Neutrophil gelatinase-associated lipocalin predicts the efficacy of tolvaptan for ascites in patients with liver cirrhosis.


Journal

Journal of gastroenterology
ISSN: 1435-5922
Titre abrégé: J Gastroenterol
Pays: Japan
ID NLM: 9430794

Informations de publication

Date de publication:
07 2023
Historique:
received: 31 01 2023
accepted: 08 04 2023
medline: 30 6 2023
pubmed: 27 4 2023
entrez: 27 4 2023
Statut: ppublish

Résumé

Acute kidney injury (AKI) is associated with liver cirrhosis (LC), water retention, diuretics to treat water retention, and a poor prognosis. Urinary neutrophil gelatinase-associated lipocalin (uNGAL) reportedly predicts a poor prognosis in decompensated LC. This study investigated the usefulness of uNGAL in predicting the short- and long-term effects of tolvaptan (TVP) and the incidence of AKI post-TVP administration. Of the LC cases with water retention, 86 with available pre-treatment uNGAL were analyzed. A short-term response was defined as weight loss of ≥ 1.5 kg within the first week; a long-term response was defined as a short-term response without early recurrence. The uNGAL usefulness in predicting the short- and long-term effects of TVP and AKI incidence post-TVP administration was investigated. Short-term effects of TVP were observed in 52 patients. Of these, 15 patients had an early recurrence. In multivariate analysis, significant short-term predictive factors were C-reactive protein (CRP) < 1.4 mg/dl, uNa/K ratio ≥ 3.51, and uNGAL < 50.2 ng/ml. Patients were classified according to these three cut-off values, with short-term response rates of 92.9%, 68.8%, 26.7%, and 0% for 0, 1, 2, and 3 points, respectively. CRP < 0.94 mg/dl and uNGAL < 50.2 ng/ml were significant factors for predicting the long-term response of TVP. The AKI incidence post-TVP was 8.1% (n = 7) and was significantly higher among those with uNGAL ≥ 38.1 ng/mL. uNGAL is a useful predictor of the short- and long-term efficacy of TVP and can be useful in predicting AKI incidence post-TVP administration.

Sections du résumé

BACKGROUND
Acute kidney injury (AKI) is associated with liver cirrhosis (LC), water retention, diuretics to treat water retention, and a poor prognosis. Urinary neutrophil gelatinase-associated lipocalin (uNGAL) reportedly predicts a poor prognosis in decompensated LC. This study investigated the usefulness of uNGAL in predicting the short- and long-term effects of tolvaptan (TVP) and the incidence of AKI post-TVP administration.
METHODS
Of the LC cases with water retention, 86 with available pre-treatment uNGAL were analyzed. A short-term response was defined as weight loss of ≥ 1.5 kg within the first week; a long-term response was defined as a short-term response without early recurrence. The uNGAL usefulness in predicting the short- and long-term effects of TVP and AKI incidence post-TVP administration was investigated.
RESULTS
Short-term effects of TVP were observed in 52 patients. Of these, 15 patients had an early recurrence. In multivariate analysis, significant short-term predictive factors were C-reactive protein (CRP) < 1.4 mg/dl, uNa/K ratio ≥ 3.51, and uNGAL < 50.2 ng/ml. Patients were classified according to these three cut-off values, with short-term response rates of 92.9%, 68.8%, 26.7%, and 0% for 0, 1, 2, and 3 points, respectively. CRP < 0.94 mg/dl and uNGAL < 50.2 ng/ml were significant factors for predicting the long-term response of TVP. The AKI incidence post-TVP was 8.1% (n = 7) and was significantly higher among those with uNGAL ≥ 38.1 ng/mL.
CONCLUSION
uNGAL is a useful predictor of the short- and long-term efficacy of TVP and can be useful in predicting AKI incidence post-TVP administration.

Identifiants

pubmed: 37103575
doi: 10.1007/s00535-023-01993-w
pii: 10.1007/s00535-023-01993-w
doi:

Substances chimiques

Lipocalin-2 0
Tolvaptan 21G72T1950
Acute-Phase Proteins 0
Lipocalins 0
Proto-Oncogene Proteins 0
Biomarkers 0
C-Reactive Protein 9007-41-4
Water 059QF0KO0R

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

656-667

Subventions

Organisme : Japan Agency for Medical Research and Development
ID : (JP21fk0310103
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210053
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210072
Organisme : Japan Agency for Medical Research and Development
ID : JP20fk0210056
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0310101
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210047
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210064
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210056
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210048
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210058
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0210066
Organisme : Japan Agency for Medical Research and Development
ID : 21fk0210067
Organisme : Japan Society for the Promotion of Science
ID : JP20K08371
Organisme : Japan Society for the Promotion of Science
ID : JP22K15954

Informations de copyright

© 2023. Japanese Society of Gastroenterology.

