Refine
Year of publication
Document Type
Language
- English (57)
Is part of the Bibliography
- yes (57)
Keywords
- Epigenetics (5)
- pregnancy (5)
- Fetal programming (4)
- Gestational diabetes (4)
- birth weight (4)
- Insulin resistance (3)
- LC-MS/MS (3)
- Metabolomics (3)
- Placenta (3)
- diabetic nephropathy (3)
- elevated plus-maze (3)
- glucocorticoid receptor (3)
- high-sodium (3)
- hypertension (3)
- linagliptin (3)
- open-field (3)
- post-natal (3)
- pre-natal (3)
- redox state (3)
- DDP-4 inhibition (2)
- DNA methylation (2)
- DOHaD (2)
- DPP-4 inhibitors (2)
- Global DNA methylation (2)
- Glucose tolerance (2)
- Hypermethylation (2)
- Kidney (2)
- Lysophosphatidylcholine (2)
- PTH (2)
- Type 2 Diabetes (2)
- chronic kidney disease (2)
- eNOS (2)
- epigenetics (2)
- fetal origins hypothesis (2)
- genes (2)
- genetics (2)
- growth restriction (2)
- later health (2)
- metabolomics (2)
- n-oxPTH (2)
- nutrient transport (2)
- patterns (2)
- proteomic analysis (2)
- repetitive elements (2)
- 1,25-Dihydroxyvitamin D-3 (1)
- 2k1c renovascular hypertension (1)
- Acute renal failure (1)
- Biomarker (1)
- Biparietal diameter (1)
- Birth Weight (1)
- Birth weight (1)
- Brain development (1)
- CORM-2 (1)
- Calcium (1)
- Cardiovascular diseases (1)
- Cardiovascular effects (1)
- Chronic Renal Failure (1)
- Chronic Renal Failure in Children (1)
- Chronic kidney disease (1)
- Clinical (1)
- Clinical trials (1)
- Contrast induced acute kidney injury (1)
- Coronary angiography (1)
- Cortisol Maternal cortisol (1)
- DPP-4 inhibition (1)
- DPP4 inhibition (1)
- Developmental programming (1)
- Diabetes (1)
- Diabetic nephropathy (1)
- Dipeptidyl peptidase IV (1)
- Endothelial nitric oxide synthase (1)
- Endothelin (1)
- Endothelin receptor antagonists (1)
- FGF23 (1)
- Free vitamin D (1)
- GLP-1 (1)
- GLP-1 receptor (1)
- Gestational diabetes mellitus (1)
- Global (1)
- Glp1r(-/-) mice (1)
- Glucocorticoid receptor (1)
- HNRNPA1 (1)
- Head circumference (1)
- Hemodialysis (1)
- High-fat-sucrose-salt diet (1)
- Hypertension (1)
- Kidney Transplantation (1)
- Klotho (1)
- Kynurenine (1)
- Long term health (1)
- Major adverse kidney event (1)
- Maternal folate treatment (1)
- Methylation (1)
- Mice (1)
- Myocardial infarction (1)
- NR3C1 gene (1)
- Nitric oxide (1)
- Nutrition (1)
- Oxidation (1)
- PCaaC38:6 (1)
- PGC1a (1)
- Paternal programming (1)
- Paternal programming; (1)
- Paternal, maternal, sex differences (1)
- Phosphate (1)
- Phosphatidylcholine acyl-alkyl C 32:1 (1)
- Preeclampsia (1)
- Pregnancy (1)
- Preinterventional biomarker (1)
- Preterm birth (1)
- Preterm delivery (1)
- Proline (1)
- Renin-angiotensin-aldosterone system (1)
- Safety (1)
- Side effects (1)
- Single nucleotide polymorphism (1)
- Small for gestational age (1)
- TGF-beta 1 (1)
- Thrifty phenotype (1)
- Vitamin D (1)
- Vitamin D binding protein (1)
- Vitamin D deficiency (1)
- Water and salt retention (1)
- YB-1 (1)
- acute kidney injury (1)
- albuminuria (1)
- alleles (1)
- angiotensin (1-7) (1)
- angiotensin II (1)
- angiotensin receptor blockers (1)
- biobanks (1)
- blood biomarker (1)
- blood pressure (1)
- cardiovascular disease (1)
- chronic renal failure (1)
- chronic renal failure in children (1)
- clusterin (1)
- collagen I (1)
- comparison (1)
- diabetes (1)
- duration of gestation (1)
- fasting blood glucose (1)
- fatty liver (1)
- fetal programing (1)
- fetal programming (1)
- fetus (1)
- fibrosis (1)
- genome-wide association study (1)
- genotype (1)
- gliptins (1)
- glycemic control (1)
- heart-type fatty acid binding protein (1)
- hemodialysis (1)
- hypotension (1)
- incretins (1)
- insulin resistance (1)
- intrauterine fetal growth (1)
- ischemia reperfusion injury (1)
- kidney (1)
- kidney injury molecule 1 (1)
- kidney transplantation (1)
- large sample size studies (1)
- low birth weight (1)
- metabolism (1)
- mothers (1)
- nephrin (1)
- neutrophil gelatinase-associated lipocalin (1)
- offspring (1)
- one dot two development signals (ODTDS) dot blot (1)
- osteopontin (1)
- oxidation (1)
- oxidative stress (1)
- phosphatidylcholine acyl-alkyl C 32:1 (1)
- placenta (1)
- preterm delivery (1)
- proline (1)
- protein quantification (1)
- proteinuria (1)
