Relationship between metformin use, vitamin B12 deficiency, hyperhomocysteinemia and vascular complications in patients with type 2 diabetes

Endocr J. 2013;60(12):1275-80. doi: 10.1507/endocrj.ej13-0332. Epub 2013 Sep 8.

Abstract

Aim of the study was to clarify the relationship between metformin-induced vitamin B12 (B12) deficiency, hyperhomocysteinemia and vascular complications in patients with type 2 diabetes. Serum B12 concentrations, homocysteine plasma levels, the presence of retinopathy and history of macroangiopathy (stroke or coronary heart disease) were analyzed in patients without renal dysfunction (serum creatinine<115 μmol/L). Firstly, B12 status was analyzed in 62 consecutive metformin-treated patients. Secondly, the relationship between B12, homocysteine and vascular complications was analyzed in 46 metformin-treated and 38 age- and sex-matched non-metformin-treated patients. Among the 62 consecutive metformin-treated patients, B12 was deficient (<150 pmol/L) in 8 (13%) and borderline-deficient (150-220 pmol/L) in 18 (29%): the larger the metformin dosage, the lower the B12 (P=0.02, Spearman's ρ=-0.30). There were independent correlations between metformin use and B12 lowering (P=0.02, r = -0.25), and B12 lowering and elevation of homocysteine (P<0.01, r=-0.34). Elevation of homocysteine was a risk for retinopathy (P=0.02, OR 1.26, 95%CI 1.04-1.52). There was no significant relation between homocysteine and macroangiopathy. Correlation between B12 and homocysteine was stronger in metformin-treated (P<0.01, r=-0.48) than non-metformin-treated (P=0.04, r=-0.38) patients. In ten B12 deficient patients, B12 supplementation (1,500 μg/day) for 2.2±1.0 months with continued use of metformin raised B12 levels: 152±42 and 299±97 pmol/L before and after treatment, respectively (P<0.01). Metformin-induced B12 lowering in diabetes was associated with elevation of homocysteine, and hyperhomocysteinemia was independently related to retinopathy. Metformin-induced B12 deficiency was correctable with B12 supplementation.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Coronary Disease / chemically induced
  • Coronary Disease / complications
  • Coronary Disease / epidemiology
  • Coronary Disease / physiopathology
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetic Angiopathies / chemically induced*
  • Diabetic Angiopathies / complications
  • Diabetic Angiopathies / epidemiology
  • Diabetic Angiopathies / physiopathology
  • Diabetic Retinopathy / chemically induced
  • Diabetic Retinopathy / complications
  • Diabetic Retinopathy / epidemiology
  • Diabetic Retinopathy / physiopathology
  • Dietary Supplements
  • Dose-Response Relationship, Drug
  • Female
  • Homocysteine / agonists
  • Homocysteine / blood
  • Humans
  • Hyperhomocysteinemia / chemically induced*
  • Hyperhomocysteinemia / complications
  • Hyperhomocysteinemia / epidemiology
  • Hyperhomocysteinemia / physiopathology
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / adverse effects*
  • Hypoglycemic Agents / therapeutic use
  • Japan / epidemiology
  • Male
  • Metformin / administration & dosage
  • Metformin / adverse effects*
  • Metformin / therapeutic use
  • Middle Aged
  • Prevalence
  • Risk Factors
  • Severity of Illness Index
  • Stroke / chemically induced
  • Stroke / complications
  • Stroke / epidemiology
  • Stroke / physiopathology
  • Vitamin B 12 / antagonists & inhibitors
  • Vitamin B 12 / blood
  • Vitamin B 12 / therapeutic use
  • Vitamin B 12 Deficiency / chemically induced*
  • Vitamin B 12 Deficiency / complications
  • Vitamin B 12 Deficiency / diet therapy
  • Vitamin B 12 Deficiency / epidemiology

Substances

  • Hypoglycemic Agents
  • Homocysteine
  • Metformin
  • Vitamin B 12