Références

European Association for the Study of the Liver. EASL clinical practice guidelines for the management of patients with decompensated cirrhosis. J Hepatol. 2018;69:406–60.
doi: 10.1016/j.jhep.2018.03.024
Biggins SW, Angeli P, Garcia-Tsao G, et al. Diagnosis, evaluation, and management of ascites, spontaneous bacterial peritonitis and hepatorenal syndrome: 2021 practice guidance by the American association for the study of liver diseases. Hepatology. 2021;74:1014–48.
pubmed: 33942342 doi: 10.1002/hep.31884
Yoshiji H, Nagoshi S, Akahane T, et al. Evidence-based clinical practice guidelines for liver cirrhosis 2020. J Gastroenterol. 2021;56:593–619.
pubmed: 34231046 pmcid: 8280040 doi: 10.1007/s00535-021-01788-x
Yoshiji H, Nagoshi S, Akahane T, et al. Evidence-based clinical practice guidelines for liver cirrhosis 2020. Hepatol Res. 2021;51:725–49.
pubmed: 34228859 doi: 10.1111/hepr.13678
Zeng X, Shi ZW, Yu JJ, et al. Sarcopenia as a prognostic predictor of liver cirrhosis: a multicentre study in China. J Cachexia Sarcopenia Muscle. 2021;12:1948–58.
pubmed: 34520115 pmcid: 8718091 doi: 10.1002/jcsm.12797
Fagundes C, Barreto R, Guevara M, et al. A modified acute kidney injury classification for diagnosis and risk stratification of impairment of kidney function in cirrhosis. J Hepatol. 2013;59:474–81.
pubmed: 23669284 doi: 10.1016/j.jhep.2013.04.036
Tsien CD, Rabie R, Wong F. Acute kidney injury in decompensated cirrhosis. Gut. 2013;62:131–7.
pubmed: 22637695 doi: 10.1136/gutjnl-2011-301255
Berl T, Quittnat-Pelletier F, Verbalis JG, et al. Oral tolvaptan is safe and effective in chronic hyponatremia. J Am Soc Nephrol. 2010;21:705–12.
pubmed: 20185637 pmcid: 2844305 doi: 10.1681/ASN.2009080857
Schrier RW, Gross P, Gheorghiade M, et al. Tolvaptan, a selective oral vasopressin V2-receptor antagonist, for hyponatremia. N Engl J Med. 2006;355:2099–112.
pubmed: 17105757 doi: 10.1056/NEJMoa065181
Torres VE, Chapman AB, Devuyst O, et al. Tolvaptan in later-stage autosomal dominant polycystic kidney disease. N Engl J Med. 2017;377:1930–42.
pubmed: 29105594 doi: 10.1056/NEJMoa1710030
Torres VE, Meijer E, Bae KT, et al. Rationale and design of the TEMPO (tolvaptan efficacy and safety in management of autosomal dominant polycystic kidney disease and its outcomes) 3–4 study. Am J Kidney Dis. 2011;57:692–9.
pubmed: 21333426 doi: 10.1053/j.ajkd.2010.11.029
Hiramine Y, Uojima H, Nakanishi H, et al. Response criteria of tolvaptan for the treatment of hepatic edema. J Gastroenterol. 2018;53:258–68.
pubmed: 28664229 doi: 10.1007/s00535-017-1366-6
Hiramine Y, Uto H, Imamura Y, et al. Efficacy of vasopressin V2 receptor antagonist tolvaptan in treatment of hepatic edema. Hepatol Res. 2017;47:542–57.
pubmed: 27448501 doi: 10.1111/hepr.12778
Kawaratani H, Fukui H, Moriya K, et al. Predictive parameter of tolvaptan effectiveness in cirrhotic ascites. Hepatol Res. 2017;47:854–61.
pubmed: 27704665 doi: 10.1111/hepr.12826
Kogiso T, Yamamoto K, Kobayashi M, et al. Response to tolvaptan and its effect on prognosis in cirrhotic patients with ascites. Hepatol Res. 2017;47:835–44.
pubmed: 27670393 doi: 10.1111/hepr.12822
Nakai M, Ogawa K, Takeda R, et al. Increased serum C-reactive protein and decreased urinary aquaporin 2 levels are predictive of the efficacy of tolvaptan in patients with liver cirrhosis. Hepatol Res. 2018;48:E311–9.
pubmed: 28984014 doi: 10.1111/hepr.12988
Uojima H, Kinbara T, Hidaka H, et al. Close correlation between urinary sodium excretion and response to tolvaptan in liver cirrhosis patients with ascites. Hepatol Res. 2017;47:E14–21.
pubmed: 27059410 doi: 10.1111/hepr.12716
Atsukawa M, Tsubota A, Kato K, et al. Analysis of factors predicting the response to tolvaptan in patients with liver cirrhosis and hepatic edema. J Gastroenterol Hepatol. 2018;33:1256–63.
pubmed: 29215154 doi: 10.1111/jgh.14047
