دورية أكاديمية

There Is No Impact of Diabetes on the Endothelial Function of Chronic Kidney Disease Patients.

التفاصيل البيبلوغرافية
العنوان: There Is No Impact of Diabetes on the Endothelial Function of Chronic Kidney Disease Patients.
المؤلفون: Coutinho MN; Federal University of São Paulo, Brazil., Carvalho AB; Federal University of São Paulo, Brazil., Dalboni MA; Federal University of São Paulo, Brazil., Mouro MG; Federal University of São Paulo, Brazil., Higa EMS; Federal University of São Paulo, Brazil., Costa-Hong V; Heart Institute (InCor) of the University of São Paulo Medical School, Brazil., Bortolotto LA; Heart Institute (InCor) of the University of São Paulo Medical School, Brazil., Figueiredo RAO; Folkälsan Research Center, Helsinki, Finland., Canziani MEF; Federal University of São Paulo, Brazil.
المصدر: Journal of diabetes research [J Diabetes Res] 2018 Nov 25; Vol. 2018, pp. 7926473. Date of Electronic Publication: 2018 Nov 25 (Print Publication: 2018).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Hindawi Limited Country of Publication: England NLM ID: 101605237 Publication Model: eCollection Cited Medium: Internet ISSN: 2314-6753 (Electronic) NLM ISO Abbreviation: J Diabetes Res Subsets: MEDLINE
أسماء مطبوعة: Publication: <2019>-: London, United Kingdom : Hindawi Limited
Original Publication: Nasr City, Cairo : Hindawi Publishing Corporation, [2013]-
مواضيع طبية MeSH: Chemokine CXCL12/*blood , Diabetes Mellitus, Type 2/*physiopathology , Endothelium, Vascular/*physiopathology , Renal Insufficiency, Chronic/*physiopathology, Aged ; Aged, 80 and over ; Diabetes Mellitus, Type 2/blood ; Diabetes Mellitus, Type 2/complications ; Endothelial Progenitor Cells ; Female ; Humans ; Male ; Middle Aged ; Nitric Oxide/blood ; Pulse Wave Analysis ; Renal Insufficiency, Chronic/blood ; Renal Insufficiency, Chronic/complications
مستخلص: Background: Patients with chronic kidney disease (CKD) and type 2 diabetes mellitus (DM) have increased risk of endothelial dysfunction, cardiovascular disease, and mortality. Several studies have separately analyzed endothelial function in these populations. However, data of patients with both CKD and DM are scarce. The aim of this study was to evaluate whether the presence of DM has any additional effect on the endothelial dysfunction of CKD patients.
Methods: We measured endothelial progenitor cells (EPCs), stromal-derived factor 1 alpha (SDF-1 α ), serum and urinary nitric oxide (NO), flow-mediated dilation (FMD), and pulse wave velocity (PWV) in 37 CKD patients with DM (CKD-DM group) and in 37 without DM (CKD group).
Results: CKD-DM group had a higher prevalence of obesity ( P < 0.01), previous myocardial infarction ( P = 0.02), myocardial revascularization ( P = 0.04), and a trend for more peripheral artery disease ( P = 0.07). Additionally, CKD-DM group had higher EPC ( P = 0.001) and PWV ( P < 0.001) values. On the other hand, no difference in SDF-1 α and serum or urinary NO and FMD was observed between the groups.
Conclusions: Endothelial dysfunction is frequent in CKD patients, and an additive effect of diabetes cannot be implicated, suggesting the predominant role of uremia in this condition.
