Gontijo CMF, Melo MN, 2004. Visceral leishmaniasis in Brazil: current status, challenges and prospects. Rev Bras Epidemiol 7: 338–349.
Ministério da Saúde, Secretaria de Vigilância em Saúde. Departamento de Vigilância Epidemiológica, Brasil, 2006. Manual de vigilância e controle da leishmaniose visceral (Série A. Normas e Manuais Técnicos). Brasília, Brazil: Ministério da Saúde.
Clementi A, Battaglia G, Floris M, Castellino P, Ronco C, Cruz DN, 2011. Renal involvement in leishmaniasis: a review of the literature. NDT Plus 4: 147–152.
Barsoum RS, 2013. Parasitic kidney disease: milestones in the evolution of our knowledge. Am J Kidney Dis 61: 501–513.
Lima Verde FA, Santos GM, Lima Verde FAA, Daher EF, Saboia Neto A, Lima Verde EM, 2008. Acid-base disturbances in visceral leishmaniasis. J Bras Neurol 30: 172–179.
Lima Verde FAA, Lima Verde FA, Daher EF, Santos GM, Saboia Neto A, Lima Verde EM, 2009. Renal tubular dysfunction in human visceral leishmaniasis (kala-azar). Clin Nephrol 71: 492–500.
Duarte MI, Silva MR, Goto H, 1983. Interstitial nephritis in human kala-azar. Rev Soc Trop Med Hyg 77: 531–537.
Dutra M, Martinelli MR, Carvalho EM, 1985. Renal involvement in visceral leishmaniasis. Am J Kidney Dis 7: 22–27.
Costa CHN, Werneck GL, Costa DL, Holanda TA, Aguiar GB, Carvalho AS, Cavalcanti JC, Santos LS, 2010. Is severe visceral leishmaniasis a systemic inflammatory response syndrome? – A case control study. Rev Soc Bras Med Trop 43: 386–392.
Rado JP, 1978. 1-Desamino-8-D-arginine vasopressin (DDAVP) concentration test. Am J Med Sci 275: 43–52.
Abyholm G, Monn E, 1979. Intranasal DDAVP-test in the study of renal concentrating capacity in children with recurrent urinary tract infections. Eur J Pediatr 130: 149–154.
Tryding N, Sterner G, Berg B, Harris A, Lundin S, 1987. Subcutaneous and intranasal administration of 1-deamino-8-d-arginine vasopressin in the assessment of renal concentration capacity. Nephron 45: 27–30.
Oster JR, 1975. A short duration renal acidification test using calcium chloride. Nephron 14: 281–292.
Oliveira RA, Diniz LF, Teotônio LO, Lima CG, Mota RM, Martins A, Sanches TR, Seguro AC, Andrade L, Silva GB Jr, Libório AB, Daher EF, 2011. Renal tubular dysfunction in patients with American cutaneous leishmaniasis. Kidney Int 80: 1099–1106.
Oliveira MJC, Silva Junior GB, Abreu KL, Rocha NA, Garcia AV, Franco LF, Mota RM, Libório AB, Daher EF, 2010. Risk factors for acute kidney injury in visceral leishmaniasis (Kala-Azar). Am J Trop Med Hyg 82: 449–453.
Wu HY, Huang JW, Peng YS, Hung KY, Wu KD, Lai MS, Chien KL, 2013. Microalbuminuria screening for detecting chronic kidney disease in the general population: a systematic review. Ren Fail 35: 607–614.
Conductier G, Blondeau N, Guyon A, Nahon JL, Rovère C, 2010. The role of monocyte chemoattractant protein MCP1/CCL2 in neuroinflammatory diseases. J Neuroimmunol 224: 93–100.
Hodgkins KS, Schnaper HW, 2012. Tubulointerstitial injury and progression of chronic kidney disease. Pediatr Nephrol 27: 901–909.
Grandaliano G, Gesulado L, Ranieri E, Monno R, Montinaro V, Marra F, Schena FP, 1996. Monocyte chemotactic peptide-1 expression in acute and chronic human nephritides: a patogenetic role in interstitial monocytes recruitment. J Am Soc Nephrol 7: 906–913.
