Renal and Vascular Effects of Uric Acid Lowering in Normouricemic Patients With Uncomplicated Type 1 Diabetes

被引:31
作者
Lytvyn, Yuliya [1 ,2 ]
Har, Ronnie [1 ]
Locke, Amy [1 ]
Lai, Vesta [1 ]
Fong, Derek [1 ]
Advani, Andrew [3 ,4 ]
Perkins, Bruce A. [5 ]
Cherney, David Z. I. [1 ]
机构
[1] Univ Toronto, Dept Med, Div Nephrol, Toronto Gen Hosp, Toronto, ON, Canada
[2] Univ Toronto, Dept Pharmacol & Toxicol, Toronto, ON, Canada
[3] St Michaels Hosp, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada
[4] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[5] Univ Toronto, Dept Med, Div Endocrinol & Metab, Mt Sinai Hosp, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
BETA-CELL REPLICATION; ADENOSINE KINASE; INSULIN-RESISTANCE; PROLIFERATION; MICE; GENE; REGENERATION; INHIBITION; EXPRESSION; EXPANSION;
D O I
10.2337/db17-0168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Higher plasma uric acid (PUA) levels are associated with lower glomerular filtration rate (GFR) and higher blood pressure (BP) in patients with type 1 diabetes (T1D). Our aim was to determine the impact of PUA lowering on renal and vascular function in patients with uncomplicated T1D. T1D patients (n = 49) were studied under euglycemic and hyperglycemic conditions at baseline and after PUA lowering with febuxostat (FBX) for 8 weeks. Healthy control subjects were studied under normoglycemic conditions (n = 24). PUA, GFR (inulin), effective renal plasma flow (para-aminohippurate), BP, and hemodynamic responses to an infusion of angiotensin II (assessment of intrarenal renin-angiotensin-aldosterone system [RAAS]) were measured before and after FBX treatment. Arterial stiffness, flow-mediated dilation (FMD), nitroglycerin-mediated dilation (GMD), urinary nitric oxide (NO), and inflammatory markers were measured before and after FBX treatment. Gomez equations were used to estimate arteriolar afferent resistance, efferent resistance (R-E), and glomerular hydrostatic pressure (P-GLO). FBX had a modest systolic BP-lowering effect in T1D patients (112 +/- 10 to 109 +/- 9 mmHg, P = 0.049) without impacting arterial stiffness, FMD, GMD, or NO. FBX enhanced the filtration fraction response to hyperglycemia in T1D patients through larger increases in R-E, P-GLO, and interleukin-18 but without impacting the RAAS. FBX lowered systolic BP and modulated the renal R-E responses to hyperglycemia but without impacting the RAAS or NO levels, suggesting that PUA may augment other hemodynamic or inflammatory mechanisms that control the renal response to hyperglycemia at the efferent arteriole. Ongoing outcome trials will determine cardiorenal outcomes of PUA lowering in patients with T1D.
引用
收藏
页码:1939 / 1949
页数:11
相关论文
共 40 条
[11]   Subcellular localization of adenosine kinase in mammalian cells: The long isoform of AdK is localized in the nucleus [J].
Cui, Xianying Amy ;
Singh, Bhag ;
Park, Jae ;
Gupta, Radhey S. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 388 (01) :46-50
[12]   Inhibition of DYRK1A Stimulates Human β-Cell Proliferation [J].
Dirice, Ercument ;
Walpita, Deepika ;
Vetere, Amedeo ;
Meier, Bennett C. ;
Kahraman, Sevim ;
Hu, Jiang ;
Dancik, Vlado ;
Burns, Sean M. ;
Gilbert, Tamara J. ;
Olson, David E. ;
Clemons, Paul A. ;
Kulkarni, Rohit N. ;
Wagner, Bridget K. .
DIABETES, 2016, 65 (06) :1660-1671
[13]   Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation [J].
Dor, Y ;
Brown, J ;
Martinez, OI ;
Melton, DA .
NATURE, 2004, 429 (6987) :41-46
[14]   Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci [J].
