Vitamin B status in patients with type 2 diabetes mellitus with and without incipient nephropathy

Wilfred A. Nix, Rudolf Zirwes, Volkhard Bangert, Raimund Peter Kaiser, Matthias Schilling, Ulrike Hostalek, Rima Obeid
2015 Diabetes Research and Clinical Practice  
Type 2 diabetes Microalbuminuria Pyridoxal 5 0 -phosphate a b s t r a c t Aim: To investigate the vitamin B status, with particular focus on vitamin B 6 , in adults with and without incipient nephropathy secondary to type 2 diabetes mellitus. Methods: Plasma and/or urine concentrations of vitamins B 6 , B 1 , B 12 , related vitamers and biomarkers (including total homocysteine, methylmalonic acid) were measured in 120 adults with type 2 diabetes (including 46 patients with microalbuminuria) and
more » ... 52 non-diabetic control subjects. Results: Plasma concentrations of pyridoxal 5 0 -phosphate (PLP) were significantly lower in patients with type 2 diabetes than in control subjects (median: 22.7 nmol/L, diabetes with microalbuminuria; 26.8 nmol/L, diabetes without microalbuminuria; 39.5 nmol/L, non-diabetic control; p < 0.0001). The prevalence of low PLP (<30 nmol/L) was 63%, 58%, and 25% in the diabetes groups with and without microalbuminuria and the control group, respectively. Plasma levels of pyridoxine and pyridoxal were also lower ( p < 0.0001), but levels of pyridoxamine, pyridoxamine 5 0 -phosphate, and pyridoxic acid were higher in both groups with diabetes compared to the control group ( p < 0.001). Thiamine deficiency was highly prevalent in all groups, whereas low vitamin B 12 and elevated methylmalonic acid were rare. Increased levels of C-reactive protein and soluble vascular cell adhesion molecule-1 were observed in the groups with diabetes ( p < 0.05, versus healthy control). Conclusions: Deficiency of vitamin B 6 (PLP, pyridoxine, pyridoxal) and vitamin B 1 (thiamine) was prevalent in type 2 diabetes. Incipient nephropathy was associated with more pronounced alterations in vitamin B 6 metabolism and stronger indications of endothelial dysfunction and inflammation.
doi:10.1016/j.diabres.2014.09.058 pmid:25458341 fatcat:6erqbjtye5ferle5gfdi7dx2bq