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囊性纤维化患儿中的假性巴特综合征:临床特征和基因发现。

Pseudo-Bartter syndrome in Chinese children with cystic fibrosis: Clinical features and genotypic findings.

机构信息

Department of Respiratory Medicine, Beijing Children's Hospital, National Center for Children's Health, Capital Medical University, Beijing, China.

出版信息

Pediatr Pulmonol. 2020 Nov;55(11):3021-3029. doi: 10.1002/ppul.25012. Epub 2020 Aug 13.

Abstract

OBJECTIVES

To characterize the clinical and genotypic features of cystic fibrosis-associated pseudo-Bartter syndrome (CF-PBS) in Chinese children.

METHODS

We recruited and characterized the clinical manifestations of 12 Chinese children with CF-PBS. Sweat test, blood and urinary analysis, sputum culture, chest and sinus computed tomography, and abdominal ultrasonography were obtained. Whole-exome sequencing, bioinformatics analysis, and Sanger sequencing validation were performed to define the genotypes.

RESULTS

CF-PBS was accompanied by recurrent and/or persistent pneumonia (91.7%), pancreatitis (83.3%), vomiting and/or diarrhea (66.7%), failure to thrive and liver disease (58.3% respectively), among our patients. The predominant organisms found in the airways were Pseudomonas aeruginosa (83.3%) and Staphylococcus aureus (75.0%). The mean concentrations of blood gas and electrolytes were pH 7.58, bicarbonate 40.8 mmol/L, sodium 125.9 mmol/L, chloride 77.5 mmol/L, and potassium 2.6 mmol/L. A high recurrence rate (50.0%) of CF-PBS was observed despite continued electrolyte supplementation during follow-up. In all, 19 different variants of CFTR gene were identified, and 10 of these were found to be novel observations (c.262_266delTTATA[p.L88FfsX21], c.579+2insACAT, c.1210-3C>G, c.1733T>C[p.L578P], c.2236_2246delGAGGCGATACTinsAAAAATC[p.E746KfsX8], c.3068T>G [p.I1023R], c.3635delT[p.V1212AfsX16], c.3859delG[p.G1287EfsX2], c.3964-7A>G and ΔE23 [c.3718-?_3873+?del]). The c.2909G>A[p.G970D] was the most common variant, with an allele frequency of 16.6%. A homozygous genotype of c.1521_1523delCTT[p.F508del] was discovered for the first time in patients of Chinese origin.

CONCLUSIONS

In China, CF-PBS usually presents early and recurs frequently in infancy, accompanied by multiple comorbidities. Recurrence of CF-PBS in school-going patients does occur but is rare. The p.G970D is the most frequent variant, with a significant ethnic tendency of Chinese origin.

摘要

目的

描述中国儿童囊性纤维化相关假性巴特综合征(CF-PBS)的临床和基因型特征。

方法

我们招募并描述了 12 名中国 CF-PBS 患儿的临床表现。进行了汗液测试、血液和尿液分析、痰培养、胸部和鼻窦计算机断层扫描以及腹部超声检查。进行了全外显子组测序、生物信息学分析和 Sanger 测序验证,以确定基因型。

结果

在我们的患者中,CF-PBS 常伴有反复和/或持续性肺炎(91.7%)、胰腺炎(83.3%)、呕吐和/或腹泻(66.7%)、生长不良和肝病(58.3%)。气道中主要发现的病原体是铜绿假单胞菌(83.3%)和金黄色葡萄球菌(75.0%)。血气和电解质的平均浓度为 pH 值 7.58、碳酸氢盐 40.8mmol/L、钠 125.9mmol/L、氯 77.5mmol/L 和钾 2.6mmol/L。尽管在随访期间继续进行电解质补充,但仍观察到 CF-PBS 的高复发率(50.0%)。共发现 19 种不同的 CFTR 基因突变,其中 10 种为新发现的突变(c.262_266delTTATA[p.L88FfsX21]、c.579+2insACAT、c.1210-3C>G、c.1733T>C[p.L578P]、c.2236_2246delGAGGCGATACTinsAAAAATC[p.E746KfsX8]、c.3068T>G[p.I1023R]、c.3635delT[p.V1212AfsX16]、c.3859delG[p.G1287EfsX2]、c.3964-7A>G 和 ΔE23[c.3718-?_3873+?del])。最常见的突变是 c.2909G>A[p.G970D],其等位基因频率为 16.6%。在中国人群中首次发现纯合子基因型 c.1521_1523delCTT[p.F508del]。

结论

在中国,CF-PBS 通常在婴儿期早期出现,且常反复发作,伴有多种合并症。在校患儿确实会出现 CF-PBS 复发,但很少见。p.G970D 是最常见的突变,具有明显的中国人群遗传倾向。

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