Concomitant genetic defects potentiate the adverse impact of prenatal alcohol exposure on cardiac outflow tract maturation. Issue 3 (3rd December 2021)

• Record Type: Journal Article
• Authors: Harvey, Drayton C.; De Zoysa, Prashan; Toubat, Omar; Choi, Jongkyu; Kishore, Jahnavi; Tsukamoto, Hidekazu; Kumar, S. Ram
• Is Part Of: Birth defects research. Volume 114:Issue 3/4(2022)
• Page Start: 105
• Page End: 115
• Publication Date: 2021-12-03
• Subjects: cardiac outflow tract -- congenital heart defect -- Notch -- prenatal alcohol; Teratology -- Periodicals; Abnormalities, Human -- Periodicals; Congenital Abnormalities; Embryo, Mammalian -- abnormalities; Teratology; Abnormalities, Human; Teratology; Periodicals; Periodicals; 616.043
• DOI: 10.1002/bdr2.1968
• Languages: English
• ISSNs: 2472-1727

Abstract

Abstract: Background: Prenatal alcohol exposure (PAE) is associated with an increased incidence of congenital heart defects (CHD), in particular outflow tract (OFT) defects. However, the variability in the incidence of CHD following PAE has not been fully explored. We hypothesize that a concomitant, relevant genetic defect would potentiate the adverse effect of PAE and partially explain the variability of PAE‐induced CHD incidence. Methods: The OFT is formed by the second heart field (SHF). Our PAE model consisted of two intraperitoneal injections (3 g/kg, separated by 6 hr) of 30% ethanol on E6.5 during SHF specification. The impact of genetic defects was studied by SHF‐specific loss of Delta‐like ligand 4 ( Dll4 ), fibroblast growth factor 8 ( Fgf8 ) and Islet1 . Results: Acute PAE alone significantly increased CHD incidence (4% vs. 26%, p = .015) with a particular increase in OFT alignment defects, viz., double outlet right ventricle (0 vs. 9%, p = .02). In embryos with a SHF genetic defect, acute PAE significantly increased CHD incidence (14 vs. 63%, p < .001), including double outlet right ventricle (6 vs. 50%, p < .001) compared to controls. PAE ( p = .01) and heterozygous loss of Dll4 ( p = .04) were found to independently contribute to CHD incidence, while neither Islet1 nor Fgf8 defects were found to be significant. Conclusions: Our model recapitulates the increased incidence of OFT alignment defects seen in the clinic due to PAE. The presence of a concomitant SHF genetic mutation increases the incidence of PAE‐related OFT defects. An apparent synergistic interaction between PAE and the loss of DLL4‐mediated Notch signaling in OFT alignment requires further analysis.