Literature DB >> 27058465

Histopathology of Septic Acute Kidney Injury: A Systematic Review of Experimental Data.

Junko Kosaka1, Yugeesh R Lankadeva, Clive N May, Rinaldo Bellomo.   

Abstract

OBJECTIVE: The histopathologic changes associated with septic acute kidney injury are poorly understood, in part, because of the lack of biopsy data in humans. Animal models of septic acute kidney injury may help define such changes. Therefore, we performed a systematic review of the histopathologic changes found in modern experimental septic acute kidney injury models. DATA SOURCES: MEDLINE, EMBASE, Cumulative Index to Nursing and Allied Health Literature, and PubMed (from January 2007 to February 2015). STUDY SELECTION: We reviewed experimental studies reporting findings on the histopathology of contemporary experimental septic acute kidney injury. DATA EXTRACTION: We focused on the presence or the absence of acute tubular necrosis, tubular cell apoptosis, and other nonspecific findings. DATA SYNTHESIS: We identified 102 studies in 1,059 animals. Among the 1,059 animals, 53 (5.0%) did not have any renal histopathologic changes, but acute tubular necrosis was found in 184 (17.4%). The prevalence of acute tubular necrosis was not related to animal size or model of sepsis and was only found in models with low cardiac output and decreased renal blood flow (p < 0.0001). Only 21 studies (170 animals) assessed the prevalence of tubular cell apoptosis, which was reported in 158 animals (92.9%). The prevalence of tubular cell apoptosis was significantly higher in studies using small animals (p < 0.0001) and in peritonitis models (p < 0.0001). Simultaneous acute tubular necrosis and tubular cell apoptosis was rare (55 animals [32.4%]) and only seen with decreased cardiac output and renal blood flow. Nonspecific changes (vacuolization of tubular cells, loss of brush border, and tubular cell swelling) were each observed in 423 (39.9%), 250 (23.6%) and 243 (22.9%) animals, respectively.
CONCLUSIONS: In models of experimental septic acute kidney injury in contemporary articles, acute tubular necrosis was relatively uncommon and, when present, reflected the presence of an associated low cardiac output or low renal blood flow syndrome. Tubular cell apoptosis seemed frequent in the few studies in which it was investigated. Nonspecific morphologic changes, however, were the most common histopathologic findings.

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Mesh:

Year:  2016        PMID: 27058465     DOI: 10.1097/CCM.0000000000001735

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  30 in total

Review 1.  Recent advances in the pathogenetic mechanisms of sepsis-associated acute kidney injury.

Authors:  Filippo Fani; Giuseppe Regolisti; Marco Delsante; Vincenzo Cantaluppi; Giuseppe Castellano; Loreto Gesualdo; Gianluca Villa; Enrico Fiaccadori
Journal:  J Nephrol       Date:  2017-12-23       Impact factor: 3.902

2.  Negative Regulation of Tec Kinase Alleviates LPS-Induced Acute Kidney Injury in Mice via theTLR4/NF-κB Signaling Pathway.

Authors:  Wei Zhang; Ping Zhou; Xiao Jiang; Zhe Fan; Xingxin Xu; Fei Wang
Journal:  Biomed Res Int       Date:  2020-06-19       Impact factor: 3.411

3.  The 10 false beliefs in adult critical care nephrology.

Authors:  Zaccaria Ricci; Stefano Romagnoli; Claudio Ronco
Journal:  Intensive Care Med       Date:  2017-12-01       Impact factor: 17.440

Review 4.  The crosstalk between hypoxia-inducible factor-1α and microRNAs in acute kidney injury.

Authors:  Zhiyu Wang; Wen Zhang
Journal:  Exp Biol Med (Maywood)       Date:  2020-01-29

5.  Renal tubular cell spliced X-box binding protein 1 (Xbp1s) has a unique role in sepsis-induced acute kidney injury and inflammation.

Authors:  Silvia Ferrè; Yingfeng Deng; Sarah C Huen; Christopher Y Lu; Philipp E Scherer; Peter Igarashi; Orson W Moe
Journal:  Kidney Int       Date:  2019-08-01       Impact factor: 10.612

6.  Postmortem Kidney Pathology Findings in Patients with COVID-19.

Authors:  Dominick Santoriello; Pascale Khairallah; Andrew S Bomback; Katherine Xu; Satoru Kudose; Ibrahim Batal; Jonathan Barasch; Jai Radhakrishnan; Vivette D'Agati; Glen Markowitz
Journal:  J Am Soc Nephrol       Date:  2020-07-29       Impact factor: 10.121

Review 7.  The intensive care medicine agenda on acute kidney injury.

Authors:  Peter Pickkers; Marlies Ostermann; Michael Joannidis; Alexander Zarbock; Eric Hoste; Rinaldo Bellomo; John Prowle; Michael Darmon; Joseph V Bonventre; Lui Forni; Sean M Bagshaw; Miet Schetz
Journal:  Intensive Care Med       Date:  2017-01-30       Impact factor: 17.440

8.  Thiamine as a Renal Protective Agent in Septic Shock. A Secondary Analysis of a Randomized, Double-Blind, Placebo-controlled Trial.

Authors:  Ari Moskowitz; Lars W Andersen; Michael N Cocchi; Mathias Karlsson; Parth V Patel; Michael W Donnino
Journal:  Ann Am Thorac Soc       Date:  2017-05

9.  Juvenile OLFM4-null mice are protected from sepsis.

Authors:  Julie E Stark; Amy M Opoka; Jaya Mallela; Prasad Devarajan; Qing Ma; Nick C Levinsky; Keith F Stringer; Hector R Wong; Matthew N Alder
Journal:  Am J Physiol Renal Physiol       Date:  2020-02-18

10.  Impaired angiotensin II type 1 receptor signaling contributes to sepsis-induced acute kidney injury.

Authors:  Daniel E Leisman; Tiago D Fernandes; Vanesa Bijol; Mabel N Abraham; Jake R Lehman; Matthew D Taylor; Christine Capone; Omar Yaipan; Rinaldo Bellomo; Clifford S Deutschman
Journal:  Kidney Int       Date:  2020-08-31       Impact factor: 10.612

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