Madras Diabetes Research Foundation & Dr. Mohan's Diabetes Specialities Centre, Chennai, India.
Clin Biochem. 2012 Nov;45(16-17):1432-8. doi: 10.1016/j.clinbiochem.2012.07.097. Epub 2012 Jul 22.
Although telomere shortening has been linked with type 2 diabetes and most variables of adiposity, a shortcoming of such studies is the measurement of telomere length in leukocytes. Therefore, we tested the association among adipocyte cell size, telomere length (both subcutaneous and visceral adipose tissue) and systemic levels of adiponectin in obese subjects and patients with type 2 diabetes compared to control subjects.
Human subcutaneous and visceral adipose tissues were obtained from the subjects who have undergone bariatric surgery or other abdominal surgeries. The study groups comprised: i) control subjects, ii) type 2 diabetes patients, iii) obese subjects without diabetes and iv) obese subjects with diabetes. Adipocyte cell size was measured by histological staining. Adiponectin levels were measured by ELISA. Telomere length was determined by Real-time PCR and lipid peroxidation was assessed by fluorimetry.
Compared to control subjects, adipocyte size (both subcutaneous and visceral) from obese, diabetic and obese-diabetic subjects was significantly larger [p<0.001]. Individuals with adipose hypertrophy also exhibited shortened telomeres and hypoadiponectinemia. Pearson correlation analysis revealed that both visceral and subcutaneous fat cell size showed a positive correlation with FBS, HbA1c, HOMA-IR, LDL, total cholesterol, triglycerides and negatively correlated with HDL and adiponectin. Regression analysis revealed that the association between shortened telomeres and hypoadiponectinemia was lost when adjusted for adipocyte cell size.
Adipocyte hypertrophy appears to be strongly associated with shortened telomeres, hypoadiponectinemia and poor glycemic and lipid control. Interestingly, these molecular alterations seen in lean diabetics reflect a state of 'metabolic obesity'.
尽管端粒缩短与 2 型糖尿病和大多数肥胖变量有关,但此类研究的一个缺点是测量白细胞中的端粒长度。因此,我们在肥胖受试者和 2 型糖尿病患者中测试了脂肪细胞大小、端粒长度(皮下和内脏脂肪组织)与全身脂联素水平之间的相关性,并与对照受试者进行了比较。
我们从接受减肥手术或其他腹部手术的受试者中获得了人体皮下和内脏脂肪组织。研究组包括:i)对照组,ii)2 型糖尿病患者,iii)无糖尿病的肥胖受试者,iv)肥胖伴糖尿病患者。通过组织学染色测量脂肪细胞大小。通过 ELISA 测量脂联素水平。通过实时 PCR 确定端粒长度,并通过荧光法评估脂质过氧化。
与对照组相比,肥胖、糖尿病和肥胖伴糖尿病受试者的脂肪细胞大小(皮下和内脏)均明显更大[P<0.001]。脂肪肥大的个体也表现出端粒缩短和脂联素减少。Pearson 相关分析显示,内脏和皮下脂肪细胞大小与 FBS、HbA1c、HOMA-IR、LDL、总胆固醇、甘油三酯呈正相关,与 HDL 和脂联素呈负相关。回归分析显示,当调整脂肪细胞大小后,缩短的端粒与脂联素减少之间的关联就消失了。
脂肪细胞肥大似乎与端粒缩短、脂联素减少以及血糖和血脂控制不良密切相关。有趣的是,瘦型糖尿病患者中出现的这些分子改变反映了一种“代谢性肥胖”状态。