Gul Kiran A, Strand Janne, Pettersen Rolf D, Brun Henrik, Abrahamsen Tore G
Department of Paediatric Research, Division of Paediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.
Pediatr Cardiol. 2020 Apr;41(4):809-815. doi: 10.1007/s00246-020-02317-y. Epub 2020 Mar 13.
In the fetus, the cardiac neural crest gives rise to both the thymus and the conotruncus of the heart. In newborn screening for severe T-cell lymphopenia neonates with congenital heart defects may be detected. In this study, we investigated the occurrence of T-cell lymphopenia in neonates with or without 22q11.2 deletion syndrome (del) suffering from heart defects. This retrospective cohort study included 125 patients with heart defects. T-cell receptor excision circles (TRECs), a measure for T-cell lymphopenia, were quantified by RT-PCR using stored newborn screening blood spots. Three patient groups were compared: non-conotruncal defects (n = 57), conotruncal defects (n = 42), and 22q11.2 del with conotruncal defects (n = 26). Significantly lower TREC values were detected in patients with 22q11.2 del and conotruncal heart defects compared to those with non-syndromic conotruncal (p < 0.001) and non-conotruncal (p < 0.001) defects. In contrast, no significant difference was found between patients with non-syndromic conotruncal and non-conotruncal heart defects (p = 0.152). Low TREC levels were obtained in neonates treated with heart surgery/intervention within 2 weeks after birth and in those with a fatal outcome (p = 0.02) independent of patient group. A correlation was found between low TREC numbers and oxygen saturation, SpO below 95% (p = 0.017). The SpO was significantly lower in the non-syndromic conotruncal group compared to non-conotruncal (p < 0.001) and 22q11.2 del group (p = 0.015). No correlation was found between low neonatal TRECs and infections needing hospitalization later in life (p = 0.135). Patients with 22q11.2 del and conotruncal defects have significantly lower TREC levels compared to patients with heart defects without this syndrome.
在胎儿期,心脏神经嵴可发育为胸腺和心脏的圆锥动脉干。在新生儿重症T细胞淋巴细胞减少症的筛查中,可能会检测出患有先天性心脏病的新生儿。在本研究中,我们调查了患有或未患有22q11.2缺失综合征(del)且患有心脏缺陷的新生儿中T细胞淋巴细胞减少症的发生率。这项回顾性队列研究纳入了125例患有心脏缺陷的患者。采用逆转录聚合酶链反应(RT-PCR),通过储存的新生儿筛查血斑对T细胞受体切除环(TRECs,一种衡量T细胞淋巴细胞减少症的指标)进行定量分析。比较了三个患者组:非圆锥动脉干缺陷组(n = 57)、圆锥动脉干缺陷组(n = 42)和伴有圆锥动脉干缺陷的22q11.2 del组(n = 26)。与非综合征性圆锥动脉干缺陷患者(p < 0.001)和非圆锥动脉干缺陷患者(p < 0.001)相比,伴有22q11.2 del和圆锥动脉干心脏缺陷的患者TREC值显著降低。相比之下,非综合征性圆锥动脉干缺陷患者和非圆锥动脉干心脏缺陷患者之间未发现显著差异(p = 0.152)。出生后2周内接受心脏手术/干预的新生儿以及有致命结局的新生儿TREC水平较低(p = 0.02),且与患者组无关。TREC数量低与血氧饱和度(SpO低于95%)之间存在相关性(p = 0.017)。与非圆锥动脉干缺陷组(p < 0.001)和22q11.2 del组(p = 0.015)相比,非综合征性圆锥动脉干缺陷组的SpO显著降低。未发现新生儿TREC水平低与日后需要住院治疗的感染之间存在相关性(p = 0.135)。与无此综合征的心脏缺陷患者相比,伴有22q11.2 del和圆锥动脉干缺陷的患者TREC水平显著降低。