Shehab-Eldin Walid, Shoker Ahmed
Royal University Hospital, Department of Medicine, Division of Nephrology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Nephron Clin Pract. 2008;110(1):c1-9. doi: 10.1159/000148207. Epub 2008 Jul 24.
Several groups identified pre-transplant factors which contribute to the development of new onset of diabetes after transplantation (NODAT).
To identify post-transplant risk factors for NODAT.
55 stable renal transplant patients were divided into group A of 34 recipients with normoglycemia and group B of 21 recipients with impaired fasting glucose. Markers including insulin, pro-insulin, soluble receptors for advanced glycated end products (sRAGE), adiponectin, malondialdehyde, homeostasis model assessment of insulin resistance (HOMA-IR), and beta-cell function were calculated at the outset and correlated, thereafter, with the later development of NODAT after a follow-up duration of 14.98 +/- 3.97 months.
11.8 and 19% of groups A and B respectively developed NODAT. Insulin, sRAGE, HOMA-IR and basal fasting plasma glucose correlated with the development of NODAT in univariate analysis. A baseline insulin level of 54.54 mU/l predicted the development of NODAT with a specificity of 95.45% and was the only significant factor in the multivariate analysis. beta-Cell function was not different among the three groups.
A long prodrome of insulin resistance (IR) exists prior to development of NODAT. 50% of patients with NODAT will remit to a normoglycemic state. IR, rather than beta-cell dysfunction, precedes the development of NODAT. Serum insulin in stable non-diabetic renal transplant patients can be used as a confirmatory test to the development of future NODAT.
多个研究小组确定了移植前因素,这些因素会导致移植后新发糖尿病(NODAT)的发生。
确定NODAT的移植后危险因素。
55例稳定的肾移植患者被分为A组(34例血糖正常的受者)和B组(21例空腹血糖受损的受者)。在研究开始时计算包括胰岛素、胰岛素原、晚期糖基化终末产物可溶性受体(sRAGE)、脂联素、丙二醛、胰岛素抵抗稳态模型评估(HOMA-IR)和β细胞功能等指标,并在此后与随访14.98±3.97个月后NODAT的发生情况进行相关性分析。
A组和B组分别有11.8%和19%的患者发生了NODAT。在单因素分析中,胰岛素、sRAGE、HOMA-IR和基础空腹血糖与NODAT的发生相关。基线胰岛素水平为54.54 mU/l时预测NODAT发生的特异性为95.4%,且是多因素分析中唯一的显著因素。三组间β细胞功能无差异。
在NODAT发生之前存在胰岛素抵抗(IR)的长期前驱期。50%的NODAT患者将恢复至血糖正常状态。IR而非β细胞功能障碍先于NODAT的发生。稳定的非糖尿病肾移植患者的血清胰岛素可作为未来NODAT发生的确诊试验。