Lê Bianca, Dahl Mar Janna, Albertine Kurt H, Sutherland Megan R, Black Mary Jane
Department of Anatomy and Developmental Biology and Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
CJC Open. 2020 Dec 28;3(5):574-584. doi: 10.1016/j.cjco.2020.12.017. eCollection 2021 May.
Adults born preterm (< 37 weeks' gestation) exhibit altered cardiac growth and are susceptible to cardiac dysfunction. Sheep studies have shown that moderate preterm birth results in maladaptive structural remodelling of the cardiac ventricles. The aim of this study was to examine ventricular structure in lambs born at a greater severity of preterm birth and ventilated postnatally.
Former-preterm lambs delivered at 128 days' gestation, and mechanically ventilated for a week after birth, were compared with unventilated lambs born at term (150 days' gestation), at 2 months (term: n = 10, former-preterm: n = 8), and 5 months (term: n = 9, former-preterm: n = 8) term-equivalent age. The right ventricle and left ventricle plus septum were analysed using immunohistochemistry, histology, and stereology.
Cardiomyocyte number, cross-sectional area, proliferation, and apoptosis were not affected by preterm birth or age. Left ventricle plus septum interstitial collagen levels increased with age ( = 0.0015) and were exacerbated by preterm birth ( = 0.0006; 2 months term: 0.57% ± 0.07%, former-preterm: 1.44% ± 0.18%; 5 months term: 1.37% ± 0.25%, former-preterm: 2.15% ± 0.31%). Right ventricle interstitial collagen levels increased with age ( = 0.012) but were not affected by preterm birth.
This study is the first to explore the effect of preterm birth combined with modern neonatal interventions on the ventricular myocardium in lambs. There was no adverse impact on cardiomyocyte growth in early postnatal life. Of concern, however, there was increased collagen deposition in the preterm hearts, which has the potential to induce cardiac dysfunction, especially if it becomes exaggerated with ageing.
早产(妊娠<37周)出生的成年人表现出心脏生长改变,且易患心脏功能障碍。绵羊研究表明,中度早产会导致心室结构发生适应性不良重塑。本研究的目的是检查出生时早产程度更严重且出生后接受通气的羔羊的心室结构。
将妊娠128天出生并在出生后机械通气一周的早产羔羊与足月(妊娠150天)出生、未通气的羔羊在相当于足月的2个月(足月:n = 10,早产:n = 8)和5个月(足月:n = 9,早产:n = 8)时进行比较。使用免疫组织化学、组织学和体视学方法分析右心室以及左心室加室间隔。
心肌细胞数量、横截面积、增殖和凋亡不受早产或年龄影响。左心室加室间隔的间质胶原水平随年龄增加(P = 0.0015),且早产会使其加剧(P = 0.0006;2个月时,足月:0.57%±0.07%,早产:1.44%±0.18%;5个月时,足月:1.37%±0.25%,早产:2.15%±0.31%)。右心室间质胶原水平随年龄增加(P = 0.012),但不受早产影响。
本研究首次探讨了早产结合现代新生儿干预措施对羔羊心室心肌的影响。在出生后早期对心肌细胞生长没有不利影响。然而,令人担忧的是,早产心脏中的胶原沉积增加,这有可能诱发心脏功能障碍,尤其是如果随着年龄增长这种情况加剧的话。