Mesangial expansion at 5 years predicts death and death-censored graft loss after renal transplantation.
Aleksandra KuklaMariam P AlexanderSandor Turkevi-NagyMassini A MerzkaniWalter ParkByron H SmithPingchuan ZhangXiomara BenavidesMatthew Ross D'CostaCatalina Morales AlvarezAleksandar DenicAndrew John BentallYogish C KudvaMark D StegallPublished in: Clinical transplantation (2020)
Death with a functioning graft and death-censored renal allograft failure remain major problems for which effective preventative protocols are lacking. The retrospective cohort study aimed to determine whether histologic changes on a 5-year surveillance kidney biopsy predict adverse outcomes after transplantation in recipients who had: both Type 2 diabetes (T2DM) and obesity (BMI ≥ 30 kg/m2 ) at the time of transplantation (T2DM/Obesity, n = 75); neither (No T2DM/No obesity, n = 78); No T2DM/Obesity (n = 41), and T2DM/No obesity (n = 47). On 5-year biopsies, moderate-to-severe mesangial expansion was more common in the T2DM/Obesity group (Banff mm score ≥2 = 49.3%; Tervaert classification MS ≥ 2b = 26.7%) compared to the other groups (p < .001 for both scores). Risk factors included older age, higher BMI, HbA1C, and triglycerides at 1-year post-transplant. Moderate-to-severe mesangial expansion correlated with death with function (HR 1.74 (1.01, 2.98), p = .045 Banff and 1.89 (1.01, 3.51) p = .045 Tervaert) and with death-censored graft loss (HR 3.2 (1.2, 8.8), p = .02 Banff and HR 3.8 (1.3, 11.5), p = .01 Tervaert) over a mean of 11.6 years of recipient follow-up post-transplant. These data suggest that mesangial expansion in recipients with T2DM and obesity may reflect systemic vascular injury and might be a novel biomarker to predict adverse outcomes post renal transplant.
Keyphrases
- type diabetes
- insulin resistance
- metabolic syndrome
- weight loss
- weight gain
- glycemic control
- high fat diet induced
- risk factors
- diabetic nephropathy
- skeletal muscle
- adipose tissue
- machine learning
- public health
- stem cells
- emergency department
- early onset
- high glucose
- cell therapy
- mass spectrometry
- ms ms
- kidney transplantation
- endothelial cells
- ultrasound guided
- mesenchymal stem cells
- electronic health record
- bone marrow