- renal impairment (1)
- single nucleotide polymorphism (1)
- thymosin beta 4 (1)
- tissue inhibitior of metalloproteinases 1 (1)
- urinary biomarker (1)
- western blot (1)
High-salt (HS) diets have recently been linked to oxidative stress in the brain, a fact that may be a precursor to behavioral changes, such as those involving anxiety-like behavior. However, to the best of our knowledge, no study has evaluated the amygdala redox status after consuming a HS diet in the pre- or postweaning periods. This study aimed to evaluate the amygdala redox status and anxiety-like behaviors in adulthood, after inclusion of HS diet in two periods: preconception, gestation, and lactation (preweaning); and only after weaning (postweaning). Initially, 18 females and 9 male Wistar rats received a standard (n = 9 females and 4 males) or a HS diet (n = 9 females and 5 males) for 120 days. After mating, females continued to receive the aforementioned diets during gestation and lactation. Weaning occurred at 21-day-old Wistar rats and the male offspring were subdivided: control-control (C-C)-offspring of standard diet fed dams who received a standard diet after weaning (n = 9-11), control-HS (C-HS)-offspring of standard diet fed dams who received a HS diet after weaning (n = 9-11), HS-C-offspring of HS diet fed dams who received a standard diet after weaning (n = 9-11), and HS-HS-offspring of HS diet fed dams who received a HS diet after weaning (n = 9-11). At adulthood, the male offspring performed the elevated plus maze and open field tests. At 152-day-old Wistar rats, the offspring were euthanized and the amygdala was removed for redox state analysis. The HS-HS group showed higher locomotion and rearing frequency in the open field test. These results indicate that this group developed hyperactivity. The C-HS group had a higher ratio of entries and time spent in the open arms of the elevated plus maze test in addition to a higher head-dipping frequency. These results suggest less anxiety-like behaviors. In the analysis of the redox state, less activity of antioxidant enzymes and higher levels of the thiobarbituric acid reactive substances (TBARS) in the amygdala were shown in the amygdala of animals that received a high-salt diet regardless of the period (pre- or postweaning). In conclusion, the high-salt diet promoted hyperactivity when administered in the pre- and postweaning periods. In animals that received only in the postweaning period, the addition of salt induced a reduction in anxiety-like behaviors. Also, regardless of the period, salt provided amygdala oxidative stress, which may be linked to the observed behaviors.
Being born large for gestational age is associated with increased global placental DNA methylation
(2020)
Being born small (SGA) or large for gestational age (LGA) is associated with adverse birth outcomes and metabolic diseases in later life of the offspring. It is known that aberrations in growth during gestation are related to altered placental function. Placental function is regulated by epigenetic mechanisms such as DNA methylation. Several studies in recent years have demonstrated associations between altered patterns of DNA methylation and adverse birth outcomes. However, larger studies that reliably investigated global DNA methylation are lacking. The aim of this study was to characterize global placental DNA methylation in relationship to size for gestational age. Global DNA methylation was assessed in 1023 placental samples by LC-MS/MS. LGA offspring displayed significantly higher global placental DNA methylation compared to appropriate for gestational age (AGA; p<0.001). ANCOVA analyses adjusted for known factors impacting on DNA methylation demonstrated an independent association between placental global DNA methylation and LGA births (p<0.001). Tertile stratification according to global placental DNA methylation levels revealed a significantly higher frequency of LGA births in the third tertile. Furthermore, a multiple logistic regression analysis corrected for known factors influencing birth weight highlighted an independent positive association between global placental DNA methylation and the frequency of LGA births (p=0.001).