Eardley KS, Zehnder D, Quinkler M, Lepenies J, Bates RL, Savage CO, Howie AJ, Adu D, Cockwell P, 2006. The relationship between albuminuria, MCP-1/CCL2, and interstitial macrophages in chronic kidney disease. Kidney Int 69: 1189–1197.
Hanemann ALP, Libório AB, Daher EF, Martins AM, Pinheiro MC, Sousa MS, Bezerra FS, 2013. Monocyte chemotactic protein-1 (MCP-1) in patients with chronic schistosomiasis mansoni: evidences of subclinical renal inflammation. PLoS ONE 8: e80421.
Heidarpour M, Soltani S, Mohri M, Khoshnegah J, 2012. Canine visceral leishmaniasis: relationships between oxidative stress, liver and kidney variables, trace elements and clinical status. Parasitol Res 111: 1491–1496.
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Visceral leishmaniasis (VL) is a re-emerging zoonosis of worldwide distribution. Monocyte chemotactic protein-1 (MCP-1) and malondialdehyde (MDA) are inflammation biomarkers that have never been investigated in VL. The aim of this study is to investigate the association between renal abnormalities and inflammation biomarkers in VL. This study is a preliminary prospective study with 16 VL adult patients evaluated before treatment compared with a group of 13 healthy volunteers and 5 VL patients evaluated after treatment. Urinary concentration and acidification tests were performed. MCP-1 and MDA were quantified in urine. Urinary concentration deficit was found in all VL patients before (100%) and four VL patients after (80%) treatment. Urinary acidification deficit was found in nine cases before (56.2%) and two cases after (40%) treatment. Urinary MCP-1 (374 ± 359 versus 42 ± 29 pg/mg creatinine, P = 0.002) as well as urinary MDA (5.4 ± 2.6 versus 2.0 ± 0.8 μmol/mL) showed significant differences between VL patients and controls. These data show that VL patients present urinary concentration and acidification deficit, which can persist even after specific treatment. Urinary MCP-1 and MDA are elevated in patients with VL, which suggests renal inflammation and incipient renal damage.
Financial support: This research was supported by the Brazilian Research Council (CNPq).
Authors' addresses: Michelle J. C. Oliveira, Aline M. Sampaio, Bárbara L. Montenegro, Marília P. Alves, and Elizabeth F. Daher, Department of Internal Medicine, Federal University of Ceara, Fortaleza, Ceara, Brazil, E-mails: mi_cavalcante@hotmail.com, aline_sampa@hotmail.com, barbararlmontenegro@hotmail.com, lilah_alves@hotmail.com, and ef.daher@uol.com.br. Geraldo B. Silva Junior, School of Medicine, Master in Collective Health, Health Sciences Center, University of Fortaleza, Fortaleza, Ceará, Brazil, E-mail: geraldobezerrajr@yahoo.com.br. Guilherme A. L. Henn and Hermano A. L. Rocha, Department of Community Health, Federal University of Ceara, Fortaleza, Ceara, Brazil, E-mails: guialhenn@gmail.com and hermanoalexandre@gmail.com. Gdayllon C. Meneses and Alice M. C. Martins, School of Pharmacy, Federal University of Ceara, Fortaleza, Ceara, Brazil, E-mail: gdayllon@yahoo.com.br and martinsalice@gmail.com.
Gontijo CMF, Melo MN, 2004. Visceral leishmaniasis in Brazil: current status, challenges and prospects. Rev Bras Epidemiol 7: 338–349.
Ministério da Saúde, Secretaria de Vigilância em Saúde. Departamento de Vigilância Epidemiológica, Brasil, 2006. Manual de vigilância e controle da leishmaniose visceral (Série A. Normas e Manuais Técnicos). Brasília, Brazil: Ministério da Saúde.
Clementi A, Battaglia G, Floris M, Castellino P, Ronco C, Cruz DN, 2011. Renal involvement in leishmaniasis: a review of the literature. NDT Plus 4: 147–152.
Barsoum RS, 2013. Parasitic kidney disease: milestones in the evolution of our knowledge. Am J Kidney Dis 61: 501–513.
Lima Verde FA, Santos GM, Lima Verde FAA, Daher EF, Saboia Neto A, Lima Verde EM, 2008. Acid-base disturbances in visceral leishmaniasis. J Bras Neurol 30: 172–179.
