Suppr超能文献

39 例先天性糖基化障碍患者的肝脏表现:明确肝脏损伤的特征并提出随访建议。

Liver manifestations in a cohort of 39 patients with congenital disorders of glycosylation: pin-pointing the characteristics of liver injury and proposing recommendations for follow-up.

机构信息

Graduate Program in Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil.

Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.

出版信息

Orphanet J Rare Dis. 2021 Jan 7;16(1):20. doi: 10.1186/s13023-020-01630-2.

Abstract

BACKGROUND

The congenital disorders of glycosylation (CDG) are a heterogeneous group of rare metabolic diseases with multi-system involvement. The liver phenotype of CDG varies not only according to the specific disorder, but also from patient to patient. In this study, we sought to identify common patterns of liver injury among patients with a broad spectrum of CDG, and to provide recommendations for follow-up in clinical practice.

METHODS

Patients were enrolled in the Frontiers in Congenital Disorders of Glycosylation natural history study. We analyzed clinical history, molecular genetics, serum markers of liver injury, liver ultrasonography and transient elastography, liver histopathology (when available), and clinical scores of 39 patients with 16 different CDG types (PMM2-CDG, n = 19), with a median age of 7 years (range: 10 months to 65 years). For patients with disorders which are treatable by specific interventions, we have added a description of liver parameters on treatment.

RESULTS

Our principal findings are (1) there is a clear pattern in the evolution of the hepatocellular injury markers alanine aminotransferase and aspartate aminotransferase according to age, especially in PMM2-CDG patients but also in other CDG-I, and that the cholangiocellular injury marker gamma-glutamyltransferase is not elevated in most patients, pointing to an exclusive hepatocellular origin of injury; (2) there is a dissociation between liver ultrasound and transient elastography regarding signs of liver fibrosis; (3) histopathological findings in liver tissue of PMM2-CDG patients include cytoplasmic glycogen deposits; and (4) most CDG types show more than one type of liver injury.

CONCLUSIONS

Based on these findings, we recommend that all CDG patients have regular systematic, comprehensive screening for liver disease, including physical examination (for hepatomegaly and signs of liver failure), laboratory tests (serum alanine aminotransferase and aspartate aminotransferase), liver ultrasound (for steatosis and liver tumors), and liver elastography (for fibrosis).

摘要

背景

先天性糖基化障碍(CDG)是一组异质性罕见代谢疾病,多系统受累。CDG 的肝脏表型不仅因具体疾病而异,而且在患者之间也存在差异。在这项研究中,我们试图确定广泛谱 CDG 患者的肝脏损伤常见模式,并为临床实践中的随访提供建议。

方法

患者被纳入先天性糖基化障碍的前沿自然史研究。我们分析了 39 名患者的临床病史、分子遗传学、肝损伤血清标志物、肝脏超声和瞬时弹性成像、肝组织病理学(如有)以及 16 种不同 CDG 类型(PMM2-CDG,n=19)的临床评分,中位数年龄为 7 岁(范围:10 个月至 65 岁)。对于可通过特定干预措施治疗的疾病患者,我们增加了肝脏参数治疗的描述。

结果

我们的主要发现是:(1)根据年龄,丙氨酸氨基转移酶和天冬氨酸氨基转移酶等肝细胞损伤标志物的演变存在明确模式,尤其是在 PMM2-CDG 患者中,但在其他 CDG-I 中也是如此,而大多数患者的γ-谷氨酰转移酶等胆管细胞损伤标志物并未升高,表明损伤仅限于肝细胞;(2)肝脏超声和瞬时弹性成像在肝纤维化迹象方面存在差异;(3)PMM2-CDG 患者肝组织的组织病理学发现包括细胞质糖原沉积;(4)大多数 CDG 类型显示不止一种类型的肝损伤。

结论

基于这些发现,我们建议所有 CDG 患者定期进行系统性、全面的肝脏疾病筛查,包括体格检查(肝肿大和肝功能衰竭迹象)、实验室检查(血清丙氨酸氨基转移酶和天冬氨酸氨基转移酶)、肝脏超声(脂肪变性和肝肿瘤)和肝脏弹性成像(纤维化)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14a7/7788939/188b1c2847a0/13023_2020_1630_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验