Predicting type 2 diabetes risk before and after solid organ transplantation using polygenic scores in a Danish cohort

被引:1
|
作者
dos Santos, Quenia [1 ]
Leung, Preston [1 ]
Thorball, Christian W. [2 ,3 ,4 ]
Ledergerber, Bruno [1 ]
Fellay, Jacques [2 ,3 ,4 ]
MacPherson, Cameron R. [1 ,5 ]
Hornum, Mads [6 ]
Terrones-Campos, Cynthia [1 ]
Rasmussen, Allan [7 ]
Gustafsson, Finn [8 ,9 ]
Perch, Michael [8 ,9 ]
Sorensen, Soren S. [6 ]
Ekenberg, Christina [1 ]
Lundgren, Jens D. [1 ]
Feldt-Rasmussen, Bo [6 ]
Reekie, Joanne [1 ]
机构
[1] Univ Copenhagen, Inst Roche Immun & Infect CHIP, Ctr Excellence Hlth, Rigshosp, Copenhagen, Denmark
[2] Lausanne Univ Hosp, Univ Lausanne, Lausanne, Switzerland
[3] Univ Lausanne, Lausanne, Switzerland
[4] Ecole Polytech Fed Lausanne, Sch Life Sci, Lausanne, Switzerland
[5] Inst Roche, Boulogne Billancourt, France
[6] Rigshosp, Dept Nephrol, Copenhagen Univ Hosp, Copenhagen, Denmark
[7] Rigshosp, Rigshospitalet, Copenhagen, Denmark
[8] Rigshosp, Dept Cardiol, Copenhagen, Denmark
[9] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark
基金
新加坡国家研究基金会;
关键词
type 2 diabetes mellitus; transplant; post-transplant diabetes mellitus; solid organ transplant recipient; polygenic risk score; MELLITUS; VARIANTS; IMPACT;
D O I
10.3389/fmolb.2023.1282412
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type 2 diabetes mellitus (T2DM) can be multifactorial where both genetics and environmental factors play a role. We aimed to investigate the use of polygenic risk scores (PRS) in the prediction of pre-transplant T2DM and post-transplant diabetes mellitus (PTDM) among solid organ transplant (SOT) patients. Using non-genetic risk scores alone; and the combination with PRS, separate logistic regression models were built and compared using receiver operator curves. Patients were assessed pre-transplant and in three post-transplant periods: 0-45, 46-365 and >365 days. A higher PRS was significantly associated with increased odds of pre-transplant T2DM. However, no improvement was observed for pre-transplant T2DM prediction when comparing PRS combined with non-genetic risk scores to using non-genetic risk scores alone. This was also true for predictions of PTDM in all three post-transplant periods. This study demonstrated that polygenic risk was only associated with the risk of T2DM among SOT recipients prior to transplant and not for PTDM. Combining PRS with a clinical model of non-genetic risk scores did not significantly improve the predictive ability, indicating its limited clinical utility in identifying patients at high risk for T2DM before transplantation, suggesting that non-genetic or different genetic factors may contribute to PTDM.
引用
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页数:10
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