scholarly journals Pet ownership in pregnancy and methylation pattern in cord blood

Author(s):  
Hanna Danielewicz ◽  
Artur Gurgul ◽  
Anna Dębińska ◽  
Grzegorz Myszczyszyn ◽  
Tomasz Szmatoła ◽  
...  
Cytokine X ◽  
2021 ◽  
pp. 100052
Author(s):  
Anne FLOECK ◽  
Nina FERRARI ◽  
Christine JOISTEN ◽  
Maria T. PUTH ◽  
Brigitte STRIZEK ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Zongzhi Liu ◽  
Wei Chen ◽  
Zilong Zhang ◽  
Junyun Wang ◽  
Yi-Kun Yang ◽  
...  

The DNA methylation of human offspring can change due to the use of assisted reproductive technology (ART). In order to find the differentially methylated regions (DMRs) in ART newborns, cord blood maternal cell contamination and parent DNA methylation background, which will add noise to the real difference, must be removed. We analyzed newborns’ heel blood from six families to identify the DMRs between ART and natural pregnancy newborns, and the genetic model of methylation was explored, meanwhile we analyzed 32 samples of umbilical cord blood of infants born with ART and those of normal pregnancy to confirm which differences are consistent with cord blood data. The DNA methylation level was lower in ART-assisted offspring at the whole genome-wide level. Differentially methylated sites, DMRs, and cord blood differentially expressed genes were enriched in the important pathways of the immune system and nervous system, the genetic patterns of DNA methylation could be changed in the ART group. A total of three imprinted genes and 28 housekeeping genes which were involved in the nervous and immune systems were significant different between the two groups, six of them were detected both in heel blood and cord blood. We concluded that there is an ART-specific DNA methylation pattern involved in neuro- and immune-system pathways of human ART neonates, providing an epigenetic basis for the potential long-term health risks in ART-conceived neonates.


2019 ◽  
Vol 34 (7) ◽  
pp. 637-649 ◽  
Author(s):  
Karl Mårild ◽  
German Tapia ◽  
Øivind Midttun ◽  
Per M. Ueland ◽  
Maria C. Magnus ◽  
...  

2009 ◽  
Vol 136 (5) ◽  
pp. A-146 ◽  
Author(s):  
Uma Mahadevan ◽  
Maria T. Abreu
Keyword(s):  

2015 ◽  
Vol 30 (5) ◽  
pp. 249-254 ◽  
Author(s):  
Michael Paulzen ◽  
Sarah E. Lammertz ◽  
Tanja Veselinovic ◽  
Tamme W. Goecke ◽  
Christoph Hiemke ◽  
...  

2017 ◽  
Vol 212 ◽  
pp. 1-6 ◽  
Author(s):  
Michael Paulzen ◽  
Tamme W. Goecke ◽  
Elmar Stickeler ◽  
Gerhard Gründer ◽  
Georgios Schoretsanitis

2021 ◽  
Vol 12 ◽  
Author(s):  
Jia-Shuan Huang ◽  
Qiao-Zhu Chen ◽  
Si-Yu Zheng ◽  
Rema Ramakrishnan ◽  
Ji-Yuan Zeng ◽  
...  

BackgroundBirth weight is associated with cardiometabolic factors at birth. However, it is unclear when these associations occur in fetal life. We aimed to investigate the associations between fetal growth in different gestational periods and cord blood cardiometabolic factors.MethodsWe included 1,458 newborns from the Born in Guangzhou Cohort Study, China. Z-scores of fetal size parameters [weight, abdominal circumference (AC), and femur length (FL)] at 22 weeks and growth at 22–27, 28–36, and ≥37 weeks were calculated from multilevel linear spline models. Multiple linear regression was used to examine the associations between fetal growth variables and z-scores of cord blood cardiometabolic factors.ResultsFetal weight at each period was positively associated with insulin levels, with stronger association at 28–36 weeks (β, 0.31; 95% CI, 0.23 to 0.39) and ≥37 weeks (β, 0.15; 95% CI, 0.10 to 0.20) compared with earlier gestational periods. Fetal weight at 28–36 (β, −0.32; 95% CI, −0.39 to −0.24) and ≥37 weeks (β, −0.26; 95% CI, −0.31 to −0.21) was negatively associated with triglyceride levels, whereas weight at 28–36 weeks was positively associated with HDL levels (β, 0.12; 95% CI, 0.04 to 0.20). Similar results were observed for AC. Fetal FL at 22 and 22–27 weeks was associated with increased levels of insulin, glucose, and HDL.ConclusionsFetal growth at different gestational periods was associated with cardiometabolic factors at birth, suggesting that an interplay between fetal growth and cardiometabolic factors might exist early in pregnancy.


