肝移植后的糖尿病和墨西哥队列糖尿病家族史的影响。

A. Fernández-Ramírez , A. Olivas-Martinez , J. Ruiz-Manriquez , E. Kauffman-Ortega , C. Moctezuma-Velázquez , E. Marquez-Guillen , A.G. Contreras , M. Vilatobá , E. González-Flores , R. Cruz-Martínez , N.C. Flores-García , I. García-Juárez
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引用次数: 0

摘要

引言和目的:移植后糖尿病(PTDM)是一种严重的长期并发症,对移植物和患者的生存有负面影响。本研究的目的是描述墨西哥队列中PTDM的发病率,并评估其与既往糖尿病家族史(FHD)的关系。方法:对接受肝移植(LT)的患者进行回顾性单中心队列研究。主要结果是从LT到PTDM的时间。PTDM的诊断采用ADA标准。采用调整后的Cox回归模型,并将移植前糖尿病前期作为媒介,进行中介分析,以确定FHD对PTDM的总影响和直接影响。结果:共纳入152例患者,中位随访时间为41个月;19.2%(n = 29)患有移植前糖尿病。在随访期间,15%的患者出现PTDM(n = 23),发病率为4.71例/100人年。FHD患者的PTDM明显高于无FHD患者(分别为8.72例/100人年和2.04例/100人岁;p = PTDM对FHD的校正危险比为4.14(95%CI 1.60-10.7),p = 0.005)和3.48(95%CI 1.35-9.01,p = 0.010)。结论:PTDM的发生率与大多数国际研究报道的相似。与2型糖尿病一样,家族史在PTDM的发展中起着重要作用,即使考虑到移植前糖尿病。FHD患者应接受更严格的代谢程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Posttransplantation diabetes mellitus after liver transplant and the impact of family history of diabetes in a Mexican cohort

Introduction and aims

Posttransplantation diabetes mellitus (PTDM) is a serious long-term complication that has a negative impact on graft and patient survival. The purpose of the present study was to describe the incidence of PTDM in a Mexican cohort and evaluate its association with a previous family history of diabetes (FHD).

Methods

A retrospective single-center cohort study was conducted on patients undergoing liver transplantation (LT). The primary outcome was time from LT to PTDM. The diagnosis of PTDM was established using the ADA criteria. A mediation analysis that used adjusted Cox regression models and considered pretransplant prediabetes a mediator was performed, to determine the total effect and direct effect of FHD on PTDM.

Results

A total of 152 patients were included, with a median follow-up time of 41 months; 19.2% (n = 29) had pretransplant diabetes. During the follow-up time, 15% of patients developed PTDM (n = 23), with an incidence rate of 4.71 cases/100 person-years. PTDM was significantly higher in patients with FHD, compared with those with no FHD (8.72 cases/100 person-years vs 2.04 cases/100 person-years, respectively; p = 0.001). The adjusted hazard ratio of PTDM for FHD was 4.14 (95% CI 1.60–10.7), p = 0.005) and 3.48 (95% CI 1.35–9.01, p = 0.010), when further controlled for pretransplant prediabetes.

Conclusion

The occurrence of PTDM was similar to that reported in most international studies. As with type 2 diabetes, family history plays an important role in the development of PTDM, even after accounting for pretransplant prediabetes. Patients with FHD should undergo a stricter metabolic program.

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