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Cell. 2006;127:1109–22.PubMedCrossRef 24. Milne JC, Lambert PD, Schenk S, Carney DP, Smith JJ, Gagne DJ, et al. Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes. Nature. 2007;450:712–6.PubMedCrossRef 25. Zillikens MC, van Meurs JB, Rivadeneira F, Amin N, Hofman A, LY333531 clinical trial Oostra BA, et al. SIRT1 genetic variation is related to BMI and risk of obesity. Diabetes. 2009;58:2828–34.PubMedCrossRef”
“To the Editor We read with interest the recent work: “Minimal change nephrotic syndrome in a patient with strongyloidiasis” [1] where Dr. Miyzaki and colleagues quote 15 reported cases RXDX-101 concentration of nephropathy associated with Strongyloides stercoralis (Ss). We would like to add to this list another case

that we reported in 2007 regarding this topic [2]. A 25-year-old

male, born in Ecuador and living in Italy from 3 years of age, developed fever, vomiting, malnutrition, Selleckchem AZD5363 abdominal pain, watery diarrhea, dehydration with arterial hypertension and edema in both lower extremities. On admission, laboratory tests showed proteinuria (4 g/day), hypoalbuminemia (1.9 g/dl), hypercholesterolemia, eosinophilia and low platelets. Renal and liver function tests, serum immunoglobulin and complement, antinuclear antibodies, ANCA were unremarkable; HAV, HBV, HCV, HIV, VDRL, BK detection and fecal and urine cultures were negative. Screening stool for rhabditiform Ss larvae was positive. Hemoculture was positive for Escherichia coli. The renal biopsy specimen contained 32 glomeruli under

light microscopy examination and all had a normal appearance. No vascular or tubularinterstitial lesions were seen. Immunofluorescent studies were negative for IgA, IgG, IgM, light chains, C1q, C3, C4 and fibrinogen. The electron microscopic examination showed disappearance of slight diaphragms and moderate fusion of foot processes of glomerular epithelial cells, associated with microvillous degeneration and sometimes with a tortuous course of the basement membrane. We made Sirolimus ic50 a diagnosis of minimal change disease. The patient was treated with prednisone (1 mg/kg/day), sulfamethoxazole−trimethoprim (800–160 mg twice a day) and albendazole (400 mg twice a day for 3 days); sepsis cleared up quickly and the patient was discharged; however, 3 months later he was admitted again because of acute renal failure, diarrhea and nephrotic syndrome. We detected rhabditiform Ss larvae and IgG anti-Ss (283 UI/ml). The patient was successfully treated with ivermectin; screening for rhabditiform Ss larvae and IgG anti-Ss became negative with recovery of normal renal function. Six months later the patient did not show any sign of parasitic infection but there was proteinuria (1 g/day) without any other sign of nephrotic syndrome. Afterwards the patient was lost to follow-up. Conflict of interest All the authors have declared no competing interest. References 1. Miyazaki M, Tamura M, Kabashima N, Serino R, Shibata T, Miyamoto T, et al.

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