Abstract: SA-PO705
Urinary Phenotyping in Mesoamerican Nephropathy
Session Information
- Fluid, Electrolyte, Acid-Base Disorders: Clinical - II
November 04, 2023 | Location: Exhibit Hall, Pennsylvania Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Fluid, Electrolytes, and Acid-Base Disorders
- 1102 Fluid, Electrolyte, and Acid-Base Disorders: Clinical
Authors
- Oomatia, Amin, University College London, London, United Kingdom
- Badri, Faisal M., University College London, London, United Kingdom
- Al-Rashed, Ali M., University College London, London, United Kingdom
- Gonzalez, Marvin Antonio, Research Centre on Health, Work and Environment at National Autonomous University of Nicaragua, Leon, Nicaragua
- Nitsch, Dorothea, London School of Hygiene & Tropical Medicine, London, United Kingdom
- Pearce, Neil, London School of Hygiene & Tropical Medicine, London, United Kingdom
- Caplin, Ben, University College London, London, United Kingdom
Group or Team Name
- The Colt/UK MRC CKDu Study Group.
Background
Mesoamerican nephropathy (MN) is a leading cause of CKD in Central America. Studies suggest an underlying tubulointerstitial nephritis with coexisting electrolyte wasting in affected individuals. The Colt-MRC cohort is a community-based study in Nicaragua, which recruited individuals at risk of MN, measuring serum creatinine (Cr) and collecting questionnaire data and biosamples at annual study visits for 7 years. In this sub-study, we aimed to compare the urinary phenotype of individuals from the cohort who develop early kidney injury (EKI) – defined by a significant decline in eGFR from a healthy baseline, with healthy controls (HC) and those with established MN (eMN).
Methods
We compared concurrent serum and urine samples from EKI cases pre and post decline in eGFR to two samples from HC matched for age, sex, community and study visit, and samples from two consecutive study visits from un-matched eMN participants (Table 1). All serum and urine samples were tested for: Cr, Na, K, PO4 & Mg, and fractional excretions (FE) of electrolytes were calculated. Urine was also tested for MCP-1 (ELISA) and corrected for urine Cr. Data were analysed using mixed-effects modelling.
Results
FE of all electrolytes were raised in the eMN group, but serum Na and Mg were lower. MCP1 was significantly raised in cases in the visit post EKI compared to pre-EKI, HC and eMN. See Table 1.
Conclusion
Urinary MCP1 levels are higher in cases after incident EKI versus HC and eMN, suggesting acute inflammation at the onset of MN that subsequently subsides. Participants with eMN had raised FE of all measured electrolytes, a common feature of CKD due to decreased nephron mass. However, they also had lower serum Na and Mg, with 50% exhibiting clinical hypomagnesemia, which is not a feature of CKD and suggests ongoing impairment of tubular function in established MN.
*p<0.001 **p<0.05 eMN vs HC & EKI ~p<0.05 post-decline EKI vs pre-decline, HC and eMN.
Funding
- Private Foundation Support