Epigenomics ◽  
2021 ◽  
Author(s):  
Diana L Juvinao-Quintero ◽  
Andres Cardenas ◽  
Patrice Perron ◽  
Luigi Bouchard ◽  
Sharon M Lutz ◽  
...  

Background: Previous studies suggest that fetal programming to hyperglycemia in pregnancy is due to modulation of DNA methylation (DNAm), but they have been limited in their maternal glycemic characterization. Methods: In Gen3G, we used a principal component analysis to integrate multiple glucose and insulin values measured during the second trimester oral glucose tolerance test. We investigated associations between principal components and cord blood DNAm levels in an epigenome-wide analysis among 430 mother–child pairs. Results: The first principal component was robustly associated with lower DNAm at cg26974062 ( TXNIP; p = 9.9 × 10-9) in cord blood. TXNIP is a well-known DNAm marker for type 2 diabetes in adults. Conclusion: We hypothesize that abnormal glucose metabolism in pregnancy may program dysregulation of TXNIP across the life course.


1962 ◽  
Vol 40 (3_Suppl) ◽  
pp. S110 ◽  
Author(s):  
V. H. T. James ◽  
E. Caie ◽  
P. H. Sanderson ◽  
G. Pinker

2019 ◽  
Vol 11 (4) ◽  
pp. 369-378 ◽  
Author(s):  
Simon-Pierre Guay ◽  
Andrée-Anne Houde ◽  
Edith Breton ◽  
Jean-Patrice Baillargeon ◽  
Patrice Perron ◽  
...  

AbstractPlacental lipids transfer is essential for optimal fetal development, and alterations of these mechanisms could lead to a higher risk of adverse birth outcomes. Low-density lipoprotein receptor (LDLR), LDL receptor-related protein 1 (LRP1), and scavenger receptor class B type 1 (SCARB1) genes are encoding lipoprotein receptors expressed in the placenta where they participate in cholesterol exchange from maternal to fetal circulation. The aim of this study was thus to investigate the association between maternal lipid changes occurring in pregnancy, placental DNA methylation (DNAm) variations at LDLR, LRP1, and SCARB1 gene loci, and newborn’s anthropometric profile at birth. Sixty-nine normoglycemic women were followed from the first trimester of pregnancy until delivery. Placental DNAm was quantified at 43 Cytosine-phosphate-Guanines (CpGs) at LDLR, LRP1, and SCARB1 gene loci using pyrosequencing: 4 CpGs were retained for further analysis. Maternal clinical data were collected at each trimester of pregnancy. Newborns’ data were collected from medical records. Statistical models included minimally newborn sex and gestational and maternal age. Maternal total cholesterol changes during pregnancy (ΔT3-T1) were correlated with DNAm variations at LDLR (r = −0.32, p = 0.01) and LRP1 (r = 0.34, p = 0.007). DNAm at these loci was also correlated with newborns’ cord blood triglyceride and leptin levels. Mediation analysis supports a causal relationship between maternal cholesterol changes, DNAm levels at LRP1 locus, and cord blood leptin concentration (pmediation = 0.02). These results suggest that LRP1 DNAm link maternal blood cholesterol changes in pregnancy and offspring adiposity at birth, which provide support for a better follow-up of blood lipids in pregnancy.


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