Thioredoxin interacting protein expression in the urinary sediment associates with renal function decline in type 1 diabetes. (2nd January 2016)

• Record Type: Journal Article
• Authors: Monteiro, Maria Beatriz; Santos-Bezerra, Daniele Pereira; Thieme, Karina; Admoni, Sharon Nina; Perez, Ricardo Vessoni; Machado, Cleide Guimarães; Queiroz, Marcia Silva; Nery, Marcia; Oliveira-Souza, Maria; Woronik, Viktoria; Passarelli, Marisa; Giannella-Neto, Daniel; Machado, Ubiratan Fabres; Corrêa-Giannella, Maria Lúcia
• Is Part Of: Free radical research. Volume 50:Number 1(2016:Jan.)
• Page Start: 101
• Page End: 110
• Publication Date: 2016-01-02
• Subjects: Diabetic complications -- diabetic kidney disease -- oxidative stress -- PBMC -- urinary sediment; Free radicals (Chemistry) -- Periodicals; Antioxidants -- Periodicals; Vitamin C -- Periodicals; Vitamin E -- Periodicals; 541.224
• DOI: 10.3109/10715762.2015.1109083
• Languages: English
• ISSNs: 1071-5762

Abstract

ABSTRACT: Aims : Thioredoxin interacting protein (TXNIP), an inhibitor of antioxidant thioredoxin (Trx), is upregulated by hyperglycemia and implicated in pathogenesis of diabetes complications. We evaluated mRNA expressions of genes encoding TXNIP and Trx ( TXN ) in urinary sediment and peripheral blood mononuclear cells (PBMC) of type 1 diabetes (T1D) patients with different degrees of chronic complications. Methods : qPCR was employed to quantify target genes in urinary sediment ( n = 55) and PBMC ( n = 161) from patients sorted by presence or absence of diabetic nephropathy (DN), retinopathy, peripheral and cardiovascular neuropathy; 26 healthy controls and 13 patients presenting non-diabetic nephropathy (focal and segmental glomerulosclerosis, FSGS) were also included. Results : Regarding the urinary sediment, TXNIP (but not TXN ) expression was higher in T1D ( p = 0.0023) and FSGS ( p = 0.0027) patients versus controls. Expressions of TXNIP and TXN were higher, respectively, in T1D patients with versus without DN ( p = 0.032) and in those with estimated glomerular filtration rate (eGFR) < 60 versus ≥60 mL/min/1.73 m 2 ( p = 0.008). eGFR negatively correlated with TXNIP ( p = 0.04, r = −0.28) and TXN ( p = 0.04, r = −0.30) expressions. T1D patients who lost ≥5 mL/min/1.73 m 2 yearly of eGFR presented higher basal TXNIP expression than those who lost <5 mL/min/1.73 m 2 yearly after median follow-up of 24 months. TXNIP ( p < 0.0001) and TXN ( p = 0.002) expressions in PBMC of T1D patients were significantly higher than in controls but no differences were observed between patients with or without chronic complications. Conclusions : TXNIP and TXN are upregulated in urinary sediment of T1D patients with diabetic kidney disease (DKD), but only TXNIP expression is associated with magnitude of eGFR decline.