Lima Verde FAA, Lima Verde FA, Daher EF, Santos GM, Saboia Neto A, Lima Verde EM, 2009. Renal tubular dysfunction in human visceral leishmaniasis (kala-azar). Clin Nephrol 71: 492–500.
Duarte MI, Silva MR, Goto H, 1983. Interstitial nephritis in human kala-azar. Rev Soc Trop Med Hyg 77: 531–537.
Dutra M, Martinelli MR, Carvalho EM, 1985. Renal involvement in visceral leishmaniasis. Am J Kidney Dis 7: 22–27.
Costa CHN, Werneck GL, Costa DL, Holanda TA, Aguiar GB, Carvalho AS, Cavalcanti JC, Santos LS, 2010. Is severe visceral leishmaniasis a systemic inflammatory response syndrome? – A case control study. Rev Soc Bras Med Trop 43: 386–392.
Rado JP, 1978. 1-Desamino-8-D-arginine vasopressin (DDAVP) concentration test. Am J Med Sci 275: 43–52.
Abyholm G, Monn E, 1979. Intranasal DDAVP-test in the study of renal concentrating capacity in children with recurrent urinary tract infections. Eur J Pediatr 130: 149–154.
Tryding N, Sterner G, Berg B, Harris A, Lundin S, 1987. Subcutaneous and intranasal administration of 1-deamino-8-d-arginine vasopressin in the assessment of renal concentration capacity. Nephron 45: 27–30.
Oster JR, 1975. A short duration renal acidification test using calcium chloride. Nephron 14: 281–292.
Oliveira RA, Diniz LF, Teotônio LO, Lima CG, Mota RM, Martins A, Sanches TR, Seguro AC, Andrade L, Silva GB Jr, Libório AB, Daher EF, 2011. Renal tubular dysfunction in patients with American cutaneous leishmaniasis. Kidney Int 80: 1099–1106.
Oliveira MJC, Silva Junior GB, Abreu KL, Rocha NA, Garcia AV, Franco LF, Mota RM, Libório AB, Daher EF, 2010. Risk factors for acute kidney injury in visceral leishmaniasis (Kala-Azar). Am J Trop Med Hyg 82: 449–453.
Wu HY, Huang JW, Peng YS, Hung KY, Wu KD, Lai MS, Chien KL, 2013. Microalbuminuria screening for detecting chronic kidney disease in the general population: a systematic review. Ren Fail 35: 607–614.
Conductier G, Blondeau N, Guyon A, Nahon JL, Rovère C, 2010. The role of monocyte chemoattractant protein MCP1/CCL2 in neuroinflammatory diseases. J Neuroimmunol 224: 93–100.
Hodgkins KS, Schnaper HW, 2012. Tubulointerstitial injury and progression of chronic kidney disease. Pediatr Nephrol 27: 901–909.
Grandaliano G, Gesulado L, Ranieri E, Monno R, Montinaro V, Marra F, Schena FP, 1996. Monocyte chemotactic peptide-1 expression in acute and chronic human nephritides: a patogenetic role in interstitial monocytes recruitment. J Am Soc Nephrol 7: 906–913.
Eardley KS, Zehnder D, Quinkler M, Lepenies J, Bates RL, Savage CO, Howie AJ, Adu D, Cockwell P, 2006. The relationship between albuminuria, MCP-1/CCL2, and interstitial macrophages in chronic kidney disease. Kidney Int 69: 1189–1197.
Hanemann ALP, Libório AB, Daher EF, Martins AM, Pinheiro MC, Sousa MS, Bezerra FS, 2013. Monocyte chemotactic protein-1 (MCP-1) in patients with chronic schistosomiasis mansoni: evidences of subclinical renal inflammation. PLoS ONE 8: e80421.
Heidarpour M, Soltani S, Mohri M, Khoshnegah J, 2012. Canine visceral leishmaniasis: relationships between oxidative stress, liver and kidney variables, trace elements and clinical status. Parasitol Res 111: 1491–1496.
Past two years | Past Year | Past 30 Days | |
---|---|---|---|
Abstract Views | 611 | 542 | 56 |
Full Text Views | 288 | 12 | 0 |
PDF Downloads | 82 | 11 | 0 |