Department of Endocrinology and Inborn Metabolic Diseases, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
PET CT Center, Division of Nuclear Medicine, Huashan Hospital, Fudan University, 518 East Wuzhong Road, Shanghai, 200235, China.
Eur J Pediatr. 2019 Aug;178(8):1161-1169. doi: 10.1007/s00431-019-03408-6. Epub 2019 Jun 19.
Congenital hyperinsulinism (CHI) is a clinically, genetically, and morphologically heterogeneous disorder. F DOPA-PET CT scanning greatly improves its clinical outcome. Here, we presented the first Chinese F DOPA-PET CT scanning-based CHI cohort highlighting the variable ethic clinical phenotypes and genotypes. Fifty CHI patients were recruited. Median age at presentation was 2 days. Median fasting time was 2 h. Mean insulin level was 25.6 μIU/ml. Fifty-two percent of patients were diazoxide-unresponsive with significantly shorter fasting tolerance time and higher serum insulin level compared with the responsive patients. Seventy-four percent of patients experienced at least one adverse drug reaction. Tremendously increased focal lesions (32%) were detected and 75% of them were cured through surgery. Thirty-one nucleotide sequence changes were identified in 48% patients. Four novel variants (Q608X, Q1347X, Q289X, F1489S) in ABCC8 gene and 2 novel variants (G132A, V138E) in KCNJ11 gene were detected. Of the variants, 87.1% harbored in ABCC and KCNJ11 genes. T1042Qfs75 in ABCC8 gene was the most common mutation.Conclusion: Highly increased portion of focal lesion was presented in Chinese CHI patients compared with that of the previous reports. Intolerance to diazoxide was much more evident in Chinese or East Asian than other populations. Certain hotspot mutations harbored in Chinese CHI patients. What is Known: • F DOPA-PET CT scanning can provide informative guidance for surgical procedure when medical therapy is not well responded in CHI patients. What is New: • Intolerance to diazoxide is much more evident in Chinese and East Asian CHI patients compared with the other ethnic populations. • Novel mutations were detected in ABCC8 and KCNJ11 gene. Hotspot mutations such as T1042Qfs75, I1511K, E501K, G111R in ABCC8 gene, and R34H in KCNJ11 gene are predominantly responsible for Chinese CHI patients.
先天性高胰岛素血症 (CHI) 是一种临床表现、遗传和形态学均具有异质性的疾病。F DOPA-PET CT 扫描极大地改善了其临床预后。在这里,我们呈现了首个基于中国 F DOPA-PET CT 扫描的 CHI 队列,突出了不同种族的临床表型和基因型。我们招募了 50 名 CHI 患者。就诊时的中位年龄为 2 天。中位禁食时间为 2 小时。平均胰岛素水平为 25.6μIU/ml。52%的患者对二氮嗪无反应,与有反应的患者相比,他们的禁食耐量时间更短,血清胰岛素水平更高。74%的患者至少经历了一次药物不良反应。发现了明显增加的局灶性病变(32%),其中 75%通过手术治愈。在 48%的患者中发现了 31 个核苷酸序列变化。在 ABCC8 基因中发现了 4 个新的变异(Q608X、Q1347X、Q289X、F1489S),在 KCNJ11 基因中发现了 2 个新的变异(G132A、V138E)。这些变异中,87.1%存在于 ABCC 和 KCNJ11 基因中。ABCC8 基因中的 T1042Qfs75 是最常见的突变。结论:与之前的报道相比,中国 CHI 患者中局灶性病变的比例明显增加。与其他人群相比,中国或东亚的 CHI 患者对二氮嗪不耐受更为明显。中国 CHI 患者存在某些热点突变。已知:• F DOPA-PET CT 扫描可为 CHI 患者的手术提供有价值的指导,当药物治疗反应不佳时。新发现:• 与其他种族人群相比,中国和东亚的 CHI 患者对二氮嗪不耐受更为明显。• 在 ABCC8 和 KCNJ11 基因中检测到新的突变。ABCC8 基因中的热点突变,如 T1042Qfs75、I1511K、E501K、G111R,以及 KCNJ11 基因中的 R34H,主要与中国 CHI 患者有关。