References: J Clin Invest. 1999 Nov;104(9):1199-211. (PMID: 10545519)
Br J Clin Pharmacol. 2000 Nov;50(5):397-404. (PMID: 11069434)
Endocr Rev. 2001 Feb;22(1):36-52. (PMID: 11159815)
J Am Coll Cardiol. 2002 Jan 16;39(2):257-65. (PMID: 11788217)
Arterioscler Thromb Vasc Biol. 2004 Jul;24(7):1246-52. (PMID: 15155385)
Am J Kidney Dis. 2004 Nov;44(5):840-9. (PMID: 15492950)
Transplantation. 2005 Apr 27;79(8):941-5. (PMID: 15849547)
Thromb Haemost. 2005 Oct;94(4):770-2. (PMID: 16270628)
Blood Purif. 2006;24(2):196-202. (PMID: 16373998)
Am J Kidney Dis. 2006 Jan;47(1):42-50. (PMID: 16377384)
Am J Transplant. 2006 Dec;6(12):2922-8. (PMID: 17061996)
Am J Physiol Renal Physiol. 2007 Apr;292(4):F1132-40. (PMID: 17200161)
J Cell Mol Med. 2009 Mar;13(3):454-71. (PMID: 19379144)
Kidney Int Suppl. 2009 Aug;(113):S1-130. (PMID: 19644521)
Nephrol Dial Transplant. 2010 Jun;25(6):1875-82. (PMID: 20083473)
Diabet Med. 2010 Jan;27(1):54-60. (PMID: 20121889)
Clin Chim Acta. 2010 Oct 9;411(19-20):1412-20. (PMID: 20598675)
Cardiovasc Res. 2011 Jul 1;91(1):9-15. (PMID: 21186243)
Diabetes Obes Metab. 2011 Aug;13(8):718-25. (PMID: 21410861)
Eur J Pharmacol. 2011 Jun 1;659(2-3):296-301. (PMID: 21453695)
Semin Dial. 2011 May-Jun;24(3):327-37. (PMID: 21682773)
Kidney Blood Press Res. 2011;34(4):284-90. (PMID: 21691132)
Exp Biol Med (Maywood). 2011 Sep;236(9):1085-92. (PMID: 21791552)
Cardiovasc Diabetol. 2011 Dec 20;10:113. (PMID: 22185563)
Diab Vasc Dis Res. 2012 Apr;9(2):109-16. (PMID: 22337893)
Circ Res. 2012 Feb 17;110(4):624-37. (PMID: 22343557)
Contraception. 2012 Jul;86(1):35-41. (PMID: 22465116)
Int J Cardiol. 2013 Sep 20;168(1):344-51. (PMID: 23041097)
Int J Cardiol. 2013 Sep 1;167(5):1688-95. (PMID: 23171577)
Lancet. 2012 Dec 15;380(9859):2095-128. (PMID: 23245604)
Eur Heart J. 2014 Aug 14;35(31):2115-22. (PMID: 24306482)
Int J Hypertens. 2013;2013:876865. (PMID: 24396591)
Arterioscler Thromb Vasc Biol. 2014 Jun;34(6):1136-43. (PMID: 24743430)
Nutr Metab Cardiovasc Dis. 2014 Aug;24(8):815-22. (PMID: 24780515)
Kidney Int. 2015 Jan;87(1):20-30. (PMID: 24786708)
Cardiovasc Diabetol. 2014 Jun 16;13:101. (PMID: 24934236)
Biomed Res Int. 2014;2014:364738. (PMID: 24949439)
Arterioscler Thromb Vasc Biol. 2014 Sep;34(9):2100-5. (PMID: 25060794)
Diabetes Care. 2014 Oct;37(10):2864-83. (PMID: 25249672)
Int J Med Sci. 2016 Feb 20;13(3):240-7. (PMID: 26941585)
Circ Res. 2016 Jun 10;118(12):1930-9. (PMID: 27073015)
Clin J Am Soc Nephrol. 2016 Aug 8;11(8):1384-91. (PMID: 27340284)
Yonsei Med J. 2016 Nov;57(6):1446-53. (PMID: 27593873)
Kidney Blood Press Res. 2016;41(6):1025-1036. (PMID: 28006782)
Circulation. 1993 Dec;88(6):2510-6. (PMID: 8080489)
Nature. 1993 Apr 29;362(6423):801-9. (PMID: 8479518)
J Am Coll Cardiol. 1996 Mar 1;27(3):567-74. (PMID: 8606266)
Lancet. 1996 Dec 21-28;348(9043):1673-4. (PMID: 8973424)
Int J Cardiol. 1997 Dec 1;62 Suppl 1:S43-8. (PMID: 9464583)
المشرفين على المادة: 0 (CXCL12 protein, human)
0 (Chemokine CXCL12)
31C4KY9ESH (Nitric Oxide)
تواريخ الأحداث: Date Created: 20190101 Date Completed: 20190415 Latest Revision: 20220330
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC6286770
DOI: 10.1155/2018/7926473
PMID: 30596103
قاعدة البيانات: MEDLINE