Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.

BACKGROUND: Acute kidney injury (AKI) complicating severe Plasmodium falciparum malaria occurs in up to 40% of adult patients. The case fatality rate reaches 75% in the absence of renal replacement therapy (RRT). The precise pathophysiology of AKI in falciparum malaria remains unclear. Histopatholog...

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Main Authors: Plewes, K, Royakkers, A, Hanson, J, Hasan, M, Alam, S, Ghose, A, Maude, R, Stassen, P, Charunwatthana, P, Lee, S, Turner, G, Dondorp, A, Schultz, M
Format: Journal article
Language:English
Published: BioMed Central 2014
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author Plewes, K
Royakkers, A
Hanson, J
Hasan, M
Alam, S
Ghose, A
Maude, R
Stassen, P
Charunwatthana, P
Lee, S
Turner, G
Dondorp, A
Schultz, M
author_facet Plewes, K
Royakkers, A
Hanson, J
Hasan, M
Alam, S
Ghose, A
Maude, R
Stassen, P
Charunwatthana, P
Lee, S
Turner, G
Dondorp, A
Schultz, M
author_sort Plewes, K
collection OXFORD
description BACKGROUND: Acute kidney injury (AKI) complicating severe Plasmodium falciparum malaria occurs in up to 40% of adult patients. The case fatality rate reaches 75% in the absence of renal replacement therapy (RRT). The precise pathophysiology of AKI in falciparum malaria remains unclear. Histopathology shows acute tubular necrosis with localization of host monocytes and parasitized red blood cells in the microvasculature. This study explored the relationship of plasma soluble urokinase-type plasminogen activator receptor (suPAR), as a proxy-measure of mononuclear cell activation, and plasma P. falciparum histidine rich protein 2 (PfHRP2), as a measure of sequestered parasite burden, with AKI in severe malaria. METHODS: Admission plasma suPAR and PfHRP2 concentrations were assessed in Bangladeshi adults with severe falciparum malaria (n=137). Patients were stratified according to AKI severity based on admission creatinine clearance. RESULTS: A total of 106 (77%) patients had AKI; 32 (23%), 42 (31%) and 32 (23%) were classified into 'mild, 'moderate' and 'severe' AKI groups, respectively. Plasma suPAR and PfHRP2 concentrations increased with AKI severity (test-for-trend P <0.0001) and correlated with other markers of renal dysfunction. Admission plasma suPAR and PfHRP2 concentrations were higher in patients who later required RRT (P <0.0001 and P=0.0004, respectively). In a multivariate analysis, both increasing suPAR and PfHRP2 were independently associated with increasing urine neutrophil gelatinase-associated lipocalin concentration, a marker of acute tubular necrosis (β=16.54 (95% CI 6.36-26.71) and β=0.07 (0.02-0.11), respectively). CONCLUSIONS: Both sequestered parasite burden and immune activation contribute to the pathogenesis of AKI in severe falciparum malaria.
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spelling oxford-uuid:0a6afdde-b5dd-4e3a-8f13-3c01bd3d23f32022-03-26T09:23:47ZCorrelation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:0a6afdde-b5dd-4e3a-8f13-3c01bd3d23f3EnglishSymplectic Elements at OxfordBioMed Central2014Plewes, KRoyakkers, AHanson, JHasan, MAlam, SGhose, AMaude, RStassen, PCharunwatthana, PLee, STurner, GDondorp, ASchultz, MBACKGROUND: Acute kidney injury (AKI) complicating severe Plasmodium falciparum malaria occurs in up to 40% of adult patients. The case fatality rate reaches 75% in the absence of renal replacement therapy (RRT). The precise pathophysiology of AKI in falciparum malaria remains unclear. Histopathology shows acute tubular necrosis with localization of host monocytes and parasitized red blood cells in the microvasculature. This study explored the relationship of plasma soluble urokinase-type plasminogen activator receptor (suPAR), as a proxy-measure of mononuclear cell activation, and plasma P. falciparum histidine rich protein 2 (PfHRP2), as a measure of sequestered parasite burden, with AKI in severe malaria. METHODS: Admission plasma suPAR and PfHRP2 concentrations were assessed in Bangladeshi adults with severe falciparum malaria (n=137). Patients were stratified according to AKI severity based on admission creatinine clearance. RESULTS: A total of 106 (77%) patients had AKI; 32 (23%), 42 (31%) and 32 (23%) were classified into 'mild, 'moderate' and 'severe' AKI groups, respectively. Plasma suPAR and PfHRP2 concentrations increased with AKI severity (test-for-trend P <0.0001) and correlated with other markers of renal dysfunction. Admission plasma suPAR and PfHRP2 concentrations were higher in patients who later required RRT (P <0.0001 and P=0.0004, respectively). In a multivariate analysis, both increasing suPAR and PfHRP2 were independently associated with increasing urine neutrophil gelatinase-associated lipocalin concentration, a marker of acute tubular necrosis (β=16.54 (95% CI 6.36-26.71) and β=0.07 (0.02-0.11), respectively). CONCLUSIONS: Both sequestered parasite burden and immune activation contribute to the pathogenesis of AKI in severe falciparum malaria.
spellingShingle Plewes, K
Royakkers, A
Hanson, J
Hasan, M
Alam, S
Ghose, A
Maude, R
Stassen, P
Charunwatthana, P
Lee, S
Turner, G
Dondorp, A
Schultz, M
Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.
title Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.
title_full Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.
title_fullStr Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.
title_full_unstemmed Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.
title_short Correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria.
title_sort correlation of biomarkers for parasite burden and immune activation with acute kidney injury in severe falciparum malaria
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