Background/Aims: Impaired birth outcomes, like low birth weight, have consistently been associated with increased disease susceptibility to hypertension in later life. Alterations in the maternal or fetal metabolism might impact on fetal growth and influence birth outcomes. Discerning associations between the maternal and fetal metabolome and surrogate parameters of fetal growth could give new insight into the complex relationship between intrauterine conditions, birth outcomes, and later life disease susceptibility. Methods: Using flow injection tandem mass spectrometry, targeted metabolomics was performed in serum samples obtained from 226 mother/child pairs at delivery. Associations between neonatal birth weight and concentrations of 163 maternal and fetal metabolites were analyzed. Results: After FDR adjustment using the Benjamini-Hochberg procedure lysophosphatidylcholines (LPC) 14:0, 16:1, and 18:1 were strongly positively correlated with birth weight. In a stepwise linear regression model corrected for established confounding factors of birth weight, LPC 16: 1 showed the strongest independent association with birth weight (CI: 93.63 - 168.94; P = 6.94x10(-11)). The association with birth weight was stronger than classical confounding factors such as offspring sex (CI: - 258.81- -61.32; P = 0.002) and maternal smoking during pregnancy (CI: -298.74 - -29.51; P = 0.017). Conclusions: After correction for multiple testing and adjustment for potential confounders, LPC 16:1 showed a very strong and independent association with birth weight. The underlying molecular mechanisms linking fetal LPCs with birth weight need to be addressed in future studies. (c) 2018 The Author(s) Published by S. Karger AG, Basel
Background/Aims: Impaired birth outcomes, like low birth weight, have consistently been associated with increased disease susceptibility to hypertension in later life. Alterations in the maternal or fetal metabolism might impact on fetal growth and influence birth outcomes. Discerning associations between the maternal and fetal metabolome and surrogate parameters of fetal growth could give new insight into the complex relationship between intrauterine conditions, birth outcomes, and later life disease susceptibility. Methods: Using flow injection tandem mass spectrometry, targeted metabolomics was performed in serum samples obtained from 226 mother/child pairs at delivery. Associations between neonatal birth weight and concentrations of 163 maternal and fetal metabolites were analyzed. Results: After FDR adjustment using the Benjamini-Hochberg procedure lysophosphatidylcholines (LPC) 14:0, 16:1, and 18:1 were strongly positively correlated with birth weight. In a stepwise linear regression model corrected for established confounding factors of birth weight, LPC 16: 1 showed the strongest independent association with birth weight (CI: 93.63 - 168.94; P = 6.94x10(-11)). The association with birth weight was stronger than classical confounding factors such as offspring sex (CI: - 258.81- -61.32; P = 0.002) and maternal smoking during pregnancy (CI: -298.74 - -29.51; P = 0.017). Conclusions: After correction for multiple testing and adjustment for potential confounders, LPC 16:1 showed a very strong and independent association with birth weight. The underlying molecular mechanisms linking fetal LPCs with birth weight need to be addressed in future studies. (c) 2018 The Author(s) Published by S. Karger AG, Basel
Being born large for gestational age is associated with increased global placental DNA methylation
(2020)
Being born small (SGA) or large for gestational age (LGA) is associated with adverse birth outcomes and metabolic diseases in later life of the offspring. It is known that aberrations in growth during gestation are related to altered placental function. Placental function is regulated by epigenetic mechanisms such as DNA methylation. Several studies in recent years have demonstrated associations between altered patterns of DNA methylation and adverse birth outcomes. However, larger studies that reliably investigated global DNA methylation are lacking. The aim of this study was to characterize global placental DNA methylation in relationship to size for gestational age. Global DNA methylation was assessed in 1023 placental samples by LC-MS/MS. LGA offspring displayed significantly higher global placental DNA methylation compared to appropriate for gestational age (AGA; p<0.001). ANCOVA analyses adjusted for known factors impacting on DNA methylation demonstrated an independent association between placental global DNA methylation and LGA births (p<0.001). Tertile stratification according to global placental DNA methylation levels revealed a significantly higher frequency of LGA births in the third tertile. Furthermore, a multiple logistic regression analysis corrected for known factors influencing birth weight highlighted an independent positive association between global placental DNA methylation and the frequency of LGA births (p=0.001).
