Nefrología (English Edition) (Mar 2016)

Glycaemic changes in patients with chronic kidney disease

  • Guillermo De’Marziani,
  • Gervasio Soler Pujol,
  • Liliana Miriam Obregón,
  • Elisa Mabel Morales,
  • Claudio Daniel Gonzalez,
  • Luciana Gonzalez Paganti,
  • Leonardo Cacciagiú,
  • Graciela Lopez,
  • Laura Schreier,
  • Alicia Elbert

DOI
https://doi.org/10.1016/j.nefroe.2016.04.001
Journal volume & issue
Vol. 36, no. 2
pp. 133 – 140

Abstract

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In Argentina, there have been no studies aimed at establishing the prevalence of dysglycaemia (impaired fasting glucose [IFG], impaired glucose tolerance [IGT] and diabetes mellitus [DM]) in patients with chronic kidney disease (CKD). Our group decided to conduct an observational study to evaluate the frequency with oral glucose tolerance test (OGTT) in CKD patients with no previous data for dysglycaemia in their medical records. OGTT was performed in 254 patients (60.62% male) with stage 3, 4 and 5 CKD under conservative treatment, haemodialysis or transplantation. Rsults for DM were found in 10 patients according to fasting glucose alone (3.94%; 95% CI: 1.35–6.53%), 11 patients with exclusively the second hour criterion (4.33%; 95% CI: 1.63–7.03%), 15 with both criteria (5.91%; 95% CI: 2.81–9.00%) and 36 patients with at least one criteria (14.17%; 95% CI: 9.69–18.66%). In a multivariate analysis, DM was associated with waist circumference (OR = 1.033 per cm; 95% CI, 1.005 to 1.062; P = .019) and with conservative treatment vs. replacement therapy (OR = 0.41; 95% CI: 0.19–0.92; P = .028). IGT was evident in 24.6% and 20.3 on conservative vs. replacement therapy, with no statistically significant difference. IFG (ADA criteria) was 19.75 vs. 9.24% in conservative vs. replacement therapy, with a statistically significant difference. OGTT is suggested for all CKD patients since it is able to detect the full range of unknown dysglycaemias, which avoids underdiagnoses and favours performing treatments to prevent progression in DM risk groups (IFG and/or IGT). It also aids in the selection of the most appropriate medication for transplantation or treatment initiation in new cases of undiagnosed DM to decrease morbidity and mortality.

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