023-01546-x
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DOI: https://doi.org/10.1038/s41440-023-01546-x