Aims/hypothesis It was shown that maternal endothelial nitric oxide synthase (eNOS) deficiency causes fatty liver disease and numerically lower fasting glucose in female wild-type offspring, suggesting that parental genetic variants may influence the offspring's phenotype via epigenetic modifications in the offspring despite the absence of a primary genetic defect. The aim of the current study was to analyse whether paternal eNOS deficiency may cause the same phenotype as seen with maternal eNOS deficiency. Methods Heterozygous (+/-) male eNOS (Nos3) knockout mice or wild-type male mice were bred with female wild-type mice. The phenotype of wild-type offspring of heterozygous male eNOS knockout mice was compared with offspring from wild-type parents. Results Global sperm DNA methylation decreased and sperm microRNA pattern altered substantially. Fasting glucose and liver glycogen storage were increased when analysing wild-type male and female offspring of +/- eNOS fathers. Wild-type male but not female offspring of +/- eNOS fathers had increased fasting insulin and increased insulin after glucose load. Analysing candidate genes for liver fat and carbohydrate metabolism revealed that the expression of genes encoding glucocorticoid receptor (Gr; also known as Nr3c1) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (Pgc1a; also known as Ppargc1a) was increased while DNA methylation of Gr exon 1A and Pgc1a promoter was decreased in the liver of male wild-type offspring of +/- eNOS fathers. The endocrine pancreas in wild-type offspring was not affected. <br /> Conclusions/interpretation Our study suggests that paternal genetic defects such as eNOS deficiency may alter the epigenome of the sperm without transmission of the paternal genetic defect itself. In later life wild-type male offspring of +/- eNOS fathers developed increased fasting insulin and increased insulin after glucose load. These effects are associated with increased Gr and Pgc1a gene expression due to altered methylation of these genes.
In vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) is associated with an increased risk of preterm (33rd-37th gestational week) and early preterm birth (20th-32nd gestational week). The underlying general and procedure related risk factors are not well understood so far. 4328 infertile women undergoing IVF/ICSI were entered into this study. The study population was divided into three groups: (a) early preterm birth group (n = 66), (b) preterm birth group (n = 675) and (c) full-term birth group (n = 3653). Odds for preterm birth were calculated by stepwise multivariate logistic regression analysis. We identified seven independent risk factors for preterm birth and four independent risk factors for early preterm birth. Older (> 39) or younger (< 25) maternal age (OR: 1.504, 95% CI 1.108-2.042, P = 0.009; OR: 2.125, 95% CI 1.049-4.304, P = 0.036, respectively), multiple pregnancy (OR: 9.780, 95% CI 8.014-11.935, P < 0.001; OR: 8.588, 95% CI 4.866-15.157, P < 0.001, respectively), placenta previa (OR: 14.954, 95% CI 8.053-27.767, P < 0.001; OR: 16.479, 95% CI 4.381-61.976, P < 0.001, respectively), and embryo reduction (OR: 3.547, 95% CI 1.736-7.249, P = 0.001; OR: 7.145, 95% CI 1.990-25.663, P = 0.003, respectively) were associated with preterm birth and early preterm birth, whereas gestational hypertension (OR: 2.494, 95% CI 1.770-3.514, P < 0.001), elevated triglycerides (OR: 1.120, 95% CI 1.011-1.240, P = 0.030) and shorter activated partial thromboplastin time (OR: 0.967, 95% CI 0.949-0.985, P < 0.001) were associated only with preterm birth. In conclusion, preterm and early preterm birth risk factors in patients undergoing assisted IVF/ICSI are in general similar to those in natural pregnancy. The lack of some associations in the early preterm group was most likely due to the lower number of early preterm birth cases. Only embryo reduction represents an IVF/ICSI specific risk factor.