PMID- 24843699 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20140520 LR - 20211021 IS - 2040-1116 (Print) IS - 2040-1124 (Electronic) IS - 2040-1116 (Linking) VI - 4 IP - 5 DP - 2013 Sep 13 TI - Serum arylhydrocarbon receptor transactivating activity is elevated in type 2 diabetic patients with diabetic nephropathy. PG - 483-91 LID - 10.1111/jdi.12081 [doi] AB - AIMS/INTRODUCTION: Evidence is emerging that exposure to persistent organic pollutants (POPs) is a risk factor for obesity-related diseases and for diabetes mellitus (DM). We found that POPs could be measured by a cell-based arylhydrocarbon receptor (AhR)-dependent reporter assay. We tested if serum AhR transactivating (AHRT) activities are a risk factor for diabetic nephropathy in people with type 2 diabetes. MATERIALS AND METHODS: We enrolled diabetic patients with normoalbuminuria (n = 36), microalbuminuria (n = 29), macroalbuminuria (n = 8) and end-stage renal disease (n = 31). Sera were tested for their AHRT activities, which were standardized by an AhR ligand, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and expressed as TCDD equivalents (TCDDeq pmol/L). RESULTS: Mean serum AHRT activities were higher in patients with microalbuminuria (40.1 +/- 7.1 pmol/L), macroalbuminuria (37.4 +/- 5.5 pmol/L) and end-stage renal disease (59.1 +/- 20.0 pmol/L) than in subjects with normoalbuminuria (12.7 +/- 5.4 pmol/L; P < 0.05 for all comparisons). Serum AhR ligands showed a correlation with estimated glomerular filtration rate (eGFR; r = -0.663, P < 0.001), serum creatinine level (r = 0.635, P < 0.001), systolic blood pressure (r = 0.223, P = 0.026), glycated hemoglobim (r = 0.339, P < 0.001) and diabetic duration (r = 0.394, P < 0.001). In a multiple regression analysis, diabetic nephropathy was found to be an independent risk factor for higher AHRT activity after controlling for the confounding factors. CONCLUSIONS: The present findings suggest serum AHRT activity, thus serum AhR ligands, is a risk factor for diabetic nephropathy. Further studies are required to clarify if an accumulation of POPs in the body is causally related to diabetic nephropathy. FAU - Kim, Jin Taek AU - Kim JT AD - Department of Internal Medicine College of Medicine Eulji University Seoul Korea. FAU - Kim, Sang Soo AU - Kim SS AD - Eulji Medi-Bio Research Institute Seoul Korea. FAU - Jun, Dae Won AU - Jun DW AD - Department of Internal Medicine College of Medicine Hanyang University Seoul Korea. FAU - Hwang, Young Hwan AU - Hwang YH AD - Department of Internal Medicine College of Medicine Eulji University Seoul Korea. FAU - Park, Wook-Ha AU - Park WH AD - Department of Physiology College of Medicine Kyung Hee University Seoul Korea. FAU - Pak, Youngmi Kim AU - Pak YK AD - Department of Physiology College of Medicine Kyung Hee University Seoul Korea. FAU - Lee, Hong Kyu AU - Lee HK AD - Department of Internal Medicine College of Medicine Eulji University Seoul Korea. LA - eng PT - Journal Article DEP - 20130422 PL - Japan TA - J Diabetes Investig JT - Journal of diabetes investigation JID - 101520702 PMC - PMC4025111 OTO - NOTNLM OT - Aryl hydrocarbon receptor ligands OT - Diabetic nephropathy OT - Persistent organic pollutants EDAT- 2014/05/21 06:00 MHDA- 2014/05/21 06:01 PMCR- 2013/09/13 CRDT- 2014/05/21 06:00 PHST- 2012/08/24 00:00 [received] PHST- 2013/02/20 00:00 [revised] PHST- 2013/02/22 00:00 [accepted] PHST- 2014/05/21 06:00 [entrez] PHST- 2014/05/21 06:00 [pubmed] PHST- 2014/05/21 06:01 [medline] PHST- 2013/09/13 00:00 [pmc-release] AID - JDI12081 [pii] AID - 10.1111/jdi.12081 [doi] PST - ppublish SO - J Diabetes Investig. 2013 Sep 13;4(5):483-91. doi: 10.1111/jdi.12081. Epub 2013 Apr 22.