MD (Biochemistry), Senior Resident, Department of Biochemistry, University College of Medical Sciences & GTB Hospital, University of Delhi, Delhi, India.
MD (Biochemistry), Professor, Department of Biochemistry, University College of Medical Sciences & GTB Hospital, University of Delhi, Delhi, India.
J Diabetes Complications. 2023 Aug;37(8):108542. doi: 10.1016/j.jdiacomp.2023.108542. Epub 2023 Jun 17.
To compare mRNA [messenger RNA] expression of PINK1 in whole blood and the levels of biomarkers of Oxidative Stress (mitochondrial DNA [mtDNA] content & Total Antioxidant status [TAS]) in newly diagnosed lean and obese patients with T2DM.
Newly diagnosed patients of T2DM were enrolled in this study. The patients were divided into two groups of 30 patients each, lean (BMI < 18.5 kg/m) and obese (BMI > 25 kg/m). mRNA expression of PINK1 & mtDNA content was measured by real time PCR. Serum TAS was measured using a commercially available kit.
There was a 1.78-fold decrease in mRNA expression of PINK1 in obese group compared to the lean group. Mean mtDNA content was 300.82 ± 169.66 in the obese group and 332.78 ± 147.07 in the lean group (p = 0.06). Mean levels of TAS was 5.39 ± 2.28 μM Trolox Equivalents in the obese group and 3.85 ± 3.33 μM Trolox Equivalents in the lean group (p = 0.001).
The T2DM patient with obesity had greater OS than the lean patients. Thus, there is a compensatory increase in antioxidants in obese patients with T2DM. Our findings also suggest that decreased levels of PINK1 in obese group are unable to protect the mitochondria against OS leading to decreased mtDNA content. Does it also result in beta cell dysfunction or contribute to insulin resistance in obese patients with T2DM needs to be explored.
比较新诊断的瘦型和肥胖 2 型糖尿病(T2DM)患者全血中 PINK1mRNA 表达和氧化应激生物标志物(线粒体 DNA [mtDNA]含量和总抗氧化状态 [TAS])水平。
本研究纳入了新诊断的 T2DM 患者。将患者分为两组,每组 30 例,瘦型(BMI<18.5kg/m)和肥胖型(BMI>25kg/m)。通过实时 PCR 测量 PINK1mRNA 表达和 mtDNA 含量。使用市售试剂盒测量血清 TAS。
与瘦型组相比,肥胖组 PINK1mRNA 表达降低了 1.78 倍。肥胖组 mtDNA 含量的平均值为 300.82±169.66,瘦型组为 332.78±147.07(p=0.06)。肥胖组 TAS 水平的平均值为 5.39±2.28μM Trolox 当量,瘦型组为 3.85±3.33μM Trolox 当量(p=0.001)。
肥胖的 T2DM 患者的 OS 高于瘦型患者。因此,肥胖的 T2DM 患者抗氧化剂代偿性增加。我们的发现还表明,肥胖组 PINK1 水平降低无法保护线粒体免受 OS 影响,导致 mtDNA 含量降低。这是否也导致肥胖的 T2DM 患者的β细胞功能障碍或有助于胰岛素抵抗,需要进一步探索。