Increased global placental DNA methylation levels are associated with gestational diabetes

被引:107
作者
Reichetzeder, C. [1 ,2 ,4 ]
Putra, S. E. Dwi [1 ,5 ]
Pfab, T. [4 ,6 ]
Slowinski, T. [3 ]
Neuber, C. [2 ]
Kleuser, B. [2 ]
Hocher, B. [1 ,7 ,8 ]
机构
[1] Univ Potsdam, Inst Nutr Sci, Dept Expt Nutr Med, Arthur Scheunert Allee 114-116, D-14558 Potsdam, Germany
[2] Univ Potsdam, Inst Nutr Sci, Dept Toxicol, Nuthetal, Germany
[3] Campus Charite Mitte, Dept Nephrol, Berlin, Germany
[4] Univ Hosp Charite, Campus Charite Mitte, CCR, Berlin, Germany
[5] Univ Surabaya, Fac Biotechnol, Surabaya, Indonesia
[6] Diaverum Deutschland, Potsdam, Germany
[7] Inst Lab Med, Berlin, Germany
[8] Hunan Normal Univ, Dept Basic Med, Coll Med, Changsha, Hunan, Peoples R China
来源
CLINICAL EPIGENETICS | 2016年 / 8卷
关键词
Placenta; Gestational diabetes; Insulin resistance; LC-MS/MS; Global DNA methylation; Epigenetics; Hypermethylation; BLOOD-CELL DNA; OXIDATIVE STRESS; CORD BLOOD; REPETITIVE ELEMENTS; INSULIN-RESISTANCE; MELLITUS; HYPERMETHYLATION; CANCER; METHYLTRANSFERASE; PREECLAMPSIA;
D O I
10.1186/s13148-016-0247-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Gestational diabetes mellitus (GDM) is associated with adverse pregnancy outcomes. It is known that GDM is associated with an altered placental function and changes in placental gene regulation. More recent studies demonstrated an involvement of epigenetic mechanisms. So far, the focus regarding placental epigenetic changes in GDM was set on gene-specific DNA methylation analyses. Studies that robustly investigated placental global DNA methylation are lacking. However, several studies showed that tissue-specific alterations in global DNA methylation are independently associated with type 2 diabetes. Thus, the aim of this study was to characterize global placental DNA methylation by robustly measuring placental DNA 5-methylcytosine (5mC) content and to examine whether differences in placental global DNA methylation are associated with GDM. Methods: Global DNA methylation was quantified by the current gold standard method, LC-MS/MS. In total, 1030 placental samples were analyzed in this single-center birth cohort study. Results: Mothers with GDM displayed a significantly increased global placental DNA methylation (3.22 +/- 0.63 vs. 3.00 +/- 0.46 %; p = 0.013; +/- SD). Bivariate logistic regression showed a highly significant positive correlation between global placental DNA methylation and the presence of GDM (p = 0.0009). Quintile stratification according to placental DNA 5mC levels revealed that the frequency of GDM was evenly distributed in quintiles 1-4 (2.9-5.3 %), whereas the frequency in the fifth quintile was significantly higher (10.7 %; p = 0.003). Bivariate logistic models adjusted for maternal age, BMI, ethnicity, recurrent miscarriages, and familiar diabetes predisposition clearly demonstrated an independent association between global placental DNA hypermethylation and GDM. Furthermore, an ANCOVA model considering known predictors of DNA methylation substantiated an independent association between GDM and placental DNA methylation. Conclusions: This is the first study that employed a robust quantitative assessment of placental global DNA methylation in over a thousand placental samples. The study provides large scale evidence that placental global DNA hypermethylation is associated with GDM, independent of established risk factors.
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页数:10
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