Vitamin Status as a Determinant of Serum Homocysteine Concentration in Type 2 Diabetic Retinopathy

Author:

Fotiou Pandelis1ORCID,Raptis Athanasios2,Apergis George3,Dimitriadis George2,Vergados Ioannis4,Theodossiadis Panagiotis1

Affiliation:

1. 2nd Department of Ophthalmology, “Attikon” University Hospital, Athens University Medical School, 1 Rimini Street, 12462 Athens, Greece

2. 2nd Department of Internal Medicine-Propaedeutic, Research Institute and Diabetes Center, “Attikon” University Hospital, Athens University Medical School, 1 Rimini Street, 12462 Athens, Greece

3. Department of Molecular Diagnosis, “Hippokration” General Hospital, 114 Vasilissis Sofias Avenue, 11527 Athens, Greece

4. Athens Eye Hospital, 45 Vouliagmenis Avenue, 16675 Athens, Greece

Abstract

We investigated the association of serum homocysteine levels and vitamin status with type 2 diabetic retinopathy. This study included 65 patients with and 75 patients without diabetic retinopathy. Patients with diabetic retinopathy had significantly higher serum homocysteine levelsP<0.001, higher prevalence of hyperhomocysteinemiaP<0.001, lower serum folic acidP<0.001, and vitamin B12(P=0.014) levels than those without diabetic retinopathy. Regression analysis revealed that homocysteine was an independent risk factor for diabetic retinopathy and there was a threshold in its serum level (13.7 μmol/L), above which the risk of diabetic retinopathy greatly increases (OR=1.66,P=0.001). Folic acid was associated with decreased odds for diabetic retinopathy (OR=0.73,P<0.001). There was a threshold in serum vitamin B12level (248.4 pg/mL), below which serum homocysteine concentration significantly increases with decreasing serum vitamin B12(P=0.003). Our findings suggest that hyperhomocysteinemia is an independent risk factor for the development and progression of diabetic retinopathy. Decreased serum levels of folic acid and vitamin B12, through raising serum homocysteine concentrations, may also affect the diabetic retinopathy risk.

Publisher

Hindawi Limited

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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