Literature DB >> 15996650

Complement activation and diabetic vascular complications.

Jakob Østergaard1, Troels Krarup Hansen, Steffen Thiel, Allan Flyvbjerg.   

Abstract

Diabetes mellitus is a major and increasing health problem worldwide. One of the most serious consequences of diabetes is the development of diabetic angiopathy, which includes cardiovascular disease, neuropathy, retinopathy and nephropathy. Diabetic nephropathy alone affects 15-25% of patients with type 1 diabetes and 30-40% of patients with type 2 diabetes and is the single-most important cause of end-stage renal failure in the Western World. Existing research has demonstrated the involvement of glycation factors, growth factors/cytokines, hemodynamic factors and intracellular changes in the pathogenesis of diabetic kidney disease. An emerging amount of recent data suggests that the complement system, especially the MBL pathway, plays an important role in the pathogenesis of diabetic vascular complications. Although the numerous therapeutic interventions available today may delay the development and progression of diabetes vascular complications, there is an ongoing need for new therapeutic strategies. In this article the evidence for a connection between the complement system and vascular dysfunction will be reviewed, with a special focus on the relation to diabetic kidney disease. Several ways of specifically manipulating the complement system already exist. However, whether or not these drugs provide new targets for intervention on diabetic vascular complications is still unknown.

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Year:  2005        PMID: 15996650     DOI: 10.1016/j.cccn.2005.04.028

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  30 in total

Review 1.  Complement activation in progressive renal disease.

Authors:  Amy Fearn; Neil Stephen Sheerin
Journal:  World J Nephrol       Date:  2015-02-06

2.  Plasma levels of MASP-1, MASP-3 and MAp44 in patients with type 2 diabetes: influence of glycaemic control, body composition and polymorphisms in the MASP1 gene.

Authors:  S S Krogh; C B Holt; R Steffensen; K L Funck; P Høyem; E Laugesen; P L Poulsen; S Thiel; T K Hansen
Journal:  Clin Exp Immunol       Date:  2017-04-20       Impact factor: 4.330

3.  Diabetes-induced renal injury in rats is attenuated by suramin.

Authors:  Midhun C Korrapati; Brooke E Shaner; Benjamin A Neely; Joseph L Alge; John M Arthur; Rick G Schnellmann
Journal:  J Pharmacol Exp Ther       Date:  2012-06-26       Impact factor: 4.030

4.  The mannose-binding lectin pathway is a significant contributor to reperfusion injury in the type 2 diabetic heart.

Authors:  Laura R La Bonte; Betsy Dokken; Grace Davis-Gorman; Gregory L Stahl; Paul F McDonagh
Journal:  Diab Vasc Dis Res       Date:  2009-07       Impact factor: 3.291

Review 5.  Role of the Immune System in Diabetic Kidney Disease.

Authors:  Fionnuala B Hickey; Finian Martin
Journal:  Curr Diab Rep       Date:  2018-03-12       Impact factor: 4.810

6.  Mannose-binding lectin deficiency attenuates renal changes in a streptozotocin-induced model of type 1 diabetes in mice.

Authors:  J Østergaard; S Thiel; M Gadjeva; T K Hansen; R Rasch; A Flyvbjerg
Journal:  Diabetologia       Date:  2007-05-01       Impact factor: 10.122

7.  Enhanced complement activation is part of the unfavourable cardiovascular risk profile in South Asians.

Authors:  M A Siezenga; P K Chandie Shaw; R N van der Geest; T E Mollnes; M R Daha; T J Rabelink; S P Berger
Journal:  Clin Exp Immunol       Date:  2009-07       Impact factor: 4.330

8.  Mannose-Binding Lectin and Diabetic Nephropathy in Type 1 Diabetes.

Authors:  Shi-Qi Zhao; Zhao Hu
Journal:  J Clin Lab Anal       Date:  2015-07-24       Impact factor: 2.352

9.  Complement C5a induces mesenchymal stem cell apoptosis during the progression of chronic diabetic complications.

Authors:  Ming Zhu; Xiao He; Xiao-Hui Wang; Wei Qiu; Wei Xing; Wei Guo; Tian-Chen An; Luo-Quan Ao; Xue-Ting Hu; Zhan Li; Xiao-Ping Liu; Nan Xiao; Jian Yu; Hong Huang; Xiang Xu
Journal:  Diabetologia       Date:  2017-06-03       Impact factor: 10.122

10.  Mice lacking C1q are protected from high fat diet-induced hepatic insulin resistance and impaired glucose homeostasis.

Authors:  Antoinette D Hillian; Megan R McMullen; Becky M Sebastian; Sanjoy Roychowdhury; Sanjoy Rowchowdhury; Sangeeta R Kashyap; Philip R Schauer; John P Kirwan; Ariel E Feldstein; Laura E Nagy
Journal:  J Biol Chem       Date:  2013-06-20       Impact factor: 5.157

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