Circulating microRNAs overexpressed in macrosomia: an experimental and bioinformatic approach.
Alejandra Ortiz-DosalElvira Del Carmen Arellanes-LiceaPatricia Rodil-GarcíaLuis A Salazar-OlivoPublished in: Journal of developmental origins of health and disease (2020)
Low birth weight (LBW) and macrosomia have been associated with later-in-life metabolic alterations. The aim of this study was to elucidate whether the expression levels of circulating microRNAs (c-miRNAs) associated with adult metabolic diseases are also dysregulated in newborns with LBW or macrosomia. The expression levels of five microRNAs (miRNAs) associated with metabolic diseases were quantified in dried blood spots of newborns with adequate birth weight, LBW and macrosomia by stem-loop real-time polymerase chain reaction. miR-29a-5p, miR-126-3p, miR-221-3p, and miR-486-5p were significantly overexpressed in newborns with macrosomia and showed no significant change in the LBW group compared to normal weight controls. miR-320a showed no statistical difference among groups. We predicted the putative target genes and pathways of the overexpressed miRNAs with bioinformatic tools. Bioinformatic analyses of overexpressed miRNAs predicted target genes involved in carbohydrate metabolism, participate in FoxO and PI3K/Akt signaling pathways, and are associated with diabetes, obesity, and cardiovascular diseases. The overexpression of circulating miR-29a-5p, miR-126-3p, miR-221-3p, and miR-486-5p may explain the increased risk of obesity and diabetes associated with macrosomia. The use of dried blood spots from newborn screening cards to quantify miRNAs expression levels could be an early and minimally invasive predictive tool for these metabolic alterations.
Keyphrases
- low birth weight
- pi k akt
- signaling pathway
- gestational age
- poor prognosis
- cell proliferation
- weight gain
- type diabetes
- birth weight
- cardiovascular disease
- preterm infants
- preterm birth
- human milk
- weight loss
- minimally invasive
- pregnant women
- metabolic syndrome
- insulin resistance
- long non coding rna
- body mass index
- glycemic control
- cell cycle arrest
- cord blood
- genome wide
- skeletal muscle
- dna methylation
- adipose tissue
- young adults
- high fat diet induced
- long noncoding rna
- oxidative stress
- cardiovascular events
- childhood cancer
- bioinformatics analysis
- genome wide analysis