首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Relationship between the content of lysyl oxidase-dependent cross-links in skin collagen nonenzymatic glycosylation and long-term complications in type I diabetes mellitus.
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Relationship between the content of lysyl oxidase-dependent cross-links in skin collagen nonenzymatic glycosylation and long-term complications in type I diabetes mellitus.

机译:Ⅰ型糖尿病患者皮肤胶原中赖氨酰氧化酶依赖性交联的含量非酶糖基化与长期并发症之间的关系。

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摘要

Many abnormalities in collagen have been reported in insulin-dependent diabetes mellitus, some or all of which have been attributed to increased cross-linking. Although recent work has focused on the role of glucose-derived collagen cross-links in the pathogenesis of diabetic complications, relatively few studies have investigated the role of lysyl oxidase-dependent (LOX) cross-links. In the present study, LOX cross-links and nonenzymatic glycosylation were quantified in skin collagen from diabetic subjects. There was an increase in the difunctional cross-link dihydroxylysinonorleucine (DHLNL) as well as in one of its trifunctional maturation products, hydroxypyridinium. All other LOX crosslinks were normal. Nonenzymatic glycosylation was increased in diabetic skin collagen, and this increase was correlated with increases in DHLNL (P less than 0.001). The biochemical results were examined for correlations with clinical data from the same subjects. Increases in DHLNL content were associated with duration of diabetes (P less than 0.003), glycohemoglobin levels (P less than 0.001), hand contractures (P less than 0.05), skin changes (P less than 0.005), and microalbuminuria (P less than 0.01). In nondiabetic subjects age was not correlated with collagen cross-link content with the exception that his-HLNL increased with age (r = 0.79, P less than 0.02). In diabetic subjects, PA levels decreased with age (r = 0.51, P less than 0.02). With increased duration of diabetes, DHLNL content was increased (r = 0.55, P less than 0.003) and OHP was increased (r = 0.59, P less than 0.01), whereas PA levels were decreased (r = -0.48, P less than 0.04). Nonenzymatic glycosylation of collagen was also increased with increased duration of diabetes (hex-lys, r = 0.47, P less than 0.02; hex-hyl, r = 0.39, P less than 0.05). We conclude that: (a) lysyl oxidase-dependent cross-linking is increased in skin collagen in diabetes and (b) that these changes in skin collagen are correlated with duration of diabetes, glycemic control, and long-term complications.
机译:在胰岛素依赖型糖尿病中已经报道了许多胶原蛋白异常,其中一些或全部归因于交联的增加。尽管最近的工作集中于葡萄糖衍生的胶原蛋白交联在糖尿病并发症发病机理中的作用,但相对较少的研究已经研究了赖氨酰氧化酶依赖性(LOX)交联的作用。在本研究中,LOX交联和非酶糖基化被量化在糖尿病受试者皮肤胶原蛋白中。双功能交联二羟基赖氨酸正亮氨酸(DHLNL)及其三功能成熟产物之一羟基吡啶鎓的含量有所增加。所有其他LOX交叉链接均正常。糖尿病皮肤胶原蛋白的非酶糖基化增加,并且这种增加与DHLNL的增加相关(P小于0.001)。检查了生化结果与来自同一受试者的临床数据的相关性。 DHLNL含量的增加与糖尿病持续时间(P小于0.003),糖化血红蛋白水平(P小于0.001),手挛缩(P小于0.05),皮肤变化(P小于0.005)和微量白蛋白尿(P小于0.01)。在非糖尿病受试者中,年龄与胶原蛋白交联含量无关,只是他的-HLNL随着年龄的增长而增加(r = 0.79,P小于0.02)。在糖尿病患者中,PA水平随年龄而降低(r = 0.51,P小于0.02)。随着糖尿病持续时间的增加,DHLNL含量增加(r = 0.55,P小于0.003),OHP升高(r = 0.59,P小于0.01),而PA水平降低(r = -0.48,P小于0.04)。 )。糖尿病的持续时间也增加了胶原蛋白的非酶糖基化作用(hex-lys,r = 0.47,P小于0.02; hex-hyl,r = 0.39,P小于0.05)。我们得出以下结论:(a)糖尿病患者皮肤胶原中赖氨酰氧化酶依赖性交联增加,并且(b)皮肤胶原中的这些变化与糖尿病持续时间,血糖控制和长期并发症相关。

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