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Type 2 Diabetes, Skin Autof luorescence, and Brain Atrophy

机译:2型糖尿病,皮肤自发荧光和脑萎缩

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摘要

Type 2 diabetes mellitus (T2DM) is associated with brain atrophy, but the mechanisms underlying this link are unknown. Advanced glycation end products (AGEs) accumulate in T2DM, resulting in inflammation, oxida-tive stress, and protein cross-linking, which are known contributors to neurodegeneration. We aimed to study whether tissue AGE accumulation is associated with T2DM-related brain atrophy. We performed brain magnetic resonance imaging, cognitive tests, and noninva-sive skin autofluorescence (SAF; a measure of tissue AGE levels) on people aged >55 years with and without T2DM. Multivariable linear regression was used to study the relationships among T2DM, SAF, and gray matter volume (GMV). There were 486 people included in the study. T2DM was associated with greater SAF. Greater SAF, T2DM, and cognitive impairment were each associated with lower GMV independently of age, sex, and total intracranial volume. SAF partially mediated the association between T2DM and GMV. Longitudinal studies may help confirm whether tissue AGE accumulation is associated with brain atrophy in T2DM.
机译:2型糖尿病(T2DM)与脑萎缩相关,但这种联系的潜在机制尚不清楚。晚期糖基化终产物(AGEs)积累在T2DM中,导致炎症,氧化应激和蛋白质交联,这是导致神经退行性变的已知原因。我们旨在研究组织AGE积累是否与T2DM相关的脑萎缩相关。我们对患有和不患有T2DM的> 55岁人群进行了脑磁共振成像,认知测试和无创皮肤自发荧光(SAF;组织AGE水平的测定)。多变量线性回归用于研究T2DM,SAF和灰质体积(GMV)之间的关系。该研究包括486人。 T2DM与更高的SAF相关。独立于年龄,性别和总颅内体积,较高的SAF,T2DM和认知障碍均与较低的GMV相关。 SAF部分介导了T2DM与GMV之间的关联。纵向研究可能有助于确认组织AGE积累是否与T2DM中的脑萎缩有关。

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  • 来源
    《Diabetes》 |2015年第1期|279-283|共5页
  • 作者单位

    Stroke and Ageing Research Group, Department of Medicine, Southern Clinical School, Monash University, Melbourne, Victoria, Australia,Neurosciences, Monash Medical Centre, Monash Health, Melbourne, Australia;

    Department of Pharmacology, School of Medicine, University of Western Sydney, New South Wales, Australia,Molecular Medicine Research Group, University of Western Sydney, New South Wales, Australia;

    Translational Research Institute, Mater University of Queensland, Brisbane, Queensland, Australia,Mater Clinical School, University of Queensland, Brisbane, Queensland, Australia;

    Stroke and Ageing Research Group, Department of Medicine, Southern Clinical School, Monash University, Melbourne, Victoria, Australia,Neurosciences, Monash Medical Centre, Monash Health, Melbourne, Australia,Developmental Imaging, Murdoch Children's Research Institute, Melbourne, Australia;

    Menzies Research Institute Tasmania, Hobart, Tasmania, Australia;

    Menzies Research Institute Tasmania, Hobart, Tasmania, Australia;

    Stroke and Ageing Research Group, Department of Medicine, Southern Clinical School, Monash University, Melbourne, Victoria, Australia,Neurosciences, Monash Medical Centre, Monash Health, Melbourne, Australia;

    Stroke and Ageing Research Group, Department of Medicine, Southern Clinical School, Monash University, Melbourne, Victoria, Australia,Neurosciences, Monash Medical Centre, Monash Health, Melbourne, Australia,Developmental Imaging, Murdoch Children's Research Institute, Melbourne, Australia;

    Stroke and Ageing Research Group, Department of Medicine, Southern Clinical School, Monash University, Melbourne, Victoria, Australia,Neurosciences, Monash Medical Centre, Monash Health, Melbourne, Australia,Menzies Research Institute Tasmania, Hobart, Tasmania, Australia;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:46:14

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