PERSONAL DE APOYO
HEISECKE PERALTA Silvina Lidia
artículos
Título:
Genes, exposures, and interactions on preterm birth risk: an exploratory study in an Argentine population
Autor/es:
ELIAS, DARIO E.; SANTOS, MARIA R.; CAMPAÑA, HEBE; POLETTA, FERNANDO A.; HEISECKE, SILVINA L.; GILI, JUAN A.; RATOWIECKI, JULIA; COSENTINO, VIVIANA; URANGA, ROCIO; MÁLAGA, DIANA ROJAS; NETTO, ALICE BRINCKMANN OLIVEIRA; BRUSIUS-FACCHIN, ANA CAROLINA; SALEME, CÉSAR; RITTLER, MÓNICA; KRUPITZKI, HUGO B.; CAMELO, JORGE S. LOPEZ; GIMENEZ, LUCAS G.
Revista:
Journal of Community Genetics
Editorial:
Springer Science and Business Media Deutschland GmbH
Referencias:
Año: 2022 vol. 13 p. 557 - 565
ISSN:
1868-310X
Resumen:
Preterm birth (PTB) is the main condition related to perinatal morbimortality worldwide. The aim of this study was to identify associations of spontaneous PTB with genetic variants, exposures, and interactions between and within them. We carried out a retrospective case–control study including parental sociodemographic and obstetric data, and fetal genetic variants. We sequenced the coding and flanking regions of five candidate genes from the placental blood cord of 69 preterm newborns and 61 at term newborns. We identify the characteristics with the greatest predictive power of PTB using penalized regressions, in which we include exposures (E), genetic variants (G), and two-way interactions. Few prenatal visits (< 5) was the main predictor of PTB from 26 G, 35 E, 299 G × G, 564 E × E, and 875 G × E evaluated terms. Within the fetal genetic characteristics, we observed associations of rs4845397 (KCNN3, allele T) variant; G × G interaction between rs12621551 (COL4A3, allele T) and rs73993878 (COL4A3, allele A), which showed sensitivity to anemia; and G × G interaction between rs11680670 (COL4A3, allele T) and rs2074351 (PON1, allele A), which showed sensitivity to vaginal discharge. The results of this exploratory study suggest that social disparities and metabolic pathways linked to uterine relaxation, inflammation/infections, and collagen metabolism would be involved in PTB etiology. Future studies with a larger sample size are necessary to confirm these findings and to analyze a greater number of exposures.