Mortensen H B
Dan Med Bull. 1985 Dec;32(6):309-28.
The introduction briefly describes the necessity of maintaining a good metabolic control in children with diabetes mellitus. Thereupon, the object of the study is defined, viz. the wish to elucidate glycation of hemoglobin by means of reaction and biokinetic studies and to evaluate the applicability of the glycated hemoglobin fraction HbA1c in the clinical control of children with diabetes mellitus. In the subsequent historical section the most important studies on glycated hemoglobin are reviewed, with a particular view to the formation of this hemoglobin fraction and its clinical applicability. A brief description follows of the pathway in which hemoglobin A, via condensation with glucose, first forms a labile intermediate adduct, designated HbA1d, which is thereafter rearranged to the more stable HbA1c form. The methods used for determining glycated hemoglobin are described and their specificity assessed. In addition, an account is given of the reasons for choosing isoelectric focusing for a further elucidation of the glycation of hemoglobin. Among the results of the present studies it may be mentioned that by using the method of isoelectric focusing for separation of hemoglobin it is possible to: separate HbA1d and HbA1c and to determine the rate and equilibrium constants for the formation and dissociation of these glycated hemoglobin fractions; calculate, by the use of a biokinetic model, that HbA1c reflects the mean blood glucose concentration of the preceding 4 weeks; ascertain that HbA1c is preferable to HbA1 as a parameter for assessing the glycemic control; demonstrate that in children with newly diagnosed diabetes mellitus HbA1c is a useful index for defining the start and cessation of the remission period and for predicting the length of this period; demonstrate that HbA1c in children with diabetes mellitus is positively correlated to the clinical control and negatively correlated to linear growth; demonstrate a seasonal variation in the HbA1c substance fraction which shows the lowest level in the months of June and July; demonstrate that the transport of glucose across the erythrocyte membrane in children with diabetes mellitus is not notably affected by the glycemic control. The final section deals with the possibility whether glycation of hemoglobin and of other proteins can be a contributory cause of long-term diabetic complications.
引言简要描述了对糖尿病患儿维持良好代谢控制的必要性。据此,明确了研究目的,即希望通过反应和生物动力学研究阐明血红蛋白的糖化作用,并评估糖化血红蛋白组分HbA1c在糖尿病患儿临床控制中的适用性。在随后的历史部分,回顾了关于糖化血红蛋白的最重要研究,特别关注该血红蛋白组分的形成及其临床适用性。接下来简要描述了血红蛋白A通过与葡萄糖缩合首先形成不稳定的中间加合物(称为HbA1d),然后重排为更稳定的HbA1c形式的途径。描述了用于测定糖化血红蛋白的方法并评估了其特异性。此外,还说明了选择等电聚焦进一步阐明血红蛋白糖化作用的原因。在本研究结果中,可以提到通过使用等电聚焦方法分离血红蛋白能够:分离HbA1d和HbA1c,并确定这些糖化血红蛋白组分形成和解离的速率和平衡常数;通过使用生物动力学模型计算得出HbA1c反映了前4周的平均血糖浓度;确定HbA1c作为评估血糖控制的参数比HbA1更可取;证明在新诊断的糖尿病患儿中,HbA1c是确定缓解期开始和结束以及预测该期长度的有用指标;证明糖尿病患儿的HbA1c与临床控制呈正相关,与线性生长呈负相关;证明HbA1c物质组分存在季节性变化,在6月和7月水平最低;证明糖尿病患儿红细胞膜上葡萄糖的转运不受血糖控制的显著影响。最后一部分探讨了血红蛋白和其他蛋白质的糖化是否可能是长期糖尿病并发症的促成因素。