CYSTATIN C AS A MARKER OF IMMUNE COMPLEX–ASSOCIATED RENAL IMPAIRMENT IN A SUDANESE POPULATION WITH VISCERAL LEISHMANIASIS

AMIR IBRAHIM ELSHAFIE Department of Clinical Pathology and Microbiology, Alribat University Hospital, Khartoum, Sudan; Department of Immunology, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia; Department of Microbiology and Immunology, University of Khartoum, Khartoum, Sudan; Department of Oncology, Radiology and Clinical Immunology, University of Uppsala, Uppsala, Sweden; Department of Medical Sciences, University of Uppsala, Uppsala, Sweden

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GEHAD ELGHAZALI Department of Clinical Pathology and Microbiology, Alribat University Hospital, Khartoum, Sudan; Department of Immunology, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia; Department of Microbiology and Immunology, University of Khartoum, Khartoum, Sudan; Department of Oncology, Radiology and Clinical Immunology, University of Uppsala, Uppsala, Sweden; Department of Medical Sciences, University of Uppsala, Uppsala, Sweden

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JOHAN RÖNNELID Department of Clinical Pathology and Microbiology, Alribat University Hospital, Khartoum, Sudan; Department of Immunology, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia; Department of Microbiology and Immunology, University of Khartoum, Khartoum, Sudan; Department of Oncology, Radiology and Clinical Immunology, University of Uppsala, Uppsala, Sweden; Department of Medical Sciences, University of Uppsala, Uppsala, Sweden

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PER VENGE Department of Clinical Pathology and Microbiology, Alribat University Hospital, Khartoum, Sudan; Department of Immunology, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia; Department of Microbiology and Immunology, University of Khartoum, Khartoum, Sudan; Department of Oncology, Radiology and Clinical Immunology, University of Uppsala, Uppsala, Sweden; Department of Medical Sciences, University of Uppsala, Uppsala, Sweden

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Renal function was studied in visceral leishmaniasis (VL) and post-kala-azar dermal leishmaniasis (PKDL) by means of the specific marker cystatin C and related to circulating immune complexes and cytokine production. Forty patients with VL (23 with sub-acute disease and 17 with acute disease), 17 patients with PKDL, and 22 healthy controls were included. Cystatin C, but not creatinine, was significantly raised in VL (P = 0.004). The highest levels of cystatin C were found in those with acute disease (P < 0.0001). In VL, cystatin C levels were positively correlated to circulating immune complexes and production of granulocyte-macrophage colony stimulating factor (GM-CSF), but negatively correlated to aspartate aminotransferase and lactate dehydrogenase. We conclude that cystatin C is a superior marker of glomerular function in leishmaniasis and that immune complex deposition and GM-CSF are two functions that most likely are causally involved in the mechanisms leading to glomerular dysfunction in leishmaniasis.

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