The Role of Immune Markers in Predicting Infectious Complications in Children with Congenital Heart Defects.

IF 1.6 Q3 PEDIATRICS Current Pediatric Reviews Pub Date : 2025-03-26 DOI:10.2174/0115733963325523250320065040
Degtyareva Elena, Mwela Bupe Mumba, Prodeus Andrey, Ovsyannikov Dmitry, Kantemirova Marina, Alekseeva Olga, Kudlay Dmitry, Kim Alexey, Nefedova Inessa, Rogova Tatyana, Tumanyan Margarita, Korsunsky Iliya
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Abstract

The literature review presents data from a limited number of available studies conducted over the last two decades on immunological deficiency in congenital heart defects (CHDs), which is the cause of frequent infectious complications before and after cardiac surgery. Several studies based on screenings at various levels indicate the presence of primary and secondary immunodeficiency in CHDs, in particular about 13 genetic syndromes in which CHD is combined with immunodeficiency. The available data suggests a greater severity of immunological disorders in patients with critical CHDs, cyanotic CHDs, and conotruncal defects with T-cell dysfunction and deficiency of immunoglobulins (especially the IgG class, mainly IgG4) than in patients with shunts and obstructive defects. To identify defects in the T- and B-cell components of the immune system, quantification of the DNA of T-cell receptor excision circles (TRECs) and K-deleting recombination excision circles (KRECs)-by-products of the maturation of T- and B-cell receptors- has proven helpful in the world practice of neonatal screening. It allows the evaluation of a number of functionally mature T- and B-cells. In Russia, however, its widespread use started only in 2023. Data on the use of this assay in infants with CHDs are represented by isolated case reports. In Russia, a combination of CHD and primary immunodeficiency was found in 37% of cases in the Sverdlovsk Region. We conducted our own study of 200 children with CHD; 5% of cases were syndromic forms of CHD. 48.5% of children were admitted to the cardiac surgery clinic in critical condition. A decrease in the TREC level was detected in 23.5% of cases, including all children with syndromic CHD. In the group of patients with immunological disorders, there were significantly more children with cyanotic CHD, children admitted in critical condition, and children with conotruncal defects. Infectious complications in the postoperative period (sepsis, pneumonia, tracheobronchitis, postoperative wound infection) were observed significantly more often in 47 children with reduced TREC levels compared to children with normal TREC levels (P = .00000, in 36% and 3.6%, respectively). The analysis of publications confirms the prognostic value of TREC and KREC screening for targeted preoperative preparation to reduce postoperative complications and decrease the risk of mortality in CHDs.

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免疫标记物在预测先天性心脏缺陷儿童感染并发症中的作用
文献综述介绍了过去二十年来对先天性心脏缺陷(CHDs)的免疫缺陷进行的有限数量的现有研究的数据,先天性心脏缺陷(CHDs)是心脏手术前后常见感染并发症的原因。几项基于不同水平筛查的研究表明,冠心病中存在原发性和继发性免疫缺陷,特别是13种冠心病合并免疫缺陷的遗传综合征。现有数据表明,危重型冠心病、青紫型冠心病和伴有t细胞功能障碍和免疫球蛋白(特别是IgG类,主要是IgG4)缺乏的锥形锥体缺陷患者的免疫功能障碍比分流和梗阻性缺陷患者更严重。为了识别免疫系统中T细胞和b细胞成分的缺陷,T细胞受体切除环(TRECs)和k删除重组切除环(KRECs)的DNA定量- T细胞和b细胞受体成熟的副产物-已被证明在新生儿筛查的世界实践中有帮助。它允许对一些功能成熟的T细胞和b细胞进行评估。然而,在俄罗斯,它的广泛使用直到2023年才开始。在患有冠心病的婴儿中使用这种检测方法的数据是由个别病例报告代表的。在俄罗斯,斯维尔德洛夫斯克地区37%的病例中发现冠心病和原发性免疫缺陷的结合。我们对200名患有冠心病的儿童进行了研究;5%的病例为综合征型冠心病。48.5%患儿入院时病情危重。在23.5%的病例中检测到TREC水平下降,包括所有患有综合征型冠心病的儿童。在免疫功能障碍组中,青紫型冠心病患儿、危重型患儿和圆锥体缺损患儿明显较多。47例TREC水平降低的患儿术后感染性并发症(脓毒症、肺炎、气管支气管炎、术后伤口感染)发生率明显高于TREC水平正常的患儿(P = 0.00000,分别为36%和3.6%)。文献分析证实了TREC和KREC筛查对冠心病患者术前准备的预后价值,可减少术后并发症,降低死亡风险。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
66
期刊介绍: Current Pediatric Reviews publishes frontier reviews on all the latest advances in pediatric medicine. The journal’s aim is to publish the highest quality review articles dedicated to clinical research in the field. The journal is essential reading for all researchers and clinicians in pediatric medicine.
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