Department of Internal Medicine, Mitochondrial Research Unit, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Gene. 2013 Dec 1;531(2):370-6. doi: 10.1016/j.gene.2013.08.020. Epub 2013 Aug 14.
To identify the mitochondrial DNA (mtDNA) single nucleotide polymorphisms (SNPs) in the control region and elucidate their role in metabolic phenotypes and oxidative stress.
A total of 861 nondiabetic subjects were enrolled, including 250 impaired fasting glucose (IFG) and 370 obese subjects (body mass index [BMI]>25 kg/m(2)). Antioxidant status presented as total free thiol level was determined from serum samples. DNA was extracted from peripheral blood leucocytes, and the sequences were analyzed using the DNASTAR software. SNPs were identified by comparison with the Cambridge Reference Sequence.
After adjusting odds ratios for age, sex, and BMI, the selected independently significant SNPs indicated 4 susceptible SNPs: SNP-16126C and SNP-16261T, which were related to abdominal obesity (P=0.009; 0.06); SNP-16390A, related to hypertension (HTN) (P=0.007); and SNP-16092C, related to decreased antioxidant capacity (P=0.015). In the obese subgroup, 3 susceptible SNPs included SNP-16189C and SNP-16260T, which showed significantly higher IFG prevalence (P=0.016 and 0.024, respectively), and SNP-16519C, which was significantly higher in the HTN group (P=0.036). As to protective SNPs, 5 protective SNPs were identified in all subjects but only one SNP-16093C is consistent in obese group, which showed a significantly lower prevalence in patients with abdominal obesity and was associated with a higher antioxidant status (P<0.001).
SNPs in the mtDNA control region are associated with metabolic phenotypes and oxidative stress markers. Some SNPs are relating to the interaction between obesity and genetic factors. The beneficial effects of these protective SNPs were insignificant and some susceptible SNPs became dominant within the obese subgroup. Subjects harboring these SNPs should avoid excessive weight gain.
鉴定控制区线粒体 DNA(mtDNA)单核苷酸多态性(SNP),阐明其在代谢表型和氧化应激中的作用。
共纳入 861 例非糖尿病患者,包括 250 例空腹血糖受损(IFG)和 370 例肥胖患者(BMI>25kg/m2)。采用血清总游离巯基水平测定抗氧化状态。从外周血白细胞中提取 DNA,采用 DNASTAR 软件进行序列分析。通过与剑桥参考序列比较鉴定 SNP。
在调整年龄、性别和 BMI 的比值比后,选择的独立显著 SNP 表明有 4 个易感 SNP:SNP-16126C 和 SNP-16261T 与腹型肥胖相关(P=0.009;0.06);SNP-16390A 与高血压(HTN)相关(P=0.007);SNP-16092C 与抗氧化能力降低相关(P=0.015)。在肥胖亚组中,有 3 个易感 SNP,包括 SNP-16189C 和 SNP-16260T,IFG 发生率显著较高(P=0.016 和 0.024),SNP-16519C 在 HTN 组中显著较高(P=0.036)。至于保护 SNP,在所有受试者中鉴定出 5 个保护 SNP,但只有 SNP-16093C 在肥胖组中一致,该 SNP 在腹型肥胖患者中发生率较低,与较高的抗氧化状态相关(P<0.001)。
mtDNA 控制区的 SNP 与代谢表型和氧化应激标志物相关。一些 SNP 与肥胖和遗传因素之间的相互作用有关。这些保护 SNP 的有益作用不显著,一些易感 SNP 在肥胖亚组中占主导地位。携带这些 SNP 的受试者应避免体重过度增加。