Heredity of type 2 diabetes confers increased susceptibility to oxidative stress and inflammation

Introduction and objectiveHeredity of type 2 diabetes mellitus (T2DM) is associated with greater risk for developing T2DM. Thus, individuals who have a first-degree relative with T2DM (FDRT) provide a natural model to study factors of susceptibility towards development of T2DM, which are poorly unde...

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Veröffentlicht in:BMJ open diabetes research & care 2020-01, Vol.8 (1), p.e000945, Article 000945
Hauptverfasser: Baig, Sonia, Shabeer, Muhammad, Parvaresh Rizi, Ehsan, Agarwal, Madhur, Lee, Michelle H, Ooi, Delicia Shu Qin, Chia, Chelsea, Aung, Nweni, Ng, Geelyn, Teo, Yvonne, Chhay, Vanna, Magkos, Faidon, Vidal-Puig, Antonio, Seet, Raymond C S, Toh, Sue-Anne
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Sprache:eng
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Zusammenfassung:Introduction and objectiveHeredity of type 2 diabetes mellitus (T2DM) is associated with greater risk for developing T2DM. Thus, individuals who have a first-degree relative with T2DM (FDRT) provide a natural model to study factors of susceptibility towards development of T2DM, which are poorly understood. Emerging key players in T2DM pathophysiology such as adverse oxidative stress and inflammatory responses could be among possible mechanisms that predispose FDRTs to develop T2DM. Here, we aimed to examine the role of oxidative stress and inflammatory responses as mediators of this excess risk by studying dynamic postprandial responses in FDRTs.Research design and methodsIn this open-label case-control study, we recruited normoglycemic men with (n=9) or without (n=9) a family history of T2DM. We assessed plasma glucose, insulin, lipid profile, cytokines and F2-isoprostanes, expression levels of oxidative and inflammatory genes/proteins in circulating mononuclear cells (MNC), myotubes and adipocytes at baseline (fasting state), and after consumption of a carbohydrate-rich liquid meal or insulin stimulation.ResultsPostprandial glucose and insulin responses were not different between groups. Expression of oxidant transcription factor NRF2 protein (p
ISSN:2052-4897
2052-4897
DOI:10.1136/bmjdrc-2019-000945