Komiyama Y, Kurosaki M, Nakanishi H, et al. Prediction of diuretic response to tolvaptan by a simple, readily available spot urine Na/K ratio. PLoS One. 2017;12: e0174649.
pubmed: 28362879 pmcid: 5375149 doi: 10.1371/journal.pone.0174649
Sakaida I, Terai S, Kurosaki M, et al. Effectiveness and safety of tolvaptan in liver cirrhosis patients with edema: interim results of post-marketing surveillance of tolvaptan in liver cirrhosis (START study). Hepatol Res. 2017;47:1137–46.
pubmed: 27958663 doi: 10.1111/hepr.12852
Nakai M, Suda G, Kubo A, et al. Durable response without recurrence to tolvaptan improves long-term survival. J Gastroenterol. 2020;55:1150–61.
pubmed: 32851487 doi: 10.1007/s00535-020-01721-8
Uojima H, Hidaka H, Nakayama T, et al. Efficacy of combination therapy with natriuretic and aquaretic drugs in cirrhotic ascites patients: a randomized study. World J Gastroenterol. 2017;23:8062–72.
pubmed: 29259382 pmcid: 5725301 doi: 10.3748/wjg.v23.i45.8062
Barasch J, Mori K. Cell biology: iron thievery. Nature. 2004;432:811–3.
pubmed: 15602535 doi: 10.1038/432811a
Mishra J, Dent C, Tarabishi R, et al. Neutrophil gelatinase-associated lipocalin (NGAL) as a biomarker for acute renal injury after cardiac surgery. The Lancet. 2005;365:1231–8.
doi: 10.1016/S0140-6736(05)74811-X
Tsuchimoto A, Shinke H, Uesugi M, et al. Urinary neutrophil gelatinase-associated lipocalin: a useful biomarker for tacrolimus-induced acute kidney injury in liver transplant patients. PLoS One. 2014;9: e110527.
pubmed: 25329716 pmcid: 4203804 doi: 10.1371/journal.pone.0110527
Angeli P, Gines P, Wong F, et al. Diagnosis and management of acute kidney injury in patients with cirrhosis: revised consensus recommendations of the international club of ascites. J Hepatol. 2015;62:968–74.
pubmed: 25638527 doi: 10.1016/j.jhep.2014.12.029
Ohara M, Suda G, Kimura M, et al. Analysis of the optimal psoas muscle mass index cut-off values, as measured by computed tomography, for the diagnosis of loss of skeletal muscle mass in Japanese people. Hepatol Res. 2020;50:715–25.
pubmed: 32202371 doi: 10.1111/hepr.13499
Kanda Y. Investigation of the freely available easy-to-use software “EZR” for medical statistics. Bone Marrow Transplant. 2013;48:452–8.
pubmed: 23208313 doi: 10.1038/bmt.2012.244
Mazzaferro V, Regalia E, Doci R, et al. Liver transplantation for the treatment of small hepatocellular carcinomas in patients with cirrhosis. N Engl J Med. 1996;334:693–9.
pubmed: 8594428 doi: 10.1056/NEJM199603143341104
Malinchoc M, Kamath PS, Gordon FD, et al. A model to predict poor survival in patients undergoing transjugular intrahepatic portosystemic shunts. Hepatology. 2000;31:864–71.
pubmed: 10733541 doi: 10.1053/he.2000.5852
Kamath PS, Kim WR, Advanced Liver Disease Study G. The model for end-stage liver disease (MELD). Hepatology. 2007;45:797–805.
pubmed: 17326206 doi: 10.1002/hep.21563
Kim WR, Biggins SW, Kremers WK, et al. Hyponatremia and mortality among patients on the liver-transplant waiting list. N Engl J Med. 2008;359:1018–26.
pubmed: 18768945 pmcid: 4374557 doi: 10.1056/NEJMoa0801209
Bellos I, Kontzoglou K, Perrea DN. Predictors of tolvaptan short-term response in patients with refractory ascites: a meta-analysis. J Gastroenterol Hepatol. 2020;35:182–91.
pubmed: 31323125 doi: 10.1111/jgh.14784
Khwaja A. KDIGO clinical practice guidelines for acute kidney injury. Nephron Clin Pract. 2012;120:c179–84.
pubmed: 22890468 doi: 10.1159/000339789
Schmidt-Ott KM. Neutrophil gelatinase-associated lipocalin as a biomarker of acute kidney injury–where do we stand today? Nephrol Dial Transplant. 2011;26:762–4.
pubmed: 21310736 doi: 10.1093/ndt/gfr006
Hirsch R, Dent C, Pfriem H, et al. NGAL is an early predictive biomarker of contrast-induced nephropathy in children. Pediatr Nephrol. 2007;22:2089–95.
pubmed: 17874137 doi: 10.1007/s00467-007-0601-4
