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Increased Plasma Soluble Interleukin-2 Receptor Alpha Levels in Patients With Long-Term Type 1 Diabetes With Vascular Complications Associated With IL2RA and PTPN2 Gene Polymorphisms

Keindl, Magdalena (författare)
University of Bergen
Fedotkina, Olena (författare)
University of Bergen
du Plessis, Elsa (författare)
University of Bergen
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Jain, Ruchi (författare)
Lund University,Lunds universitet,Diabetes - öpatofysiologi,Forskargrupper vid Lunds universitet,Diabetes - Islet Patophysiology,Lund University Research Groups
Bergum, Brith (författare)
Karolinska Institutet
Mygind Jensen, Troels (författare)
Steno Diabetes Center Copenhagen,University of Southern Denmark
Laustrup Moller, Cathrine (författare)
Steno Diabetes Center Copenhagen
Falhammar, Henrik (författare)
Karolinska Institutet,Karolinska Institute,Karolinska University Hospital
Nyström, Thomas (författare)
Karolinska Institutet
Catrina, Sergiu-Bogdan (författare)
Karolinska Institute,Karolinska University Hospital
Jörneskog, Gun (författare)
Danderyd Hospital
Groop, Leif (författare)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups,Institute for Molecular Medicine Finland (FIMM),University of Helsinki
Eliasson, Mats (författare)
Umeå University,Umeå universitet,Avdelningen för medicin
Eliasson, Björn, 1959 (författare)
Gothenburg University,Göteborgs universitet,University of Gothenburg,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
Brismar, Kerstin (författare)
Karolinska Institutet
Nilsson, Peter M. (författare)
Lund University,Lunds universitet,Internmedicin - epidemiologi,Forskargrupper vid Lunds universitet,Internal Medicine - Epidemiology,Lund University Research Groups
Berg, Tore Julsrud (författare)
University of Oslo
Appel, Silke (författare)
University of Bergen
Lyssenko, Valeriya (författare)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups,University of Bergen
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 (creator_code:org_t)
2020-10-30
2020
Engelska.
Ingår i: Frontiers in Endocrinology. - : Frontiers Media S.A.. - 1664-2392. ; 11
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Type 1 diabetes (T1D) is largely considered an autoimmune disease leading to the destruction of insulin-producing pancreatic beta cells. Further, patients with T1D have 3-4-fold increased risk of developing micro- and macrovascular complications. However, the contribution of immune-related factors contributing to these diabetes complications are poorly understood. Individuals with long-term T1D who do not progress to vascular complications offer a great potential to evaluate end-organ protection. The aim of the present study was to investigate the association of inflammatory protein levels with vascular complications (retinopathy, nephropathy, cardiovascular disease) in individuals with long-term T1D compared to individuals who rapidly progressed to complications. We studied a panel of inflammatory markers in plasma of patients with long-term T1D with (n = 81 and 26) and without (n = 313 and 25) vascular complications from two cross-sectional Scandinavian cohorts (PROLONG and DIALONG) using Luminex technology. A subset of PROLONG individuals (n = 61) was screened for circulating immune cells using multicolor flow cytometry. We found that elevated plasma levels of soluble interleukin-2 receptor alpha (sIL-2R) were positively associated with the complication phenotype. Risk carriers of polymorphisms in the IL2RA and PTPN2 gene region had elevated plasma levels of sIL-2R. In addition, cell surface marker analysis revealed a shift from naive to effector T cells in T1D individuals with vascular complications as compared to those without. In contrast, no difference between the groups was observed either in IL-2R cell surface expression or in regulatory T cell population size. In conclusion, our data indicates that IL2RA and PTPN2 gene variants might increase the risk of developing vascular complications in people with T1D, by affecting sIL-2R plasma levels and potentially lowering T cell responsiveness. Thus, elevated sIL-2R plasma levels may serve as a biomarker in monitoring the risk for developing diabetic complications and thereby improve patient care.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

cardiovascular disease
Cluster of Differentiation 25 (CD25)
diabetes complications
nephropathy
regulatory T cells
retinopathy
sIL-2R
cardiovascular disease
Cluster of Differentiation 25 (CD25)
diabetes complications
nephropathy
regulatory T cells
retinopathy
sIL-2R

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ref (ämneskategori)
art (ämneskategori)

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