Gaulton, Kyle J. ;
Ferreira, Teresa ;
Lee, Yeji ;
Raimondo, Anne ;
Maegi, Reedik ;
Reschen, Michael E. ;
Mahajan, Anubha ;
Locke, Adam ;
Rayner, N. William ;
Robertson, Neil ;
Scott, Robert A. ;
Prokopenko, Inga ;
Scott, Laura J. ;
Green, Todd ;
Sparso, Thomas ;
Thuillier, Dorothee ;
Yengo, Loic ;
Grallert, Harald ;
Wahl, Simone ;
Franberg, Mattias ;
Strawbridge, Rona J. ;
Kestler, Hans ;
Chheda, Himanshu ;
Eisele, Lewin ;
Gustafsson, Stefan ;
Steinthorsdottir, Valgerdur ;
Thorleifsson, Gudmar ;
Qi, Lu ;
Karssen, Lennart C. ;
van Leeuwen, Elisabeth M. ;
Willems, Sara M. ;
Li, Man ;
Chen, Han ;
Fuchsberger, Christian ;
Kwan, Phoenix ;
Ma, Clement ;
Linderman, Michael ;
Lu, Yingchang ;
Thomsen, Soren K. ;
Rundle, Jana K. ;
Beer, Nicola L. ;
van de Bunt, Martijn ;
Chalisey, Anil ;
Kang, Hyun Min ;
Voight, Benjamin F. ;
Abecasis, Goncalo R. ;
Almgren, Peter ;
Baldassarre, Damiano ;
Balkau, Beverley ;
Benediktsson, Rafn .
NATURE GENETICS, 2015, 47 (12) :1415-+
[15]   p16Ink4a-induced senescence of pancreatic beta cells enhances insulin secretion [J].
Helman, Aharon ;
Klochendler, Agnes ;
Azazmeh, Narmen ;
Gabai, Yael ;
Horwitz, Elad ;
Anzi, Shira ;
Swisa, Avital ;
Condiotti, Reba ;
Granit, Roy Z. ;
Nevo, Yuval ;
Fixler, Yaakov ;
Shreibman, Dorin ;
Zamir, Amit ;
Tornovsky-Babeay, Sharona ;
Dai, Chunhua ;
Glaser, Benjamin ;
Powers-, Alvin C. ;
Shapiro, A. M. James ;
Magnuson, Mark A. ;
Dor, Yuval ;
Ben-Porath, Ittai .
NATURE MEDICINE, 2016, 22 (04) :412-+
[16]   Chronic hyperglycemia triggers loss of pancreatic β cell differentiation in an animal model of diabetes [J].
Jonas, JC ;
Sharma, A ;
Hasenkamp, W ;
Ilkova, H ;
Patanè, G ;
Laybutt, R ;
Bonner-Weir, S ;
Weir, GC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (20) :14112-14121
[17]   PDX-1 haploinsufficiency limits the compensatory islet hyperplasia that occurs in response to insulin resistance [J].
Kulkarni, RN ;
Jhala, US ;
Winnay, JN ;
Krajewski, S ;
Montminy, M ;
Kahn, CR .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (06) :828-836
[18]   RIP-Cre revisited, evidence for impairments of pancreatic β-cell function [J].
Lee, JY ;
Ristow, M ;
Lin, XY ;
White, MF ;
Magnuson, MA ;
Hennighausen, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (05) :2649-2653
[19]   DYRK1A protein kinase promotes quiescence and senescence through DREAM complex assembly [J].
Litovchick, Larisa ;
Florens, Laurence A. ;
Swanson, Selene K. ;
Washburn, Michael P. ;
DeCaprio, James A. .
GENES & DEVELOPMENT, 2011, 25 (08) :801-813
[20]   β-Cell replication is the primary mechanism subserving the postnatal expansion of β-cell mass in humans [J].
Meier, Juris J. ;
Butler, Alexandra E. ;
Saisho, Yoshifumi ;
Monchamp, Travis ;
Galasso, Ryan ;
Bhushan, Anil ;
Rizza, Robert A. ;
Butler, Peter C. .
DIABETES, 2008, 57 (06) :1584-1594