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Published on: August 21, 2020
Metabolic acidosis in pediatric kidney transplant recipients
Stella Kilduff1,2, Nicole Hayde3, Shankar Viswanathan4
1The Children's Hospital at Montefiore/Einstein, Bronx, NY, USA. skilduff@montefiore.org.
Insights
Metabolic acidosis is common in pediatric kidney transplant recipients (KTRs) within the first year. This condition is linked to a significant decline in kidney function (eGFR) during follow-up.
Area of Science:
- Nephrology
- Pediatric Transplantation
- Metabolic Disorders
Background:
- Metabolic acidosis is a known risk factor for kidney function decline in chronic kidney disease and adult kidney transplant recipients.
- The prevalence and impact of metabolic acidosis in pediatric kidney transplant recipients (KTRs) remain less understood.
Purpose of the Study:
- To investigate the prevalence of metabolic acidosis in pediatric KTRs.
- To determine the association between metabolic acidosis and allograft function in this population.
Main Methods:
- A retrospective study included pediatric KTRs from 2010 to 2018.
- Metabolic acidosis was defined as serum bicarbonate < 22 mEq/L or receipt of alkali therapy.
- Regression models adjusted for demographic and transplant-related factors.
Main Results:
- Metabolic acidosis was prevalent in 44% at baseline and ranged from 58-70% in the first year post-transplant.
- Older age at transplant was associated with lower odds of acidosis.
- Metabolic acidosis independently predicted an 8.2 ml/min/1.73 m² lower eGFR during follow-up.
Conclusions:
- Metabolic acidosis is highly prevalent in pediatric KTRs during the first year after transplantation.
- The presence of metabolic acidosis is associated with worse kidney allograft function (eGFR) during follow-up.
Background:
Metabolic acidosis is a risk factor for faster kidney function decline in chronic kidney disease (CKD) and in adult kidney transplant recipients (KTRs). We hypothesized that metabolic acidosis would be highly prevalent and associated with worse allograft function in pediatric KTRs.
Methods:
Pediatric KTRs at Montefiore Medical Center from 2010 to 2018 were included. Metabolic acidosis was defined as serum bicarbonate < 22 mEq/L or receiving alkali therapy. Regression models were adjusted for demographic factors and donor/recipient characteristics.
Results:
Sixty-three patients were identified with a median age at transplant of 10.5 (interquartile range (IQR) 4.4-15.2) years and post-transplant follow-up of 3 (IQR 1-5) years. Baseline serum bicarbonate was 21.7 ± 2.4 mEq/L, serum bicarbonate < 22 mEq/L was present in 28 (44%), and 44% of all patients were receiving alkali therapy. The prevalence of acidosis ranged from 58 to 70% during the first year of follow-up. At baseline, each 1-year higher age at transplant and every 10 ml/min/1.73 m2 higher eGFR were associated with 0.16 mEq/L (95% CI: 0.03-0.3) and 0.24 mEq/L (95% CI: 0.01-0.5) higher serum bicarbonate, respectively. Older age at transplant was associated with lower odds of acidosis (OR: 0.84; 95% CI: 0.72-0.97). During follow-up, metabolic acidosis was independently associated with 8.2 ml/min/1.73 m2 (95% CI 4.4-12) lower eGFR compared to not having acidosis; furthermore, eGFR was significantly lower among KTRs with unresolved acidosis compared with resolved acidosis.
Conclusions:
Among pediatric KTRs, metabolic acidosis was highly prevalent in the first year post-transplantation and was associated with lower eGFR during follow-up. A higher resolution version of the Graphical abstract is available as Supplementary information.
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