Liebetrau C, Gaede L, Doerr O, et al. Neutrophil gelatinase-associated lipocalin (NGAL) for the early detection of contrast-induced nephropathy after percutaneous coronary intervention. Scand J Clin Lab Invest. 2014;74:81–8.
pubmed: 24304491 doi: 10.3109/00365513.2013.860615
Gomes BC, Silva Junior JM, Tuon FF. Evaluation of urinary NGAL as a diagnostic tool for acute kidney injury in critically ill patients with infection: an original study. Can J Kidney Health Dis. 2020;7:2054358120934215.
pubmed: 32612844 pmcid: 7307396 doi: 10.1177/2054358120934215
Mishra J, Ma Q, Prada A, et al. Identification of neutrophil gelatinase-associated lipocalin as a novel early urinary biomarker for ischemic renal injury. J Am Soc Nephrol. 2003;14:2534–43.
pubmed: 14514731 doi: 10.1097/01.ASN.0000088027.54400.C6
Mishra J, Mori K, Ma Q, et al. Amelioration of ischemic acute renal injury by neutrophil gelatinase-associated lipocalin. J Am Soc Nephrol. 2004;15:3073–82.
pubmed: 15579510 doi: 10.1097/01.ASN.0000145013.44578.45
Nickolas TL, O’Rourke MJ, Yang J, et al. Sensitivity and specificity of a single emergency department measurement of urinary neutrophil gelatinase-associated lipocalin for diagnosing acute kidney injury. Ann Intern Med. 2008;148:810–9.
pubmed: 18519927 pmcid: 2909852 doi: 10.7326/0003-4819-148-11-200806030-00003
Gambino C, Piano S, Stenico M, et al. Diagnostic and prognostic performance of urinary neutrophil gelatinase-associated lipocalin in patients with cirrhosis and AKI. Hepatology. 2022. https://doi.org/10.1002/hep.32799 .
doi: 10.1002/hep.32799
Ariza X, Graupera I, Coll M, et al. Neutrophil gelatinase-associated lipocalin is a biomarker of acute-on-chronic liver failure and prognosis in cirrhosis. J Hepatol. 2016;65:57–65.
pubmed: 26988732 doi: 10.1016/j.jhep.2016.03.002
Jiang QQ, Han MF, Ma K, et al. Acute kidney injury in acute-on-chronic liver failure is different from in decompensated cirrhosis. World J Gastroenterol. 2018;24:2300–10.
pubmed: 29881239 pmcid: 5989244 doi: 10.3748/wjg.v24.i21.2300
Lei L, Li LP, Zeng Z, et al. Value of urinary KIM-1 and NGAL combined with serum Cys C for predicting acute kidney injury secondary to decompensated cirrhosis. Sci Rep. 2018;8:7962.
pubmed: 29784944 pmcid: 5962573 doi: 10.1038/s41598-018-26226-6
Hiramine Y, Uto H, Mawatari S, et al. Impact of acute kidney injury on prognosis and the effect of tolvaptan in patients with hepatic ascites. J Gastroenterol. 2021;56:54–66.
pubmed: 32959093 doi: 10.1007/s00535-020-01727-2
Tamaki S, Sato Y, Yamada T, et al. Tolvaptan reduces the risk of worsening renal function in patients with acute decompensated heart failure and preserved left ventricular ejection fraction- prospective randomized controlled study. Circ J. 2017;81:740–7.
pubmed: 28202885 doi: 10.1253/circj.CJ-16-1122

Auteurs

Masato Nakai (M)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Kenichi Morikawa (K)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Takashi Sasaki (T)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Risako Kohya (R)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Sonoe Yoshida (S)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Shunichi Hosoda (S)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Akinori Kubo (A)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Yoshimasa Tokuchi (Y)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Takashi Kitagataya (T)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Ren Yamada (R)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Masatsugu Ohara (M)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Takuya Sho (T)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Goki Suda (G)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Koji Ogawa (K)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan.

Naoya Sakamoto (N)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-Ku, Sapporo-shi, Hokkaido, 060-8638, Japan. sakamoto@med.hokudai.ac.jp.

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