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鞘氨醇-1-磷酸裂解酶缺乏症内分泌疾病的回顾性分析:病例系列及文献综述

A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review.

作者信息

Maharaj Avinaash, Kwong Ruth, Williams Jack, Smith Christopher, Storr Helen, Krone Ruth, Braslavsky Debora, Clemente Maria, Ram Nanik, Banerjee Indraneel, Çetinkaya Semra, Buonocore Federica, Güran Tülay, Achermann John C, Metherell Louise, Prasad Rathi

机构信息

Centre for Endocrinology, John Vane Science Centre, Queen Mary University of London, London, UK.

Birmingham Children's Hospital, Birmingham, UK.

出版信息

Endocr Connect. 2022 Jul 25;11(8). doi: 10.1530/EC-22-0250. Print 2022 Aug 1.

Abstract

Sphingosine-1-phosphate lyase (SGPL1) insufficiency syndrome (SPLIS) is an autosomal recessive multi-system disorder, which mainly incorporates steroid-resistant nephrotic syndrome and primary adrenal insufficiency. Other variable endocrine manifestations are described. In this study, we aimed to comprehensively annotate the endocrinopathies associated with pathogenic SGPL1 variants and assess for genotype-phenotype correlations by retrospectively reviewing the reports of endocrine disease within our patient cohort and all published cases in the wider literature up to February 2022. Glucocorticoid insufficiency in early childhood is the most common endocrine manifestation affecting 64% of the 50 patients reported with SPLIS, and a third of these individuals have additional mineralocorticoid deficiency. While most individuals also have nephrotic syndrome, SGPL1 variants also account for isolated adrenal insufficiency at presentation. Primary gonadal insufficiency, manifesting with microphallus and cryptorchidism, is reported in less than one-third of affected boys, all with concomitant adrenal disease. Mild primary hypothyroidism affects approximately a third of patients. There is paucity of data on the impact of SGPL1 deficiency on growth, and pubertal development, limited by the early and high mortality rate (approximately 50%). There is no clear genotype-phenotype correlation overall in the syndrome, with variable disease penetrance within individual kindreds. However, with regards to endocrine phenotype, the most prevalent disease variant p.R222Q (affecting 22%) is most consistently associated with isolated glucocorticoid deficiency. To conclude, SPLIS is associated with significant multiple endocrine disorders. While endocrinopathy in the syndrome generally presents in infancy, late-onset disease also occurs. Screening for these is therefore warranted both at diagnosis and through follow-up.

摘要

鞘氨醇-1-磷酸裂解酶(SGPL1)功能不全综合征(SPLIS)是一种常染色体隐性多系统疾病,主要包括类固醇抵抗性肾病综合征和原发性肾上腺功能不全。还描述了其他可变的内分泌表现。在本研究中,我们旨在通过回顾性分析我们患者队列中的内分泌疾病报告以及截至2022年2月更广泛文献中所有已发表病例,全面注释与致病性SGPL1变异相关的内分泌疾病,并评估基因型与表型的相关性。儿童早期的糖皮质激素功能不全是最常见的内分泌表现,影响了报告的50例SPLIS患者中的64%,其中三分之一的个体还存在盐皮质激素缺乏。虽然大多数个体也患有肾病综合征,但SGPL1变异也可导致孤立性肾上腺功能不全。不到三分之一的患病男孩报告有原发性性腺功能不全,表现为小阴茎和隐睾症,所有这些男孩都伴有肾上腺疾病。轻度原发性甲状腺功能减退影响约三分之一的患者。由于早期和高死亡率(约50%),关于SGPL1缺乏对生长和青春期发育影响的数据很少。该综合征总体上没有明确的基因型与表型相关性,在个体家族中疾病外显率各不相同。然而,就内分泌表型而言,最常见的疾病变异p.R222Q(占22%)最一致地与孤立性糖皮质激素缺乏相关。总之,SPLIS与多种严重内分泌疾病相关。虽然该综合征的内分泌病通常在婴儿期出现,但也会发生迟发性疾病。因此,在诊断时和随访过程中都有必要进行筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf2c/9346324/6d12e2c060d3/EC-22-0250fig1.jpg

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