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婴儿期醛固酮信号缺陷:单中心报告及综述。

Aldosterone signaling defect in young infants: single-center report and review.

机构信息

Department of Pediatrics, The First affiliated Hospital, Sun Yat-Sen University, No. 58, Zhongshan II Rd, Guangzhou, 510080, P. R. China.

出版信息

BMC Endocr Disord. 2021 Jul 9;21(1):149. doi: 10.1186/s12902-021-00811-9.

Abstract

BACKGROUND

Aldosterone (Ald) is a crucial factor in maintaining electrolyte and water homeostasis. Defect in either its synthesis or function causes salt wasting (SW) manifestation. This disease group is rare, while most reported cases are sporadic. This study aimed to obtain an overview of the etiology and clinical picture of patients with the above condition and report our rare cases.

METHODS

A combination of retrospective review and case studies was conducted at the Pediatric Endocrine unit of The First Affiliated Hospital Sun Yat Sen University from September 1989 to June 2020.

RESULTS

A total of 187 patients with SW were enrolled, of which 90.4% (n = 169) were diagnosed with congenital adrenal hyperplasia (CAH). SW type 21-hydroxylase deficiency accounted for 98.8% (n = 167) of CAH diagnosis, while 1.2% (n = 2) was of lipoid CAH. Non-CAH comprised 9.6% (n = 18) of the total patients whose etiologies included SF-1 gene mutation (n = 1), X-linked adrenal hypoplasia congenita (n = 9), aldosterone synthase deficiency (ASD, n = 4), and pseudo-hypoaldosteronism type 1 (PHA1, n = 1). Etiologies were not identified in three patients. All of patients with ASD and PHA1 exhibited SW syndrome in their early neonatal period. DNA sequencing showed mutations of CYP11B2 for P1-P4 and NR3C2 for P5. P1 and P2 were sibling brothers affected by compound heterozygous mutations of c.1121G > A (p.R374Q) and c.1486delC p.(L496fs); likewise, P4 was identified with compound heterozygous mutations of c.1200 + 1G > A and c.240-1 G > T; meanwhile P3 demonstrated c.1303G > A p.(G435S) homozygous mutation in CYP11B2 gene. Lastly, P5 showed c.1768 C > T p.(R590*) heterozygous mutation in the NR3C2 gene.

CONCLUSION

Etiology of infant with aldosterone defect was mostly congenital. Renal and adrenal imaging are recommended to exclude renal causes. If clinical picture is suggestive, normal plasma Ald in early infancy cannot rule out aldosterone insufficiency.

摘要

背景

醛固酮(Ald)是维持电解质和水稳态的关键因素。其合成或功能缺陷会导致盐耗竭(SW)表现。这类疾病较为罕见,而大多数报道的病例都是散发性的。本研究旨在概述具有上述情况的患者的病因和临床表现,并报告我们的罕见病例。

方法

回顾性研究和病例研究相结合,在中山大学附属第一医院儿科内分泌科进行,时间为 1989 年 9 月至 2020 年 6 月。

结果

共纳入 187 例 SW 患者,其中 90.4%(n=169)诊断为先天性肾上腺皮质增生症(CAH)。SW 型 21-羟化酶缺陷占 CAH 诊断的 98.8%(n=167),而 1.2%(n=2)为脂质 CAH。非 CAH 占总患者的 9.6%(n=18),其病因包括 SF-1 基因突变(n=1)、X 连锁肾上腺发育不全(n=9)、醛固酮合酶缺乏症(ASD,n=4)和假性低醛固酮血症 1 型(PHA1,n=1)。有 3 例患者病因不明。所有 ASD 和 PHA1 患者均在新生儿早期表现出 SW 综合征。DNA 测序显示 CYP11B2 的 P1-P4 和 NR3C2 的 P5 突变。P1 和 P2 是受复合杂合突变 c.1121G > A(p.R374Q)和 c.1486delC p.(L496fs)影响的同胞兄弟;同样,P4 被鉴定为复合杂合突变 c.1200 + 1G > A 和 c.240-1 G > T;同时,P3 在 CYP11B2 基因中表现出纯合突变 c.1303G > A p.(G435S)。最后,P5 在 NR3C2 基因中表现出 c.1768 C > T p.(R590*)杂合突变。

结论

婴儿醛固酮缺陷的病因主要为先天性。建议进行肾和肾上腺影像学检查以排除肾脏病因。如果临床表现提示,新生儿期正常血浆 Ald 不能排除醛固酮不足。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb11/8272273/ee0f93c5cbaa/12902_2021_811_Fig1_HTML.jpg

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