Albumin of People with Diabetes Mellitus Is More Reduced at Low HbA1c.
Margret PaarGerhard CvirnGerd HoerlGilbert ReibneggerHarald SourijCaren SourijHarald KojzarKarl OettlPublished in: International journal of molecular sciences (2023)
Oxidative stress is involved in the development, progression, and complications of diabetes mellitus (DM). Oxidative modification of human serum albumin's cysteine-34 is a marker for oxidative stress-related pathological conditions. We aimed to evaluate the redox state of albumin in patients with DM to investigate possible correlations with age, diabetes duration, and disease control status. Plasma aliquots were collected from 52 participants (26 type 1 and 26 type 2 DM). Patients were divided into two groups according to their glycated hemoglobin levels less than or equal to and greater than 58 mmol/L. Albumin redox state was assessed with high-performance liquid chromatography by fractionating it into human mercaptalbumin (HMA) and human nonmercaptalbumin 1 and 2 (HNA1 and HNA2). Albumin redox fractions were differently related to the age of study participants. In age-matched T1DM and T2DM groups, the albumin redox state was essentially the same. Irreversibly oxidized HNA2 was positively correlated with diabetes duration, especially in the T1DM group. HNA was increased in people with an increased HbA1c (>58 mmol/mol). Our results support the hypothesis that oxidative stress plays a crucial role in DM pathogenesis and emphasize the importance of diabetes control on systemic oxidative burden.
Keyphrases
- glycemic control
- oxidative stress
- type diabetes
- high performance liquid chromatography
- endothelial cells
- cardiovascular disease
- end stage renal disease
- newly diagnosed
- human serum albumin
- mass spectrometry
- chronic kidney disease
- ejection fraction
- diabetic rats
- peritoneal dialysis
- induced pluripotent stem cells
- adipose tissue
- pluripotent stem cells
- simultaneous determination
- signaling pathway