Department of Transplantation Medicine, Oslo University Hospital, Rikshospitalet, P.O.Box 4950, 0424, Oslo, Nydalen, Norway.
Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway.
BMC Nephrol. 2019 Jan 10;20(1):12. doi: 10.1186/s12882-018-1171-3.
The use of HbA1c ≥6.5% for diagnosis of diabetes has been challenged for post-transplantation diabetes mellitus (PTDM) also known as new onset diabetes after transplantation (NODAT) due to a low sensitivity early after renal transplantation. PTDM diagnosed with an oral glucose tolerance test (OGTT) is highly predictable for long-term patient mortality. HbA1c was introduced for diagnosis based on the risk of developing diabetic retinopathy. The utility of HbA1c measures versus glucose criteria has not been widely assessed in stable transplant patients but still HbA1c is widely used in this population. The aim of the present analyses was to validate the utility of fasting plasma glucose (FPG) together with HbA1c in diagnosing PTDM in stable renal transplant recipients (RTRs).
OGTT's were performed one year after transplantation in 494 consecutive RTRs without diabetes. FPG and HbA1c were obtained the same day, before starting the OGTT. Validation was performed using C-statistics and logistic regression analyses.
PTDM was diagnosed in 51 patients (10.3%) by glucose criteria, 38 (74%) patients were diagnosed by FPG ≥7.0 mmol/L [126.1 mg/dl], and 13 (26%) only by 2-h plasma glucose. Six of the latter had HbA1c ≥6.5%. Only seven patients out of the 51 (13.7%) PTDM patients remained undiagnosed when HbA1c ≥6.5% was used together with FPG, and five of these regressed to normal after a median follow-up of 14 months. ROC curves including FPG and HbA1c versus OGTT derived criteria revealed an AUC of 0.858.
Combining standard diagnostic FPG and HbA1c criteria captured almost all patients with persistent PTDM in stable RTRs. The combined use of the criteria appears to be an applicable diagnostic strategy for PTDM without the need of an OGTT one year post-transplant.
Retrospectively registered.
由于肾移植后早期 HbA1c 检测诊断糖尿病的敏感性较低,因此其用于诊断移植后糖尿病(PTDM),也称为移植后新发糖尿病(NODAT)的方法受到了挑战。通过口服葡萄糖耐量试验(OGTT)诊断的 PTDM 与长期患者死亡率高度相关。HbA1c 用于诊断的依据是发生糖尿病视网膜病变的风险。在稳定的移植患者中,尚未广泛评估 HbA1c 测量值与血糖标准的实用性,但该指标仍在该人群中广泛使用。本分析的目的是验证在稳定的肾移植受者(RTR)中,空腹血糖(FPG)联合 HbA1c 用于诊断 PTDM 的实用性。
对 494 例无糖尿病的连续 RTR 进行移植后 1 年的 OGTT。同一天进行 OGTT 前,获取 FPG 和 HbA1c。采用 C 统计量和逻辑回归分析进行验证。
根据血糖标准诊断出 51 例(10.3%)PTDM 患者,38 例(74%)患者通过 FPG≥7.0mmol/L[126.1mg/dl]诊断,13 例(26%)仅通过 2 小时血浆葡萄糖诊断。后 13 例中有 6 例 HbA1c≥6.5%。当使用 HbA1c≥6.5% 联合 FPG 时,51 例 PTDM 患者中仅有 7 例(13.7%)仍未被诊断,其中 5 例在中位随访 14 个月后恢复正常。包括 FPG 和 HbA1c 与 OGTT 衍生标准的 ROC 曲线显示 AUC 为 0.858。
联合使用标准诊断 FPG 和 HbA1c 标准可捕获稳定 RTR 中几乎所有持续 PTDM 患者。联合使用这些标准似乎是一种适用于 PTDM 的诊断策略,无需在移植后 1 年进行 OGTT。
回顾性注册。