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Intact and total proinsulin: new aspects for diagnosis and treatment of type 2 diabetes mellitus and insulin resistance.

机译:完整胰岛素原和总胰岛素原:诊断和治疗2型糖尿病和胰岛素抵抗的新方面。

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摘要

Proinsulin, the precursor of insulin during physiological insulin production, has been demonstrated in the past to stimulate PAI-1 secretion and consecutively block fibrinolysis. Therefore, proinsulin is contributing as an independent factor to the increased cardiovascular risk of patients with type 2 diabetes. However, development of insulin resistance in the course of type 2 diabetes leads to increased insulin demands and finally to an impairment of beta-cell function in later disease stages. Appearance of intact proinsulin in the peripheral blood has been shown to be a good laboratory marker for this phenomenon since it indicates an exhaustion of the cleavage capacity of the intracellular processing enzymes. However, the close relation of the two pathophysiological entities also makes it a very specific marker for insulin resistance per se. During the past years, new immunoassays have been developed that are able to distinguish between intact proinsulin and its specific and unspecific cleavage products. Use of these assays in recent epidemiological and intervention studies has helped to get a better understanding about beta-cell dysfunction and its relation to insulin resistance and cardiovascular risk. In a large cross-sectional study with 4270 orally treated patients, elevation of fasting intact proinsulin was very closely related to insulin resistance, as assessed by iv glucose tolerance test in a subgroup, and by HOMA analysis in the entire patient population. Effective treatment of insulin resistance (e.g. with thiazolidindiones) led to a decrease in elevated proinsulin levels and to a decrease of the cardiovascular risk profile, while the levels remained high during sulfonylurea therapy. These results suggest to reconsider intact and total proinsulin as valuable diagnostic tools in diagnosis and treatment of type 2 diabetes. Based on the published data of the new specific immunoassays, patients with elevated intact proinsulin levels (> 10 pmol/L) should be regarded and treated as being insulin-resistant, while elevation of total proinsulin (>45 pmol/l) may help to identify the high cardiovascular risk patients. Both assays can thus be used to assess beta-cell function, to facilitate the selection of the most promising therapy, and may also serve to monitor treatment success in the further course of the disease.
机译:胰岛素原是生理性胰岛素生产过程中胰岛素的前体,过去已被证明可刺激PAI-1分泌并连续阻断纤维蛋白溶解。因此,胰岛素原是导致2型糖尿病患者心血管风险增加的独立因素。但是,在2型糖尿病的过程中胰岛素抵抗的发展导致胰岛素需求增加,并最终导致疾病后期的β细胞功能受损。外周血中完整胰岛素原的出现已被证明是该现象的良好实验室标记,因为它表明细胞内加工酶的切割能力已经耗尽。然而,两个病理生理实体的紧密联系也使其成为胰岛素抵抗本身的非常特殊的标志。在过去的几年中,已经开发出了新的免疫分析方法,能够区分完整的胰岛素原及其特异性和非特异性裂解产物。在最近的流行病学和干预研究中使用这些检测方法有助于更好地了解β细胞功能障碍及其与胰岛素抵抗和心血管风险的关系。在一项对4270例经口服治疗的患者进行的大型横断面研究中,空腹完整胰岛素原的升高与胰岛素抵抗密切相关,如通过亚组的iv葡萄糖耐量试验以及整个患者群体的HOMA分析所评估的。有效治疗胰岛素抵抗(例如用噻唑烷二酮)导致升高的胰岛素原水平降低和心血管风险特征的降低,而在磺酰脲治疗期间水平仍然很高。这些结果表明,应将完整胰岛素原和总胰岛素原重新考虑为诊断和治疗2型糖尿病的有价值的诊断工具。根据新的特异性免疫测定的公开数据,完整胰岛素原水平升高(> 10 pmol / L)的患者应被视为胰岛素抵抗,而总胰岛素原水平升高(> 45 pmol / l)可能有助于确定高心血管风险患者。因此,两种测定法都可用于评估β细胞功能,以帮助选择最有希望的疗法,并且还可用于监测疾病进一步进程中的治疗成功。

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